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Gastrointestinal stromal tumor natural history

Introduction

Overview

Overview

If left untreated, patients with gastrointestinal stromal tumors (GIST) may progress to develop abdominal pain, abdominal distension and perforation. A benign GIST may remain unchanged for years before its progression into malignancy. A GIST may rupture and lead to intra-abdominal or gastrointestinal bleeding. Ultimately, the GIST may metastasize and turn fatal. Common complications of GIST include bowel obstruction, bowel perforation, and peritonitis. Depending on the extent of the tumor at the time of diagnosis, the prognosis of GIST may vary. Prognosis of GIST depends upon size, location, spread and mitotic rate of the tumor. A benign GIST treated with surgical resection has much more better outcome as compared to patients with malignant GIST.

Natural history

Natural history

Complications

Complications

Common complications of GIST include:[2]

Prognosis

Prognosis

Refrences

Refrences

  1. ↑ Antonopoulos P, Leonardou P, Barbagiannis N, Alexiou K, Demonakou M, Economou N (2014). “Gastrointestinal and extragastrointestinal stromal tumors: report of two cases and review of the literature”. Case Rep Gastroenterol. 8 (1): 61–6. doi:10.1159/000354724. PMCΒ 3975174. PMIDΒ 24707244.
  2. ↑ Sorour MA, Kassem MI, Ghazal A, El-Riwini MT, Abu Nasr A (2014). “Gastrointestinal stromal tumors (GIST) related emergencies”. Int J Surg. 12 (4): 269–80. doi:10.1016/j.ijsu.2014.02.004. PMIDΒ 24530605. Vancouver style error: initials (help)
  3. ↑ “Risk Assessment and Prognosis”.
  4. ↑ Dematteo RP, Heinrich MC, El-Rifai WM, Demetri G (2002). “Clinical management of gastrointestinal stromal tumors: before and after STI-571”. Hum. Pathol. 33 (5): 466–77. PMIDΒ 12094371.
  5. ↑ Crosby JA, Catton CN, Davis A, Couture J, O’Sullivan B, Kandel R, Swallow CJ (2001). “Malignant gastrointestinal stromal tumors of the small intestine: a review of 50 cases from a prospective database”. Ann. Surg. Oncol. 8 (1): 50–9. PMIDΒ 11206225.
  6. ↑ Conlon KC, Casper ES, Brennan MF (1995). “Primary gastrointestinal sarcomas: analysis of prognostic variables”. Ann. Surg. Oncol. 2 (1): 26–31. PMIDΒ 7834450.
  7. ↑ GΓΌller U, Tarantino I, Cerny T, Schmied BM, Warschkow R (2015). “Population-based SEER trend analysis of overall and cancer-specific survival in 5138 patients with gastrointestinal stromal tumor”. BMC Cancer. 15: 557. doi:10.1186/s12885-015-1554-9. PMCΒ 4518595. PMIDΒ 26223313.
  8. ↑ Carney JA (1999). “Gastric stromal sarcoma, pulmonary chondroma, and extra-adrenal paraganglioma (Carney Triad): natural history, adrenocortical component, and possible familial occurrence”. Mayo Clin. Proc. 74 (6): 543–52. doi:10.4065/74.6.543. PMIDΒ 10377927.


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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Akshun Kalia M.B.B.S.[2]