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무증상 단백뇨로 나타난 막성 신병증과 동반된 조기위암 1예
김용진,김익수,서경희,이중기,이덕현,이동엽,우창근,신경순,황중하,제석준 대한신장학회 1998 Kidney Research and Clinical Practice Vol.17 No.6
The nephrotic syndrome in association with extrarenal malignancy is not an uncommon event. The membranous nephropathy is most frequently associated with various carcinomas of the lung, breast, stomach and colon. Though the exact causal relationship has not been determined completely, deposition of the immune complexes composed of antitumor antibody and tumor antigens in the subepithelium is most favorably accepted. We experienced a patient with previously diagnosed membranous nephropathy and subsequently demonstrated early gastric cancer during patient follow-up. After surgical resection proteinuria improved significantly. All physicians are strongly recommended to examine thoroughly and search carefully for possibility of concomitant occult malignancy when an aged patient, especially over 40 years old, is diagnosed as a nephrotic syndrome.
이창기,이상문,이중기,백효종,김석준,박진석,우창근,권소정 대한소화기내시경학회 1997 Clinical Endoscopy Vol.17 No.6
Gastric leiomyoblastoma is an uncommon intramural tumor, Its been regarded as a tumor of smooth muscle origin by its histological and electronmicroscopic characteristics. However, recent immunohistochemical staining techniques have shown that tumors diagnosed as leiomyoblastoma may have different tumor origins. We report a case of multiple leiomyoblastoma of the stomach thought to be of unknown derivation by Immunohistochemical study.
이동환 ( Dong Hwan Lee ),권소정 ( So Jeong Kwon ),박진석 ( Jin Seouk Park ),우창근 ( Chang Keun Woo ),이창기 ( Chang Ki Lee ),황중하 ( Joong Ha Hwang ),이병기 ( Byung Ki Lee ),이중기 ( Chong Ki Lee ) 대한류마티스학회 1997 대한류마티스학회지 Vol.4 No.2
Relapsing polychondritis is an uncommon disease manifested by episodes of progressive inflammation and destruction of cartilage. While the cause remains unknown, an autoimmune pathogenesis appears likely. Characteristic features include auricular chondritis, arthritis, nasal chondritis, ocular inflammation, respiratory tract involvement and audiovestibular damage. The clinical course of patients may vary from a relatively benign illness free of clinically evident visceral involvement, to one of episodic or smoldering activity with variable intensity, to a fulminant illness and death within months of diagnosis. Dapsone, corticosteroid and immunosuppressive agent remain the effective therapies. We have experienced a case of relapsing polychondritis and active pulmonary tuberculosis in a 69-year-old man. He suffered from arthralgia and swelling of joints for several months on the first admission and initially was diagnosed as pseudo gout based on polyarthritis and chondrocalcinosis of right knee joint. During follow-up, chondritis of both auricles and nose, which was proved by the biosy of right auricle, and relapse of polyarthritis were developed. His sputum smear for acid-fast bacillus was postive on the second admission. Then he was diagnosed as relapsing polychondritis and active pulmonary tuberculosis and has achieved improvement with medication of dapsone and antituberculosis drugs according to susceptability test during followed-up. Thus we report this case with literature review.
남근하(Keun Ha Nam),권범찬(Bum Chan Kweon),이한균(Han Kyun Lee),이동욱(Dong Wook Lee),권소정(So Jung Kweon),우창근(Chang Keun Woo),박진석(Jin Seouk Park),황중하(Joong Ha Hwang),이중기(Choong Ki Lee) 대한내과학회 1998 대한내과학회지 Vol.54 No.4
Mesenteric fibromatosis is a rare nonmetastasizing fibrous tumor, characterized by fibroblastic proliferation without evidence of inflammatory response or definite neoplasia. It appears at any age, but mainly in the second to fifth decades as incidence of two to four desmoid tumor cases per 1 rnillion people per annum. It is pseudoencapsulated and locally invasive and has a tendency to recur, but metastases are rare. It is more frequent with Gardner`s syndrome(adenomatosis coli) in which 50% of them will appear as mesenteric fibromatosis. Trauma, especially that of previous surgery, has been associated with the subsequent development of desmoid tumor. The treatment of choice is a wide margin resection of the tumor. we experienced a case of mesenteric fibromatosis without Gardner`s syndrome 2 years after appendectomy in a 31-year old man and recurred at 21 months after resection and report with a review of literatures.