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Sirolimus for Kaposiform Hemangioendothelioma and Kasabach-Merritt Phenomenon in a Neonate.
Cabrera, Trevor B; Speer, Allison L; Greives, Matthew R; Goff, Donna A; Menon, Neethu M; Reynolds, Eric W.
Afiliación
  • Cabrera TB; Department of Pediatrics, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
  • Speer AL; Department of Pediatric Surgery, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
  • Greives MR; Department of Pediatric Plastic Surgery, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
  • Goff DA; Department of Pediatric Cardiology, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
  • Menon NM; Department of Pediatric Hematology, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
  • Reynolds EW; Department of Neonatal/Perinatal Medicine, University of Texas Health Science Center at Houston/McGovern Medical School, Houston, Texas.
AJP Rep ; 10(4): e390-e394, 2020 Oct.
Article en En | MEDLINE | ID: mdl-33214934
ABSTRACT
We present a case of a neonate born with kaposiform hemangioendothelioma (KHE), complicated by Kasabach-Merritt phenomenon (KMP) and other serious conditions, who was successfully treated with sirolimus. In addition to complications from thrombocytopenia and fluid overload, during the course of therapy, our patient experienced supratherapeutic drug levels at the commonly accepted starting dose of sirolimus. Patients with KHE and KMP should be closely monitored for potential complications of both the initial disease and unexpected side effects of treatments.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: AJP Rep Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: AJP Rep Año: 2020 Tipo del documento: Article
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