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Neonatal kaposiform hemangioendothelioma of the spleen associated with Kasabach-Merritt phenomenon.

Abstract：

:Kaposiform hemangioendothelioma is a rare locally aggressive vascular tumor that usually manifests during early childhood. Typically the lesion presents with skin, soft tissue and bone involvement and is characterized histologically by ill-defined nodularity and the presence of spindle cells with resemblance to Kaposi's sarcoma. We report a rare neonatal case of a splenic kaposiform hemangioendothelioma associated with Kasabach-Merritt phenomenon that was diagnosed with radiographic imaging. Because of the rapid onset of thrombocytopenia and anemia, the patient required urgent splenectomy with subsequent resolution of the blood dyscrasias.

journal_name

J Pediatr Surg

journal_title

Journal of pediatric surgery

authors

Shabtaie SA,Wang B,Owyong M,Ruiz-Mesa C,Corrales-Medina FF,Rojas CP,Infante JC,Neville HL,Perez EA,Sola JE,Hogan AR

doi

10.1016/j.jpedsurg.2016.03.014

subject

Has Abstract

pub_date

2016-06-01 00:00:00

pages

1047-50

issue

6

eissn

0022-3468

issn

1531-5037

pii

S0022-3468(16)30008-2

journal_volume

51

pub_type

杂志文章

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