Kasabach-Merritt phenomenon: a single centre experience

Eur J Haematol. 2010 Feb 1;84(2):97-104. doi: 10.1111/j.1600-0609.2009.01370.x. Epub 2009 Nov 3.

Abstract

Objective: Kasabach-Merritt phenomenon (KMP) can lead to life-threatening bleeding, and its optimum treatment has not been established. We review the experience of managing KMP in a single institution.

Methods: A retrospective chart review on all children with KMP treated at the Hospital for Sick Children, Toronto, over an 18 yr period was carried out.

Results: All 15 patients had profound thrombocytopenia and hypofibrinogenemia at presentation, half had bleeding symptoms, and three had cardiac failure. All patients received corticosteroids. Five responded to steroids alone, given for an average of 13 wk, increasing platelets to >20 x 10(9)/L at a mean of 6.2 d and fibrinogen >1 g/dL at 25.6 d. Ten patients received at least one other therapeutic modality in addition to steroids, including vincristine, interferon, anti-platelet agents and pentoxifylline. Five patients received vincristine, for a mean of 6 wk, with two patients responding. Eight patients received interferon, for a mean of 4 months, with two patients responding. Overall, the mean time to increasing platelets >20 x 10(9)/L was 56 d, to >150 x 10(9)/L was 88 d and fibrinogen >1 g/dL 49 d. Ten patients showed a partial response to embolisation, with a mean of 2.8 procedures performed. Thrombotic complications occurred in 7%. Twelve patients remain alive, with relapse in six patients, all treated successfully. One patient died, and two patients have been lost to follow-up.

Conclusion: KMP is a rare condition, with significant morbidity and mortality. The therapeutic approach should include a multidisciplinary team and consensus on guidelines.

MeSH terms

  • Adrenal Cortex Hormones / administration & dosage*
  • Antineoplastic Agents, Phytogenic / administration & dosage
  • Female
  • Hematologic Diseases / blood
  • Hematologic Diseases / drug therapy*
  • Hematologic Diseases / mortality*
  • Humans
  • Infant
  • Infant, Newborn
  • Interferons / administration & dosage
  • Male
  • Pentoxifylline / administration & dosage
  • Platelet Aggregation Inhibitors / administration & dosage
  • Platelet Count
  • Retrospective Studies
  • Vincristine / administration & dosage

Substances

  • Adrenal Cortex Hormones
  • Antineoplastic Agents, Phytogenic
  • Platelet Aggregation Inhibitors
  • Vincristine
  • Interferons
  • Pentoxifylline