scholarly journals Hypothalamic Hypogonadism in Hemochromatosis: A Case Report

1988 ◽  
Vol 2 (1) ◽  
pp. 31-34
Author(s):  
Igor Matwijiw ◽  
Gerald D. Iliffe ◽  
Adi E. Mehta ◽  
Charles Faiman
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Early Development ◽  
Hypogonadotropic Hypogonadism ◽  
Gonadotropin Secretion

A 42-year-old man developed hypogonadotropic hypogonadism due to primary hemochromatosis. Endocrine evaluation indicated a hypothalamic defect in the control of gonadotropin secretion. Although cirrhosis was present on liver biopsy, ocher major features of the hemochromatosis syndrome were not manifest. Patients with hemochromacosis arc now being diagnosed at earlier stages of disease. Clinicians should be alert to possible early development of hypothalamopituitary dysfunction and should be prepared co perform derailed endocrinological investigations in such patients.

Liver Biopsy Culture in the Diagnosis of Miliary Tuberculosis: A Case Report

1952 ◽  
Vol 22 (1) ◽  
pp. 124-127 ◽  
Author(s):  
John M. Rumball ◽  
George L. Baum
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Miliary Tuberculosis

Case Report: The Coincidence of Biliary Atresia and the Heterozygous State of Galactosemia

PEDIATRICS ◽  
1965 ◽  
Vol 35 (6) ◽  
pp. 1008-1010
Author(s):  
A. F. ROBERTSON
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Biliary Atresia ◽  
Heterozygous State

A case is presented in which biliary atresia and the heterozygous state of galactosemia occurred coincidentally. The mother was also heterozygous for galactosemia. A liver biopsy revealed changes compatible with biliary atresia and no evidence of galactosemia cirrhosis.

scholarly journals Early Development and Rupture of De Novo Aneurysm. Case Report.

2002 ◽  
Vol 42 (8) ◽  
pp. 334-337 ◽  
Author(s):  
Jae Hong SIM ◽  
Soo Chun KIM ◽  
Moo Seong KIM
Keyword(s):  
Case Report ◽  
Early Development ◽  
De Novo ◽  
De Novo Aneurysm

scholarly journals Reye Syndrome – A Case Report with Review of Literature .

2008 ◽  
Vol 47 (169) ◽  
Author(s):  
Arnab Ghosh ◽  
S Pradhan ◽  
R Swami ◽  
S R KC ◽  
O P Talwar
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Needle Biopsy ◽  
Differential Diagnoses ◽  
Low Grade ◽  
Loss Of Consciousness ◽  
Reye Syndrome ◽  
Supportive Treatment ◽  
Review Of Literature ◽  
Drug Ingestion

Here we describe a case of Reye syndrome diagnosed at postmortem liver biopsy of a three-year oldgirl who presented with vomiting, low grade fever for three days and loss of consciousness for 18hours. Clinically, the differential diagnoses were meningitis, encephalitis and septicemia. No historyof past illness or any drug ingestion including aspirin were present. Laboratory investigationsindicated a diagnosis of Reye syndrome. The child was given supportive treatment but died aftertwo days of admission and postmortem needle-biopsy of the liver showed microvesicular steatosisconsistent with Reye syndrome.Key words: Microvesicular steatosis, mitochondrial hepatopathy, Reye syndrome, Reye-like syndrome

scholarly journals Hypogonadotropic hypogonadism presenting with arhinia: a case report

2013 ◽  
Vol 7 (1) ◽  
Author(s):  
Jeanie B Tryggestad ◽  
Shibo Li ◽  
Steven D Chernausek
Keyword(s):  
Case Report ◽  
Hypogonadotropic Hypogonadism

scholarly journals Cardiac MRI prior to liver biopsy in a Fontan patient: A case report

2020 ◽  
Vol 8 (9) ◽  
pp. 1781-1785
Author(s):  
Pier Paolo Bassareo ◽  
Kevin Patrick Walsh ◽  
John Gerard Murray
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Cardiac Mri ◽  
Fontan Patient

Gallbladder Perforation During Liver Biopsy Diagnosed Using Hepatobiliary Scintigraphy: A Case Report

1990 ◽  
Vol 15 (2) ◽  
pp. 95-96 ◽  
Author(s):  
CPT KENNETH G. DENNISON ◽  
CPT DOUGLAS KHOURY ◽  
LTC JAMES D. HEIRONIMUS
Keyword(s):  
Case Report ◽  
Liver Biopsy ◽  
Gallbladder Perforation ◽  
Hepatobiliary Scintigraphy
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