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Case Report: Late-onset liver cirrhosis in an elderly patient with FBN1-related Geleophysic Dysplasia. [PDF]
Front Endocrinol (Lausanne)Liu Y, Wang Y, Teng X, Wang X.
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Heart Failure in Adult Congenital Heart Disease. [PDF]
Methodist Debakey Cardiovasc JRichardson JN, Martin CM.
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Overview of Non-Cirrhotic Portal Hypertension in Pediatric Patients. [PDF]
J Clin MedWalecha A +2 more
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Congenital hepatic fibrosis of heterotopic hepatic tissue
Pathology Research and Practice, 1998We describe a unique case of a one-month-old infant with congenital hepatic fibrosis in the heterotopic liver within the adrenal gland. The main (orthotopic) liver was normal. Complex congenital heart disease and asplenia were associated.
M, Zlatković, S, Duricić, P, Plamenac
exaly +3 more sources
Journal of Hepatology, 1988
We report the clinical features of 7 men (mean age 22 years, range 7-53 years) with congenital hepatic fibrosis (CHF). Five patients presented with variceal bleeding and/or hepatosplenomegaly due to portal hypertension. Cholangitis was the presenting symptom in the other 2 cases. Diagnosis was established by histological examination of a surgical wedge
M, De Vos, F, Barbier, C, Cuvelier
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We report the clinical features of 7 men (mean age 22 years, range 7-53 years) with congenital hepatic fibrosis (CHF). Five patients presented with variceal bleeding and/or hepatosplenomegaly due to portal hypertension. Cholangitis was the presenting symptom in the other 2 cases. Diagnosis was established by histological examination of a surgical wedge
M, De Vos, F, Barbier, C, Cuvelier
openaire +4 more sources
Journal of Pediatric Gastroenterology and Nutrition, 1984
One family with four of seven siblings with congenital hepatic fibrosis. is reported. The proband, the only member of this family with symptoms referable to the disease, was hospitalized because of an upper gastrointestinal hemorrhage. He had a presinusoidal type of portal hypertension. The other three siblings had the latent form of congenital hepatic
J, Pereira-Lima +3 more
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One family with four of seven siblings with congenital hepatic fibrosis. is reported. The proband, the only member of this family with symptoms referable to the disease, was hospitalized because of an upper gastrointestinal hemorrhage. He had a presinusoidal type of portal hypertension. The other three siblings had the latent form of congenital hepatic
J, Pereira-Lima +3 more
openaire +4 more sources
Australasian Annals of Medicine, 1962
SUMMARYA family with a high incidence of hepatomegaly, normal liver function and stillbirths is described. In one member biopsy material confirmed the diagnosis of congenital hepatic fibrosis. This patient's sister probably died of the same disorder. Unusual hepatic sinusoidal prominence was present in the patient described and in one of her daughters,
J B, HICKIE, J M, GARVAN
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SUMMARYA family with a high incidence of hepatomegaly, normal liver function and stillbirths is described. In one member biopsy material confirmed the diagnosis of congenital hepatic fibrosis. This patient's sister probably died of the same disorder. Unusual hepatic sinusoidal prominence was present in the patient described and in one of her daughters,
J B, HICKIE, J M, GARVAN
openaire +2 more sources