SciELO - Scientific Electronic Library Online

 
vol.39 número1Megacolon tóxico secundario a enfermedad de Hirschsprung. Reporte de un casoTratamiento laparoscópico de la hernia paraesofágica y la utilización de mallas índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Cirujano general

versão impressa ISSN 1405-0099

Resumo

URIBE GONZALEZ, Guillermo  e  SIGLER MORALES, Luis. McCune-Albright syndrome in an adolescent youngster. Cir. gen [online]. 2017, vol.39, n.1, pp.37-40.  Epub 26-Mar-2020. ISSN 1405-0099.

Introduction:

This is a non-hereditary, very rare syndrome, present since birth or youth; it is due to an alteration in the chromosome 20. The objective of this work is to present the case of a male adolescent who consulted because of an ulcer in the sole of the right foot; he also showed signs of this syndrome.

Case report:

16-year-old male who lived in a distant rural zone; he complained of an ulcer in the sole of the right foot for several months. There was shortness of the right lower extremity, cafe-au-lait pigmented skin lesions, abnormal development of limbs and alopecia areata of the scalp. Cleaning of the ulcer, bandages, sole protector, and rest were recommended. A future work-up with X rays and consultations was planned, but he never came back. Later, he changed his address. Clinical findings were the basis of the diagnosis of McCune-Albright syndrome.

Palavras-chave : McCune-Albright syndrome; adolescent male; alopecia areata.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )