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Gastric antral vascular ectasia in a patient with GIST after treatment with imatinib: case report and literature review.

Abstract
Imatinib mesylate is a receptor kinase inhibitor approved by the Food and Drug Administration for the treatment of malignant metastatic and/or unresectable gastrointestinal stromal tumors and chronic myelogenous leukemia. Although imatinib is generally well tolerated, certain adverse drug reactions are common. These include gastrointestinal side-effects such as diarrhea, nausea and vomiting, as well as hematological side-effects and other miscellaneous side-effects such as fatigue, edema, dermatitis and dyspnea. We present a previously unreported adverse effect of imatinib, gastric antral vascular ectasia, in a 74-year-old woman with gastrointestinal stromal tumor in remission treated with adjuvant imatinib. Endoscopy performed prior to starting imatinib showed normal gastric mucosa, but 8 months after starting imatinib showed diffuse gastric inflammation. Repeat endoscopy 1 month after discontinuing imatinib showed significant improvement in gastric inflammation.
AuthorsEhab Saad Aldin, Fadi Mourad, Arafat Tfayli
JournalJapanese journal of clinical oncology (Jpn J Clin Oncol) Vol. 42 Issue 5 Pg. 447-50 (May 2012) ISSN: 1465-3621 [Electronic] England
PMID22422898 (Publication Type: Case Reports, Journal Article, Review)
Chemical References
  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Imatinib Mesylate
  • Protein-Tyrosine Kinases
Topics
  • Aged
  • Antineoplastic Agents (administration & dosage, adverse effects)
  • Benzamides
  • Endoscopy, Digestive System
  • Female
  • Gastric Antral Vascular Ectasia (chemically induced, complications)
  • Gastrointestinal Hemorrhage (chemically induced, etiology)
  • Gastrointestinal Neoplasms (drug therapy, pathology)
  • Gastrointestinal Stromal Tumors (drug therapy, pathology)
  • Humans
  • Imatinib Mesylate
  • Liver Neoplasms (drug therapy, secondary)
  • Piperazines (administration & dosage, adverse effects)
  • Protein Kinase Inhibitors (adverse effects)
  • Protein-Tyrosine Kinases (antagonists & inhibitors)
  • Pyrimidines (administration & dosage, adverse effects)

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