<?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">WJCS</journal-id><journal-title-group><journal-title>World Journal of Cardiovascular Surgery</journal-title></journal-title-group><issn pub-type="epub">2164-3202</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wjcs.2014.44009</article-id><article-id pub-id-type="publisher-id">WJCS-44965</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>
 
 
  A Rare Retroperitoneal Mass: Leiomyosarcoma of the Inferior Vena Cava
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ram</surname><given-names>Baram</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>Zirak</surname><given-names>Anwar Tayeb</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>Delan</surname><given-names>Ahmed Bakir</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Thoracic and Cardiovascular Surgery, Faculty of Medical Sciences, School of Medicine, 
University of Sulaimani, Fran?ois Mitterrand Street, Sulaymaniyah, 46001, Iraq </addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>aram.baramm@gmail.com(RB)</email>;<email>dr.zirak@gmail.com(ZAT)</email>;<email>deelan_83@yahoo.com(DAB)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>09</day><month>04</month><year>2014</year></pub-date><volume>04</volume><issue>04</issue><fpage>51</fpage><lpage>55</lpage><history><date date-type="received"><day>7</day>	<month>February</month>	<year>2014</year></date><date date-type="rev-recd"><day>7</day>	<month>March</month>	<year>2014</year>	</date><date date-type="accepted"><day>15</day>	<month>March</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>
 
 
  Leiomyosarcoma of the inferior vena cava (IVC) is a rare soft tissue tumor, mesenchymal in origin that arises from smooth muscles of tunica media; it accounts for about 0.5% of all soft tissue sarcomas, and it is the commonest vascular leiomyosarcoma. The tumor progression is slow, and it is asymptomatic until advanced stage in which involvement of surrounding structures even when the symptoms present are nonspecific. Presentation of Case: A 60 years old lady presented with upper abdominal pain for 3 months duration. Past surgical history was significant for Hysterectomy 15 years ago. On examination: soft abdomen, palpable non pulsating right hypochondrial mass. Ultrasound of the abdomen showed tumor of the head of pancreas. CT scan showed large retroperitoneal tumor extending from the head of pancreas to IVC. Trans abdominal CT guided FNAC showed retroperitoneal sarcoma while Immunohistochemistry (IHC) was proved to be Leiomyosarcoma of the IVC. Discussion: Leiomyosarcoma of inferior vena cava (IVC) is a rare soft tissue tumor, mesenchymal in origin that arises from smooth muscles of tunica media; it accounts for about 0.5% of all soft tissue sarcomas, and it is the commonest vascular leiomyosarcoma. The type of surgical management is a matter of debate and includes resection alone, primary repair/cavoplasty, or replacement with a graft. Reconstruction of the IVC is not always required especially in chronic occlusions. Conclusion: Despite all the advanced modalities, surgery remains the most effective method for treatment of Leiomyosarcoma.
 
