Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site

Hemangiopericytoma was first described in 1942 by Stout and Murray as a distinctive soft tissue neoplasm of pericytic orgin characterized by ‘staghorn’ branching pattern. It is no longer considered a specific entity but rather a growth pattern shared by many unrelated benign and malignant neoplasms....

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Main Authors: Neelam Sood, Kumar Sharad Sinha
Format: Article
Language:English
Published: Krishna Institute of Medical Sciences University 2017-01-01
Series:Journal of Krishna Institute of Medical Sciences University
Subjects:
Online Access:http://www.jkimsu.com/jkimsu-vol6no1/JKIMSU,%20Vol.%206,%20No.%201,%20Jan-Mar%202017%20Page%20120-126.pdf
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spelling doaj-ceafd785b4634da8ae5572eb9ecd2f642020-11-25T01:06:12ZengKrishna Institute of Medical Sciences UniversityJournal of Krishna Institute of Medical Sciences University2231-42612231-42612017-01-0161120126Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual SiteNeelam Sood0Kumar Sharad Sinha1Department of Pathology, Deen Dayal Upadhyay Hospital, Govt. of NCT, Harinagar, Delhi-(Delhi) IndiaDepartment of Pathology, Deen Dayal Upadhyay Hospital, Govt. of NCT, Harinagar, Delhi-(Delhi) IndiaHemangiopericytoma was first described in 1942 by Stout and Murray as a distinctive soft tissue neoplasm of pericytic orgin characterized by ‘staghorn’ branching pattern. It is no longer considered a specific entity but rather a growth pattern shared by many unrelated benign and malignant neoplasms. The pathogenesis of Areteriovenous malformations is not well understood. Rarely, it has been reported with associated arteriovenous malformations. We present a rare case of combination of Hemangiopericytoma with arteriovenous malformations and epidermal inclusion cyst in the same lesion in leg. A 62 year male patient presented with a polypoidal cutaneous growth over posterior aspect of right thigh measuring 8x8x5 cm for past 25 years, firm in consistency. Radiological features revealed an areteriovenous malformation with soft tissue attenuation vascular mass. Cytological findings of the swelling were suggestive of a vascular lesion with cystic degeneration. Excision of the mass was performed and specimen was received as a large skin covered polypoidal mass measuring 14x10x5 cm. To the best of our knowledge, no prior report mentions a tumour of this size, associated with arteriovenous malformation and epidermal inclusion cyst of lower extremity.http://www.jkimsu.com/jkimsu-vol6no1/JKIMSU,%20Vol.%206,%20No.%201,%20Jan-Mar%202017%20Page%20120-126.pdfArteriovenous MalformationEpidermal inclusion cystHemangiopericytomaVascular lesion
collection DOAJ
language English
format Article
sources DOAJ
author Neelam Sood
Kumar Sharad Sinha
spellingShingle Neelam Sood
Kumar Sharad Sinha
Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
Journal of Krishna Institute of Medical Sciences University
Arteriovenous Malformation
Epidermal inclusion cyst
Hemangiopericytoma
Vascular lesion
author_facet Neelam Sood
Kumar Sharad Sinha
author_sort Neelam Sood
title Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
title_short Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
title_full Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
title_fullStr Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
title_full_unstemmed Conventional (Adult Type) Hemangiopericytoma of Thigh in Association with Arteriovenous Malformation and Epidermal Inclusion Cyst: A Rare Combination, At an Unusual Site
title_sort conventional (adult type) hemangiopericytoma of thigh in association with arteriovenous malformation and epidermal inclusion cyst: a rare combination, at an unusual site
publisher Krishna Institute of Medical Sciences University
series Journal of Krishna Institute of Medical Sciences University
issn 2231-4261
2231-4261
publishDate 2017-01-01
description Hemangiopericytoma was first described in 1942 by Stout and Murray as a distinctive soft tissue neoplasm of pericytic orgin characterized by ‘staghorn’ branching pattern. It is no longer considered a specific entity but rather a growth pattern shared by many unrelated benign and malignant neoplasms. The pathogenesis of Areteriovenous malformations is not well understood. Rarely, it has been reported with associated arteriovenous malformations. We present a rare case of combination of Hemangiopericytoma with arteriovenous malformations and epidermal inclusion cyst in the same lesion in leg. A 62 year male patient presented with a polypoidal cutaneous growth over posterior aspect of right thigh measuring 8x8x5 cm for past 25 years, firm in consistency. Radiological features revealed an areteriovenous malformation with soft tissue attenuation vascular mass. Cytological findings of the swelling were suggestive of a vascular lesion with cystic degeneration. Excision of the mass was performed and specimen was received as a large skin covered polypoidal mass measuring 14x10x5 cm. To the best of our knowledge, no prior report mentions a tumour of this size, associated with arteriovenous malformation and epidermal inclusion cyst of lower extremity.
topic Arteriovenous Malformation
Epidermal inclusion cyst
Hemangiopericytoma
Vascular lesion
url http://www.jkimsu.com/jkimsu-vol6no1/JKIMSU,%20Vol.%206,%20No.%201,%20Jan-Mar%202017%20Page%20120-126.pdf
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