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Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur.
Qiu, Tong; Lan, Yuru; Zhou, Jiangyuan; Yang, Kaiying; Gong, Xue; Zhang, Zixin; Chen, Siyuan; Ji, Yi.
Afiliação
  • Qiu T; Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
  • Lan Y; Med-X Center for Informatics, Sichuan University, Chengdu, China.
  • Zhou J; Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
  • Yang K; Med-X Center for Informatics, Sichuan University, Chengdu, China.
  • Gong X; Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
  • Zhang Z; Med-X Center for Informatics, Sichuan University, Chengdu, China.
  • Chen S; Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
  • Ji Y; Med-X Center for Informatics, Sichuan University, Chengdu, China.
Front Pediatr ; 10: 995340, 2022.
Article em En | MEDLINE | ID: mdl-36405826
Kaposiform hemangioendothelioma (KHE) is a rare borderline vascular tumor that usually presents as a mass of skin or deep soft tissue. We report a unique case of an 8-year-old KHE patient with bilateral symmetrical sites involving both femurs. The laboratory, radiographic, and pathological findings of the patient were minutely described. During the 6-month follow-up, the symptoms of pain and dysfunction of this patient were relieved. This study aimed to arouse clinicians' concern about the symmetrical sites of KHE patients.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China