克-特综合征中主要的内脏受累及异位骨化

Predominant visceral involvement and heterotopic ossification in Klippel-Trenaunay syndrome.

作者信息

Yaynishet Yodit Abraham, Abera Michael Teklehaimanot, Hagos Kidist Amare, Aklilu Woubedel Kiflu, Abebe Nebyou Seyoum, Hailu Samuel Sisay

机构信息

Addis Ababa University, College of Health Sciences, Department of Radiology, Addis Ababa, Ethiopia.

Lancet Specialized Internal Medicine and Surgical Center, Addis Ababa, Ethiopia.

出版信息

Radiol Case Rep. 2025 Jan 15;20(4):1834-1839. doi: 10.1016/j.radcr.2024.12.053. eCollection 2025 Apr.

Klippel-Trenaunay Syndrome (KTS) is a complex vascular malformation disorder that primarily involves capillary, venous, and lymphatic anomalies, along with limb hypertrophy. This case report presents an atypical instance of KTS characterized by predominant visceral involvement and heterotopic ossification in a 6-year-old male patient. The child underwent surgical management with a favorable outcome.