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국소형 췌소도세포증(Nesidioblastosis) 1예
강봉수(Bong Su Kang),강성일(Sung Il Kang),구혜영(Hye Young Koo),이성배(Sung Bae Lee),강혜윤(Hye Yun Kang),박석원(Seok-Won Park),정철운(Chul-Woon Chung) 한국간담췌외과학회 2008 한국간담췌외과학회지 Vol.12 No.4
Nesidioblastosis is a rare disorder, and it usually considered as a cause of neonatal hyperinsulinemic hypoglycemia. A 35 year-old-woman with hyperinsulinemic hypoglycemia was admitted in an unconscious condition. Abdominal CT, pancreas MRI and celiac angiography with an intra-arterial calcium stimulation test revealed a suspicious insulin-producing tumorous lesion in the head of pancreas. The patient underwent enucleation of the pancreas head tumor under the initial diagnosis of insulinoma. However, the tumor was confirmed histologically as nesidioblastosis that showed ductoendocrine proliferations and numerous small endocrine cell groups. Nesidioblastosis is classified into a focal type and a diffuse type, which are characterized by different clinical outcomes. The patient in our case showed a normal blood glucose level after operation, which is often the case for the focal type. Herein, we report this very rare case of adult nesiodioblastosis that was successfully treated by surgical resection.
일란성 쌍태 중 일측 태아의 인어체기형 (Sirenomelia)
정상근 ( Jeong Sang Geun ),김현철 ( Kim Hyeon Cheol ),김유신 ( Kim Yu Sin ),김윤아 ( Kim Yun A ),김조영 ( Kim Jo Yeong ),김지연 ( Kim Ji Yeon ),신승주 ( Sin Seung Ju ),김낙근 ( Kim Nag Geun ),강혜윤 ( Kang Hye Yun ),박정선 ( Park 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.4
Sirenomelia is a lethal congenital malformation characterized by single or fused lower limbs associated with other severe genitourinary and lower gastrointestinal tract anomalies. Associated anomalies include malformation of vertebrae and pelvis, oligohyd
조상호,홍천수,박중원,고원기,윤영연,강혜윤 대한알레르기학회 1999 천식 및 알레르기 Vol.19 No.3
Episodic angioedema with eosinophilia was described by Gleich, et al. as a distinct entity characterized by recurrent angioedema, urticaria, leukocytoeis with remarkable eosinophilia, fever and periadically increased body weight. Since then, several cases of this disorder have been reported in the United States, Europe and Japan. We present a Korean patient whose clinical, histopathologic, and laboratory findings are consistent with the syndrome of episodic angioedema with eosinophilia. This case supports the previous study that revealed some differences between Asian and Caucasian patients.