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中华妇幼临床医学杂志(电子版) ›› 2018, Vol. 14 ›› Issue (05) : 508 -514. doi: 10.3877/cma.j.issn.1673-5250.2018.05.003

所属专题: 文献

论著

卵巢支持细胞-间质细胞瘤的临床分析
刘星辰1, 赵倩颖1, 刘辉1,()   
  1. 1. 610041 成都,四川大学华西第二医院妇产科、出生缺陷与相关妇儿疾病教育部重点实验室
  • 收稿日期:2018-05-18 修回日期:2018-09-08 出版日期:2018-10-01
  • 通信作者: 刘辉

Clinical analysis of Sertoli-Leydig cell tumors

Xingchen Liu1, Qianying Zhao1, Hui Liu1,()   

  1. 1. Department of Obstetrics and Gynecology, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China
  • Received:2018-05-18 Revised:2018-09-08 Published:2018-10-01
  • Corresponding author: Hui Liu
  • About author:
    Corresponding author: Liu Hui, Email:
  • Supported by:
    Key Research and Development Program of Science & Technology Department of Sichuan Province(2018SZ0164)
引用本文:

刘星辰, 赵倩颖, 刘辉. 卵巢支持细胞-间质细胞瘤的临床分析[J]. 中华妇幼临床医学杂志(电子版), 2018, 14(05): 508-514.

Xingchen Liu, Qianying Zhao, Hui Liu. Clinical analysis of Sertoli-Leydig cell tumors[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2018, 14(05): 508-514.

目的

探讨卵巢支持细胞-间质细胞瘤(SLCTs)的临床表现及活组织病理学检查特征,提高临床对该病的认识。

方法

选取2011年1月1日至2017年12月31日,四川大学华西第二医院收治的经术后活组织病理学检查确诊为卵巢SLCTs的6例患者为研究对象,其年龄为24~57岁。采用回顾性分析方法,采集其临床患者资料,并对卵巢SLCTs患者的临床表现、术后活组织病理学检查结果、辅助检查结果、免疫组化结果、治疗及预后进行总结。本研究遵循的程序符合2013年修订的《世界医学协会赫尔辛基宣言》要求。

结果

对纳入研究的6例卵巢SLCTs患者的研究结果显示,①SLCTs均发生于单侧卵巢。术中,2例卵巢SLCTs的瘤体肉眼可见,其余4例肉眼见卵巢外观无明显异常,均为术后活组织病理学检查时,光学显微镜下查见Sertoli-Leydig细胞。②按照国际妇产科联盟(FIGO)临床分期,均为ⅠA期;按照恶性肿瘤的病理分级:Ⅰ级(高分化)为2例,Ⅱ级(中分化)为2例(其中患者2伴睾丸网相似结构),另2例分化程度不明确而未能分级。③免疫组化结果显示,α-抑制素(inhibin)均呈阳性,4例钙(视)网膜蛋白(CR)呈阳性,3例抗体波形蛋白(VIM)呈阳性,3例CD99呈阳性,3例CD10呈阴性,4例上皮膜抗原(EMA)呈阴性,5例Ki-67均≤5%。④ 2例患者术前睾酮水平均升高,其中1例术后下降至正常。术前超声检查提示5例患者一侧附件占位。⑤手术治疗中,患者2为卵巢中分化SLCTs伴睾丸网相似结构,行患侧附件切除术,术后对其采用BEP(博来霉素+依托泊苷+顺铂)联合化疗方案化疗3个疗程。对这6例患者术后随访9~79个月,无一例复发。

结论

卵巢SLCTs极为少见,术前睾酮水平增高结合超声检查结果可予以辅助诊断,术后活组织病理学检查是诊断卵巢SLCTs的"金标准"。卵巢SLCTs的明确诊断,对于手术方案制定及其预后评估具有重要意义。FIGO临床分期较早的卵巢SLCTs患者预后较好。

Objective

To investigate the clinical manifestations and pathological features of ovarian Sertoli-Leydig cell tumors (SLCTs), so as to improve the recognition of this disease.

Methods

From January 1, 2011 to December 31, 2017, 6 patients with ovarian SLCTs who were diagnosed by pathological examination at the West China Second University Hospital, Sichuan University were selected as the research subjects. Their age ranged from 24 to 57 years old. The clinical data of those 6 patients were collected so as to summarize clinical characteristics, pathological examination results, auxiliary examination results, immunohistochemical results, and the process of diagnosis and treatment of SLCTs by retrospective analysis method. This study met the requirements of the World Medical Association Declaration of Helsinki revised in 2013.

