<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJGas</journal-id><journal-title-group><journal-title>Open Journal of Gastroenterology</journal-title></journal-title-group><issn pub-type="epub">2163-9450</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojgas.2017.71003</article-id><article-id pub-id-type="publisher-id">OJGas-73696</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Role of Ultrasonically Guided Fine Needle Cytology in the Diagnosis of Focal Liver Lesions in Sulaimani-Kurdistan Region, Iraq
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Taha</surname><given-names>A. Alkarboly</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohammed</surname><given-names>Omer Mohammed</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kawa</surname><given-names>Abdullah Mahmood</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Muhsin</surname><given-names>Abubakir</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Kurdistan Center for Gastroenterology and Hepatology (KCGH), Asulaimaneyah, Iraq</addr-line></aff><aff id="aff1"><addr-line>School of Medicine, Faculty of Medical Sciences, University of Sulaimani, Sulaymaniyah, Iraq</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>alkarbolytaha@gmail.com(TAA)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>06</day><month>01</month><year>2017</year></pub-date><volume>07</volume><issue>01</issue><fpage>18</fpage><lpage>27</lpage><history><date date-type="received"><day>April</day>	<month>9,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>January</month>	<year>19,</year>	</date><date date-type="accepted"><day>January</day>	<month>22,</month>	<year>2017</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Fine Needle Aspiration Cytology (FNAC) under image guidance has gained increasing acceptance as the diagnostic procedure of choice for patients with focal hepatic lesions. It can be performed percutaneously or endoscopically. FNA may also be performed at laparoscopy or laparotomy under direct vision when image guided FNA fails to provide diagnostic tissue. In experienced hands, FNA is safe, minimally invasive, accurate, and cost
  -
  effective. However, the main aim of this study is to assess the role of FNAC in the evaluation of focal liver lesions. Patients and method: This prospective study was conducted over one year,
   
  on 100 patients in Kurdistan Center for Gastroenterology and Hepatology (KCGH) and in Sulaimani General Teaching Hospital. All patients were properly assessed by history analyses and thorough clinical examination. Laboratory investigations including hematological, biochemical, viral markers, and tumor markers were requested. Thus, ultrasonically guided FNA was performed after obtaining a written informed consent from the patients. Results
  :
   FNAC showed that eighty patients (80%) had secondary liver metastasis. Ten patients (10%) had HCC
  ; 
  three patients had 
  h
  emangioma
  ; 
  one patient had abscess
  ; 
  and 6 patients had inconclusive result
  ; 
  two patients had simple cyst. Apart from mild post procedure pain, no complication or mortality had been recorded. Conclusion: FNAC is simple, easy, rapid and a minimally invasive procedure that has an acceptable diagnostic yield for focal liver lesions.
 
</p></abstract><kwd-group><kwd>FNAC</kwd><kwd> Ultrasound</kwd><kwd> Focal Liver Lesion</kwd><kwd> KCGH</kwd><kwd> Sulaimani</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Fine Needle Aspiration (FNA) under image guidance has gained increasing acceptance as the diagnostic procedure of choice for patients with focal hepatic lesions. It can be performed percutaneously or endoscopically. However, the latter approach is technically difficult for lesions located far away from the tip of the echoendoscope and lesion near the 2nd or 3rd portion of the duodenum due to poor visualization [<xref ref-type="bibr" rid="scirp.73696-ref1">1</xref>] .</p><p>FNA may also be performed at laparoscopy or laparotomy under direct vision when imaged guided FNA fails to provide diagnostic tissue [<xref ref-type="bibr" rid="scirp.73696-ref2">2</xref>] .</p><p>The specificity of FNA cytology of the liver approaches 100% and the sensitivity ranges from 67% - 100%, averaging about 85% [<xref ref-type="bibr" rid="scirp.73696-ref3">3</xref>] - [<xref ref-type="bibr" rid="scirp.73696-ref9">9</xref>] .</p><p>FNA alone is superior to core biopsy alone because the needle is longer and can be guided, and the procedure can be easily repeated. FNA is often preferred in sampling deeply placed lesions, sites adjacent to major vessels, or in situations in which needles are to be passed through the bowel wall. However, both methods are complimentary to each other [<xref ref-type="bibr" rid="scirp.73696-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref13">13</xref>] .