>
Fa   |   Ar   |   En
   Type 2 segmental glomangioma - Case report  
   
نویسنده cabral c.r. ,de oliveira filho j. ,matsumoto j.l. ,cignachi s. ,tebet a.c.f. ,nasser k.r.
منبع journal brazilian annals of dermatology - 2015 - دوره : 90 - شماره : 3 - صفحه:S97 -S100
چکیده    Glomus tumors originate from modified perivascular muscle cells. the most common form is the solitary one. the multiple form may be associated with dominant genetic inheritance. we report a case of a patient with hemangiomatous lesions on the calcaneus and wrist since birth. in 6 years,there was progression of lesions throughout the body. multiple glomangiomas are asymptomatic and more common in childhood. they can be confused with other vascular malformations. histopathological diagnosis is essential. the case shows a type 2 segmental manifestation that can be explained by genetic mutation leading to the loss of heterozygosity. as the child grows,the lesions may disseminate due to mutation in distant parts of the skin. literature shows few reports. the treatment is conservative. © 2015 by anais brasileiros de dermatologia.
کلیدواژه Classification; Congenital abnormalities; Glomus tumor; International classification of diseases; Vascular malformations
آدرس universidade de santo amaro (unisa),santo amaro,sp, Brazil, universidade de santo amaro (unisa),santo amaro,sp, Brazil, universidade de santo amaro (unisa),santo amaro,sp, Brazil, universidade de santo amaro (unisa),santo amaro,sp, Brazil, universidade de santo amaro (unisa),santo amaro,sp, Brazil, universidade de santo amaro (unisa),santo amaro,sp, Brazil
 
     
   
Authors
  
 
 

Copyright 2023
Islamic World Science Citation Center
All Rights Reserved