A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report

<p>Abstract</p> <p>Introduction</p> <p>Steroid cell tumors are microscopically characterized by abundant eosinophilic or vacuolated cytoplasm that is often positive for fat stains. These tumors could be of ovarian or ectopic adrenal origin. We present a rare case of a s...

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Main Authors: Louis Robert, Murhekar Kanchan, Majhi Urmila
Format: Article
Language:English
Published: BMC 2011-10-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/5/1/517
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spelling doaj-a73d67f0938f494593365874d7c5c2252020-11-25T00:05:39ZengBMCJournal of Medical Case Reports1752-19472011-10-015151710.1186/1752-1947-5-517A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case reportLouis RobertMurhekar KanchanMajhi Urmila<p>Abstract</p> <p>Introduction</p> <p>Steroid cell tumors are microscopically characterized by abundant eosinophilic or vacuolated cytoplasm that is often positive for fat stains. These tumors could be of ovarian or ectopic adrenal origin. We present a rare case of a steroid cell tumor arising from the pelvic mesentery.</p> <p>Case presentation</p> <p>A 31-year-old Asian woman was undergoing treatment for infertility and virilizing symptoms. She underwent laparoscopy followed by laprotomy for a suspected ovarian cyst/pelvic mass. During the laprotomy, a mass of 9 × 7 cm was detected in the pelvic mesentery.</p> <p>Microscopically, the tumor showed large cells arranged predominantly in sheets with abundant granular cytoplasm and large vesicular nuclei with prominent nucleoli. The tumor was seen infiltrating surrounding adipose tissue. Immunohistochemically, the tumor cells showed strong positivity for kertain, inhibin, vimentine, melan-A, neuron-specific enolase, chromogranin, and S-100 protein and focal positivity to epithelial membrane antigen. An MIB1 index showed 4% nuclear positivity. The tumor cells were negative for calretinin, desmin, and muscle actin. Considering the clinical findings, histomorphology, and immunohistochemistry, we made the diagnosis of extraovarian and extra-adrenal steroid cell tumor (not otherwise specified) of the pelvic mesentery.</p> <p>Conclusions</p> <p>We report an extremely rare case of an extraovarian and extra-adrenal steroid cell tumor of the pelvic mesentery. The tumor was a cause of virilizing symptoms and infertility in the patient. Surgical removal of the tumor reverted the symptoms of virilization, and the patient subsequently conceived. Steroid cell tumors should be considered in differential diagnosis among women presenting with infertility and symptoms of virilization.</p> http://www.jmedicalcasereports.com/content/5/1/517
collection DOAJ
language English
format Article
sources DOAJ
author Louis Robert
Murhekar Kanchan
Majhi Urmila
spellingShingle Louis Robert
Murhekar Kanchan
Majhi Urmila
A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
Journal of Medical Case Reports
author_facet Louis Robert
Murhekar Kanchan
Majhi Urmila
author_sort Louis Robert
title A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
title_short A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
title_full A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
title_fullStr A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
title_full_unstemmed A rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
title_sort rare occurrence of a steroid cell tumor of the pelvic mesentery: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2011-10-01
description <p>Abstract</p> <p>Introduction</p> <p>Steroid cell tumors are microscopically characterized by abundant eosinophilic or vacuolated cytoplasm that is often positive for fat stains. These tumors could be of ovarian or ectopic adrenal origin. We present a rare case of a steroid cell tumor arising from the pelvic mesentery.</p> <p>Case presentation</p> <p>A 31-year-old Asian woman was undergoing treatment for infertility and virilizing symptoms. She underwent laparoscopy followed by laprotomy for a suspected ovarian cyst/pelvic mass. During the laprotomy, a mass of 9 × 7 cm was detected in the pelvic mesentery.</p> <p>Microscopically, the tumor showed large cells arranged predominantly in sheets with abundant granular cytoplasm and large vesicular nuclei with prominent nucleoli. The tumor was seen infiltrating surrounding adipose tissue. Immunohistochemically, the tumor cells showed strong positivity for kertain, inhibin, vimentine, melan-A, neuron-specific enolase, chromogranin, and S-100 protein and focal positivity to epithelial membrane antigen. An MIB1 index showed 4% nuclear positivity. The tumor cells were negative for calretinin, desmin, and muscle actin. Considering the clinical findings, histomorphology, and immunohistochemistry, we made the diagnosis of extraovarian and extra-adrenal steroid cell tumor (not otherwise specified) of the pelvic mesentery.</p> <p>Conclusions</p> <p>We report an extremely rare case of an extraovarian and extra-adrenal steroid cell tumor of the pelvic mesentery. The tumor was a cause of virilizing symptoms and infertility in the patient. Surgical removal of the tumor reverted the symptoms of virilization, and the patient subsequently conceived. Steroid cell tumors should be considered in differential diagnosis among women presenting with infertility and symptoms of virilization.</p>
url http://www.jmedicalcasereports.com/content/5/1/517
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