A case of Dubin-Johnson syndrome with a pigmented neurofibroma / 대한내과학회지
Korean Journal of Medicine
;
: S6-S9, 2009.
Artículo
en Coreano
| WPRIM
| ID: wpr-183140
ABSTRACT
Clinically, Dubin-Johnson syndrome is characterized by mild icterus without specific symptoms or signs. The icterus is so mild that it is usually noted only during another illness, pregnancy, or the use of oral contraceptives. There is no pruritus in ubin-Johnson syndrome. The physical examination is usually normal, except for the icterus, although hepatosplenomegaly is seen occasionally. Histologically, the liver is normal, except for the presence of dense pigment making it appear black grossly. Pigmentation of tissues other than the liver in patients with Dubin-Johnson syndrome has been reported only in a few cases. We experienced a case of Dubin-Johnson syndrome with extrahepatic pigmentation in the skin with a neurofibroma in a 66-year-old man.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Examen Físico
/
Prurito
/
Piel
/
Pigmentación
/
Neurofibromatosis
/
Anticonceptivos Orales
/
Ictericia
/
Ictericia Idiopática Crónica
/
Hígado
/
Neurofibroma
Límite:
Anciano
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
Korean Journal of Medicine
Año:
2009
Tipo del documento:
Artículo
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