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하유정 ( You Jung Ha ),정상윤 ( Sang Youn Jung ),이광훈 ( Kwang Hoon Lee ),최준정 ( Jun Jung Choi ),이광길 ( Kwang Kil Lee ),이수곤 ( Soo Kon Lee ),박용범 ( Yong Beom Park ) 대한류마티스학회 2009 대한류마티스학회지 Vol.16 No.4
Dermatomyositis is a rare inflammatory myopathy with characteristic skin manifestations and accompanied by muscular weakness. Vesicle formation in dermatomyositis is rare. We report a case of dermatomyositis associated with ovarian cancer in a 62-year-old woman who had vesicles and bullae on her arms. She had erythema and edema on the face, chest, abdomen, and shoulder for 2 months. Diagnosis of dermatomyositis was established by clinical manifestations, muscle enzyme elevation, and a characteristic electromyogram. She was successfully treated with cyclosporin and high doses of steroids.
폐쇄성 대장암 상부에 발생한 ischemic colitis
김춘규(Choon Kyu Kim),김남규(Nam Kyu Kim),지훈상(Hoon Sang Chi),이광길(kwang Kil Lee),최인준(In Joon choi) 대한소화기학회 1984 대한소화기학회지 Vol.16 No.1
The ischemic colitis proximal to ohstructive colon cancer was firstly reported by MacCallum and Kaisch in 1947 Nowadays, its clinical importar.ce and the study of pathogenesis is reported frequently. Because of the rare incidence of this complicated condition this lesion could be overlooked, v hich then could result in anastomotic leakage, fecal fistula and peritonitis. Differential diagnosis from idiop thic ulcerative colitis will be needed because it is similar with idiopathic ulcerative colitis in view of clinical symptoms and operative findings. We have experienced 2 cases of the ischemic colitis proximal to obstructive sigmoid colon cancer and then reported these cases zvith literature reviev .
강진경(Jin Kyung Kang),박인서(In Suh Park),문영명(Young Myung Moon),정재복(Jae Bock Chung),이상인(Sang In Lee),지훈상(Hoon Sang Chi),이광길(kwang Kil Lee),정준표(Jun Pyo Chung),박영년(Young Nyun Park) 대한소화기학회 1993 대한소화기학회지 Vol.25 No.4
Gastronic neurofibroma is rare. Most of the reported cases were associated with von Recklingh-ausens disease. We experieced a case of solitary gastric neurofibroma. A 28-year old male patient was aclmitted with epigastric pain for 4 months and tarry stool for 4 days. Neither cafe-au-lait spots nor superficial tumors were found. Gastroscopic exminatio showed a large (3: 2 cm) polypoid mass with a superfcial ulceration and a bridging fold on the anterior wall of the anrum. UGI series showed a large polipoid mass with the central ulceration on the antrunl. Antrectomy with gastrojejunostomy was performed. Grossly, the mass was 3.2*2.7*1.5cm sizecl, well-circumscribed submucosal tumor with central ulceration Microscopically, the mass was not encapsulated. The arrangement of the tumor cells was -coarse and wavy with the myxomatous matrix. Each of the tumor cells had oval shaped nucleus and spindle shaped cytoplasm. Nuclear atypism and frequent mitosis were not observed. We report a rare case of solitary gastric neurofibroma with review of the literatures.