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
1952 ◽  
Vol 22 (1) ◽  
pp. 124-127 ◽  
Author(s):  
John M. Rumball ◽  
George L. Baum

PEDIATRICS ◽  
1965 ◽  
Vol 35 (6) ◽  
pp. 1008-1010
Author(s):  
A. F. ROBERTSON

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.


2008 ◽  
Vol 47 (169) ◽  
Author(s):  
Arnab Ghosh ◽  
S Pradhan ◽  
R Swami ◽  
S R KC ◽  
O P Talwar

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


1988 ◽  
Vol 2 (1) ◽  
pp. 31-34
Author(s):  
Igor Matwijiw ◽  
Gerald D. Iliffe ◽  
Adi E. Mehta ◽  
Charles Faiman

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.


1990 ◽  
Vol 15 (2) ◽  
pp. 95-96 ◽  
Author(s):  
CPT KENNETH G. DENNISON ◽  
CPT DOUGLAS KHOURY ◽  
LTC JAMES D. HEIRONIMUS

Ultrasound ◽  
2008 ◽  
Vol 16 (4) ◽  
pp. 196-198 ◽  
Author(s):  
Roberto Chiavaroli ◽  
Pierfrancesco Grima ◽  
Paola Calabrese ◽  
Piero Grima

Sarcoidosis is a systemic disease characterised by non-caseating multiple granulomas involving virtually any organ in the body. The aetiology and natural history of sarcoidosis remains obscure. Hepatosplenic sarcoidosis is rare with image-based diagnosis difficult if no other organ is already involved. This case report describes a patient with asymptomatic liver and spleen involvement in which a final diagnosis was achieved with contrast enhanced ultrasound (CEUS) guided liver biopsy.


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