</p></abstract><kwd-group><kwd>Ivc Leiomyosarcoma</kwd><kwd> Retroperitoneal Tumor</kwd><kwd> Resection</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Background</title><p>Leiomyosarcoma of inferior vena cava (IVC) is a rare soft tissue tumor, mesenchymal in origin that arises from smooth muscles of tunica media; it accounts for about 0.5% of all soft tissue sarcomas [<xref ref-type="bibr" rid="scirp.44965-ref1">1</xref>] , and it is the commonest vascular leiomyosarcoma [<xref ref-type="bibr" rid="scirp.44965-ref2">2</xref>] .</p><p>Patterns of the tumor growth are extraluminal which is the commonest, intraluminal which is rare, around 1/3 of the cases have both extra and intraluminal tumor growth [<xref ref-type="bibr" rid="scirp.44965-ref3">3</xref>] .</p><p>According to the site involved IVC leiomyosarcomas are divided into 3 levels, Level 1 proximal to the level of Hepatic veins, Level 2 between the level of renal veins and hepatic veins, Level 3 distal to the entry of renal veins to IVC [<xref ref-type="bibr" rid="scirp.44965-ref4">4</xref>] -[<xref ref-type="bibr" rid="scirp.44965-ref6">6</xref>]</p><p>The tumor progression is slow [<xref ref-type="bibr" rid="scirp.44965-ref7">7</xref>] , and it is asymptomatic until advanced stage in which involvement of surrounding structures and distal metastasis occur [<xref ref-type="bibr" rid="scirp.44965-ref8">8</xref>] , even when the symptoms are present are nonspecific, that is why the disease is usually diagnosed after several years [<xref ref-type="bibr" rid="scirp.44965-ref9">9</xref>] . Imaging studies has a major role in diagnosis, demonstration of origin and extension of such tumors [<xref ref-type="bibr" rid="scirp.44965-ref10">10</xref>] .</p></sec><sec id="s2"><title>2. Case Report</title><p>A 60 years old lady presented with upper abdominal pain of 3 months duration, pain was persistent, dull in nature, aggravated by heavy meals, no weight loss. She has long history of Arterial Hypertension. Past surgical history significant for Hysterectomy 15 years before presentation, for which details are not known, results of the biopsy are not available, cancers are not known in the family.</p><p>On examination: soft abdomen, audible bowel sounds, palpable non pulsating right hypochondrial mass, Hepatomegaly. Initial laboratory investigations including CBC and Biochemical tests were within normal limits. Ultrasound of the abdomen showed Tumor of the head of Pancreas. CT scan showed large retroperitoneal tumor extending from the head of pancreas to IVC, both renal veins and caudate lobe of the liver [<xref ref-type="fig" rid="fig1">Figure 1</xref>]. Trans abdominal CT guided FNAC showed retroperitoneal sarcoma while by Immunohistochemistry (IHC) proved to be Leiomyosarcoma of the IVC. IVC venogram showed subtotal occlusion of IVC with a floating filling defect in the lumen [<xref ref-type="fig" rid="fig2">Figure 2</xref>].</p><p>She disappeared from follow-up because she went to another institution where high risk resection decided with cardiopulmonary bypass and repair by graft decided for which a midline laparotomy performed, unfortunately intraoperative decision was to terminate the operation because the mass found was not respectable.</p><p>In front of this disappointment she returned back to our center, few days after arrival, she was to be found tired, with tachypnea and jaundice and huge swelling of both lower limbs in Phlegmasiaalbadolens, Doppler study of both lower limbs showed extensive DVT reaching IVC.</p><p>Oncologist and Vascular Surgeon care started, the patient received 6 cycles of chemotherapy along with systemic anticoagulation and compression stocking of lower limbs. At 11 months later, after down-staging of the tumor, clinical examination revealed no palpable mass, multiple large dilated anterior and posterior abdominal wall veins, and performance status was one. New CT-scan of abdomen showed more than 50% reduction in the tumor size [<xref ref-type="fig" rid="fig3">Figure 3</xref>] and radiological signs of respectability. Doppler study shows chronic DVT, Mild Post Post-thrombotic syndrome, OGD was normal, IVU showed right kidney hydronephrosis. Resection of the residual tumor decided.</p></sec><sec id="s3"><title>3. Operation</title><p>Through the previous midline laparotomy abdomen opened, tumor noted to originate from IVC, resectability assessed, dissection of the mass from aorta, duodenum, portal vein, caudate lobe of the liver and right kidney done. Proximal and distal control done, Resection of the mass done en-bloc with renal veins and IVC, tumor margins at the time of resection were negative. Postoperative sample examination revealed tumor free excisional margins.</p></sec><sec id="s4"><title>4. Post-Operative Period</title><p>After the surgery she developed high output renal failure (urine output about 3000 ml/24 hrs.) with elevation of serum creatinine which reached 3.9 mg/dl. At 5th post-operative day renal function returned to normal. Systemic anticoagulation was administered through out perioperative period. She discharged from hospital at 9th postoperative day.</p></sec><sec id="s5"><title>5. Discussion</title><p>Leiomyosarcoma of inferior vena cava (IVC) is a rare soft tissue tumor, mesenchymal in origin that arises from smooth muscles of tunica media; it accounts for about 0.5% of all soft tissue sarcomas [<xref ref-type="bibr" rid="scirp.44965-ref1">1</xref>] , and it is the commonest vascular leiomyosarcoma [<xref ref-type="bibr" rid="scirp.44965-ref2">2</xref>] .</p><p>Patterns of the tumor growth are extraluminal which is the commonest, intraluminal which is rare, around 1/3 of the cases have both extra and intraluminal tumor growth [<xref ref-type="bibr" rid="scirp.44965-ref3">3</xref>] .</p><p>According to the site involved IVC leiomyosarcomas are divided into 3 levels, level 1 proximal to the level of Hepatic veins, level 2 between the level of renal veins and hepatic veins, level 3 distal to the entry of renal veins to IVC [<xref ref-type="bibr" rid="scirp.44965-ref4">4</xref>] -[<xref ref-type="bibr" rid="scirp.44965-ref6">6</xref>] .</p><p>The tumor progression is slow [<xref ref-type="bibr" rid="scirp.44965-ref7">7</xref>] , and it is asymptomatic until advanced stage in which involvement of surrounding structures and distal metastasis occur [<xref ref-type="bibr" rid="scirp.44965-ref8">8</xref>] , even when the symptoms present are nonspecific such as dyspnea, malaise, weight loss, abdominal pain, or back pain, that is why the disease is usually diagnosed after several years [<xref ref-type="bibr" rid="scirp.44965-ref9">9</xref>] . Imaging studies have a major role in diagnosis, demonstration of origin and extension of such tumors [<xref ref-type="bibr" rid="scirp.44965-ref10">10</xref>] .Computed tomography (CT), magnetic resonance imaging (MRI), individually or in combination with cavography, ultrasound (US), and echocardiography, allow an early and accurate preoperative diagnosis [<xref ref-type="bibr" rid="scirp.44965-ref9">9</xref>] .</p><p>Despite advancing imaging technology, biopsy is still indicated for formal diagnosis. Histopathology of leiomyosarcoma reveals spindle tumor cells, which are positive for markers of smooth muscle activity includingvimentin, muscle actin, alpha-smooth muscle actin, and desmin [<xref ref-type="bibr" rid="scirp.44965-ref11">11</xref>] .</p><p>Chemotherapy, using adriamycin-ifosfamide or chemotherapy combined with radiation therapy offers potential adjuvant treatment options [<xref ref-type="bibr" rid="scirp.44965-ref4">4</xref>] .</p><p>The surgical management of partial resections of the IVC is a matter of current debate and includes ligation, primary repair/cavoplasty, or replacement with a graft. Reconstruction of the IVC is not always required, because gradual occlusion of the IVC allows the development of venous collaterals. However, when pararenal leiomyosarcoma of the IVC is present, reconstruction of the IVC and the renal vein are necessary to prevent transient or permanent renal dysfunction [<xref ref-type="bibr" rid="scirp.44965-ref1">1</xref>] .</p><p>In summary, despite all advanced modalities, surgery remains the most important method for treatment for Leiomyosarcoma.</p></sec><sec id="s6"><title>Conflict of Interest</title><p>No conflict of interest attributed.</p></sec><sec id="s7"><title>Consent</title><p>Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the editor of this journal.</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.44965-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Alexander, A., Rehders, A., Raffel, A., Poremba, C., Knoefel, W.T. and Eisenberger, C.F. 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