Cargando…

Glomeruloid Hemangioma in Normal Individuals

Glomeruloid hemangioma is a rare, histologically distinctive, cutaneous, benign vascular tumor, originally described by Chan et al. Glomeruloid hemangioma appears specific to polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome (POEMS), and is usually, but n...

Descripción completa

Detalles Bibliográficos
Autores principales: Gupta, Jyoti, Kandhari, Rajat, Ramesh, V, Singh, Avninder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657245/
https://www.ncbi.nlm.nih.gov/pubmed/23716835
http://dx.doi.org/10.4103/0019-5154.108088
_version_ 1782270120781938688
author Gupta, Jyoti
Kandhari, Rajat
Ramesh, V
Singh, Avninder
author_facet Gupta, Jyoti
Kandhari, Rajat
Ramesh, V
Singh, Avninder
author_sort Gupta, Jyoti
collection PubMed
description Glomeruloid hemangioma is a rare, histologically distinctive, cutaneous, benign vascular tumor, originally described by Chan et al. Glomeruloid hemangioma appears specific to polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome (POEMS), and is usually, but not always, related to Castleman's disease. We herein report two cases with glomeruloid hemangioma, without any features of the POEMS syndrome. Glomeruloid hemangioma requires a high index of suspicion for diagnosis. It could rarely present as a solitary finding, without any evidence of an underlying POEMS syndrome.
format Online
Article
Text
id pubmed-3657245
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-36572452013-05-28 Glomeruloid Hemangioma in Normal Individuals Gupta, Jyoti Kandhari, Rajat Ramesh, V Singh, Avninder Indian J Dermatol E-Case Report Glomeruloid hemangioma is a rare, histologically distinctive, cutaneous, benign vascular tumor, originally described by Chan et al. Glomeruloid hemangioma appears specific to polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome (POEMS), and is usually, but not always, related to Castleman's disease. We herein report two cases with glomeruloid hemangioma, without any features of the POEMS syndrome. Glomeruloid hemangioma requires a high index of suspicion for diagnosis. It could rarely present as a solitary finding, without any evidence of an underlying POEMS syndrome. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3657245/ /pubmed/23716835 http://dx.doi.org/10.4103/0019-5154.108088 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle E-Case Report
Gupta, Jyoti
Kandhari, Rajat
Ramesh, V
Singh, Avninder
Glomeruloid Hemangioma in Normal Individuals
title Glomeruloid Hemangioma in Normal Individuals
title_full Glomeruloid Hemangioma in Normal Individuals
title_fullStr Glomeruloid Hemangioma in Normal Individuals
title_full_unstemmed Glomeruloid Hemangioma in Normal Individuals
title_short Glomeruloid Hemangioma in Normal Individuals
title_sort glomeruloid hemangioma in normal individuals
topic E-Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657245/
https://www.ncbi.nlm.nih.gov/pubmed/23716835
http://dx.doi.org/10.4103/0019-5154.108088
work_keys_str_mv AT guptajyoti glomeruloidhemangiomainnormalindividuals
AT kandharirajat glomeruloidhemangiomainnormalindividuals
AT rameshv glomeruloidhemangiomainnormalindividuals
AT singhavninder glomeruloidhemangiomainnormalindividuals