Angiomyomatous hamartoma of the inguinal lymph node

Angiomyomatous hamartoma is a rare disease of the lymph nodes, particularly inguinal and femoral lymph nodes. It was first identified as a distinct entity by Chan et al. in 1992. Histologically, it is characterized by the replacement of lymph nodal parenchyma with irregularly distributed thick-walle...

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Main Authors: Supriya Verma, Gauri Nakra, Anchana Gulati
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Archives of Medicine and Health Sciences
Subjects:
Online Access:http://www.amhsjournal.org/article.asp?issn=2321-4848;year=2022;volume=10;issue=2;spage=285;epage=287;aulast=Verma
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author Supriya Verma
Gauri Nakra
Anchana Gulati
author_facet Supriya Verma
Gauri Nakra
Anchana Gulati
author_sort Supriya Verma
collection DOAJ
description Angiomyomatous hamartoma is a rare disease of the lymph nodes, particularly inguinal and femoral lymph nodes. It was first identified as a distinct entity by Chan et al. in 1992. Histologically, it is characterized by the replacement of lymph nodal parenchyma with irregularly distributed thick-walled variable-sized blood vessels, haphazardly arranged smooth muscle cells, and variable amounts of fat and fibrous tissue in a sclerotic lymphatic stroma. Only a few atrophic lymphatic follicles are seen in the subcapsular area. The exact pathogenesis is still controversial. Although this entity is very rare, its recognition is important in discriminating it from other benign and malignant vascular lesions of lymph nodes.
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spelling doaj.art-ed1e276e6a4c443a8daa4b2c91b4eb3a2023-01-12T11:05:32ZengWolters Kluwer Medknow PublicationsArchives of Medicine and Health Sciences2321-48482022-01-0110228528710.4103/amhs.amhs_245_21Angiomyomatous hamartoma of the inguinal lymph nodeSupriya VermaGauri NakraAnchana GulatiAngiomyomatous hamartoma is a rare disease of the lymph nodes, particularly inguinal and femoral lymph nodes. It was first identified as a distinct entity by Chan et al. in 1992. Histologically, it is characterized by the replacement of lymph nodal parenchyma with irregularly distributed thick-walled variable-sized blood vessels, haphazardly arranged smooth muscle cells, and variable amounts of fat and fibrous tissue in a sclerotic lymphatic stroma. Only a few atrophic lymphatic follicles are seen in the subcapsular area. The exact pathogenesis is still controversial. Although this entity is very rare, its recognition is important in discriminating it from other benign and malignant vascular lesions of lymph nodes.http://www.amhsjournal.org/article.asp?issn=2321-4848;year=2022;volume=10;issue=2;spage=285;epage=287;aulast=Vermaangiomyomatous hamartomabenign vascular diseaseinguinal lymph node
spellingShingle Supriya Verma
Gauri Nakra
Anchana Gulati
Angiomyomatous hamartoma of the inguinal lymph node
Archives of Medicine and Health Sciences
angiomyomatous hamartoma
benign vascular disease
inguinal lymph node
title Angiomyomatous hamartoma of the inguinal lymph node
title_full Angiomyomatous hamartoma of the inguinal lymph node
title_fullStr Angiomyomatous hamartoma of the inguinal lymph node
title_full_unstemmed Angiomyomatous hamartoma of the inguinal lymph node
title_short Angiomyomatous hamartoma of the inguinal lymph node
title_sort angiomyomatous hamartoma of the inguinal lymph node
topic angiomyomatous hamartoma
benign vascular disease
inguinal lymph node
url http://www.amhsjournal.org/article.asp?issn=2321-4848;year=2022;volume=10;issue=2;spage=285;epage=287;aulast=Verma
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