</p><p>The occurrence of complications after hepatic FNA is rare with about 0.5% minor complications, 0.05% major complications requiring surgery, and less than 0.01% mortality [<xref ref-type="bibr" rid="scirp.73696-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref17">17</xref>] . They are limited largely to hemorrhage. The frequency of complications is often related to the vascularity and the location of the lesions as well as the needle size [<xref ref-type="bibr" rid="scirp.73696-ref18">18</xref>] . Another concern is the subcutaneous seeding of tumor along the needle tract during percutaneous liver FNA. It is still an extremely rare complication when using a needle of 23 gauges or less [<xref ref-type="bibr" rid="scirp.73696-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref20">20</xref>] .</p><p>Absolute contraindications for FNA of liver include uncorrectable bleeding diathesis, lack of a safe access route, e.g. vascular structure in the biopsy path, hydatid cyst and uncooperative patients.</p><p>Several studies have shown that the assistance of cytopathologists during the procedure increases overall accuracy [<xref ref-type="bibr" rid="scirp.73696-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref23">23</xref>] . The latter is attributed to the ability to assess specimen adequacy at the time of procedure and to determine if additional tissue is required for diagnosis and/or ancillary studies such as flow cytometry [<xref ref-type="bibr" rid="scirp.73696-ref24">24</xref>] .</p><p>A markedly elevated serum AFP level, &gt;1000 ng/ml, is highly suggestive of HCC or in children, hepatoblastoma. A moderate increase in serum AFP, however, is non-specific and can be seen in a wide variety of benign and malignant conditions [<xref ref-type="bibr" rid="scirp.73696-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref25">25</xref>] .</p><p>Aspirates of normal liver consist predominantly of hepatocytes and scattered bile duct epithelial cells. Other cell types such as endothelial cells and Kupffer’s cells are infrequently noted [<xref ref-type="bibr" rid="scirp.73696-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref26">26</xref>] .</p><p>Hepatocellular carcinoma (HCC) is the most common primary hepatic malignancy [<xref ref-type="bibr" rid="scirp.73696-ref26">26</xref>] . Cirrhosis may be sampled by FNA when a dominant nodule mimics a HCC radiologically. The cytology of cirrhotic liver is similar to that of normal liver [<xref ref-type="bibr" rid="scirp.73696-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref28">28</xref>] . AFP level and the finding of a single lesion with or without satellite lesions on imaging, favor a primary tumor over metastatic disease [<xref ref-type="bibr" rid="scirp.73696-ref27">27</xref>] .</p><p>Up to the knowledge of the researcher, no previous scientific study has been conducted about ultrasonically guided FNA in Sulaimani city or Kurdistan region. Therefore, the purpose of this study is to examine the diagnostic value of ultrasonically guided percutaneous FNA cytology in the diagnosis of focal liver lesions.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This is a prospective study conducted in Kurdistan center for Gastroenterology and Hepatology and the Sulaimani General Teaching Hospital over one year. After the agreement by the ethical committee of the School of Medicine, University of Sulaimani, one hundred patients with Focal liver lesions were studied.</p><p>Inclusion Criteria</p><p>Adult patients with Focal liver lesion(s) that were identified by imaging studies (ultrasound, Computerized Tomography, Magnetic Resonant Imaging) were included.</p><p>Exclusion Criteria</p><p>1. All cystic lesions proved by imaging studies.</p><p>2. Any lesion less than 1 cm in diameter (difficult to target).</p><p>3. Any inaccessible lesion deeper than the length of 22 G &#215; 3<sub>1/2</sub> spinal needle</p><p>4. Gross Ascites.</p><p>5. Un-cooperative patients.</p><p>6. Uncorrectable coagulopathy (INR &gt; 2.5), by fresh frozen plasma and/or Vitamin K</p><p>7. Patient’s refusal.</p><p>We obtained informed consent from the patients, and after taking proper history and performing a thorough examination, ten ml venous blood were aspirated for the following laboratory tests; (complete blood Count, ESR, TSB, AST, ALT, PT, INR, Serum Albumin, Blood Urea, Blood glucose, Serum Alkaline Phosphatase, Alfa feto protein, Carcinoembryonic Antigen, CA<sub>19-9</sub>, CA 125, HBs Ag, HCV Ab).</p><p>Using sterile technique, the skin was cleansed with povidone Iodine USP 10% (1% available Iodine). The ultrasound guidance was done by an experienced ultrasonographer using SONAC 8000 Live (prime) MEDISON device with a probe of 3.5 MHz, convex free hand technique. After the localization of the lesion (s), the needle (spinal needle 22 G &#215; 3<sub>1/2</sub>) was advanced under continuous ultrasound guide through the skin and soft tissue and into the target mass. After ensuring the correct position of the needle tip, the trocar was removed and a 10 ml syringe was attached; then a 2 - 3 ml negative pressure was applied while performing 2 - 4 punctures of the wall and central part of the lesion, then the needle was withdrawn and the specimen was distributed over slides which were immediately placed into a 95% alcohol solution for 20 minutes, and then, it was left to dry and later sent for cytological examination.</p><p>All slides were studied by two expert pathologists. Follow up was done for all patients after the procedure for 6 hours to observe any complications. Statistical analysis was done using SPSS Software version 17.