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Poorly Differentiated Chordoma of the Clivus With Loss of SMARCB1 Expression in a Pediatric Patient: A Case Report.
Yasue, Shiho; Ozeki, Michio; Endo, Saori; Kanayama, Tomohiro; Suzui, Natsuko; Nakamura, Sayaka; Kishimoto, Kenji; Kosaka, Yoshiyuki; Miyazaki, Tatsuhiko; Demizu, Yusuke; Soejima, Toshinori; Kawamura, Atsufumi; Ohnishi, Hidenori.
Afiliação
  • Yasue S; Department of Pediatrics, Gifu University Graduate School of Medicine.
  • Ozeki M; Department of Pediatrics, Gifu University Graduate School of Medicine.
  • Endo S; Department of Pediatrics, Gifu University Graduate School of Medicine.
  • Kanayama T; Department of Pathology, Gifu University Hospital, Gifu.
  • Suzui N; Department of Pathology, Gifu University Hospital, Gifu.
  • Nakamura S; Depertment of Hematology and Oncology, Children's Cancer Center.
  • Kishimoto K; Depertment of Hematology and Oncology, Children's Cancer Center.
  • Kosaka Y; Depertment of Hematology and Oncology, Children's Cancer Center.
  • Miyazaki T; Department of Pathology, Gifu University Hospital, Gifu.
  • Demizu Y; Department of Radiation Oncology, Hyogo Ion Beam Medical Center Kobe Proton Center, Kobe, Japan.
  • Soejima T; Department of Radiation Oncology, Hyogo Ion Beam Medical Center Kobe Proton Center, Kobe, Japan.
  • Kawamura A; Depertment of Neurosurgery, Childhood Cancer Medical Center, Hyogo Prefectural Kobe Children's Hospital.
  • Ohnishi H; Department of Pediatrics, Gifu University Graduate School of Medicine.
J Pediatr Hematol Oncol ; 44(8): 465-470, 2022 11 01.
Article em En | MEDLINE | ID: mdl-35091519
Poorly differentiated chordoma (PDC) is a rare, aggressive subtype of chordoma. A two-year-old girl presented with cervical pain, limb paralysis and respiratory failure. Magnetic resonance imaging and positron emission tomography-computed tomography revealed a tumor compressing the pons at the clivus and osteoblastic metastatic lesions of the left upper arm and right iliac bone. Her tumors shrank substantially after treatment with chemotherapy and proton beam therapy. Our initial diagnosis was an atypical teratoma/rhabdoid tumor, but final diagnosis of PDC was made on the basis of the immunohistochemical expression of brachyury. In addition, the detection of SMARCB1/INI1 mutation confirmed the diagnosis of PDC.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teratoma / Cordoma / Tumor Rabdoide / Neuroblastoma Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Female / Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teratoma / Cordoma / Tumor Rabdoide / Neuroblastoma Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Female / Humans Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article