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Hepatoblastoma Arising in a Pigmented ß-catenin-activated Hepatocellular Adenoma: Case Report and Review of the Literature.
Louie, Christine Y; Concepcion, Waldo; Park, Joseph K; Rangaswami, Arun; Finegold, Milton J; Hazard, Florette K.
Afiliação
  • Louie CY; Departments of *Pathology †Surgery ‡Pediatrics, Stanford University School of Medicine, Stanford, CA Departments of §Pathology ∥Immunology and Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX.
Am J Surg Pathol ; 40(7): 998-1003, 2016 07.
Article em En | MEDLINE | ID: mdl-27096257
ABSTRACT
Hepatoblastoma is the most common malignant liver tumor in childhood. It has been associated with a variety of constitutional syndromes and gene mutations. However, there are very few reports of associations with pediatric hepatocellular adenomas (HCAs) and no reported associations with pigmented HCAs (P-HCAs). We present a unique case of hepatoblastoma arising in a background of 2 ß-catenin-activated HCAs, one of which is pigmented, in a 4-year-old child. The gross, histologic, and immunohistochemical features are described for each tumor. In addition, the literature is reviewed with specific emphasis on the clinical and pathologic features of B-HCAs. Although the potential of ß-catenin-activated HCAs to progress to hepatocellular carcinoma has been well documented, there are very few reports of their potential to progress to hepatoblastoma. We not only present such a case, but, to our knowledge, we also present the first case of a P-HCA in a child.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatoblastoma / Adenoma de Células Hepáticas / Neoplasias Hepáticas / Neoplasias Primárias Múltiplas Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatoblastoma / Adenoma de Células Hepáticas / Neoplasias Hepáticas / Neoplasias Primárias Múltiplas Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article