원발성 난관 이행세포암 1예
A case of primary transitional cell carcinoma of the fallopian tube
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초록
원발성 난관암은 여성 생식기에서 발생하는 악성 종양 중 그 빈도가 1% 정도의 매우 드문 질환으로 대부분 술 중 또는 술 후 진단된다. 특히 원발성 난관 이행세포암은 극히 드물며 전 세계적으로 십 여건만이 보고되어 있다. 조직학적으로 난관암은 거의 대부분 유두상 선암이며 그 외 자궁내막양암, 투명세포암, mixed carcinoma 등이 소수 보고되고 있다. 원발성 난관암에서 이행세포암은 그 희귀성으로 인해 아직까지 그 임상병리학적 특성이 정확히 밝혀져 있지 않다. 본 저자들은 원발성 이행세포암으로 확진된 1예를 경험하였기에 간단한 문헌 고찰과 함께 그 임상적 특성과 치료에 대해 보고하는 바이다.
Abstract
Primary carcinoma of the fallopian tube is a rare entity that accounts for about 1% of all gynecologic malignancies, and most are discovered during or after surgery. Primary transitional cell carcinoma of the fallopian tube is an extremely rare tumor that is reported only occasionally in the worldwide literature. Histologically, fallopian tube carcinomas are almost always papillary adenocarcinomas, but other histologic types such as endometrioid carcinoma, clear cell carcinoma, and mixed carcinoma have been reported. As primary transitional cell carcinoma (TCC) of the fallopian tube is so rare, the clinicopathologic characteristics are as yet unknown. The authors recently experienced a case of primary transitional cell carcinoma arising in the fallopian tube, and thus report the clinical features, management, and also a review of the past pertinent literature.
참고문헌 (20)
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