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건강한 젊은 남자에서의 자발성 신동맥 및 복강동맥 박리 1예
허종훈 ( Jong Hun Heo ),박건태 ( Geon Tae Park ),송준휘 ( Jun Whee Song ),임상우 ( Sang Woo Yim ),김정훈,조성 ( Sung Cho ),김성록 ( Sung Rok Kim ) 대한신장학회 2008 Kidney Research and Clinical Practice Vol.27 No.5
Spontaneous dissection of peripheral arteries unrelated to the aorta is rare. Cases reported in the literature have involved the renal arteries, the coronary arteries, the cerebral arteries, and visceral arteries, in order of incidence. There is no consensus yet on indications for medical or surgical therapeutic modality. As a consequence of the rarity of spontaneous dissection of peripheral arteries, its natural history has been poorly described. A healthy 37-year-old male with normotension was admitted with an acute onset of left flank pain. Physical examination turned out an unremarkable result. Right renal infarction and splenic infarction was diagnosed by abdominal computed tomography. A spiral CT angiogram and angiography showed dissection of main right renal artery and celiac artery with involvement of branches. One year later, he has remained well and normotensive without treatment. To our knowledge, this is the first case of spontaneous renal and celiac artery dissection in normotensive patient in Korea.
이진호 ( Jin Ho Lee ),허종훈 ( Jong Hun Heo ),권경아 ( Kyung A Kwon ),한대희 ( Dae Hui Han ),황종운 ( Jong Woon Hwang ),조성 ( Seong Cho ),김성록 ( Sung Rok Kim ) 대한내과학회 2009 대한내과학회지 Vol.76 No.2
Allopurinol is widely used to reduce serum uric acid levels and, generally, has mild side effects. Rarely, allopurinol hypersensitivity syndrome occurs and this consists of severe systemic skin lesions, fever, reduced kidney and liver function, and leukocytosis with eosinophilia. Extremely rarely, allopurinol-induced pure red cell aplasia is reported. We report a case of allopurinol hypersensitivity syndrome and pure red cell aplasia following allopurinol therapy for eight weeks and the disease response to steroid therapy in a patient with chronic renal insufficiency. (Korean J Med 76:220-224, 2009)