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[卵巢颗粒细胞瘤的临床与病理分析]

[Clinical and pathological analysis on ovarian granulosa cell tumors].

作者信息

You Xiao-Lin, Yin Ru-Tie, Li Ke-Min, Wang Dan-Qing, Li Lei, Yang Kai-Xuan

机构信息

Department of Gynecology & Obstetric, West China Second Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2010 May;41(3):467-70.

PMID:20629323
Abstract

OBJECTIVE

To identify different clinical and pathological features for adult and juvenile granulosa cell tumors.

METHODS

The clinical records of 42 patients with granulosa cell tumors of ovary, including pathological features, treatments and follow up results between April 2001 and September 2009 were reviewed.

RESULTS

  1. There were 38 newly diagnosed cases after 2001, and 4 cases were relapsed cases diagnosed before 2001. The 38 cases accounted for 3.13% of ovarian cancer cases treated in our hospital. 2) Twenty nine of the 38 cases (76.3%) were Adult Type, while the other 9 (23.7%) were Juvenile Type. The median onset age were 53 and 25 years old for the Adult Type and Juvenile Type, respectively, which shows significant difference (z = -2.990, P = 0.003). 3) The most common symptoms and signs were abdominal pain (44.7%), vaginal bleeding (42.1%), and abdominal mass (76.3%). The most common complications were endometrial hyperplasia (52.6%) and hysteromyoma (21.1%). 4) Stage I, II and III comprised 73.7%, 23.7% and 2.6% of the 38 cases, respectively. Ten patients ng the underwent conservative unilateral oophorectomy or ovarian enucleation. Twenty patients underwent total abdominal hysterectomy plus bilateral salpingo-oophorectomy. Eight patients underwent cytoreductive surgery. The 42 patients had been followed up for 7 to 175 months, with 14 patients lost of contact. No death was recorded. Inhibin, calretinin, and vimentin were demonstrated to be useful for the diagnosis of granulose cell tumors.

CONCLUSION

With low incidence rate, ovarian granulosa cell tumor is a low-grade malignant and functional tumor. Most are unilateral diseases. Most Adult-type granulosa cell tumors occur in middle aged and elderly people, while most juvenile granulosa cell tumors occur in adolescents and children. Acute abdomen symptom may occur but ascites are less likely to occur in patients with granular cell tumors than those with epithelial ovarian cancers. Ovarian granulosa cell tumors are usually detected early, but easily relapse. Long-term follow-up is needed.

摘要

目的

明确成人型和青少年型颗粒细胞瘤不同的临床和病理特征。

方法

回顾性分析2001年4月至2009年9月间42例卵巢颗粒细胞瘤患者的临床资料,包括病理特征、治疗方法及随访结果。

结果

1)2001年后新诊断38例,2001年前诊断的复发患者4例。38例占我院卵巢癌治疗病例的3.13%。2)38例中成人型29例(76.3%),青少年型9例(23.7%)。成人型和青少年型的中位发病年龄分别为53岁和25岁,差异有统计学意义(z = -2.990,P = 0.003)。3)最常见的症状和体征为腹痛(44.7%)、阴道流血(42.1%)和腹部肿块(76.3%)。最常见的并发症为子宫内膜增生(52.6%)和子宫肌瘤(21.1%)。4)38例中Ⅰ期、Ⅱ期和Ⅲ期分别占73.7%、23.7%和2.6%。10例患者行保守性单侧卵巢切除术或卵巢肿瘤剥除术。20例患者行全腹子宫切除术加双侧输卵管卵巢切除术。8例患者行肿瘤细胞减灭术。42例患者随访7至175个月,14例失访。无死亡病例。抑制素、钙视网膜蛋白和波形蛋白对颗粒细胞瘤的诊断有帮助。

结论

卵巢颗粒细胞瘤发病率低,是一种低级别恶性功能性肿瘤。多数为单侧病变。多数成人型颗粒细胞瘤发生于中老年,而多数青少年型颗粒细胞瘤发生于青少年和儿童。可出现急腹症症状,但与上皮性卵巢癌患者相比,颗粒细胞瘤患者腹水较少见。卵巢颗粒细胞瘤通常早期发现,但易复发,需要长期随访。

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1
[Clinical and pathological analysis on ovarian granulosa cell tumors].[卵巢颗粒细胞瘤的临床与病理分析]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2010 May;41(3):467-70.
2
[Granulosa cell tumors: a population-based study from two counties].[颗粒细胞瘤:来自两个县的基于人群的研究]
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Androgenic granulosa cell tumors of the ovary. A clinicopathologic analysis of 17 cases and review of the literature.
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[Clinical pathological study of granulosatheca cell tumor].颗粒卵泡膜细胞瘤的临床病理研究
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