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Rapidly involuting congenital hemangioma associated with profound, transient thrombocytopenia.
Rangwala, Sophia; Wysong, Ashley; Tollefson, Megha M; Khuu, Phuong; Benjamin, Latanya T; Bruckner, Anna L.
Afiliación
  • Rangwala S; Baylor College of Medicine, Houston, TexasDepartment of Dermatology, School of Medicine, Stanford University, Palo Alto, CaliforniaDepartment of Pediatrics, School of Medicine, Stanford University, Palo Alto, CaliforniaDepartment of Dermatology, Mayo Clinic, Rochester, MinnesotaDepartments of Dermatology and Pediatrics, School of Medicine, University of Colorado, Denver, Colorado.
Pediatr Dermatol ; 31(3): 402-4, 2014.
Article en En | MEDLINE | ID: mdl-22937785
Rapidly involuting congenital hemangioma (RICH) is an uncommon, often high-flow vascular tumor that presents at birth and involutes within the first year of life. It is clinically and histologically distinct from infantile hemangioma, kaposiform hemangioendothelioma, and tufted angioma, the latter two being associated with Kasabach-Merritt phenomenon. We present a female infant with RICH and profound, transient thrombocytopenia and review the extent and clinical course of thrombocytopenia in the context of congenital vascular tumors.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sarcoma de Kaposi / Neoplasias Cutáneas / Trombocitopenia / Neoplasias Vasculares / Síndrome de Kasabach-Merritt / Hemangioendotelioma / Hemangioma Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Newborn Idioma: En Revista: Pediatr Dermatol Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sarcoma de Kaposi / Neoplasias Cutáneas / Trombocitopenia / Neoplasias Vasculares / Síndrome de Kasabach-Merritt / Hemangioendotelioma / Hemangioma Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Newborn Idioma: En Revista: Pediatr Dermatol Año: 2014 Tipo del documento: Article