A Rare Case of a Solitary Fibrous Tumor in a Child, Presenting as a Congenital Mass, Displaying <i>NAB2ex4::STAT6ex2</i> Gene Fusion with an Incidental Ganglioneuroblastoma.

Rao, Vidya; Rekhi, Bharat; Abraham, Latha K; Bapat, Prachi

A Rare Case of a Solitary Fibrous Tumor in a Child, Presenting as a Congenital Mass, Displaying NAB2ex4::STAT6ex2 Gene Fusion with an Incidental Ganglioneuroblastoma.

Rao, Vidya; Rekhi, Bharat; Abraham, Latha K; Bapat, Prachi.

Afiliação

Rao V; Department of Surgical Pathology, Tata Memorial Hospital (TMH), Narayana Health, Bengaluru, India.
Rekhi B; Department of Surgical Pathology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI) University, Parel, Mumbai, Maharashtra, India.
Abraham LK; Division of Molecular Pathology and Translational Medicine, Tata Memorial Hospital (TMH), Homi Bhabha National Institute (HBNI) University, Parel, Mumbai, Maharashtra, India.
Bapat P; Department of Pathology, Rajagiri Hospital, Aluva, Kerala, India.

Int J Surg Pathol ; 31(3): 321-331, 2023 May.

Article em En | MEDLINE | ID: mdl-35711164

Assuntos

Ganglioneuroblastoma; Tumores Fibrosos Solitários; Humanos; Masculino; Criança; Lactente; Ganglioneuroblastoma/genética; Tumores Fibrosos Solitários/patologia; Fusão Gênica; Éxons

Palavras-chave

NAB2::STAT6; STAT6; Solitary fibrous tumor; pediatric soft tissue tumors; rare tumors; sarcoma

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ganglioneuroblastoma / Tumores Fibrosos Solitários Limite: Child / Humans / Infant / Male Idioma: En Revista: Int J Surg Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Índia

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