• Journal of Chest Surgery
• /
• 제48권1호
• /
• pp.70-73
• /
• 2015

Lower limb ischemia caused by multiple stenosis of the thoracoabdominal aorta is one of the rare clinical manifestations of Takayasu arteritis. The optimal management of such mid-aortic syndrome related with Takayasu arteritis has not been established to date. Here we report a case of extra-anatomic aortic bypass through minimally invasive techniques to treat lower limb ischemia caused by Takayasu arteritis.

• Journal of Chest Surgery
• /
• 제25권3호
• /
• pp.330-334
• /
• 1992

Takayasu`s arteritis is a non-specific arteritis involving the aorta and its major branches. Because of the complexity in the feature of vessel involvement, it represents various clinical presentations according to the sites of involvement. In general, the medical and the surgical treatment of this progressive disease are known to be unsatisfactory but the surgical treatment can provide symptomatic relief and prolong life in selected cases. Recently we experienced one case of Takayasu`s arteritis involving the aortic arch and its major branches. A 45 year-old male patient admitted with the complaints of dizziness, headache, visual disturbance and coldness of upper extremities. Ascending aortogram revealed total occlusion of innominate artery and near total occlusion of left common carotid artery at the site of origin of both vessels. Under the clinical diagnosis of Takayasu`s arteritis, aorto-bicarotid-right subclavian bypass was performed. Postoperative course was uneventful and most of symptoms were relieved except mild residual visual disturbance.

• Journal of Chest Surgery
• /
• 제34권11호
• /
• pp.870-874
• /
• 2001

Takayasu 동맥염은 만성 비특이성 동맥염으로 젊은 여자에 호발하며 대동맥궁의 분지 혈관이나 신동맥 등 여러 혈관들을 광범위하게 침범하여 폐쇄를 일으키는 질환으로 알려져 있다. 최근 나이가 많은 52세의 여자 환자에서 신동맥 이하의 복부 대동맥에만 국한적으로 침범하여 삭did(cord-like) 폐쇄를 일으킨 Takayasu 동맥염의 비교적 드문 예를 경험하고 18mm PTFE(polytetrafluoroethylene) 인조혈관을 이용하여 하행 흉부 대동맥과 총장골동맥 분기 직상부 복부 대동맥 사이에 측단 우회술을 시행하여 좋은 결과를 얻었기에 보고한다.

• Journal of Chest Surgery
• /
• 제19권4호
• /
• pp.688-694
• /
• 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
• /
• 제27권5호
• /
• pp.394-398
• /
• 1994

Takayasu`s arteritis is one of chronic inflammatory disease characteristically involving the aorta and it`s major branches. We experienced two surgical cases of Takayasu`s arteritis associated with the stenosis of the descending thoracic aorta. One case was 15 year-old girl and she was admitted because of dyspnea on exertion for 12 months. Aortogram showed the stenosis of the descending thoracic aorta from just below left subclavian artery to the 9th thoracic vetebra. The other case was 10 year-old girl and she was admitted because of URI and hypertension. Aortogram showed narrowing of right innominate artery, but developed collateral circulation, and the stenosis of the descending thoracic aorta near the 9th thoracic vertebra. In each case, bypass graft from the ascending aorta to the abdominal aorta just above the inferior mesenteric artery was performed with satisfactory result.

• Journal of Chest Surgery
• /
• 제34권12호
• /
• pp.944-947
• /
• 2001

Takayasu 동맥염에서 관상동맥의 침범은 비교적 드물게 나타나며 일단 동반되면 치명적이지만 외과적으로 교정될 수 있는 질환이다. 환자는 28세 여자로 내원 2개월 전부터 발생한 심계항진을 동반한 어지럼증 및 두통과 좌상지의 파행(claudication)을 주소로 내원하였다. 대동맥조영술 및 관상동맥조영술 시행 결과 양측 관상동맥 개구부 협착을 동반한 Takayasu 동맥염으로 진단되어 복재정맥을 이용한 첨포이식편(patch graft)으로 양측 관상동맥 개구부 성형술을 받은 후 별 다른 문제없이 퇴원하였다. 이에 문헌고찰과 함께 보고하는 바이다.

