Kaposiform Hemangioendothelioma Presenting as Hydrops Fetalis

被引：4

作者：

Sobrino-Fernandez, Elena ^{[1
]}

Campos-Dominguez, Minia ^{[2
]}

Gregorio-Hernandez, Rebeca ^{[1
]}

Huerta-Aragones, Jorge ^{[3
]}

Belendez-Bieler, Cristina ^{[3
]}

Lancharro-Zapata, Angel ^{[4
]}

Luisa Franco-Fernandez, Maria ^{[1
]}

Bernardo-Atienza, Belen ^{[1
]}

Sanchez-Luna, Manuel ^{[1
]}

机构：

[1] Hosp Gen Univ Gregorio Maranon, Sect Neonatol, Dept Pediat, Madrid, Spain

[2] Hosp Gen Univ Gregorio Maranon, Dept Dermatol, C Doctor Esquerdo 46, Madrid 28007, Spain

[3] Hosp Gen Univ Gregorio Maranon, Dept Pediat, Sect Pediat Oncol, Madrid, Spain

[4] Hosp Gen Univ Gregorio Maranon, Dept Radiol, Sect Pediat Radiol, Madrid, Spain

来源：

PEDIATRIC DERMATOLOGY | 2017年 / 34卷 / 03期

关键词：

D O I：

10.1111/pde.13101

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

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.

引用

页码：E128 / E129

页数：2

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