| Literature DB >> 27342010 |
Samuel A Shabtaie1, Bo Wang1, Mark Owyong1, Catalina Ruiz-Mesa2, Fernando F Corrales-Medina2, Claudia P Rojas3, Juan C Infante4, Holly L Neville1, Eduardo A Perez1, Juan E Sola1, Anthony R Hogan5.
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.Entities:
Keywords: Kaposiform hemangioendothelioma; Kasabach-Merritt phenomenon; Neonatal kaposiform hemangioendothelioma; Splenic mass; Vascular tumor
Mesh:
Year: 2016 PMID: 27342010 DOI: 10.1016/j.jpedsurg.2016.03.014
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545