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Rom J Morphol Embryol ; 53(4): 1077-80, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23303036

RESUMO

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.


Assuntos
Tumor Glômico/diagnóstico , Neoplasias Cutâneas/diagnóstico , Adolescente , Tumor Glômico/genética , Tumor Glômico/patologia , Humanos , Masculino , Neoplasias Cutâneas/genética , Neoplasias Cutâneas/patologia
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