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[腹主动脉解剖显示高安氏病:几内亚的一个病例]

[Dissection of the abdominal aorta revealing Takayasu´s disease: about a case in Guinea].

作者信息

Sory Barry Ibrahima, Yaya Balde El Hadj, Abdoulaye Camara, Aly Samoura, Diarra Koivogui, Kokoulo Koivogui, Morlaye Soumaoro, Djibril Sylla, Bassirou Bah Mamadou, Mariame Beavogui, Dadhi Balde Mamadou, Mamady Conde

机构信息

Service de Cardiologie de l´Hôpital National Ignace Deen, Centre Hospitalier Universitaire de Conakry, Conakry, République de Guinée.

Service des Urgences Médico-Chirurgicales de l'Hôpital National Donka, Centre Hospitalier Universitaire de Conakry, Conakry, République de Guinée.

出版信息

Pan Afr Med J. 2020 Sep 8;37:34. doi: 10.11604/pamj.2020.37.34.21441. eCollection 2020.

Abstract

Takayasu´s disease (TD) is a chronic inflammatory arteriopathy affecting the aorta, its main branches and the pulmonary arteries. It was first described in 1908 by the Japanese ophthalmologist Mikito Takayasu. The study involved a 78-year-old patient with no known history of cardiovascular disease, admitted with abdominal pain, pain in the right lower limb when walking, insomnia. These symptoms had progressed over 1 year. Physical examination showed normal heart rate of 87 beats per minute without pathological noises, with absence of right pedal pulse, blood pressure 120/78 mmhg, free lungs, flexible abdomen, and a beating mass in the right iliac fossa whose auscultation showed continuous murmur. The remainder of the physical examination was normal. Abdominal CT angiography confirmed extensive aortic dissection at the abdominal aorta with synchronous opacification of both channels, thrombotic aneurysm of the primitive iliac arteries measuring 48mmx100mm on the right and 38mm x 90mm on the left, with no visible fissurization. We report a case abdominal aorta dissection associated with thrombus formation in the primary iliac arteries revealing Takayashu´s disease treated in the Department of Cardiology at the Ignace Deen National Hospital. The rate of abdominal aorta dissection in patients with Takayasu´s disease is rare. It is most often diagnosed in the occlusive phase. Prognosis depends on possible complications.

摘要

高安氏病(TD)是一种慢性炎症性动脉病,累及主动脉、其主要分支及肺动脉。1908年由日本眼科医生高安道仁首次描述。该研究涉及一名78岁患者,无已知心血管疾病史,因腹痛、行走时右下肢疼痛、失眠入院。这些症状已持续1年。体格检查显示心率正常,每分钟87次,无病理性杂音,右足背动脉搏动消失,血压120/78 mmHg,肺部正常,腹部柔软,右髂窝有一搏动性肿块,听诊显示连续性杂音。其余体格检查正常。腹部CT血管造影证实腹主动脉广泛夹层,双腔同步显影,原始髂动脉血栓性动脉瘤,右侧大小为48mm×100mm,左侧为38mm×90mm,未见破裂。我们报告一例腹主动脉夹层合并原发性髂动脉血栓形成,揭示在伊格纳西·迪恩国立医院心内科治疗的高安氏病。高安氏病患者腹主动脉夹层发生率罕见。最常在闭塞期诊断。预后取决于可能出现的并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/506e/7648487/f20ca0266309/PAMJ-37-34-g001.jpg

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