海南医学
海南醫學
해남의학
HAINAN MEDICAL JOURNAL
2014年
22期
3404-3406
,共3页
余绍兰%徐基成%刘丹丹%李晓琼%王青青
餘紹蘭%徐基成%劉丹丹%李曉瓊%王青青
여소란%서기성%류단단%리효경%왕청청
卵巢肿瘤%类癌%病理学%免疫组织化学
卵巢腫瘤%類癌%病理學%免疫組織化學
란소종류%유암%병이학%면역조직화학
Ovarian tumor%Carcinoid%Pathology%Immunohistochemistry
目的:探讨卵巢原发性类癌的临床病理特征。方法报道2例卵巢原发性类癌,并结合相关文献进行临床病理分析。结果病例1为岛状型类癌,肿瘤细胞呈圆形或多角形,排列成岛状或假菊团状,行单侧附件切除术;病例2为梁状型类癌,肿瘤细胞呈柱状,小梁由单至多层瘤细胞构成,瘤细胞核长轴与小梁走向垂直,其临床上有便秘的症状,术后缓解,行全子宫加双附件切除术。术后随访45个月和63个月均未见复发证据。免疫组化肿瘤细胞均呈不同程度的Syn(+)、CK(+);α-inhibin、CD99、TTF-1、ER、PR均(-);Ki-67增殖指数<1%。结论卵巢原发性类癌临床罕见,诊断需和颗粒细胞瘤、支持细胞瘤等鉴别,并排除转移性类癌。作为一种低度恶性肿瘤,卵巢类癌多数预后良好。
目的:探討卵巢原髮性類癌的臨床病理特徵。方法報道2例卵巢原髮性類癌,併結閤相關文獻進行臨床病理分析。結果病例1為島狀型類癌,腫瘤細胞呈圓形或多角形,排列成島狀或假菊糰狀,行單側附件切除術;病例2為樑狀型類癌,腫瘤細胞呈柱狀,小樑由單至多層瘤細胞構成,瘤細胞覈長軸與小樑走嚮垂直,其臨床上有便祕的癥狀,術後緩解,行全子宮加雙附件切除術。術後隨訪45箇月和63箇月均未見複髮證據。免疫組化腫瘤細胞均呈不同程度的Syn(+)、CK(+);α-inhibin、CD99、TTF-1、ER、PR均(-);Ki-67增殖指數<1%。結論卵巢原髮性類癌臨床罕見,診斷需和顆粒細胞瘤、支持細胞瘤等鑒彆,併排除轉移性類癌。作為一種低度噁性腫瘤,卵巢類癌多數預後良好。
목적:탐토란소원발성유암적림상병리특정。방법보도2례란소원발성유암,병결합상관문헌진행림상병리분석。결과병례1위도상형유암,종류세포정원형혹다각형,배렬성도상혹가국단상,행단측부건절제술;병례2위량상형유암,종류세포정주상,소량유단지다층류세포구성,류세포핵장축여소량주향수직,기림상상유편비적증상,술후완해,행전자궁가쌍부건절제술。술후수방45개월화63개월균미견복발증거。면역조화종류세포균정불동정도적Syn(+)、CK(+);α-inhibin、CD99、TTF-1、ER、PR균(-);Ki-67증식지수<1%。결론란소원발성유암림상한견,진단수화과립세포류、지지세포류등감별,병배제전이성유암。작위일충저도악성종류,란소유암다수예후량호。
Objective To investigate the clinicopathological features of primary ovarian carcinoid. Methods Two primary ovarian carcinoid cases from the clinicpathology perspective were reported and ana-lyzed, in combination with relevant literature reviews. Results Case 1 was isular carcinoid. The tumor cells were round or polygonal, and arranged in a shape of island or pseudorosettes. And unilateral adnexectomy was performed. Case 2 was trabecular carcinoid. The tumor cells were columnar, and the trabecula was made up of monolayer or multi-layer tumor cells. The long axes of the tumor cell nucleus were perpendicular to the trend of the trabecula. The consti-pation symptom was relieved after surgery of total hysterectomy and bilateral adnexectomy. There was no evidence of relapse after the respective follow-up of 45 months and 63 months. Immunohistochemical tumor cells showed differ-ent level of positive to Syn and CK in bothcases, while negative toα-inhibin, CD99, TTF-1, ER, and PR, with Ki-67 proliferation index<1%. Conclusion Primary ovarian carcinoid is relatively rare, therefore its diagnosing should be differentiated from that of the granulosa cell tumor, Sertoli cell tumor and metastatic carcinoid. Ovarian carcinoid is a low-grade malignant tumor with favorable prognosis.