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Post-transplant gastric antral vascular ectasia after intra-venous busulfan regimen.

Abstract
Gastric antral vascular ectasia (GAVE) is an angiodysplastic disorder that causes gastric bleeding. GAVE can develop as a complication of hematopoietic stem cell transplantation (HSCT-GAVE), and it has been suggested that it may be associated with oral administration of busulfan. We report two cases of HSCT-GAVE after a conditioning regimen containing intra-venous busulfan (ivBu), not oral busulfan. The first case, a 42-year-old woman with blastic plasmacytoid dendritic cell neoplasm, underwent second allogeneic HSCT with conditioning regimen consisting of cyclophosphamide (120 mg/kg) and ivBu (12.8 mg/kg). HSCT-GAVE developed on day 84 post-transplant, and argon plasma coagulation (APC) was performed successfully. The second case, a 60-year-old woman with acute myelogenous leukemia, underwent allogeneic HSCT with the conditioning regimen consisting of ivBu (12.8 mg/kg) and fludarabine (150 mg/kg). She developed melena and was diagnosed with GAVE by endoscopy on day 145 post-transplant. Although complete hemostasis was not achieved despite four administrations of APCs, the melena spontaneously terminated on day 235 post-transplant. To our knowledge, this is the first report describing HSCT-GAVE after ivBU-based HSCT. Although there is no established therapy for HSCT-GAVE, APC may be an option for HSCT-GAVE.
AuthorsKuniyoshi Fukuda, Naoki Kurita, Tatsuhiro Sakamoto, Hidekazu Nishikii, Yasushi Okoshi, Masato Sugano, Shigeru Chiba
JournalInternational journal of hematology (Int J Hematol) Vol. 98 Issue 1 Pg. 135-8 (Jul 2013) ISSN: 1865-3774 [Electronic] Japan
PMID23632949 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Myeloablative Agonists
  • Busulfan
Topics
  • Adult
  • Argon Plasma Coagulation
  • Busulfan (administration & dosage, adverse effects, therapeutic use)
  • Female
  • Gastric Antral Vascular Ectasia (chemically induced, surgery)
  • Hematopoietic Stem Cell Transplantation (adverse effects)
  • Humans
  • Infusions, Intravenous
  • Middle Aged
  • Myeloablative Agonists (administration & dosage, adverse effects, therapeutic use)
  • Transplantation Conditioning (adverse effects)
  • Treatment Outcome

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