Literature DB >> 23303036

Multiple disseminated glomuvenous malformations: do we know enough?

C Solovan1, Elena Chiticariu, Doina Beinsan, Sabina Zurac, Flavia Baderca.   

Abstract

Multiple glomuvenous malformations (GVMs), also known as glomangiomas, are uncommon entities with histological features of both glomus cells proliferation and venous malformation. A 14-year-old boy was admitted to our clinic with multiple dermal blue nodules, disseminated in different segments of the body. The patient's family history was positive for similar lesions; his mother and maternal grandmother had some asymptomatic blue nodules on their body. Histological examination showed a tumor composed of multiple caveronous vessels surrounded by glomus cells, positive for alpha smooth muscle actin, HHF35 (pan-actin), and h-caldesmon. This is a case of multiple GVMs, a rare disease caused by mutations in glomulin gene, with an autosomal dominant pattern of inheritance. The clinical and histopathological features are briefly discussed.

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Year:  2012        PMID: 23303036

Source DB:  PubMed          Journal:  Rom J Morphol Embryol        ISSN: 1220-0522            Impact factor:   1.033


  3 in total

1.  Type 2 segmental glomangioma--Case report.

Authors:  Camila Raposo Cabral; Jayme de Oliveira Filho; Julliene Lika Matsumoto; Stela Cignachi; Ana Carolina Franco Tebet; Kássila da Rosa Nasser
Journal:  An Bras Dermatol       Date:  2015 May-Jun       Impact factor: 1.896

2.  Multiple glomuvenous malformations presenting in a child: follow-up over a period of 8 years.

Authors:  Shehab Jabir; Quentin Frew; Mahir Petkar; Peter Dziewulski
Journal:  BMJ Case Rep       Date:  2013-07-13

3.  Congenital plaque-like glomangioma: report of two cases.

Authors:  Nivea Godinho Alves de Souza; Gisele Alborghetti Nai; Gláucia Ferreira Wedy; Marilda Aparecida Milanez Morgado de Abreu
Journal:  An Bras Dermatol       Date:  2017       Impact factor: 1.896

  3 in total

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