Results

①Among 6 ovarian SLCTs patients, all the tumors occurred in the unilateral ovary. Only 2 cases of the 6 patients had visible tumors to the naked eye during the operation. And the remaining 4 cases, the Sertoli-Keydig cells were observed under the light microscope, without obvious abnormality in appearance. ② Six patients were staged by the International Federation of Obstetrics and Gynecology (FIGO), all in ⅠA phase. There were 2 cases with high differentiation, 2 cases with middle differentiation (patient 2 with reticular component) and 2 cases with unclear degree of differentiation. ③ Immunohistochemical results of 6 patients showed that α-inhibin was positive in 6 patients, calretinin (CR) was positive in 4 patients, vimentin (VIM) was positive in 3 patients, CD99 was positive in 3 patients, CD10 was negative in 3 patients, epithelial membrane antigen (EMA) was negative in 4 patients, and Ki-67≤5% in 5 patients. ④ Testosterone levels increased in two cases before operation and decreased to normal in one case after operation. Among 6 patients, 5 showed adnexa uteri space-occupying by ultrasouad examination. ⑤Among them, patient 2 had ovarian moderately differentiated SLCTs with reticular components, underwent ipsilateral adnexectomy, and received three courses of BEP chemotherapy regimen (bleomycin + etoposide + cisplatin) after surgery. All the patients were followed up for 9 to 79 months, and none of them had recurrence.

Conclusions

Ovarian SLCTs are extremely rare. Preoperative testosterone levels combined with ultrasound examination results can help diagnose. Postoperative biopsy findings are of great significance to the diagnosis, surgical plan, and prognosis of ovarian SLCTs. Patients with earlier FIGO staging have a better prognosis.

表1 本组6例卵巢SLCTs患者年龄及相关临床患者资料比较
编号(No.) 年龄(岁) 临床表现 超声检查结果 手术方式 术后活组织病理学检查结果 病理学分级 Ki-67 是否保留生育功能 FIGO临床分期 随访结果
1 47 右侧附件实性弱回声团(6.9 cm×4.3 cm×5.5 cm ) 全子宫切除术+双侧附件切除术 右侧卵巢硬化性间质瘤,左侧卵巢微小SLCTs 分化程度不明确而未能分级 <5% A 随访3年5个月,无复发
2 24 月经紊乱0.5年(经期延长至60 d) 右侧附件囊实性占位(5.3 cm×4.2 cm×5.0 cm) 右侧附件切除术 右侧卵巢SLCTs伴睾丸网相似结构 Ⅱ级(中分化) 约为5% A 随访9个月,接受BEP联合化疗方案化疗3个疗程,无复发
3 56 月经紊乱2个月(经期延长至10 d) 双侧附件未见确切占位;多发性子宫肌瘤(最大直径约为9 cm) 全子宫切除术+双侧附件切除术 右侧卵巢SLCTs Ⅰ级(高分化) 约为3% A 随访6年2个月,无复发
4 53 子宫肌瘤10年 左侧附件实性结节(2.4 cm×2.3 cm× 2.5 cm)。子宫肌瘤直径约为5 cm 全子宫切除术+双侧附件切除术+大网膜切除术+阑尾切除术+盆腔淋巴结清扫术 左侧卵巢SLCTs Ⅱ级(中分化) <2% A 随访1年2个月,无复发
5 37 左侧卵巢无性细胞瘤再次手术 左侧附件实性弱回声团(6.4 cm×3.5 cm×3.8 cm) 全子宫切除术+双侧附件切除术+大网膜切除术+阑尾切除术+盆腔淋巴结清扫术 右侧卵巢SLCTs 分化程度不明确而未能分级 <5% A 随访4年1个月,无复发
6 57 体检发现盆腔右侧附件包块 右侧附件查见囊实性占位(6.9 cm×5.1 cm×6.7 cm) 全子宫切除术+双侧附件切除术+阑尾切除术 右侧卵巢成熟性囊性畸胎瘤,左侧卵巢微小SLCTs Ⅰ级(高分化) A 随访6年7个月,无复发
图1 1例卵巢高分化SLCTs患者(女性,56岁)术后活组织病理学检查结果显示,Sertoli细胞排列成中空小管状,周围有散在Leydig细胞(HE染色,低倍)
图2 1例卵巢中分化SLCTs患者(女性,24岁)术后活组织病理学检查结果显示,伴睾丸网相似结构,Sertoli细胞呈巢片状,细胞质稀少,混杂片状排列的Leydig细胞,其间可见网状间隙(HE染色,低倍)
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