<?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">OJRad</journal-id><journal-title-group><journal-title>Open Journal of Radiology</journal-title></journal-title-group><issn pub-type="epub">2164-3024</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojrad.2014.42027</article-id><article-id pub-id-type="publisher-id">OJRad-46908</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>BIOMEDICAL &amp; LIFE SCIENCES</subject><subject>PHYSICS &amp; MATHEMATICS</subject></subj-group></article-categories><title-group><article-title>Assessment of Visceral Leishmaniasis Consequences Using Ultrasound</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mustafa</surname><given-names>Z. Mahmoud</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Radiology and Medical Imaging Department, College of Applied Medical Sciences, Salman bin Abdulaziz
University, Al-Kharj, KSA;
Basic Sciences Department, College of Medical Radiological Sciences, Sudan University of Science and
Technology, Khartoum, Sudan</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>m.alhassen@sau.edu.sa</email></corresp></author-notes><pub-date pub-type="epub"><day>28</day><month>03</month><year>2014</year></pub-date><volume>04</volume><issue>02</issue><fpage>201</fpage><lpage>206</lpage><history><date date-type="received"><day>27</day>	<month>April</month>	<year>2014</year></date><date date-type="rev-recd"><day>22</day>	<month>May</month>	<year>2014</year>	</date><date date-type="accepted"><day>29</day>	<month>May</month>	<year>2014</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
and Aim: Visceral leishmaniasis (VL), also known as kala azar, is a parasitic
disease that caused by infection with Leishmania parasites, which are spread by
the bite of phlebotomine sand flies. An ultrasound examination is strongly
advocated for the promote diagnosis and treatment of VL for long term follow up
and evaluation of unresponsive cases. The aim of this study was to assess the
consequences of VL in the liver, spleen and pancreas of affected participants
by using ultrasound. Materials and Methods: A prospective cohort study was
conducted in the period of January 2012 to March 2014 in the ultrasound
department of Tropical Disease Hospital (TDH) in Khartoum-Sudan, among a group
of 100 participants (84% males, 16% females and their ages ranges from 15 to 45
years) positive to VL and had been diagnosed by laboratory tests; either serological
or Napier’s Aldehyde test. The Aloka portable ultrasound machine equipped with
3.5 MHz convex probe was used for abdominal ultrasound scanning. Standard
Statistical Package for the Social Sciences (SPSS) was used to analyze the
results. Results: The commonest ultrasound findings in VL participants were
hepatomegaly (100%), splenomegaly (100%) and ascites (50%). Other complications
such as lymphadenopathy (35%), focal splenic lesions (34%), dilated portal vein
(7%) and shrinkage liver (4%) were detected. Conclusion: Ultrasound scanning
presents an effective role in VL, because of its ability to detect the
consequences of this disease in various abdominal organs such as liver, spleen
and pancreas earlier, which in turn allowing the possibility to treat these
complications and prevents the deterioration of a patient’s health status.

	
</p></abstract><kwd-group><kwd>Napier’s Aldehyde Test</kwd><kwd> Ultrasound</kwd><kwd> Serological Tests</kwd><kwd> Visceral Leishmaniasis</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Visceral leishmaniasis (VL), known as kala azar in India, is the cause of much death and disease in developing countries. It is one of several diseases caused by over 20 species of Leishmania; it is transmitted by Sandfly bi- tes [<xref ref-type="bibr" rid="scirp.46908-ref1">1</xref>] . The infection of humans appears with multiple clinical manifestations, including cutaneous (CL), muco- cutaneous, diffuse and VL. The latter is responsible for approximately 59,000 deaths per year, a parasitic disease surpassed only by malaria [<xref ref-type="bibr" rid="scirp.46908-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.46908-ref3">3</xref>] . There are two types of VL, anthroponotic and zoonotic. Zoonotic VL (ZVL) is widespread and occurs in Latin America, Northern Africa, Southern Europe and in areas of the Middle East and Asia [<xref ref-type="bibr" rid="scirp.46908-ref2">2</xref>] -[<xref ref-type="bibr" rid="scirp.46908-ref4">4</xref>] . Two forms of leishmaniasis (VL and CL) present in Europe are caused by Leishmania infan- tum [<xref ref-type="bibr" rid="scirp.46908-ref4">4</xref>] . While cases of cutaneous leishmaniosis were reported in France, Italy and Spain, ZVL is endemic in all countries bordering the Mediterranean Sea [<xref ref-type="bibr" rid="scirp.46908-ref5">5</xref>] .</p><p>Geographically, the distribution of leishmaniasis is limited by the distribution of its vector Sandfly species. The Sandfly vectors are mainly active during the night, and therefore the highest risk for contracting the infec- tive stages of the parasite from Sandfly bites is between dusk and dawn [<xref ref-type="bibr" rid="scirp.46908-ref6">6</xref>] . The reservoirs of the pathogen can be several wild and domestic canid and rodent species, but domestic dogs are considered as the main reservoir of Leishmania infantum playing a key role as the source of human infection. Indeed, there is a clear association between a high rate of infection in dogs and an increased risk of human disease [<xref ref-type="bibr" rid="scirp.46908-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.46908-ref7">7</xref>] .</p><p>VL is endemic in 62 countries, with a total of 200 million people at risk, an estimated 500,000 new cases each year worldwide, and 41,000 recorded deaths in the year 2000 [<xref ref-type="bibr" rid="scirp.46908-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.46908-ref9">9</xref>] . As is the case for other tropical diseases, epidemiological data are incomplete, and official figures are likely to underestimate grossly the real prevalence of the disease [<xref ref-type="bibr" rid="scirp.46908-ref10">10</xref>] . Both the number of recorded cases and the geographic areas affected have grown in the past two decades [<xref ref-type="bibr" rid="scirp.46908-ref11">11</xref>] .</p><p>Delays and difficulty in diagnosis are common due to the long incubation period of the agent, nonspecific symptoms, and the difficulty of identifying the intracellular protozoa (Donovan bodies) in tissue aspirates. It is usually diagnosed by serology or bone marrow examination. Liver biopsy is rarely required for diagnosis [<xref ref-type="bibr" rid="scirp.46908-ref12">12</xref>] . The role of imaging techniques as diagnostic tools remains to be established in VL [<xref ref-type="bibr" rid="scirp.46908-ref13">13</xref>] . This study designed with an aim to assess the consequences of VL in the liver, spleen and pancreas of the affected participants by using ultrasound, which will contribute in the treatment of the disease in an early period, before the exacerbation of complications and the condition become difficult to control.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Selection and Description of Participants</title><p>This prospective cohort study was performed in the period of January 2012 to March 2014. Participants were scanned in the ultrasound department of Tropical Disease Hospital (TDH) in Khartoum-Sudan. Prior to partici- pants scanning, a formal approval was obtained from Ethics and Scientific Committee of TDH and has therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and all subsequent revisions.</p><p>After the nature of the procedure was fully explained, informed consents were obtained from participants and the ultrasound department. Sudanese participants were included in this study, after they were diagnosed to be affected by VL on the basis of noninvasive laboratory tests, either immunodiagnostic (serological tests) or non- specific serological tests (Napier’s Aldehyde test). Participants were excluded if they were pregnant or breast- feeding, human immunity virus (HIV) positive, had a serious concurrent infection such as tuberculosis, bacterial pneumonia, malaria or if they had a granulocyte count &lt;1 &#215; 109/l, hemoglobin concentration &lt;40 g/l, or platelet count &lt;40 &#215; 109/l.</p></sec><sec id="s2_2"><title>2.2. Technical Information Identifies</title><p>Abdominal ultrasound scanning was performed using Aloka (SSD-500) portable ultrasound machine equipped with 3.5 MHz convex probe (serial number of 1028924YM7, manufactured date of February 2010 and made by the Yokogawa medical system, Ltd. 7 - 127 Asahigaoka 4-chome Hino-shi Tokyo, Japan). Printing facility is- sued through the ultrasound-digital graphic-printer (serial number of 3-619-GBI-01 made by Sony Corporation- Japan), 100 V; 1.5 A; and 50/60 Hz.</p></sec><sec id="s2_3"><title>2.3. Abdominal Ultrasound Scanning Technique</title><p>Abdominal ultrasound scanning technique used was in accordance with the protocols established by the Ameri- can Institute of Ultrasound in Medicine (AIUM) [<xref ref-type="bibr" rid="scirp.46908-ref14">14</xref>] . The examination of the liver should include long-axis and transverse views. The liver parenchyma should be evaluated for focal and/or diffuse abnormalities. If possible, the echogenicity of the liver should be compared with that of the right kidney [<xref ref-type="bibr" rid="scirp.46908-ref15">15</xref>] -[<xref ref-type="bibr" rid="scirp.46908-ref17">17</xref>] . Whenever possible, all portions of the pancreas -head, uncinate process, body, and tail-should be identified. Orally administered water may afford better visualization of the pancreas [<xref ref-type="bibr" rid="scirp.46908-ref18">18</xref>] -[<xref ref-type="bibr" rid="scirp.46908-ref20">20</xref>] . Representative views of the spleen in long-axis and transverse projections should be obtained. Splenic length measurement may be helpful in assessing enlargement. Echogenicity of the left kidney should be compared to splenic echogenicity when possible.