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한국인에서 위상피하 종양의 유병률에 대한 연구: 단일기관 경험
이정훈 ( Jung Hoon Lee ),이항락 ( hang Lak Lee ),안영우 ( Yong Woo Ahn ),이강녕 ( Kang Nyeong Lee ),전대원 ( Dae Won Jun ),이오영 ( Oh Young Lee ),한동수 ( Dong Soo Han ),윤병철 ( Byung Chul Yoon ),최호순 ( Ho Soon Choi ) 대한소화기학회 2015 대한소화기학회지 Vol.66 No.5
Background/Aims: The incidental finding of gastrointestinal subepithelial tumors (SETs) is increasing with national cancer screening endoscopy. In a Swedish population, screening endoscopy found a prevalence of SETs of 0.36%. However, the prevalence of gastric SETs in Korean patients has not been described. Therefore, this study evaluated the prevalence of SETs of the stomach in a Korean patient population. Methods: We reviewed endoscopic reports of 11,712 subjects who underwent screening esophagogastroduodenoscopy (EGD) at Hanyang University Hospital between July 2012 and June 2013. Results: Among 11,712 patients, 194 (1.7%) had SET of the stomach. Of these, 71 (prevalence, 0.6%) were male and 123 (prevalence, 1.1%) were female. When grouped by age, the prevalence of SET was as follows: 1.0% for patients in their twenties, 6.2% for those in their thirties, 19.1% for those in their forties, 33.0% for those in their fifties, 30.4% for those in their sixties, and 10.3% for those over 70 years of age. Conclusions: The overall prevalence of gastric SET among healthy examinees was 1.7%. The prevalence of gastric SET increased with age and was higher in female. (Korean J Gastroenterol 2015;66:274-276)
이정훈 ( Jung Hoon Lee ),홍승표 ( Seung Pyo Hong ),고준권 ( Jun Kwon Ko ),이은영 ( Eun Young Lee ),이강록 ( Kang Lok Lee ),정승준 ( Sung Jun Chung ),구건우 ( Gun Woo Koo ),방소영 ( So Young Bang ),이혜순 ( Hye Soon Lee ) 대한류마티스학회 2015 대한류마티스학회지 Vol.22 No.4
피부비후뼈막증은 곤봉형 수지, 피부비후, 뼈막증을 특징으로 하는 일차성 비대성 뼈관절병증으로서 드문 유전질환이다. 미분류형 관절염으로 치료받고 있던 환자에서 발생한 양측 곤봉형 수지, 이마와 두피의 피부비후, 손과 발의 다한증 및 X선 검사에서 관찰되는 뼈막증 등의 소견으로 PDP로 진단받은 본 증례를 통하여 미분류형 관절염의 다양한 원인질환 중 하나로서 드물지만 PDP를 고려해야 할 것으로 생각된다. Pachydermoperiostosis (PDP) is a primary hypertrophic osteoarthropathy characterized by digital clubbing, pachydermia, and periostosis, which is inherited as an autosomal dominant or recessive trait. We report on a patient suffering from bilateral knee arthritis for 6 years who was newly diagnosed as PDP. PDP was confirmed by bilateral digital clubbing, hyperhidrosis, and cutis verticis gyrata, findings of pachydermatosis on the forehead and scalp, X-ray findings of proliferative periostitis. This case indicates that PDP is one of several possible rare diseases that should be considered in patients with undifferentiated arthritis. (J Rheum Dis 2015;22:256-259)