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Updated: Jun 3, 2026

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
Published on: April 3, 2026
Gastrointestinal stromal tumors in Addis Ababa, Ethiopia
Wegatha Tesfay1, Paul Komminoth, Jakob Schneider
1Gondar University, School of Health Science, Department of Pathology.
Background:
The last decade brought a deeper understanding of gastrointestinal stromal tumors (GIST). The cell of origin is the pacemaker cell of Cajal which has an intermediate function between the autonomic nervous system and the smooth muscle cells of the gastrointestinal tract. These cells express KIT/CD117 and less consistently CD34. Based on this facts new diagnostic and therapeutic methods have been developed. In this study we applied the current immunohistochemical methods on tumor tissue previously diagnosed as stromal tumor.
Method:
Histological specimens diagnosed as GISTs during 3 years (2005-2007) in the Department of Pathology, Tikur Anbessa Hospital, Addis Ababa, Ethiopia were reviewed and the available blocks were used for immunohistochemical assessment of KIT/CD]17 and CD34 expression.
Results:
Tumor specimens of 17 patients were analyzed histologically. Most tumors were purely spindle celled (82%), the rest were mixed (spindle cells/epithelioid cells). Blocks of 14 tumors allowed immunohistochemical investigation. KIT/CD117 positivity could be shown in 11 of 14 tumors, CD34 positivity in 9 of 13 tumors. In contrast to the reported cases from Western countries Ethiopian patients with GISTs were younger, their tumors were larger and the most common sites were small and large intestine, not the stomach.
Conclusions:
GISTs became probably not more common but gave rise to increased interest during the last decade because of growing understanding of origin, behavior, and molecular mechanism. GISTs seen in Ethiopia differ from those reported in Western countries in age, size and location within the gastrointestinal tract.