</p><p>An attempt should be made to demonstrate the left hemi diaphragm and the adjacent pleural space [<xref ref-type="bibr" rid="scirp.46908-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.46908-ref22">22</xref>] . The potential benefits and risks of each examination should be considered. The ALARA (as low as reasonably achievable) principle should be observed when adjusting controls that affect the acoustic output and by consi- dering transducer dwell times.</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>Data were initially summarized as mean &#177; SD in a form of comparison tables. Statistical analysis was performed using the standard Statistical Package for the Social Sciences (SPSS Inc., Chicago, IL, USA) version 15 for windows.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Study population comprised 100 positive participants to VL (84% males and 16% females). Participants’ ages ranged from 15 to 45 years; with a mean age of (29.8 &#177; 2.2) years (<xref ref-type="table" rid="table1">Table 1</xref>). Out of the scanned participants, a total of 34 subjects were in the age group (35 - 39) years, representatives (34%) of the population. The age group of (40 - 45) years was the smallest and representing only (6%) of the population (<xref ref-type="table" rid="table1">Table 1</xref>). The highest mean &#177; SD of ages was (43 &#177; 1.4) years and found in the age group 40 - 45 years, while the lowest mean &#177; SD of ages was (18 &#177; 1.4) years found in the age group 15 - 19 years (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>Regarding symptoms and signs of VL; abdominal distention was detected in (50%) of participants, while he- pato-splenomegaly, weight loss and fever were present in (100%) of participants. Cough and diarrhoea were the least clinical features detected only in (2%) of participants for each (<xref ref-type="table" rid="table2">Table 2</xref>). Sonographically, hepatic compli- cations of VL were hepatic lesions as hepatomegaly (100%), increased liver echogenicity (18%), dilated portal vein (7%), and shrinkage liver (4%) (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>In the Spleens of the affected participants, ultrasound detects features of splenomegaly (100%), hypoechoic spleen (19%), and focal splenic lesion (34%). While in pancreas, acute pancreatitis (2%) and decreased pancrea- tic echogenicity (1%) were the commonest sonographic findings (<xref ref-type="table" rid="table3">Table 3</xref>). Other complications of VL such as ascites (50%) and lymphadenopathy (35%) were also detected (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>Kala azar is a protozoal infection common in developing countries; there are an estimated 500,000 new cases</p><table-wrap id="table1"  position="float"><object-id pub-id-type="pii">Table 1</object-id><label>Table 1</label><caption><p>. Distribution of participant’s ages (years).</p></caption><table><thead><tr><th align="center" valign="middle" >Age ranges (years)</th><th align="center" valign="middle" >Percentage (%)</th><th align="center" valign="middle" >Mean &#177; SD (years)</th></tr></thead><tbody><tr><td align="center" valign="middle" >15 - 19</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >18 &#177; 1.4</td></tr><tr><td align="center" valign="middle" >20 - 24</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >23 &#177; 2.4</td></tr><tr><td align="center" valign="middle" >25 - 29</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >27 &#177; 2.7</td></tr><tr><td align="center" valign="middle" >30 - 34</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >33 &#177; 2.3</td></tr><tr><td align="center" valign="middle" >35 - 39</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >35 &#177; 3.1</td></tr><tr><td align="center" valign="middle" >40 - 45</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >43 &#177; 1.4</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >100%</td><td align="center" valign="middle" >29.8 &#177; 2.2 years</td></tr></tbody></table></table-wrap><table-wrap id="table2"  position="float"><object-id pub-id-type="pii">Table 2</object-id><label>Table 2</label><caption><p>. Distribution of symptoms and signs in VL participants.</p></caption><table><thead><tr><th align="center" valign="middle" >Symptoms and Signs</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tbody><tr><td align="center" valign="middle" >Abdominal distention</td><td align="center" valign="middle" >50</td></tr><tr><td align="center" valign="middle" >Hepato-splenomegaly</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >Weight loss</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >Fever</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >Cough</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Diarrhoea</td><td align="center" valign="middle" >2</td></tr></tbody></table></table-wrap><table-wrap id="table3"  position="float"><object-id pub-id-type="pii">Table 3</object-id><label>Table 3</label><caption><p>. Ultrasound findings in the liver, spleen and pancrease of VL participants.