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Invasive aspergillosis causing gastric necrosis and perforation: A case report

Aspergillosis is an opportunistic infection commonly seen in immunocompromised patients. Patients with hematological malignancies, postorgan transplantation, or those with comorbid conditions are susceptible to the development of invasive aspergillosis. Lungs are the main portal of entry and are thu...

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Autores principales: Kulkarni, Aditya Atul, Aruni, Amaresh, Rastogi, Pulkit, Rana, Surinder, Gupta, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008170/
https://www.ncbi.nlm.nih.gov/pubmed/32055703
http://dx.doi.org/10.1002/jgh3.12157
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author Kulkarni, Aditya Atul
Aruni, Amaresh
Rastogi, Pulkit
Rana, Surinder
Gupta, Rajesh
author_facet Kulkarni, Aditya Atul
Aruni, Amaresh
Rastogi, Pulkit
Rana, Surinder
Gupta, Rajesh
author_sort Kulkarni, Aditya Atul
collection PubMed
description Aspergillosis is an opportunistic infection commonly seen in immunocompromised patients. Patients with hematological malignancies, postorgan transplantation, or those with comorbid conditions are susceptible to the development of invasive aspergillosis. Lungs are the main portal of entry and are thus most commonly involved. Aspergillosis can involve the gut, causing vascular thrombosis leading to ischemia and necrosis of the gut wall, resulting in perforation. Primary gastric involvement has been rarely seen, with few case reports in the literature. We report a rare case of primary invasive gastric aspergillosis in a 60‐year‐old diabetic and cirrhotic woman, who presented with clinical features of perforation peritonitis. Exploratory laparotomy was performed, and a 6 cm × 6 cm perforation with necrotizing inflammation was found in the distal stomach, pylorus, and duodenum. Distal gastrectomy with Billroth II reconstruction was performed. Pathology demonstrated septate fungal hyphae invading the gastric wall transmurally. The morphology was compatible with those of Aspergillus spp. Liposomal amphotericin B was started immediately after surgery based on the presence of unusually large areas of necrosis and perforation with blackish exudate covering the ulcer base. Unfortunately, the patient succumbed to rapidly progressive fungal septicemia despite early surgical intervention and critical care management. We recommend that any large confluent areas of gastric ulceration and necrosis with blackish exudates in an appropriate setting should evoke suspicion of invasive fungal infection. These patients should be started on prophylactic broadspectrum antifungal therapy immediately, which may be switched over to specific therapy once the diagnosis is confirmed.
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spelling pubmed-70081702020-02-13 Invasive aspergillosis causing gastric necrosis and perforation: A case report Kulkarni, Aditya Atul Aruni, Amaresh Rastogi, Pulkit Rana, Surinder Gupta, Rajesh JGH Open Case Reports Aspergillosis is an opportunistic infection commonly seen in immunocompromised patients. Patients with hematological malignancies, postorgan transplantation, or those with comorbid conditions are susceptible to the development of invasive aspergillosis. Lungs are the main portal of entry and are thus most commonly involved. Aspergillosis can involve the gut, causing vascular thrombosis leading to ischemia and necrosis of the gut wall, resulting in perforation. Primary gastric involvement has been rarely seen, with few case reports in the literature. We report a rare case of primary invasive gastric aspergillosis in a 60‐year‐old diabetic and cirrhotic woman, who presented with clinical features of perforation peritonitis. Exploratory laparotomy was performed, and a 6 cm × 6 cm perforation with necrotizing inflammation was found in the distal stomach, pylorus, and duodenum. Distal gastrectomy with Billroth II reconstruction was performed. Pathology demonstrated septate fungal hyphae invading the gastric wall transmurally. The morphology was compatible with those of Aspergillus spp. Liposomal amphotericin B was started immediately after surgery based on the presence of unusually large areas of necrosis and perforation with blackish exudate covering the ulcer base. Unfortunately, the patient succumbed to rapidly progressive fungal septicemia despite early surgical intervention and critical care management. We recommend that any large confluent areas of gastric ulceration and necrosis with blackish exudates in an appropriate setting should evoke suspicion of invasive fungal infection. These patients should be started on prophylactic broadspectrum antifungal therapy immediately, which may be switched over to specific therapy once the diagnosis is confirmed. Wiley Publishing Asia Pty Ltd 2019-02-27 /pmc/articles/PMC7008170/ /pubmed/32055703 http://dx.doi.org/10.1002/jgh3.12157 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Kulkarni, Aditya Atul
Aruni, Amaresh
Rastogi, Pulkit
Rana, Surinder
Gupta, Rajesh
Invasive aspergillosis causing gastric necrosis and perforation: A case report
title Invasive aspergillosis causing gastric necrosis and perforation: A case report
title_full Invasive aspergillosis causing gastric necrosis and perforation: A case report
title_fullStr Invasive aspergillosis causing gastric necrosis and perforation: A case report
title_full_unstemmed Invasive aspergillosis causing gastric necrosis and perforation: A case report
title_short Invasive aspergillosis causing gastric necrosis and perforation: A case report
title_sort invasive aspergillosis causing gastric necrosis and perforation: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008170/
https://www.ncbi.nlm.nih.gov/pubmed/32055703
http://dx.doi.org/10.1002/jgh3.12157
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