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단백질 C와 S 결핍증 환자에서 발생한 자발성 신동맥 박리
임예지 ( Ye Jee Lim ),이래석 ( Rae Seok Lee ),유현아 ( Hyun Ah Yu ),장경윤 ( Kyung Yoon Chang ),서재현 ( Jae Hyun Seo ),이관현 ( Kwan Hyun Lee ),황대연 ( Dae Yeon Hwang ) 대한내과학회 2013 대한내과학회지 Vol.84 No.1
Spontaneous renal artery dissection without aortic dissection in normotensive patients is rarely reported. Spontaneous renal artery dissection is also an uncommon cause of renal infarction that occurs, though rarely, in patients with hypercoagulable states such as protein C and S deficiency. We report here a case of spontaneous renal artery dissection and renal infarction associated with protein C and S deficiency. (Korean J Med 2013;84:116-119)
즐례 : 대장내시경 시행 중 회장 삽관을 통해 우연히 발견된 무증상의 소장 림프종
김은희 ( Eun Hee Kim ),이래석 ( Rae Seok Lee ),허주연 ( Joo Yeun Hu ),최윤석 ( Yoon Seok Choi ),김교희 ( Gyo Hui Kim ),오정환 ( Jung Hwan Oh ),노상영 ( Sang Young Roh ) 대한내과학회 2014 대한내과학회지 Vol.86 No.1
Primary lymphoma of the small intestine is commonly diagnosed after serious complications, such as bowel perforation and bleeding. It results from vague symptoms and the lack of routine screening programs due to low prevalence. Ileal intubation can be used for screening and diagnosis of various small intestinal diseases. However, the value of routine terminal ileum intubation during colonoscopy remains controversial because of its low diagnostic yield. In Korea, there has been no report of asymptomatic primary lymphoma of the small intestine discovered through ileal intubation during colonoscopy. Thus, we report a case of asymptomatic primary lymphoma of the small intestine diagnosed incidentally through terminal ileum intubation during screening colonoscopy, and we review the literature on small intestinal lymphoma and the value of routine ileal intubation. (Korean J Med 2014;86:49-53)
김민재 ( Min Jae Kim ),최영 ( Young Choi ),윤건중 ( Gun Jung Youn ),이래석 ( Rae Seok Lee ),박종호 ( Jong Ho Park ),이주용 ( Jue Young Lee ),주연호 ( Yeon Ho Joo ),이윤복 ( Yun Bok Lee ) 대한췌장담도학회 2014 대한췌담도학회지 Vol.19 No.2
Extrahepatic bile duct can be compressed by right hepatic artery (RHA) and cause a variety of hepatobiliary symptoms. This condition is referred to as RHA syndrome. A 20-year-old man was admitted because of jaundice. No stones or tumor were visible on CT scan and endoscopic retrograde cholangiopancreatography. However, RHA was seen traversing and compressing the mid common bile duct (CBD) with resultant upstream dilatation. The patient was diagnosed with obstructive jaundice due to compression of the CBD by variant RHA originating from gastroduodenal artery. After separation and mobilization of the variant RHA, obstructive jaundice was resolved. Herein, we report a case of a variant form of RHA syndrome that was successfully managed by surgery.