</p></caption><table><thead><tr><th align="center" valign="middle"  colspan="4"  >Ultrasound Findings in VL Participants</th></tr></thead><tbody><tr><td align="center" valign="middle" >Liver</td><td align="center" valign="middle" >Spleen</td><td align="center" valign="middle" >Pancreas</td><td align="center" valign="middle" >Others</td></tr><tr><td align="center" valign="middle" >Hepatomegaly (100%)</td><td align="center" valign="middle" >Splenomegaly (100%)</td><td align="center" valign="middle" >Acute pancreatitis (2%)</td><td align="center" valign="middle" >Ascites (50%)</td></tr><tr><td align="center" valign="middle" >Increased echogenicity (18%)</td><td align="center" valign="middle" >Hypoechoic spleen (19%)</td><td align="center" valign="middle" >Decreased echogenicity (1%) </td><td align="center" valign="middle" >Lymphadenopathy (35%)</td></tr><tr><td align="center" valign="middle" >Dilated portal vein (7%)</td><td align="center" valign="middle" >Focal splenic lesions (34%)</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Shrinkage liver (4%)</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap><p>every year and there were 41,000 recorded deaths in the year 2000 [<xref ref-type="bibr" rid="scirp.46908-ref23">23</xref>] . From the early 1900s, VL has been among the most important health problems in Sudan, particularly in the main endemic area in the eastern and central regions. Several major epidemics have occurred—in the Western Upper Nile province in southern Sudan, detected in 1988—and the most recent claiming over 100,000 lives [<xref ref-type="bibr" rid="scirp.46908-ref24">24</xref>] .</p><p>Delay and difficulty in diagnosis are common, especially in the early stage of the disease, due to non-specific symptomatology and difficulty in demonstrating intracellular protozoa in tissue aspirates [<xref ref-type="bibr" rid="scirp.46908-ref25">25</xref>] . In this study there was a wild diversity in clinical patterns (<xref ref-type="table" rid="table2">Table 2</xref>) and this was caused because the pathogenicity depends mainly on parasite genotype versus host immungenetic profile [<xref ref-type="bibr" rid="scirp.46908-ref26">26</xref>] .</p><p>Study results showed that abdominal ultrasound can detect the changes occur in organ size as well as to dem- onstrate the echo texture changes—hyper or hypo echogenicity—in case of VL complications in liver, spleen and pancreases (<xref ref-type="table" rid="table3">Table 3</xref>). Such findings were confirmed in another study of ultrasound findings in patients with VL, where their results showed that abdominal ultrasound can detect the changes in organ size in an appropriate manner as well as to demonstrate the echo texture changes as hyper or hypo echogenicity in case of inflamma- tion as pancreatitis and renal inflammatory diseases resulted from VL [<xref ref-type="bibr" rid="scirp.46908-ref27">27</xref>] .</p><p>Also ultrasound findings of hepatosplenomegaly, and abdominal lymphadenopathy secondary to VL had been reported when VL was diagnosed by ultrasound guided fine needle aspiration of an axillary node and when ul- trasound is used to study changes occur in the organ parenchyma in VL participants [<xref ref-type="bibr" rid="scirp.46908-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.46908-ref29">29</xref>] .</p><p>Abdominal ultrasound has the capability to diagnose VL and differentiating it from mimicking conditions, in complement with other laboratory tests. Delayed diagnosis due to a typical manifestation can lead to fatal out- come in patients. Instead of relying solely on the classical clinical features of visceral leishmaniasis, simple ab- dominal ultrasound examination can help to make an early diagnosis even in atypical cases, thereby reducing the mortality of visceral leishmaniasis. The use of ultrasound as a primary model in the diagnosis of patients with VL, and characterization of the signs and complications in Tropical Sudanese hospitals is enlightening.</p><p>This study is limited because the obtained results cannot be applied to the whole society in Sudan, because it was conducted only in Khartoum state rather than other states in Sudan.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, ultrasound scanning presents to be an effective tool in the diagnosis of VL consequences because of its ability to detect these complications in various abdominal organs such as liver, spleen and pancreas, which in turn allowing the possibility of prevent and treat related deterioration in the patient’s health status.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The author would like to thank the staff of the ultrasound department at the Tropical Disease Hospital (TDH) for their cooperation and support during data collection.</p></sec></body><back><ref-list><title>References</title><ref id="scirp.46908-ref1"><label>1</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>DESJEUX</surname><given-names> P. </given-names></name>,<etal>et al</etal>. 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