Papas Theofanis T, Georgiadis George S, Maltezos Chrysostomos K, Lazarides Miltos K
Department of Vascular Surgery, Demokritos University Hospital, Alexandroupolis, Greece.
Wien Klin Wochenschr. 2007;119(5-6):186-8. doi: 10.1007/s00508-007-0772-9.
Adventitial cystic disease (ACD) is an uncommon and rare vascular entity characterized by a highly viscous and mucinous cyst located in the adventitia of an artery. Although first described in the external iliac artery, the disease is more frequently sited in the popliteal artery. ACD characteristically occurs in young adults, mostly male, with intermittent claudication as the initial presenting symptom. As the cyst enlarges, it leads to vascular compression with stenosis or occlusion. Because cystic formation of the popliteal artery is uncommon, the disease is often unrecognized. We report a case of popliteal artery ACD in a 54-year-old woman who was successfully treated surgically.
外膜囊肿性疾病(ACD)是一种罕见的血管病变,其特征是动脉外膜存在高度黏稠的黏液性囊肿。尽管该病最初是在髂外动脉中被描述,但更常见于腘动脉。ACD典型地发生于年轻人,以男性居多,首发症状为间歇性跛行。随着囊肿增大,会导致血管受压,出现狭窄或闭塞。由于腘动脉的囊性形成并不常见,该病常常未被识别。我们报告一例54岁女性腘动脉ACD患者,其经手术成功治疗。