</p></sec><sec id="s3"><title>3. Results</title><p>One hundred patients with focal liver lesion (s) were enrolled in this study, 54 patients were male (54%), and 46 were female (46%). Age of the patients ranged between 23 to 88 years with (a mean age + SD) of 55 &#177; 5.36 year. The majority (64%) of patients were above 60 years (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The most common presenting symptoms among the patients were fatigue and weight loss (90% and 78% respectively), while the most common sign was hepatomegaly (38%). Therefore, the rest of the symptoms and signs are illustrated in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Anemia and high ESR was found in (54% and 90% respectively) and low serum albumin in (64%), <xref ref-type="table" rid="table2">Table 2</xref>.</p><p>Viral markers had been performed for all the patients, and only 8 patients (8%) had positive results of HBs Ag. Four HBs Ag positive cases had secondaries and four cases had hepatocellular carcinoma by FNAC. None were positive for HCV.</p><p><xref ref-type="table" rid="table3">Table 3</xref> revealed levels of tumor markers. Ultrasonic findings and distribution of liver masses are shown in <xref ref-type="table" rid="table4">Table 4</xref>.</p><p><xref ref-type="table" rid="table5">Table 5</xref> demonstrates the sites of primary tumors.</p><p><xref ref-type="table" rid="table6">Table 6</xref> compares the trans-abdominal ultrasound of the studied patients with the results of ultrasonic guided FNAC.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Clinical characteristics of the studied patients (N = 100)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Clinical features</th><th align="center" valign="middle" >Patients No.</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle"  colspan="3"  >HISTORY</td></tr><tr><td align="center" valign="middle" >Fatigue</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >90</td></tr><tr><td align="center" valign="middle" >Weight loss</td><td align="center" valign="middle" >78</td><td align="center" valign="middle" >78</td></tr><tr><td align="center" valign="middle" >Anorexia</td><td align="center" valign="middle" >76</td><td align="center" valign="middle" >76</td></tr><tr><td align="center" valign="middle" >Rt. Hypochondrial and epigastric Pain</td><td align="center" valign="middle" >60</td><td align="center" valign="middle" >60</td></tr><tr><td align="center" valign="middle" >Constipation</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >40</td></tr><tr><td align="center" valign="middle" >Pallor</td><td align="center" valign="middle" >31</td><td align="center" valign="middle" >31</td></tr><tr><td align="center" valign="middle" >Jaundice</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >28</td></tr><tr><td align="center" valign="middle" >Itching</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >12</td></tr><tr><td align="center" valign="middle"  colspan="3"  >EXAMINATION</td></tr><tr><td align="center" valign="middle" >Hepatomegaly</td><td align="center" valign="middle" >38</td><td align="center" valign="middle" >38</td></tr><tr><td align="center" valign="middle" >Leg edema</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >15</td></tr><tr><td align="center" valign="middle" >Palmer erythema</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >14</td></tr><tr><td align="center" valign="middle" >Ascites</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10</td></tr><tr><td align="center" valign="middle" >Clubbing</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >8</td></tr><tr><td align="center" valign="middle" >Duputyrens’ contracture</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Flapping tremor</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Gynaecomastia</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Splenomegaly</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Hematological, biochemical investigations of the study population (N = 100)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Hematologic Parameters</th><th align="center" valign="middle" >Low No. (%)</th><th align="center" valign="middle" >Normal No. (%)</th><th align="center" valign="middle" >High No. (%)</th></tr></thead><tr><td align="center" valign="middle" >PCV%</td><td align="center" valign="middle" >54 (54)</td><td align="center" valign="middle" >46 (46)</td><td align="center" valign="middle" >0 (0)</td></tr><tr><td align="center" valign="middle" >WBC</td><td align="center" valign="middle" >14 (14)</td><td align="center" valign="middle" >74 (74)</td><td align="center" valign="middle" >12 (12)</td></tr><tr><td align="center" valign="middle" >ESR</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >10 (10)</td><td align="center" valign="middle" >90 (90)</td></tr><tr><td align="center" valign="middle" >Platelet</td><td align="center" valign="middle" >4 (4)</td><td align="center" valign="middle" >93 (93)</td><td align="center" valign="middle" >2 (2)</td></tr><tr><td align="center" valign="middle" >TSB</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >78 (78)</td><td