• Tuberculosis and Respiratory Diseases
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• 제57권2호
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• pp.188-192
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• 2004

폐동맥만을 침범한 타카야수 동맥염은 매우 드물고 폐혈전증과 동반되어 갑상선기능항진증으로 증상이 악화된 경우를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Tuberculosis and Respiratory Diseases
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• 제43권2호
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• pp.267-273
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• 1996

저자들은 최근 다발성 폐동맥 폐쇄를 동반한 Takayasu 동맥염 1예을 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Tuberculosis and Respiratory Diseases
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• 제56권6호
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• pp.677-682
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• 2004

저자들은 타카야수동맥염에 전형적인 맥박 감소, 사지 혈압의 차이, 사지 파행 등의 증상 없이 기침, 흉통, 객혈과 체중 감소의 호흡기 증상과 전신증상을 주소로 내원한 17세 남자 환자에서 진찰소견과 폐혈관조영술을 통해 폐동맥염을 확인하고, 대동맥조영술을 통해 쇄골하동맥과 온목동맥의 협착을 관찰하여 타카야수동맥염으로 진단한 증례를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제19권4호
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• pp.688-694
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• 1986

Takayasu`s disease is an arteritis of unknown etiology involving larger elastic arteries such as aorta and its branches, pulmonary arteries and rarely coronary arteries. Especially, aortic root involvement with the valvular leaflets has been reported in several cases of Takayasu`s arteritis. Recently we have experienced one case of Takayasu`s arteritis involving left subclavian artery, descending aorta, left renal artery and multiple valvular leaflets. The patient was 33 year-old female and admitted with complaints of cough, dyspnea and general weakness. Aortogram revealed extensive type of arteritis showing dilatation of ascending aorta, segmental narrowing of thoracic aorta and Riolan`s anastomosis. Double valve replacement [mitral and aortic valve] and tricuspid valve annuloplasty were performed. The patient made an excellent postoperative recovery and has shown striking improvement in cardiac status, NYHA functional class II eight months after operation.

• Journal of Chest Surgery
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• 제19권3호
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• pp.489-493
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• 1986

Takayasu`s arteritis is an arteritis of unknown etiology involving larger elastic arteries such as aorta and its branches, pulmonary arteries, and rarely coronary arteries. The late pathologic feature is vascular obstructive change and the resulting clinical manifestations are local ischemic symptoms such as syncope, visual disturbance, claudication of extremities, hypertension, and angina. the disease occurs predominantly in females, with the age of onset between 10 and 30 years. Recently we have experienced one case of Takayasu`s arteritis involving aortic arch and all its major branches. The patient was 36 year-old female and she was admitted because of headache, blurred vision, and easy fatigability and motor weakness of upper extremities. Aortogram revealed total obstruction of both carotid arteries at the site of its origin and partial irregular obstructive change in the innominate artery and both subclavian arteries. Bypass graft surgery using Gore-Tex grafts was performed with successful result.

• Tuberculosis and Respiratory Diseases
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• 제48권6호
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• pp.964-972
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• 2000

저자들은 타카야수동맥염에 의한 만성 폐고혈압 환자 3예를 대상으로 혈관확장제 (NO 및 molsidomine)가 이들의 폐고혈압을 완화시킬 수도 있음을 관찰하였으며, 이와 관련하여 보다 많은 연구가 이루어져야 하리라 생각된다.

• Journal of Chest Surgery
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• 제23권2호
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• pp.402-406
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• 1990

Recently we have experienced a case of Takayasu’s arteritis involving both common carotid artery, left subclavian artery, left renal artery, and the right pulmonary artery. The patients was 27 year-old female and she was admitted because of neck pain, dizziness and palpitation. Renal artery angioplasty with Griintzig balloon catheter was performed with successful result. And then bypass graft surgery using bifurcated Gore- Text graft was performed with satisfactory result.

• 대한핵의학회지
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• 제20권2호
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• pp.73-78
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• 1986

Of 18 patients with Takayasu's arteritis who underwent $^{99m}Tc-MAA$ (macroaggregated albumin) perfusion luing scanning, 9 (50%) showed perfusion defects. Chest X-rays of them were nonspecific. One patient underwent $^{99m}Tc-DTPA$ radio aerosol inhalation lung scanning simultaneously, which revealed normal. So routine screening radioisotope perfusion lung scanning is helpful to evaluate pulmonary arterial involnmement in Takayasu's arteritis patients. And Takayasu's arteritis should be included in differential diagnosis of pulmonary embolism.

• Clinical and Experimental Pediatrics
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• 제59권sup1호
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• pp.145-148
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• 2016

Takayasu arteritis (TA) is a chronic inflammatory disease of unknown etiology that affects mainly the aorta, main aortic branches, and pulmonary arteries. Diverse neurological manifestations of TA have rarely been reported in children. Posterior reversible encephalopathy syndrome (PRES) is a neuroradiological condition that presents with headache, seizure, visual disturbances, and characteristic lesions on imaging. Inflammatory condition and severe hypertension in TA can cause PRES. We report of a 5-year-old girl with presumed TA who presented with PRES and chronic total occlusion in the renal artery. The findings on magnetic resonance imaging suggested PRES. Left nephrectomy was performed for total occlusion of the left renal artery, and the confirmatory diagnosis of TA was based on the pathologic findings of the renal artery.

• Childhood Kidney Diseases
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• 제6권1호
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• pp.114-119
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• 2002

다카야스 동맥염은 주로 대동맥과 대동맥의 주분지를 침범하는 만성 혈관염으로 자가면역질환의 일종으로 생각되며 우리나라에서는 결핵과 관련된 예 들이 주로 보고되어 있다 저자들은 특발성으로 대동맥과 그의 주분지들을 모두 침범하여 심한 허혈성 증상과 상지의 무맥현상을 보였던 중증의 다카야스 동맥염 1례를 진단하고 스테로이드와 세포독성약제의 병합요법으로 치료하여 증상의 관해를 경험하였기에 문헌고찰과 함께 보고하는 바이다.