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一名患有克-特综合征患者的腘窝淋巴结血管肌性错构瘤:病例报告

Angiomyomatous hamartoma of the popliteal lymph nodes in a patient with Klippel-Trenaunay syndrome: case report.

作者信息

Prusac Ivana Kuzmic, Juric Ivo, Lamovec Janez, Culic Vida

机构信息

Department of Pathology, Clinical Hospital Split Centre, Split, Croatia.

出版信息

Fetal Pediatr Pathol. 2011;30(5):320-4. doi: 10.3109/15513815.2011.572962. Epub 2011 May 24.

Abstract

We present a case of angiomyomatous hamartoma (AMH) in the popliteal region of a patient with Klippel-Trenaunay syndrome. A 14-year-old boy with a right popliteal mass and recurrent edema of the right leg was admitted to a local hospital where a diagnosis of Klippel-Trenaunay syndrome was made. Three lymph nodes in the right popliteal fossa were removed. Histopathologic examination showed angiomyomatous hamartomas. Postoperatively, the patient was followed for 6 years. He had occasional mild edema of the right leg, but no signs of inflammation or recurrence of the angiomyomas. Our case is the first reported case of angiomyomatous hamartoma in a patient with Klippel-Trenaunay (KT) syndrome.

摘要

我们报告1例患有Klippel-Trenaunay综合征患者腘窝区域的血管肌性错构瘤(AMH)。一名14岁男孩因右腘窝肿物及右腿反复水肿入住当地医院,诊断为Klippel-Trenaunay综合征。切除了右腘窝的3个淋巴结。组织病理学检查显示为血管肌性错构瘤。术后对患者随访6年。他偶尔有右腿轻度水肿,但无炎症迹象或血管肌瘤复发。我们的病例是首例报道的患有Klippel-Trenaunay(KT)综合征患者的血管肌性错构瘤。

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