align="center" valign="middle" >22 (22)</td></tr><tr><td align="center" valign="middle" >AST</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >74 (74)</td><td align="center" valign="middle" >26 (26)</td></tr><tr><td align="center" valign="middle" >ALT</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >86 (86)</td><td align="center" valign="middle" >14 (14)</td></tr><tr><td align="center" valign="middle" >S. Albumin</td><td align="center" valign="middle" >64 (64)</td><td align="center" valign="middle" >36 (36)</td><td align="center" valign="middle" >0 (0)</td></tr><tr><td align="center" valign="middle" >Bl. Urea</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >75 (74)</td><td align="center" valign="middle" >25 (25)</td></tr><tr><td align="center" valign="middle" >PT/INR</td><td align="center" valign="middle" >0 (0)</td><td align="center" valign="middle" >58 (58)</td><td align="center" valign="middle" >42 (42)</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Tumor markers of the studied patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >High level Tumor markers</th><th align="center" valign="middle" >HCC</th><th align="center" valign="middle" >Secondary</th><th align="center" valign="middle" >Abscess</th><th align="center" valign="middle" >Hemangioma</th><th align="center" valign="middle" >Inconclusive</th><th align="center" valign="middle" >Total</th></tr></thead><tr><td align="center" valign="middle" >AFP</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >20</td></tr><tr><td align="center" valign="middle" >CEA</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >32</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >34</td></tr><tr><td align="center" valign="middle" >CA 19-9</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >38</td></tr><tr><td align="center" valign="middle" >CA 125</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >46</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >80</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> U/S distribution of liver lesions (N = 100)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Ultrasonic findings</th><th align="center" valign="middle" >No.</th><th align="center" valign="middle" >Percent</th></tr></thead><tr><td align="center" valign="middle" >Multiple</td><td align="center" valign="middle" >80</td><td align="center" valign="middle" >80</td></tr><tr><td align="center" valign="middle" >Single</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >20</td></tr><tr><td align="center" valign="middle" >Rt. Lobe</td><td align="center" valign="middle" >38</td><td align="center" valign="middle" >39</td></tr><tr><td align="center" valign="middle" >Rt. and Left</td><td align="center" valign="middle" >58</td><td align="center" valign="middle" >57</td></tr><tr><td align="center" valign="middle" >Lt lobe</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4</td></tr></tbody></table></table-wrap><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> The primary sites of liver secondaries</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Primary sites</th><th align="center" valign="middle" >No (%)</th><th align="center" valign="middle" >Histology</th><th align="center" valign="middle" >Diagnostic techniques</th></tr></thead><tr><td align="center" valign="middle" >Breast</td><td align="center" valign="middle" >13 (13)</td><td align="center" valign="middle" >Invasive ductal carcinoma</td><td align="center" valign="middle" >Previous Mastectomy</td></tr><tr><td align="center" valign="middle" >Stomach</td><td align="center" valign="middle" >12 (12)</td><td align="center" valign="middle" >Adenocarcinoma</td><td align="center" valign="middle" >OGD-Histopathology</td></tr><tr><td align="center" valign="middle" >Pancreas</td><td align="center" valign="middle" >8 (8)</td><td align="center" valign="middle" >Adenocarcinoma</td><td align="center" valign="middle" >Ultrasonography-FNAC</td></tr><tr><td align="center" valign="middle" >Colon</td><td align="center" valign="middle" >7 (7)</td><td align="center" valign="middle" >Adenocarcinoma</td><td align="center" valign="middle" >OGD- Histopathology</td></tr><tr><td align="center" valign="middle" >Esophagus</td><td align="center" valign="middle" >4 (4)</td><td align="center" valign="middle" >Adenocarcinoma</td><td align="center" valign="middle" >OGD- Histopathology</td></tr><tr><td align="center" valign="middle" >Bronchus</td><td align="center" valign="middle" >2 (2)</td><td align="center" valign="middle" >Squamous cell carcinoma</td><td align="center" valign="middle" >Bronchoscopy-Histopathology</td></tr><tr><td align="center" valign="middle" >Prostate</td><td align="center" valign="middle" >2 (2)</td><td align="center" valign="middle" >Adenocarcinoma</td><td align="center" valign="middle" >Previous prostatectomy</td></tr><tr><td align="center" valign="middle" >Retro peritoneal</td><td align="center" valign="middle" >2 (2)</td><td align="center" valign="middle" >Sarcoma</td><td align="center" valign="middle" >Ultrasonography-FNA</td></tr><tr><td align="center" valign="middle" >Unidentified</td><td align="center" valign="middle" >30 (30)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >80 (80)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Age and gender distribution of cases (N = 100), P-value = 0.64 (there is no significant difference between age groups and no significant difference between ≥ 60 years and &lt;60 years; P = 0.89)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-1900333x2.png"/></fig><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Ultrasonography findings vs. FNAC results</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Age group (year)</th><th align="center" valign="middle"  colspan="5"  >Ultrasound Finding</th><th align="center" valign="middle"  colspan="5"  >FNAC</th><th align="center" valign="middle" >Total</th></tr></thead><tr><td align="center" valign="middle" >Abscess</td><td align="center" valign="middle" >Heman</td><td align="center" valign="middle" >HCC</td><td align="center" valign="middle" >2nd</td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >Abscess</td><td align="center" valign="middle" >Heman</td><td align="center" valign="middle" >HCC</td><td align="center" valign="middle" >2nd</td><td align="center" valign="middle" >Inco</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >20 - 29</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >30 - 39</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >40 - 49</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >8</td></tr><tr><td align="center" valign="middle" >50 - 59</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >22</td></tr><tr><td align="center" valign="middle" >60 and More</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >58</td><td align="center" valign="middle" >64</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >53</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >62</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >80</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>Sixty two (62%) patients (38% males and 24% females) were found to be free from pain during and after the procedure, while 38 (38%) patients (16% males and 22% females) had developed mild and transient right hypochondrial pain.</p></sec><sec id="s4"><title>4. Discussion</title><p>Focal liver lesions (FLL) have been a common reason for the consultation faced by gastroenterologists and hepatologists. It is important to consider not only malignant liver lesions, but also benign solid and cystic liver lesions such as hemangioma, focal nodular hyperplasia, hepatocellular adenoma, and hepatic cysts in the differential diagnosis [<xref ref-type="bibr" rid="scirp.73696-ref28">28</xref>] . Fine Needle Aspiration cytology is a safe and effective method of establishing a definitive diagnosis of either metastatic or primary malignancy [<xref ref-type="bibr" rid="scirp.73696-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref30">30</xref>] . FNA cytology is usually guided by ultrasound or CT [<xref ref-type="bibr" rid="scirp.73696-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref32">32</xref>] .</p><p>The use of Fine Needle technique has been shown to shorten the length of hospitalization, obviate the need for more invasive procedures including laparoscopy and considerably lower the cost of hospitalization in many situations [<xref ref-type="bibr" rid="scirp.73696-ref33">33</xref>] .</p><p>The Sonographic FNA technique requires no more time than a routine abdominal scan which is usually less considerable. This technique also may be performed portably or outside the ultrasound laboratory when necessary [<xref ref-type="bibr" rid="scirp.73696-ref30">30</xref>] .</p><p>This study was performed on 100 patients. However, most of them were adult and elderly age groups, 18 patients (18%) between 50 to 59 years and 64 patients (64%) were beyond 60 years of age, which indicates that the liver masses are most common in the elderly age group as it is a usual age for malignancy.</p><p>The most common presenting symptoms among the patients were fatigue and weight loss (90% and 78% respectively), while the most common signs were hepatomegaly, which is comparable to other study [<xref ref-type="bibr" rid="scirp.73696-ref34">34</xref>] .</p><p>Anemia and high ESR found in (54% and 90% respectively) and low serum albumin in 64% is expected in people with malignancy [<xref ref-type="bibr" rid="scirp.73696-ref35">35</xref>] .</p><p>Most of the patients in our study proved by FNAC as cases of secondaries (80%) were close to that found by ultrasound (90%) which means that the (p) value of FNAC is (0.001), which indicated the significance of FNA in comparison to radiological findings. Furthermore, we did not compare our procedure to histopathological examination which is definitive diagnosis of benign or malignant lesions, because it is unwise to do laparotomy for suspicion of multiple secondaries in elderly and end stage patients.</p><p>The finding of high percent (80%) of secondary lesions in the liver in our study was similar to another study which found the overall accuracy to be 92% and 94% respectively. The specificity of the procedure was 100%. Ultrasonically guided fine-needle aspiration cytology followed by cytological examination appears indispensable in the diagnosis and differentiation between benign and malignant hepatic and pancreatic focal lesions [<xref ref-type="bibr" rid="scirp.73696-ref36">36</xref>] .