http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
십이지장에 발생한 Enteritis Cystica Profunda 1 예
정호경(Ho Kyeong Jeong),김진관(Jin Kwan Kim),황인석(In Seog Hwang),김미영(Mi Young Kim),김영묵(Yeong Muk Kim),이동윤(Dong Yun Lee),이준상(Joon Sang Lee) 대한소화기학회 2002 대한소화기학회지 Vol.39 No.1
Enteritis cystica profunda (ECP) is a very rare condition of the small intestine. It is characterized by mucin-filled cystic space and partially lined by nonneoplastic epithelium predominant in the submucosa of the small bowel. It has the identical histopathologic features to those of colitis cystica profunda (CCP), which is a rare benign lesion of the distal colon and rectum of uncertain cause. ECP appears to occur much less than CCP and all reported ECP was associated with intestinal disease, such as Peutz-Jeghers syndrome, Crohn`s disease, hamartomatous polyp, and multiple congenital anomalies. Among the reported ECP cases, only one case was located in duodenum and it was associated with hamartomatous polyps. Interestingly, we experienced a case of ECP in the duodenum without any intestinal disease. The diagnosis was made based on the endoscopic finding and histologic features of the resected specimen. We report this rare case of ECP located in the duodenum without associated small intestinal disease. (Korean J Gastroenterol 2002;39:55-58)
김미영(Mi Young Kim),황인석(In Seog Hwang),유흥선(Heung Sun Yu),박자영(Ja Young Park),서보정(Bo Jeung Seo),이상익(Sang Ik Lee) 대한신장학회 2001 Kidney Research and Clinical Practice Vol.20 No.5
A 45-year-old man presented with muscle pain, skin nodules and persistent hypereosinophilia over a period of 4 months. Laboratory data excluded the diagnosis of trichinosis or any other parasite infection. The patient's course of the disease over the 9 months was compatible with idiopathic hypereosinophilic syndrome. In a muscle biopsy, eosinophilic and lymphoplasma cells are predominantly infiltrated. Authors report a case of rhabdomyolysis due to eosinophilic polymyositis in idiopathic hypereosinophilic syndrome.
원위부 신세뇨관성 산증과 급성 췌장염이 동반된 Sjogren증후군
권형주(Hyoung Ju Koun),서보정(Bo Jeong Seo),이무열(Moo Yeol Lee),유흥선(Heung Sun Yu),황인석(In Seog Hwang),김미영(Mi Young Kim),김진관(Jin Kwan Kim) 대한신장학회 2000 Kidney Research and Clinical Practice Vol.19 No.2
Distal renal tubular acidosis is classified into primary and secondary. Sjogren Syndrome is the most common cause of secondary distal RTA. We experienced a 51 year-old female patient who had many manifestations of primary Sjogren syndrome which showes Distal renal tubular acidosis, acute pancreatitis, acute renal failure, possibly nephrogenic diabetes insipidus, but We found other atypical find-ings including ANA negative serology, high anion gap metabo1ic acidosis.
이달의 X-선 : 척추 경막외 기종이 동반된 기관지 천식 1례
이철호 ( Lee Cheol Ho ),권형주 ( Kwon Hyeong Ju ),박영우 ( Park Yeong U ),이무열 ( Lee Mu Yeol ),유흥선 ( Yu Heung Seon ),황인석 ( Hwang In Seog ),김진관 ( Kim Jin Gwan ),김미영 ( Kim Mi Yeong ),신미정 ( Sin Mi Jeong ),황순철 ( Hw 대한결핵 및 호흡기학회 2000 Tuberculosis and Respiratory Diseases Vol.49 No.3
유흥선 ( Heung Sun Yu ),이철호 ( Cheol Ho Lee ),황인석 ( In Seog Hwang ),김미영 ( Mi Young Kim ),김진관 ( Jin Kwan Kim ),이충원 ( Choong Won Lee ) 대한류마티스학회 2001 대한류마티스학회지 Vol.8 No.3
Dermatomyositis is a disorder of unknown etiology characterized by an inflammatory myopathy involving striated skeletal muscle and associated characteristic skin lesions. The relationship between dermatomyositis and malignant tumor remains controversial, but we must be concerned about evaluation of suspected malignancy in a patient with dermatomyositis. We present a case of dermatomyositis associated with lung cancer. A 51-yearold male has suffered proximal muscle weakness and facial erythema for 2 months. Pathologic results showed adenocarcinoma and pneumonectomy of the left lung was performed. Myositis resolved completely after removing the malignant mass. Few cases of malignant tumors associated with dermatomyositis were reported in Korea, but dermatomyositis associated with non-small cell lung cancer and complete remission of myositis after the tumor resection has not been reported previously.
정기적인 혈액투석중에 발생되어 자연 퇴화전 방추 세포형 흉선종
권형주(Hyoung Ju Koun),박영우(Young U Park),이철호(Chul Ho Lee),서보정(Bo Jeong Seo),이무열(Moo Yeol Lee),유흥선(Heung Sun Yu),황인석(In Seog Hwang),김미영(Mi Young Kim),김진관(Jin Kwan Kim) 대한신장학회 2000 Kidney Research and Clinical Practice Vol.19 No.2
A 34-year-old male who has recieved regular hemodialysis three times a week for 2years due to chronic renal failure was admitted due to chest pain. Chest x-ray and computed tomography showed large sized anterior mediastinal mass compressing heart and great vessels posteriorly. Open lung biopsy was performed and the result was spindle cell type thy-moma. We recommanded surgical resection but he refused and discharged. After 8months, we observed marked regression of the thymoma without any other treatment. We report a case of spontaneous regression of thymoma in patient with chronic renal failure during regular hemodialysis.
김미영,이철호,김영묵,박영우,이동윤,이준상,김진관,이무열,권형주,황인석,유흥선 대한소화기내시경학회 2000 Clinical Endoscopy Vol.20 No.6
Behcet's disease is a multisystemic, chronie inflammatory disease with a triad of symptoms including oral ulcers, genital ulcers, and inflammatory ocular lesions. While intestinal Behcet's disease commonly affects the ileocecal region, esophageal ulceration with odynophagia is very uncommon. A 38-year-old male patient was admitted due to odynophagia, a postprandial epigastric burning sensation, and right lower quadrant abdominal pain. He had a history of recurrent oral and genital ulcerations, An esophagogastroduodenoscopy revealed relatively well demarcated ulcerative lesions with mucosal nodiularities on the mid to distal esophagus which was suspected to be esophageal cancer. But repeated biopsies showed lymphocytic and plasma cell infiltrations on the lamina propria. A colonoscopy revealed a well demarcated, deep ulcerative lesion with stenotic narrowing in the ileocecal valve. The diagnosis of intestinal Behcct's disease with an esophageal ulcer was made on the basis of clinical and pathological findings. The patient was treated with steroids and sulfasalazine and the response was favorable.