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.
克-特综合征（KTS）是一种复杂的血管畸形疾病，主要累及毛细血管、静脉和淋巴管异常，以及肢体肥大。本病例报告展示了一例非典型的KTS，其特征为一名6岁男性患者主要累及内脏并伴有异位骨化。该患儿接受了手术治疗，效果良好。
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