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A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia.
Coskun, Çagri; Aksu, Tekin; Gümrük, Fatma; Ünal, Sule.
Afiliación
  • Coskun Ç; Department of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
  • Aksu T; Department of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
  • Gümrük F; Department of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
  • Ünal S; Department of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Turk J Pediatr ; 65(1): 124-128, 2023.
Article en En | MEDLINE | ID: mdl-36866992
BACKGROUND: Klippel-Trenaunay syndrome (KTS) is an overgrowth syndrome associated with capillary/venous/ lymphatic malformations with limb hypertrophy and cancer risk. Various cancers, mostly Wilms tumor, have been reported in patients with KTS, but not leukemia. Chronic myeloid leukemia (CML) is also a rare disease in children, where there is no known disease or syndrome to predispose to CML. CASE: We report a case of CML incidentally diagnosed in a child with KTS when he was bleeding from surgery of the left groin for vascular malformation. CONCLUSIONS: This case reflects the variety of cancer types that may accompany KTS and provides information about CML prognosis in such patients.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Síndrome de Klippel-Trenaunay-Weber / Neoplasias Renales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Turk J Pediatr Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Síndrome de Klippel-Trenaunay-Weber / Neoplasias Renales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Turk J Pediatr Año: 2023 Tipo del documento: Article