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복부 대동맥 가동맥류를 동반한 Bechet씨병 : 4예 4 case report
문인성,박장상,고용복,박삼곤 대한혈관외과학회 1994 Vascular Specialist International Vol.10 No.1
Behgets disease is a multisystemic disorder characterized by vasculitis. The clinical triad of relapsing uveitis with recurrent oral and genital ulceration was descibed by Hulusi Behget, a Turkish dermatologist, in 1937. It's etiology remains unknown. Later, it was realized that there may be some other systemic manifestation of the disease at the time of diagnosis, including vascular lesions, central nervous system involvement, arthritis, pulmonary and gastrointestinal involvement. Behqets disease may also begin with the manifestation of vascular involvement instead of the classical triad of symptoms. Behcets disease is of interest to not only dermatologists and ophthalmologists but also to physicians of virtually every other specialty because it is a systemic disease that spares no organ in the body. Although vascular lesions are not listed among the criteria for diagnosis of Behqets disease, up to 25-35% of patients develop vascular complications and probably an even greater proportion of patient may have small vessel vasculitis as the pathological basis of systemic manifestation. Here, we report 4 cases of Behqet disease, involuing dbdominal aorta and its main branches with review of literature.