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Bullous Kaposiform Hemangioendothelioma Masquerading as Aplasia Cutis Congenita.
Steen, Aaron J; Shin, Joseph H; Pace, Nicole C; Edgar, Mark; Clay, Michael R; Linos, Konstantinos; Barton, Dorothea T; Mann, Julianne A.
Afiliação
  • Steen AJ; Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
  • Shin JH; Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
  • Pace NC; Department of Surgery, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Edgar M; Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
  • Clay MR; Division of Dermatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Linos K; Department of Pathology, Emory University Hospital, Atlanta, Georgia.
  • Barton DT; Department of Pathology, Emory University Hospital, Atlanta, Georgia.
  • Mann JA; Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
Pediatr Dermatol ; 33(5): e267-9, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27339319
ABSTRACT
We present the case of a male infant with violaceous bullae on the scalp that were initially thought to be bullous aplasia cutis but at 3 months of age were diagnosed as a kaposiform hemangioendothelioma. This diagnosis should be considered when evaluating newborns with bullous plaques on the scalp that do not heal in the first 2-3 weeks of life. Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor that typically presents as a violaceous to purpuric plaque at birth or early infancy. It may be associated with Kasabach-Merritt phenomenon (KMP), a potentially life-threatening consumptive coagulopathy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Kaposi / Couro Cabeludo / Displasia Ectodérmica / Síndrome de Kasabach-Merritt / Hemangioendotelioma Tipo de estudo: Diagnostic_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Kaposi / Couro Cabeludo / Displasia Ectodérmica / Síndrome de Kasabach-Merritt / Hemangioendotelioma Tipo de estudo: Diagnostic_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article