A case of Dubin-Johnson syndrome with a pigmented neurofibroma / 대한내과학회지
Korean Journal of Medicine
; : S6-S9, 2009.
Article
de Ko
| WPRIM
| ID: wpr-183140
Bibliothèque responsable:
WPRO
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.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Examen physique
/
Prurit
/
Peau
/
Pigmentation
/
Neurofibromatoses
/
Contraceptifs oraux
/
Ictère
/
Ictère chronique idiopathique
/
Foie
/
Neurofibrome
Limites du sujet:
Aged
/
Humans
/
Pregnancy
langue:
Ko
Texte intégral:
Korean Journal of Medicine
Année:
2009
Type:
Article