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Pediatrics ; 150(5)2022 11 01.
Article in English | MEDLINE | ID: mdl-36193691

ABSTRACT

Kaposiform hemangioendothelioma is classified as a locally aggressive vascular tumor of childhood resulting from abnormal angiogenesis and lymphangiogenesis. Most commonly, KHE presents as a single tissue mass, ranging from an erythematous papule to a violaceous indurated tumor. Definitive diagnosis requires tissue sampling with the demonstration of ill-defined nodules and fascicles of spindle-shaped D2-40 positive endothelial cells, forming slit-like vascular channels. This newborn presented with multifocal cutaneous Kaposiform hemangioendothelioma associated with Kasabach-Merritt phenomenon confirmed on histopathology with immunostaining.


Subject(s)
Hemangioendothelioma , Kasabach-Merritt Syndrome , Sarcoma, Kaposi , Infant, Newborn , Humans , Kasabach-Merritt Syndrome/diagnosis , Kasabach-Merritt Syndrome/complications , Endothelial Cells , Hemangioendothelioma/diagnosis , Hemangioendothelioma/complications , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/complications
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