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This paper reports a case of primary squamous cell carcinoma (SCC) of the liver. The patient had a large mass between the left lateral segment of the liver and the lesser curvature of the stomach on computed tomography. Ultrasonography-guided fine needle aspiration of the mass was suggestive of a well-differentiated SCC. A left lobectomy of the liver and wedge resection of the stomach were performed. The pathology showed positive immunoreactivity for cytokeratin 19 (CK19), carcinoma-embryonic antigen and high-molecular-weight cytokeratin, and negative immunoreactivity for CK8, CK18 and hepatic-specific antigen. (Korean J Med 77:113-117, 2009)
The gastrointestinal (GI) tract is the most frequently involved site of mucosa-associated lymphoid tissue (MALT) lymphoma. Stomach is the most common site of involvement among the GI tract. However, MALT lymphoma of the large intestine is rare. A diagnosis is established by pathological examination of the surgical or endoscopic specimens. A 72-year-old man with low abdominal pain was diagnosed as a sigmoid MALT lymphoma, which was noted as an obstructing mass in a colonoscopic examination. A left hemicolectomy was performed, and the patient has had no recurrence postoperatively without any chemotherapy. (Korean J Gastroenterol 2009;54:126-129)
정창길 ( Chang Kil Jung ),이태영 ( Tae Yeong Lee ),장채령 ( Chae Ryung Jang ),문성훈 ( Sung Hun Moon ),이종훈 ( Jong Hun Lee ),노명환 ( Myung Hwan Roh ),한상영 ( San Young Han ),신우원 ( Woo Won Shin ),최석렬 ( Suk Ryul Choi ) 대한소화기학회 2002 대한소화기학회 추계학술대회 Vol.2002 No.-
이창민 ( Chang Min Lee ),노명환 ( Myung Hwan Roh ),정창길 ( Chang Kil Jung ),원종진 ( Jong Jin Won ),백양현 ( Yang Hyun Baek ),이성욱 ( Sung Wook Lee ),최석렬 ( Seok Ryeol Choi ),조진한 ( Jin Han Cho ) 대한소화기학회 2009 대한소화기학회지 Vol.53 No.6
Autoimmune pancreatitis is a distinct disease characterized by the presence of autoantibodies and hyper-gammaglobulinemia, inflammation of the pancreatic parenchyma, and irregular stricture of the pancreatic duct. The involvement of distal common bile duct is frequently observed, but intrahepatic bile duct involvement is very rare, which seem to have similar feature to primary sclerosing cholangitis. We report a case of the patient with autoimmune pancreatitis combined with extensive involvement of extrahepatic and intrahepatic bile duct, which had a favorable response to steroid therapy. (Korean J Gastroenterol 2009;53:383-387)
The main causes of biliary obstruction are stones and cancers. Fascioliasis is a very rare case which causes biliary obstruction. Fascioliasis is a zoonosis caused by Fasciola hepatica which infects herbivores like sheep and cattle. F. hepatica lives in the biliary system or the liver parenchyma of a host. In Korea, the occurrence of this infection in human is very rare and only few cases have been reported. A 32-year-old male presented with upper abdominal pain and jaundice. His laboratory finding revealed elevated liver transaminases. Abdomen CT scan showed mild left intrahepatic bile duct dilatation. On ERCP, adult F. hepatica worms were found and were thus removed. Concurrently, clonorchiasis was diagnosed by stool exam and serologic enzyme-linked immunosorbent assay test. Clonorchiasis was treated with praziquantel. Herein, we report a case of intrahepatic bile duct dilatation due to F. hepatica infection with concurrent Clonorchis sinensis infestation. (Korean J Gastroenterol 2014,64:298-301)
김충현 ( Chung-hyoun Kim ),김선영 ( Sun-young Kim ),정창길 ( Chang-kil Jung ),최정필 ( Jung-pil Choi ),서금수 ( Keum-soo Seo ),이준호 ( Jun-ho Lee ),최제형 ( Jae-hyung Choi ) 영남대학교 의과대학 2017 Yeungnam University Journal of Medicine Vol.34 No.1
Leiomyosarcoma (LMS) of the small intestine is a rare tumor, accounting for about 1% of all malignant mesenchymal lesions in the gastrointestinal tract. Since small bowel tumors are initially asymptomatic and nonspecific, delayed diagnosis and treatment are common. We found that a 44-year-old male patient who came in for lower abdominal pain had partial obstruction in the small bowel. Multiple ascites and ileal tumors involving peritoneal seeding were observed from his abdominal computed tomography. He was diagnosed as epithelioid LMS involving peritoneal transition after surgical resection, and the outpatient department has planned for a conservative therapy with observation. To the best of our knowledge, ileal epithelioid LMS accompanying a huge omental mass, with a size of 18 cm in dimension, and peritoneal seeding has not yet been reported in Korea. We report this rare case with literature review.
김현수 ( Hyun Soo Kim ),천종운 ( Jong Woon Cheon ),김민수 ( Min Su Kim ),정창길 ( Chang Kil Jung ),김경록 ( Kyung Rok Kim ),최재원 ( Jae Won Choi ),강동우 ( Dong Woo Kang ),김선영 ( Sun Young Kim ) 대한소화기학회 2013 대한소화기학회지 Vol.61 No.2
Hyun Soo Kim, Jong Woon Cheon, Min Su Kim, Chang Kil Jung, Kyung Rok Kim, Jae Won Choi, Dong Woo Kang and Sun Young Kim1 Departments of Internal Medicine and Pathology1, DongKang Medical Center, Ulsan, Korea Actinomycosis is a chronic suppurative disease and caused by Actinomycosis species, principally Actinomyces israelii, which are part of the normal inhabitant on the mucous membrane of the oropharynx, gastrointestinal tract, and urogenital tract. It usually affects cervicofacial, thoracic and abdominal tissue. Cervicofacial type has the highest percentage of occurrence with 50%. Actinomycosis frequently occurs following dental extraction, jaw surgery, chronic infection or poor oral hygiene. It may also be considered as an opportunistic infection in immunocompromised patients such as malignancy, human immunodeficiency virus infection, diabetes mellitus, steroid usage or alcoholism. But, actinomycosis rarely occurs in adults with normal immunity and rare in the esophagus. We report an unusual case of esophageal actinomycosis which was developed in a patient with normal immunity and improved by therapy with intravenous penicillin G followed oral amoxicillin, and we also reviewed the associated literature.