Kaposiform hemangioendothelioma associated with nonimmune fetal hydrops.

Abstract:

:We describe the case of a 31-week fetus who died in utero with an invasive retroperitoneal kaposiform hemangioendothelioma. This rare vascular neoplasm usually presents as a localized violaceous skin lesion in infants and behaves in a benign fashion; however, kaposiform hemangioendothelioma may present as an invasive neoplasm of the chest or abdominal cavity, where it can lead to the Kasabach-Merritt syndrome, which consists of thrombocytopenia, consumptive coagulopathy, and microangiopathic anemia in association with a vascular anomaly. The case we describe is unique in that the tumor presented in utero and led to intrauterine nonimmune fetal hydrops. Kaposiform hemangioendothelioma has been described in utero; however, to our knowledge, intrauterine fetal death as a direct consequence has not been reported previously in the literature.

journal_name

Arch Pathol Lab Med

authors

Martinez AE,Robinson MJ,Alexis JB

doi

10.1043/1543-2165(2004)128<678:KHAWNF>2.0.CO;2

subject

Has Abstract

pub_date

2004-06-01 00:00:00

pages

678-81

issue

6

eissn

0003-9985

issn

1543-2165

pii

CR3094

journal_volume

128

pub_type

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