Abstract
GIST is the commonest mesenchymal tumour of the gastrointestinal tract. Jejunal GIST is rare and spontaneous perforation of asymptomatic jejunal GIST is unique. A review of the English literature reveals only fifteen cases of perforated GIST till date. Pre-operative diagnosis is difficult. Diagnosis is confirmed on histopathology and immuno-histochemistry. Complete removal with postoperative imatinib therapy entails optimal treatment. Perforated GIST is associated with high recurrence. © 2012 Roy et al.; licensee BioMed Central Ltd.
Author supplied keywords
Cite
CITATION STYLE
Roy, S. D., Khan, D., De, K. K., & De, U. (2012, November 29). Spontaneous perforation of jejunal gastrintestinal stromal tumour (gist). Case report and review of literature. World Journal of Emergency Surgery. https://doi.org/10.1186/1749-7922-7-37
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.