</p><p>FNA is superior in the diagnosis of HCC because 6 cases of HCC were diagnosed by Ultrasound. Therefore, 10 cases proved HCC by FNA, accompanied by high tumor markers (AFP) which is more supportive for HCC.</p><p>In this study, the FNA results of 7 patients (7%) were inconclusive or contained blood elements. In two of them, ultrasound had suggested secondary lesion, but CT scan showed simple cyst. Later on, FNA was done and the result was just blood. Thus, the clinical course of the patient and the tumor marker were in favor of non malignant lesion.</p><p>This was comparable to the study done by Wei Ding et al in Hangzhou, China which was performed on 46 patients. Thus, 6 patients had Red Blood Cells on aspirations which are in agreement with other study [<xref ref-type="bibr" rid="scirp.73696-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.73696-ref38">38</xref>] .</p><p>One patient had history of breast carcinoma with mastectomy, but on follow up, focal liver lesion found. The Radiologist and Oncologist suspected secondary for which FNA was done, and fortunately, the results was sheets of pus cells. The sample sent for culture and it revealed the growth of Staphylococcus aureus; and also, tumor markers and clinical course of the disease suggest non malignant lesions i.e. ultrasonic examination alone cannot differentiate benign from malignant lesion definitely and thus, it is better to decide on radiological examination, FNAC and tumor markers.</p><p>The outcome of the procedure in our study was very favorable. Therefore, only mild non persistent right hypochondrial pain was seen in 38% of the patients. Our outcome has been comparable to that reported in other studies [<xref ref-type="bibr" rid="scirp.73696-ref39">39</xref>] . At the same time, this very accepted outcome indicates that post procedure ultrasonography is unnecessary and should only be reserved when a major complication is suspected [<xref ref-type="bibr" rid="scirp.73696-ref39">39</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>Fine Needle Aspiration Cytology is minimally invasive and a rapid method for pathologic evaluation of focal hepatic masses. Early evaluation and workup is important for early management. Thus, the most common focal liver lesions are hepatic secondaries which are more common in elderly patients. Radiological examination, whether by ultrasound or CT scan alone cannot differentiate between benign or malignant lesions definitely and should be followed and confirmed by FNA under imaging scan.</p></sec><sec id="s6"><title>Cite this paper</title><p>Alkarboly, T.A., Mohammed, M.O., Mahmood, K.A. and Abubakir, M. (2017) The Role of Ultrasonically Guided Fine Needle Cytology in the Diagnosis of Focal Liver Lesions in Sulaimani-Kurdistan Region, Iraq. Open Journal of Gastroenterology, 7, 18-27. http://dx.doi.org/10.4236/ojgas.2017.71003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.73696-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Carrera Alonso, E., Garcia Gonzalez, M., Valer lopez-Fando, P., et al. (2007) Department of Gastroenterolgy. Ramon y Cajal Hospital, Madrid.</mixed-citation></ref><ref id="scirp.73696-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Hall-Craggs, M.A. and Lees, W.R. (1987) Fine Needle Biopsy: Cytology, Histology or Both. Gut, 28, 233-236. https://doi.org/10.1136/gut.28.3.233</mixed-citation></ref><ref id="scirp.73696-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Ding, W. and He, X.J. (2004) Fine Needle Aspiration Cytology in the Diagnosis of Liver Lesions. Hepatobiliary &amp; Pancreatic Diseases International, 3, 90-92.</mixed-citation></ref><ref id="scirp.73696-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Ljubicic, N., Bilic, A., Lang, N. and Bakula, B. (1992) Ultrasonically Guided Percutaneous Fine Needle Aspiration Biopsy of the Hepatic and Pancreatic Focal Lesions: Accuracy of Cytology in the Diagnosis of Malignancy. Journal of the Royal Society of Medicine, 85, 139-141.</mixed-citation></ref><ref id="scirp.73696-ref5"><label>5</label><mixed-citation publication-type="book" xlink:type="simple">Collier, J.D. and Webster, G. (2010) Liver and Biliary Tract Disease. In: Nicki, R., Brian, R., Stuart, H., et al., Eds., Davidson’s Textbook of Medicine, 18th Edition, Churchill Livingstone, New York, 927-929.</mixed-citation></ref><ref id="scirp.73696-ref6"><label>6</label><mixed-citation publication-type="book" xlink:type="simple">Carr, B.I. (2012) Tumors of the Liver and Biliary Tree. In: Longo, D.L., Fauci, A.S., Kasper, D.L., et al., Eds., Harrison’s Principles of Internal Medicine, 18th Edition, McGraw Hill, New York, 777-785.