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전상교(Sang Kyo Jeon),박정근(Jung Kun Park),김동월(Dong Wol Kim),유선영(Seon Young Yoo),김정례(Jeong Rae Kim),김재홍(Jae Hong Kim),이진석(Jin Suk Lee),두창준(Chang Joon Doo),변종훈(Jong Hoon Byun),주재식(Jae Sik Joo) 대한소화기학회 1996 대한소화기학회지 Vol.28 No.4
Acinar cell carcinoma of the exocrine pancreas is a rare tumor with reported incidence of 1 to 2 % of pancreatic carcinoma. We reported a case of pancreatic acinar cell carcinoma in 58 year-old woman. Chief complaints were palpable mass and pain in left upper abdomen. Physical exatnination revealed huge aMominal mass in left upper abdomen. Abdominal ultrasonography and computed tomography revealed a huge well demarcated heterogeneous mass at the tail of the pancreas with liver metastasis. Distal pancreatectomy and excision of rnass were carried out. Pathological examination revealed acinar cell carcinoma in pancreatic tail. She died ninth day after operation. (Korean J Gastroenterol 1996;28: 592 - 596)
김준현(Joon Hyun Kim),전상교(Sang Kyo Jeon),박정근(Jung Kun Park),김동월(Dong Wol Kim),두창준(Chang Joon Doo),변종훈(Jong Hoon Byun),이성규(Sung Kyu Lee),유선영(Seon Young Yoo),김정례(Jeong Rae Kim) 대한소화기학회 1996 대한소화기학회지 Vol.28 No.4
Leiomyosarcoma of duodenum is a rare malignant tumor, only ten percent are found in the duo- denum. The most common symptotns are abdominal pain, melena, weakness, weight loss, and jaundice, fever are rare complants. We reported a case of leiomyosarcoma with abscess formation in 54 year-old man confirmed by exploration and excisional biopsy. His chief complaints were right upper quadrant pain and high fever, a mass lesion combined with air bubbles on computerized tomography, upper gastrointestinal findings showed a duodenal mass hanging on 2nd and 3rd portion of duodenum and mucosal destruction. Excisional biopsy revealed low grade leiomyosar- coma in duodenum combined with necrosis and suppurations. (Korean J Gastroenterol 1996;28: 566 - 570)
131I-MIBG Scintigraphy 로 진단된 재발성 갈색 세포종
정동성,이귀래,한창완,조영삼,박운식,정윤형,주홍돈,박성기,김성환,김정례 ( Dong Sung Jung,Gwi Lae Lee,Chang Wan Han,Young Sam Cho,Woon Sik Park,Yoon Hyung Jung,Hong Don Joo,Sung Ki Park,Sung Hwan Kim,Jung Lyeu Kim,Dae Hyuk Moon ) 대한핵의학회 1994 핵의학 분자영상 Vol.28 No.3
Pheochromocytomas are catecholamine producing tumors of neuroect,odermal origin, and may arise wherever chromaffin cells are located. They are rare but potentially lethal and amenable to surgical cure. Once a clinical diagnosis has been established, localization becomes of importance to direct surgical approach. MIBG scintigraphy is the initial localizing procedure of choicc, due to its ability tn screen the entire body, especially in the detection of ex(raadrenal and recurrent pheochromocytoma. A case of recurrent extraadrenal pheochromocytoma diagnosed by I-MIBG scintigraphy is presented wit,h review of the literature.