IP Archives of Cytology and Histopathology Research
Official Publication of Khyati Education and Research Foundation
Official Publication of Khyati Education and Research Foundation
Print ISSN: 2581-5725
Online ISSN: 2456-9267
CODEN : IACHCL
IP Archives of Cytology and Histopathology Research (ACHR) open access, peer-reviewed quarterly journal publishing since 2016 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...Case Report
Author Details :
Volume : 5, Issue : 3, Year : 2020
Article Page : 254-257
https://doi.org/10.18231/j.achr.2020.056
Abstract
Gastrointestinal Basidiobolomycosis (GIB) is an unusual fungal disease caused by Basidiobolus ranarum, seen in the stomach, small intestine, colon, and liver. It has been rarely reported in the literature and most of the reported cases have been from US, Saudi Arabia, Kuwait, and Iran. Basidiobolus ranarum is an environmental saprophyte found worldwide. It is a member of the order Entomophthorales of the class zygomycete. The infection is generally restricted to subcutaneous tissues but the disease can also involve visceral organs.GIB usually has nonspecific clinical manifestations and its diagnosis is more challenging. Delayed diagnosis of GIB increases the risk of morbidity and mortality, especially in pediatric patient. The plan of our case report is to illustrate the wide range of clinical presentations, clinico-radiological and histopathological diagnosis, management and outcomes.
Keywords: Basidiobolomycosis, Gastrointestinal, Pediatrics, Malignancy, Entomophthorales, Immunocompetent.
How to cite : Rao R N, Verma V, Rai V, Singh A, Gastrointestinal basidiobolomycosis in children mimicking as abdominal malignancy: A rare case report. IP Arch Cytol Histopathol Res 2020;5(3):254-257
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