</mixed-citation></ref><ref id="scirp.73696-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Mitty, H.A., Efremides, S.C. and Yeh, H. (1981) Impact of Fine Needle Biopsy on the Management of Patients with Carcinoma of the Pancreas. American Journal of Roentgenology, 137, 1119-1121. https://doi.org/10.2214/ajr.137.6.1119</mixed-citation></ref><ref id="scirp.73696-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Torzilli, G., Minagawa, M., Takayama, T., et al. (1999) Accurate Preoperative Evaluation of Liver Mass Lesions without Fine Needle Biopsy. Hepathology, 30, 889-893. https://doi.org/10.1002/hep.510300411</mixed-citation></ref><ref id="scirp.73696-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Jegou, J., Peruzzi, P., Arav, E., et al. (2004) Métastases mixtes cutanéo-osseuses révélatrices d’un carcinome hépatocellulaire. Gastroentérologie Clinique et Biologique, 28, 804-806. https://doi.org/10.1016/S0399-8320(04)95132-9</mixed-citation></ref><ref id="scirp.73696-ref10"><label>10</label><mixed-citation publication-type="book" xlink:type="simple">Holm, H.H., Als, O. and Gammelgaard, J. (1979) Percutaneous Aspiration and Biopsy Procedure Under Ultrasound Visualization. In: Taylor, K.J.W., Ed., Diagnostic Ultrasound in Gastrointestinal Disease, Churchill Livingstone, New York, 137-149.</mixed-citation></ref><ref id="scirp.73696-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Ferrucci, J.T., Wittenberg, J. and Mueller, P.R. (1980) Diagnosis of Abdominal Malignancy by Radiologic Fine Needle Aspiration Biopsy. American Journal of Roentgenology, 134, 323-330. https://doi.org/10.2214/ajr.134.2.323</mixed-citation></ref><ref id="scirp.73696-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Marrero, J.A., Ahn, J. and Rajender Reddy, K. (2014) ACG Clinical Guideline: The Diagnosis and Management of Focal Liver Lesions. The American Journal of Gastroenterology, 109, 1328-1347. https://doi.org/10.1038/ajg.2014.213</mixed-citation></ref><ref id="scirp.73696-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Imoto, M., Nishimura, D., Fukuda, Y., et al. (1985) Immunohistochemical Detection of Alpha-Fetoprotein, Carcinoembryonic Antigen, and Ferritin in Formalin-Paraffin Sections from Hepatocellular Carcinoma. American Journal of Gastroenterology, 80, 902-906.</mixed-citation></ref><ref id="scirp.73696-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Craig, J.R., Peters, R.L. and Edmonson, H.A. (1989) Tumors of the Liver and Intrahepatic Bile Ducts. 2nd Edition, AFIP, Washington DC.</mixed-citation></ref><ref id="scirp.73696-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Weinberg, A.G. and Finegold, M.J. (1983) Primary Hepatic Tumors of Childhood. Human Pathology, 14, 512-537. https://doi.org/10.1016/S0046-8177(83)80005-7</mixed-citation></ref><ref id="scirp.73696-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Pak, H.Y., Yokota, S., Teplitz, R.L., et al. (1981) Rapid Staining Techniques Employed in Fine Needle Aspirations of the Lung. Acta Cytologica, 25, 178-184.</mixed-citation></ref><ref id="scirp.73696-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Miller, D.A., Carrasco, C.H., Katz, R.L., et al. (1986) Fine Needle Aspiration Biopsy: The Role of Immediate Cytologic Assessment. American Journal of Roentgenology, 147, 155-158. https://doi.org/10.2214/ajr.147.1.155</mixed-citation></ref><ref id="scirp.73696-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Austin, J.H. and Cohen, M.B. (1993) Value of Having a Cytopathologist Present during Percutaneous Fine-Needle Aspiration Biopsy of Liver: Report of 55 Cancer Patients and Metaanalysis of the Literature. American Journal of Roentgenology, 160, 175-177. https://doi.org/10.2214/ajr.160.1.8416620</mixed-citation></ref><ref id="scirp.73696-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Hamazaki, K., Matsubara, N., Mori, M., et al. (1995) Needle Tract Implantation of Hepatocellular Carcinoma after Ultrasonically Guided Needle Liver Biopsy: A Case Report. Hepato-Gastroenterology, 42, 601-606.</mixed-citation></ref><ref id="scirp.73696-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Yamada, N., Shinzawa, H., Ukai, K., et al. (1993) Subcutaneous Seeding of Small Hepatocellular Carcinoma after Fine Needle Aspiration Biopsy. Journal of Gastroenterology and Hepatology, 8, 195-198. https://doi.org/10.1111/j.1440-1746.1993.tb01513.x</mixed-citation></ref><ref id="scirp.73696-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Vergara, V., Garripoli, A., Marucci, M.M., Bonino, F. and Capussotti, L. (1993) Colon Cancer Seeding after Percutaneous Fine Needle Aspiration of Liver Metastasis. Journal of Hepatology, 18, 276-278. https://doi.org/10.1016/S0168-8278(05)80269-7</mixed-citation></ref><ref id="scirp.73696-ref22"><label>22</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Pitman</surname><given-names> M.B. </given-names></name>,<etal>et al</etal>. (<year>1998</year>)<article-title>Fine Needle Aspiration Biopsy of the Liver. Principal Diagnostic Challenges</article-title><source> Clinics in Laboratory Medicine</source><volume> 18</volume>,<fpage> 483</fpage>-<lpage>506</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.73696-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Smith, E.H. (1991) Complications of Percutaneous Abdominal Fine Needle Biopsy. Review. Radiology, 178, 253-258. https://doi.org/10.1148/radiology.178.1.1984314</mixed-citation></ref><ref id="scirp.73696-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Fornari, F., Civardi, G., Cavanna, L., et al. (1989) Complications of Ultrasonically Guided Fine-Needle Abdominal Biopsy. Results of a Multicenter