• 동의생리병리학회지
• /
• 제18권1호
• /
• pp.301-305
• /
• 2004

There were a few case reports on the treatment of Takayasu's arteritis. We had a good effect on one patient with Takayasu's arteritis by oriental medicine therapy. We use acupuncture, herbal acupuncture, electro-acupuncture, moxa, negative thrapy, kinesio taping therapy, physical therapy and exercise for 82 days. In this case, Left hemiparesis, dysarthria, pulseless, disturbances of urination, headache, dizziness improved after treatment. We experienced improvement in this symptoms of Takayasu's arteritis by oriental medicine treatment.

• Journal of Yeungnam Medical Science
• /
• 제1권1호
• /
• pp.145-151
• /
• 1984

Takayasu 동맥염은, 원인은 분명하지 않으나, 아마도 자가면역질환으로서, 초기 전신기와 후기 폐쇄기에 걸쳐 여려 다양한 증세를 초래할 수 있고, 진단은 대동맥 조영술에 의한 대동맥 및 분지의 협착을 관찰하는 것이 필수적이다.

• Journal of Chest Surgery
• /
• 제46권4호
• /
• pp.274-278
• /
• 2013

Background: Coronary involvement in Takayasu's arteritis is a rare but fatal disease. The aim of this study was to evaluate the early and mid-term results of Takayasu's arteritis patients who underwent coronary artery bypass grafting (CABG). Materials and Methods: Of 2,280 patients who underwent isolated CABG from January 1998 to June 2012, Takayasu's arteritis was identified in 5 patients. There were 3 female patients, and the mean age was $58{\pm}9$ years. Takayasu's arteritis was diagnosed during preoperative evaluation for coronary artery disease in 4 patients, and the initial manifestation was angina pectoris in 4 patients. All of the patients underwent anaortic off-pump CABG (OPCAB) using the in situ left or right internal thoracic arteries (ITA); 3 patients had severe stenosis of the proximal left subclavian artery and the in situ right ITA was used instead. Medical treatment for inflammatory arteritis during the perioperative and follow-up period was performed if indicated. Early, 1-year, and 5-year angiographic results and clinical outcomes were analyzed. Results: There was no surgical mortality, and all of the patients were discharged without complications on postoperative $8{\pm}2$ days. Early postoperative (postoperative $2{\pm}1$ days) angiography demonstrated a graft patency of 100% (12 of 12 distal anastomoses). One-year ($13{\pm}3$ months) angiography was performed in 4 patients, and all of the grafts were patent (100%, 9 of 9 distal anastomoses). Conclusion: By performing anaortic OPCAB in patients with Takayasu's arteritis, we were able to avoid complications associated with manipulating an atherosclerotic and severely calcified ascending aorta. The early and mid-term graft patency of OPCAB in Takayasu's arteritis was maintained when concomitant with medical treatment.

• Clinical and Experimental Pediatrics
• /
• 제55권7호
• /
• pp.254-258
• /
• 2012

Takayasu arteritis is a chronic inflammatory disease of unknown etiology primarily affecting the aorta and its major branches and usually occurring in the second or third decade of life. Here, we report a case of Takayasu arteritis in a 10-month-old patient. The infant presented with signs of congestive heart failure and severe aortic regurgitation. Echocardiography and computed tomography angiography showed an abnormally dilated thoracic and abdominal aorta. The infant was initially treated with prednisolone, followed by commissuroplasty of the aortic valve but neither approach ameliorated the heart failure. The patient was eventually treated with a mechanical aortic valve replacement surgery at the age of 12 months, and her condition stabilized. Although unusual, this case indicates that the diagnosis of Takayasu arteritis should be considered in children with unexplained systemic symptoms, aortic valve regurgitation, and heart failure. Because severe aortic regurgitation may be a fatal complication of Takayasu arteritis, early aortic valve replacement surgery should be considered, even in very young children.