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

Author(s):  
Melanie Thanh Phuong Le ◽  
Jochen Herrmann ◽  
Michael Groth ◽  
Konrad Reinshagen ◽  
Michael Boettcher

Background Gallbladder perforation is a very rare finding in children. Clinical and radiografic presentations are often vague. Hence it is a challenging diagnosis, often missed during initial evaluation with potentially fatal consequences. The aim of this case report and review was to identify factors that might help to diagnose and manage future cases. Methods We present a case of gallbladder perforation in an 8-year-old child after blunt abdominal trauma caused by a handlebar in which imaging modalities such as ultrasound and magnetic resonance imaging (MRI) helped us to determine proper management. We identified and evaluated comparable cases for isolated traumatic gallbladder injury. A review of the recent literature was performed by online search in Pubmed and Google Scholar using “gallbladder injury in children”, “gallbladder perforation children”, “blunt abdominal trauma children” as keywords. We focused on articles exclusively in the pediatric section. The literature from the period 2000–2020 was taken into account to review the state of the art in diagnosis and management. Results and Conclusion Recent literature for gallbladder injury in pediatrics is sparse compared to the adult counterpart. Only eight published cases of isolated gallbladder injury in children were identified. Since the onset of symptoms may not develop acutely and often develops in an indistinct manner, radiografic examinations play an important role in the diagnostic progress. The authors advise caution in cases of blunt abdominal trauma especially involving handlebars, intraperitoneal free fluid, and severe abdominal pain. We advocate high suspicion of gallbladder perforation if the gallbladder wall displays discontinuation or cannot be definitively differentiated in sonografic examination. Echogenic fluid within the gallbladder should always lead to suspicion of intraluminal bleeding. Repeated clinical and imaging examinations are mandatory since the onset of signs and symptoms may be delayed. Key Points:  Citation Format


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.


2018 ◽  
Vol 42 ◽  
pp. 104-108 ◽  
Author(s):  
Masateru Yamamoto ◽  
Hiroyuki Tahara ◽  
Michinori Hamaoka ◽  
Seiichi Shimizu ◽  
Shintaro Kuroda ◽  
...  

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.


2020 ◽  
Vol 8 (9) ◽  
pp. 1781-1785
Author(s):  
Pier Paolo Bassareo ◽  
Kevin Patrick Walsh ◽  
John Gerard Murray

2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Yueh-Lin Wu ◽  
Yi-Sheng Lin ◽  
Thomas Yu-Ren Hsueh ◽  
Wen-Ching Lo ◽  
Kuo-Chou Peng ◽  
...  

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