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기관지 내시경 하 조직 생검 중 대량 출혈을 일으킨 기관지 강 내 돌출된 결절모양의 혈관
채수엽 ( Chae Su Yeob ),유문빈 ( Yu Mun Bin ),강기훈 ( Kang Gi Hun ),이병수 ( Lee Byeong Su ),채은하 ( Chae Eun Ha ),주은현 ( Ju Eun Hyeon ),김명찬 ( Kim Myeong Chan ),조욱현 ( Jo Ug Hyeon ),오용열 ( O Yong Yeol ),이순일 ( Lee Sun 대한결핵 및 호흡기학회 2002 Tuberculosis and Respiratory Diseases Vol.53 No.2
서울 위생 병원 5일 금연 학교를 방문한 우리나라 흡연자의 특성 및 입원 금연 교육 프로그램의 효과
이병수 ( Byung Soo Lee ),강기훈 ( Ki Hoon Kang ),채은하 ( Eun Ha Chae ),김명찬 ( Myung Chan Kim ),정재일 ( Jae Il Jung ),장희종 ( Hee Jong Chang ),이상훈 ( Sang Hoon Lee ),조동식 ( Dong Sik Cho ),신재규 ( Jai Gyu Shin ),김휘정 ( H 대한결핵 및 호흡기학회 2004 Tuberculosis and Respiratory Diseases Vol.57 No.5
갑상선 기능항진증과 성장 호르몬 과분비를 동반한 비전형적인 McCune-Albright 증후군의 1예
유문빈,강기훈,이병수,채은하,김명찬,정재일,박순희,이효진,정석태 대한내분비학회 2003 Endocrinology and metabolism Vol.18 No.4
비전형적인 Mccune-Albright 증후군은 섬유성 골이형성증과 2개 이상의 내분비 계통 이상을 동반한 질환으로 저자들은 섬유성골 이형성증과 더불어 갑상선기능항진증과 성장호르몬의 과분비를 보이는 비전형적인 Mccune-Albright 증후군 1예를 경험하였기에 문헌고찰과 더불어 보고하는 바이다. McCune-Albright syndrome is characterized by polyostotic fibrous dysplasia, Cafe-au-lait pigmentation and precocious puberty or other endocrinopathy. It can be caused by substitution of His, Cys or Gly for Arg 201st amino acid of the Gs protein subunit. The case of a 32-year-old woman, with atypical McCune-Albright syndrome, is reported. She had no skin lesion or precocity puberty. The polyostotic fibrous dysplasia was examined by a simple radiological image and whole body scan. She developed hyperthyroidism, with a multinodular toxic goiter. No thyroid related autoantibodies were detected. The cause of hyperthyroidism was thought to be a non- autoimmune thyroid hyperfunction. The level of growth hormone was not suppressed by oral glucose load. After a bromocriptine suppression test, the level of growth hormone decreased. There was no mass in the pituitary gland on a sellar MRI. A case of atypical McCune-Albright syndrome, including hyperthyroidism and hypersecretion of growth hormone, is reported (J Kor SOC Endocrinol 18:426432, 2003).
재발성 정맥혈전증을 유발한 Antithrombin Ⅲ와 Protein C 복합 결핍증 1예
엄민섭,박연희,설재일,채수엽,유문빈,강기훈,이병수,채은하,박정식,정용환,안승혜,이효진 대한내과학회 2002 대한내과학회지 Vol.62 No.5
Primary venous thrombosis caused by deficiency or qualitative abnormality of antithrombin Ⅲ, protein C and protein S is usually inherited as an autosomal dominant trait. Usually, deep vein thrombosis or pulmonary thromboembolism is developed by such abnormalities, however, mesenteric vein thrombosis is rarely reported. A 27-year-old man with previous history of deep vein thrombosis underwent segmental resection of jejunum due to mesenteric vein thrombosis complicated by necrosis of jejunum. Postoperative investigation disclosed combined deficiency of antithrombin Ⅲ and protein C. His son also showed deficiency of antithrombin Ⅲ. Postoperatively, he is on life-long warfarin therapy without experiencing recurrence of venous thrombosis.