Italian Study and Review of the Literature. The Cooperative Italian Study Group. Scandinavian Journal of Gastroenterology, 24, 949-955. https://doi.org/10.3109/00365528909089239</mixed-citation></ref><ref id="scirp.73696-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Chawla, Y.K., Ramesh, G.N., Kaur, U., Bambery, P. and Dilawar, J.B. (1990) Percutaneous Liver Biopsy: A Safe Outpatient Procedure. Journal of Gastroenterology and Hepatology, 5, 94-95. https://doi.org/10.1111/j.1440-1746.1990.tb01770.x</mixed-citation></ref><ref id="scirp.73696-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Buscarini, L., Fornari, F., Bolondi, L., et al. (1990) Ultrasound-Guided Fine-Needle Biopsy of Focal Liver Lesions: Techniques, Diagnostic Accuracy and Complications. A Retrospective Study on 2091 Biopsies. Journal of Hepatology, 11, 344-348. https://doi.org/10.1016/0168-8278(90)90219-H</mixed-citation></ref><ref id="scirp.73696-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Cochand-Priollet, B., Chagnon, S., Ferrand, J., et al. (1987) Comparison of Cytologic Examination of Smears and Histologic Examination of Tissue Cores Obtained by Fine Needle Aspiration Biopsy of the Liver. Acta Cytologica, 31, 476-480.</mixed-citation></ref><ref id="scirp.73696-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Jacobsen, G.K., Gammelgaard, J. and Fuglo, M. (1983) Coarse Needle Biopsy versus Fine Needle Aspiration Biopsy in the Diagnosis of Focal Lesions of the Liver. Ultrasonically Guided Needle Biopsy in Suspected Hepatic Malignancy. Acta Cytologica, 27, 152-156.</mixed-citation></ref><ref id="scirp.73696-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Whitlatch, S., Nunez, C. and Pitlik, D.A. (1984) Fine Needle Aspiration Biopsy of the Liver. A Study of 102 Consecutive Cases. Acta Cytologica, 28, 719-725.</mixed-citation></ref><ref id="scirp.73696-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Bell, D.A., Carr, C.P. and Szyfelbein, W.M. (1986) Fine Needle Aspiration Cytology of Focal Liver Lesions. Results Obtained with Examination of Both Cytologic and Histologic Preparations. Acta Cytologica, 30, 397-402.</mixed-citation></ref><ref id="scirp.73696-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Samaratunga, H. and Wright, G. (1992) Value of Fine Needle Aspiration Biopsy Cytology in the Diagnosis of Discrete Hepatic Lesions Suspicious for Malignancy. Australian and New Zealand Journal of Surgery, 62, 540-544. https://doi.org/10.1111/j.1445-2197.1992.tb07047.x</mixed-citation></ref><ref id="scirp.73696-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Pilotti, S., Rilke, F., Claren, R., et al. (1988) Conclusive Diagnosis of Hepatic and Pancreatic Malignancies by Fine Needle Aspiration. Acta Cytologica, 32, 27-38.</mixed-citation></ref><ref id="scirp.73696-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Michielsen, P.P., Duysburgh, I.K., Francque, S.M., et al. (1998) Ultrasonically Guided Fine Needle Puncture of Focal Liver Lesions. Review and Personal Experience. Acta Gastro-Enterologica Belgica, 61, 158-163.</mixed-citation></ref><ref id="scirp.73696-ref34"><label>34</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Pitman</surname><given-names> M.B. </given-names></name>,<etal>et al</etal>. (<year>1998</year>)<article-title>Fine Needle Aspiration Biopsy of the Liver. Principal Diagnostic Challenges</article-title><source> Clinics in Laboratory Medicine</source><volume> 18</volume>,<fpage> 483</fpage>-<lpage>506</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.73696-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Guo, Z., Kurtycz, D.F., Salem, R., et al. (2002) Radiologically Guided Percutaneous Fine-Needle Aspiration Biopsy of the Liver: Retrospective Study of 119 Cases Evaluating Diagnostic Effectiveness and Clinical Complications. Diagnostic Cytopathology, 26, 283-289. https://doi.org/10.1002/dc.10097</mixed-citation></ref><ref id="scirp.73696-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Edoute, Y., Tibon-Fisher, O., Ben-Haim, S.A., et al. (1991) Imaging Guided and Non Imaging-Guided Fine Needle Aspiration of Liver Lesions: Experience with 406 Patients. Journal of Surgical Oncology, 48, 246-251. https://doi.org/10.1002/jso.2930480407</mixed-citation></ref><ref id="scirp.73696-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Bret, P.M., Sente, J.M., Bretagnolle, M., et al. (1986) Ultrasonically Guided Fine-Needle Biopsy in Focal Intrahepatic Lesions: Six Years’ Experience. Canadian Association of Radiologists Journal, 37, 5-8.</mixed-citation></ref><ref id="scirp.73696-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Babb, R.R. and Jackman, R.J. (1989) Needle Biopsy of the Liver. A Critique of Four Currently Available Methods. Western Journal of Medicine, 150, 39-42.</mixed-citation></ref><ref id="scirp.73696-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">Ten Berge, J., Hoffman, B.J., Hawes, R.H., et al. (2002) EUS-Guided Fine Needle Aspiration of the Liver: Indications Yield, and Safety Based on an International Survey of 167 Cases. Gastrointestinal Endoscopy, 55, 859-862. https://doi.org/10.1067/mge.2002.124557</mixed-citation></ref></ref-list></back></article>