A case of a diverticulum-like giant jejunal gastrointestinal stromal tumour presenting with intraperitoneal peritonitis due to rupture.

Chemotherapy Gastrointestinal stromal tumour Local resection Peritonitis Rupture of the tumour Small intestine

Journal

International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872

Informations de publication

Date de publication:
2020
Historique:
received: 13 02 2020
revised: 12 03 2020
accepted: 13 03 2020
pubmed: 14 4 2020
medline: 14 4 2020
entrez: 14 4 2020
Statut: ppublish

Résumé

Early diagnosis of small intestinal gastrointestinal stromal tumours (GISTs) is difficult. These tumours often present with peritonitis and intraperitoneal bleeding due to rupture. We experienced a case of a tumor that grows to 12 cm asymptomatic. A 46-year-old man presented with sudden abdominal pain. Computed tomography revealed free air in the abdominal cavity, a 12-cm sized dilatation in the small intestine, and pooled residues. He was diagnosed with perforation of the gastrointestinal tract, and emergency surgery was performed. Inside the abdominal cavity, approximately 500 mL of bloody ascites was observed. A diverticulum-like mass measuring approximately 12-cm long was observed on the jejunum approximately 30 cm from the Treitz ligament. There was a large hematoma inside the mass, and perforation was recognised at the neck of the diverticulum. Partial resection of the jejunum and intraperitoneal drainage were performed. Immunohistochemistry revealed that the tumour was positive for KIT and CD34, and GIST was diagnosed. The patient was discharged on postoperative day 10 without significant complications. The patient did not relapse while taking imatinib as an adjuvant chemotherapy. Gastrointestinal stromal tumours are the most common mesenchymal tumours of the gastrointestinal tract and may undergo increased diverticulum-like growth, as seen in this case. Local resection and proper chemotherapy increase long-term survival, suppress tumour growth, and reduce the risk of relapse. Diagnosing GIST can be difficult due to the absence of clinical symptoms. It is necessary to ensure local resection and careful long-term follow-up.

Identifiants

pubmed: 32283516
pii: S2210-2612(20)30159-0
doi: 10.1016/j.ijscr.2020.03.017
pmc: PMC7154945
pii:
doi:

Types de publication

Case Reports

Langues

eng

Pagination

68-71

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Ryosuke Arata (R)

Department of Gastroenterological Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Hideki Nakahara (H)

Department of Gastroenterological Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan. Electronic address: hnakahara-gi@nifty.com.

Takashi Urushihara (T)

Department of Gastroenterological Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Toshiyuki Itamoto (T)

Department of Gastroenterological Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan; Department of Gastroenterological and Transplant Surgery Applied Life Sciences, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Takashi Nishisaka (T)

Department of Pathology Clinical Laboratory, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Classifications MeSH