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Incidental Detection of a Rare Pediatric High-Grade Fibrosarcoma in a Post-traumatic Setting: The Conundrum of Intra-Abdominal Hematoma versus Neoplasia.
Khalaj, Kamand; Fattahi, Nikoo; Omo-Ogboi, Allen C; Thomas-Ogunniyi, Jaiyeola O; Ogunleye, Olanrewaju A; Khanal, Ashish; Kramer, Larry A.
Afiliação
  • Khalaj K; Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center, Houston, USA.
  • Fattahi N; Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center, Houston, USA.
  • Omo-Ogboi AC; Department of Pathology and Laboratory Medicine, University of Texas Health Science Center, Houston, USA.
  • Thomas-Ogunniyi JO; Department of Pathology and Laboratory Medicine, University of Texas Health Science Center, Houston, USA.
  • Ogunleye OA; Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center, Houston, USA.
  • Khanal A; Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center, Houston, USA.
  • Kramer LA; Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center, Houston, USA.
Case Rep Radiol ; 2023: 3178778, 2023.
Article em En | MEDLINE | ID: mdl-38089103
Infantile fibrosarcoma (IF) is a rare malignant fibroblastic tumor that affects infants and young children, occurring most commonly in the extremities. Here, we present a 14-year-old patient with an abdominal mass incidentally detected after a blunt injury to the abdomen. The initial trauma protocol CT revealed a high attenuation mesenteric lesion in the left central abdomen suggestive of mesenteric hematoma. However, the possibility of a solid neoplastic mass lesion could not be excluded. Further evaluation with dynamic contrast-enhanced serial MRI showed a progressive enhancing mass and excluded a hyperacute hematoma with active bleeding. The mass was resected, and histopathological examination and molecular analysis of tumor cells were consistent with a high-grade fibrosarcoma with KMT2D : BCOR fusion.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Radiol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Radiol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos