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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-90357d6b33514a748fac0e454a7eb11b |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT rallisgeorgiose angiomyofibroblastomaofthespermaticcordacasereport AT efstathioustamatisp angiomyofibroblastomaofthespermaticcordacasereport AT giannopoulosgeorgea angiomyofibroblastomaofthespermaticcordacasereport AT tzanakisnikolaose angiomyofibroblastomaofthespermaticcordacasereport AT nikiteasnikolaosi angiomyofibroblastomaofthespermaticcordacasereport |
_version_ |
1716758358972694528 |