Angiomyofibroblastoma of the spermatic cord: a case report

<p>Abstract</p> <p>Introduction</p> <p>Angiomyofibroblastoma is a benign soft tissue tumor with tendency to arise in the vulva.</p> <p>Case presentation</p> <p>We report a 36-year-old Greek Caucasian man presenting with a left inguinal painless m...

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Main Authors: Rallis Georgios E, Efstathiou Stamatis P, Giannopoulos George A, Tzanakis Nikolaos E, Nikiteas Nikolaos I
Format: Article
Language:English
Published: BMC 2010-03-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/4/1/79
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spelling doaj-90357d6b33514a748fac0e454a7eb11b2020-11-24T21:09:26ZengBMCJournal of Medical Case Reports1752-19472010-03-01417910.1186/1752-1947-4-79Angiomyofibroblastoma of the spermatic cord: a case reportRallis Georgios EEfstathiou Stamatis PGiannopoulos George ATzanakis Nikolaos ENikiteas Nikolaos I<p>Abstract</p> <p>Introduction</p> <p>Angiomyofibroblastoma is a benign soft tissue tumor with tendency to arise in the vulva.</p> <p>Case presentation</p> <p>We report a 36-year-old Greek Caucasian man presenting with a left inguinal painless mass. This is the second case of angiomyofibroblastoma of the spermatic cord. At operation, a 4.5 cm well-circumscribed solid tumor was found adherent to the spermatic cord. The tumor consisted of spindle-shaped cells proliferating in short fascicles between numerous medium-sized blood vessels with thin and hyalinized walls. Neoplastic cells had eosinophilic cytoplasm with neither mitotic figures nor nuclear atypia. The stroma included abundant mast cells and few mature lypocytes. Immunostaining showed positivity for vimentin, CD34, desmin and smooth muscle actin. Our patient was treated by simple excision and was followed up for five years with clinical examination and ultrasonography, revealing no evidence of local recurrence or metastasis.</p> <p>Conclusion</p> <p>This unusual neoplasm should be distinguished from aggressive angiomyxoma and other myxoid malignant tumors with widespread metastatic potential.</p> http://www.jmedicalcasereports.com/content/4/1/79
collection DOAJ
language English
format Article
sources DOAJ
author Rallis Georgios E
Efstathiou Stamatis P
Giannopoulos George A
Tzanakis Nikolaos E
Nikiteas Nikolaos I
spellingShingle Rallis Georgios E
Efstathiou Stamatis P
Giannopoulos George A
Tzanakis Nikolaos E
Nikiteas Nikolaos I
Angiomyofibroblastoma of the spermatic cord: a case report
Journal of Medical Case Reports
author_facet Rallis Georgios E
Efstathiou Stamatis P
Giannopoulos George A
Tzanakis Nikolaos E
Nikiteas Nikolaos I
author_sort Rallis Georgios E
title Angiomyofibroblastoma of the spermatic cord: a case report
title_short Angiomyofibroblastoma of the spermatic cord: a case report
title_full Angiomyofibroblastoma of the spermatic cord: a case report
title_fullStr Angiomyofibroblastoma of the spermatic cord: a case report
title_full_unstemmed Angiomyofibroblastoma of the spermatic cord: a case report
title_sort angiomyofibroblastoma of the spermatic cord: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2010-03-01
description <p>Abstract</p> <p>Introduction</p> <p>Angiomyofibroblastoma is a benign soft tissue tumor with tendency to arise in the vulva.</p> <p>Case presentation</p> <p>We report a 36-year-old Greek Caucasian man presenting with a left inguinal painless mass. This is the second case of angiomyofibroblastoma of the spermatic cord. At operation, a 4.5 cm well-circumscribed solid tumor was found adherent to the spermatic cord. The tumor consisted of spindle-shaped cells proliferating in short fascicles between numerous medium-sized blood vessels with thin and hyalinized walls. Neoplastic cells had eosinophilic cytoplasm with neither mitotic figures nor nuclear atypia. The stroma included abundant mast cells and few mature lypocytes. Immunostaining showed positivity for vimentin, CD34, desmin and smooth muscle actin. Our patient was treated by simple excision and was followed up for five years with clinical examination and ultrasonography, revealing no evidence of local recurrence or metastasis.</p> <p>Conclusion</p> <p>This unusual neoplasm should be distinguished from aggressive angiomyxoma and other myxoid malignant tumors with widespread metastatic potential.</p>
url http://www.jmedicalcasereports.com/content/4/1/79
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AT tzanakisnikolaose angiomyofibroblastomaofthespermaticcordacasereport
AT nikiteasnikolaosi angiomyofibroblastomaofthespermaticcordacasereport
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