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난소종창을 첫증상으로 한 악성임파종 1 예 : A case report
전인선 고신대학교 의학부 1985 高神大學校 醫學部 論文集 Vol.1 No.1
Ovarian involvement by lymphoma as part of a generalized process is well recognized but initial presentation of clinically unrecognized lymphoma in the ovary is very unusual and have been reported only rarely. A case of histiocytic lymphoma of the ovary in 43-year-old female was reviewed and the differential diagnosis as well as the pertinent clinical and morphological features are discussed.
이상룡,오경석,이건호,설상영,변상준,윤혜경,고원규,김오길,전진숙,김학준,안용준,하준호,김순관,전인선,김 형 대한소화기내시경학회 1999 Clinical Endoscopy Vol.19 No.1
A 69-year-old male was admitted to the neurosurgery department for traumatic intracra-nial hemorrhage in both frontal lobes. After 2 months, he complained of epigastric dis-comfort, nausea, vomiting, and loose stools. The gastric endoscopic examination found acute hemorrhagic gastritis and there were rhabditoid nematode larvae in the gastric fluid and biopsy sections. The filariform larvae of Strongyloides sp. were discovered from a fecal culture. The patient was treated with albendazole (200 mg, po bid, for 4 weeks). The epigastric discomfort disappeared and endoscopic findings improved after treatment.
자궁 내막 선암종을 동반한 Stein-Leventhal 증후군 : 1증례 보고 A Case Report
허방,전인선,허만하 고신대학교 의학부 1990 高神大學校 醫學部 論文集 Vol.6 No.1
Stein-Leventhal first described a syndrome consisting of amenorrhea, infertility, and a pathologic feature of bilateral polycystic ovries This syndrome is not infrequently associated with endometrial hyperplasia or carcinoma Through a number of possible theories regarding etiologic factors have been explored, the pathogenetic mechanisms are including hypothalamus-pituitary axis, adrenal factors, and ovarian steroidogenesis. The authors present a case of Stein-Leventhal syndrome associated with endometrial adenocarcinoma in a 30-year-old female, who complained of intermittent vaginal bleeding for 10 years and infertility for 5 years of marriage. A diagnostic endometrial curettage showed grade I endometrial adenocarcinoma Total hysterectomy with bilateral salpingo-oophorectomy was performed. Both ovaries revealed symmetrical enlargement and disclosed multiple subcapsular cystic follicles. Numerous primodial follicles were noted. However, corpus luteum and albicans were not identified. The endometrial mucosal surface showed irregular mucosal elevation which was confirmed to be endometrial adenocarcinoma. We report this case in view of its rarity and academic interest along with a literature review on the pathogenesis.