Kaposiform Hemangioendothelioma Presenting as Hydrops Fetalis.
Elena Sobrino-FernándezMinia Campos-DominguezRebeca Gregorio-HernándezJorge Huerta-AragonésCristina Beléndez-BielerÁngel Lancharro-ZapataMaría Luisa Franco-FernándezBelén Bernardo-AtienzaManuel Sánchez-LunaPublished in: Pediatric dermatology (2017)
We describe the case of a 33-week preterm infant who developed nonimmune hydrops fetalis secondary to a kaposiform hemangioendothelioma (KHE). The tumor was successfully treated with vincristine, prednisone, ticlopidine, and aspirin. KHE can be an unusual cause of hydrops fetalis; in such cases, diagnosis can be challenging since generalized edema can obscure KHE.