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. 2015 Apr;77(Suppl 1):143-6.
doi: 10.1007/s12262-015-1208-9. Epub 2015 Mar 24.

A Sporadic Small Jejunal GIST Presenting with Acute Lower Gastrointestinal Hemorrhage: A Review of the Literature and Management Guidelines

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A Sporadic Small Jejunal GIST Presenting with Acute Lower Gastrointestinal Hemorrhage: A Review of the Literature and Management Guidelines

Sridar Govindaraj et al. Indian J Surg. 2015 Apr.

Abstract

Gastrointestinal stromal tumors (GISTs) represent the majority of primary nonepithelial neoplasms of the digestive tract, most frequently expressing the KIT protein detected by immunohistochemical staining for the CD117 antigen. Jejunal GISTs account for approximately 10 % of GISTs. Patients usually present with abdominal discomfort. Jejunal GISTs may cause symptoms secondary to obstruction or hemorrhage. Pressure necrosis and ulceration of the overlying mucosa may cause gastrointestinal bleeding, and patients who experience significant blood loss may suffer from malaise and fatigue. Literature has classified small-bowel GISTs on the basis of size, and various established guidelines have advised conservative management of small jejunal GISTs (<2 cm). We here report the clinical, macroscopic, and immunohistological features of a small jejunal GIST presenting with acute lower gastrointestinal hemorrhage in a 50-year-old postmenopausal woman necessitating an emergency laparotomy to control the bleed. The management of very small (<2 cm) small-bowel GISTs is controversial. While guidelines are primarily based on the risk of malignancy in GISTs, no guideline predicting the risk of complications in small-bowel GISTs exists. Hence, these tumors should be removed even if incidentally detected.

Keywords: GIST; Jejunal GIST; Lower GI bleed.

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Figures

Fig. 1
Fig. 1
a, b CT mesenteric angiogram showing an enhancing lesion just below the left kidney. c, d Jejunal hyperenhancing lesion seen on cross-sectional images
Fig. 2
Fig. 2
EGIST of the greater omentum: I intraoperative photograph showing jejunal GIST, II tumor cells in high power (H & E ×400), III tumor cells showing CD34 positivity, and IV tumor cells showing CD117 positivity

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