A Case of Romberg Syndrome / 대한피부과학회지
Korean Journal of Dermatology
; : 349-352, 1995.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-51445
Biblioteca responsável:
WPRO
ABSTRACT
Romberg syndrome is a rare disease and characterized by unilaeril atrophy of the skin, subcutaneous tissue and the underlying structure of half the face. The lesion does not usually cross the midline of the scalp. Roriberg syndrome is sometimes mildsnosed as linear scleroderma, although they differ widely in their clinical and histological apperance. A 13-year-old boy was present with a one year history of idefined atrophic patch on the left side of face and neck. We involved skin was not bound down to the underlying structure. The history revealed no prcvious trauma or disease, He had no abnormal neurologic finding. Computerized tomography demonstrated a diminished subcutaneouat volume and also decreased thickness of back muscle is the left side face from cheek to neck.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Atrofia
/
Couro Cabeludo
/
Esclerodermia Localizada
/
Pele
/
Bochecha
/
Tela Subcutânea
/
Doenças Raras
/
Músculos do Dorso
/
Pescoço
/
Manifestações Neurológicas
Limite:
Adolescente
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
1995
Tipo de documento:
Artigo