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妇科疾病影像学(六):卵巢未成熟畸胎瘤的临床及超声特征。

Imaging of gynecological disease (6): clinical and ultrasound characteristics of ovarian dysgerminoma.

机构信息

Department of Obstetrics and Gynecology, University of Cagliari, Cagliari, Italy.

出版信息

Ultrasound Obstet Gynecol. 2011 May;37(5):596-602. doi: 10.1002/uog.8958. Epub 2011 Apr 5.

Abstract

OBJECTIVES

To describe the clinical history and ultrasound findings in patients with ovarian dysgerminoma.

METHODS

This was a retrospective study of patients with a histological diagnosis of ovarian dysgerminoma who had undergone preoperative ultrasound examination. The patients were identified from the databases of 11 ultrasound centers. The tumors were described by the principal investigator at each contributing center on the basis of ultrasound images, ultrasound reports and research protocols (when applicable) using the terms and definitions of the International Ovarian Tumor Analysis (IOTA) group. In addition, three authors reviewed all available electronic ultrasound images (gray-scale images and color/power Doppler images were available for 18 patients and 14 patients, respectively) and described them using subjective evaluation of gray-scale and color Doppler ultrasound findings (here called pattern recognition).

RESULTS

Twenty-one patients with ovarian dysgerminoma were identified (including one woman with bilateral masses). Twenty patients had a primary ovarian dysgerminoma (including the one with bilateral masses) and one patient had a recurrence of dysgerminoma in her retained ovary. One of the 21 patients was pregnant. All tumors except one were pure dysgerminomas, one being a mixed germinal cell tumor with 30% dysgerminoma component. Median age was 20 (range, 16-31) years. Information on clinical symptoms was available for 18 patients. In four patients, the tumor was detected incidentally, whereas 14 patients presented with one or more of the following symptoms: acute pain (n = 4), chronic pain (n = 8), bloating (n = 8), menstrual disorders (n = 5) and infertility problems (n = 1). One (5%) patient had ascites. Using the IOTA terms and definitions, all but one dysgerminoma were moderately (43%) or very well (50%) vascularized solid tumors. One tumor was multilocular-solid. According to pattern recognition, most dysgerminomas were highly vascularized, purely solid tumors with heterogeneous internal echogenicity divided into several lobules, had a smooth and sometimes lobulated contour and were well-defined relative to the surrounding organs.

CONCLUSION

The ultrasound finding of a highly vascularized, large, solid, lobulated adnexal mass with irregular internal echogenicity in a woman 20-30 years old should raise the suspicion of ovarian dysgerminoma.

摘要

目的

描述卵巢未成熟畸胎瘤患者的临床病史和超声表现。

方法

这是一项回顾性研究,纳入了在术前超声检查中诊断为卵巢未成熟畸胎瘤并接受治疗的患者。这些患者是从 11 个超声中心的数据库中筛选出来的。每个参与中心的主要研究者根据超声图像、超声报告和研究方案(适用时),使用国际卵巢肿瘤分析(IOTA)组的术语和定义对肿瘤进行描述。此外,有三位作者对所有可用的电子超声图像进行了回顾(18 例患者有灰阶图像,14 例患者有彩色/能量多普勒图像),并使用灰阶和彩色多普勒超声结果的主观评估(称为模式识别)对其进行了描述。

结果

共确定了 21 例卵巢未成熟畸胎瘤患者(包括 1 例双侧肿块的患者)。20 例为原发性卵巢未成熟畸胎瘤(包括 1 例双侧肿块的患者),1 例为保留卵巢的未成熟畸胎瘤复发。其中 1 例患者为妊娠。除 1 例外,所有肿瘤均为单纯未成熟畸胎瘤,1 例为含 30%未成熟畸胎瘤成分的混合生殖细胞肿瘤。中位年龄为 20 岁(范围 16-31 岁)。18 例患者的临床症状信息可用。4 例患者为偶然发现,14 例患者出现以下一种或多种症状:急性疼痛(n=4)、慢性疼痛(n=8)、腹胀(n=8)、月经紊乱(n=5)和不孕问题(n=1)。1 例(5%)患者有腹水。根据 IOTA 术语和定义,除 1 例外,所有未成熟畸胎瘤均为中度(43%)或高度(50%)血管化实性肿瘤。1 例肿瘤为多房实性。根据模式识别,大多数未成熟畸胎瘤为高度血管化、大的、实性、分叶状附件肿块,内部回声不均匀,分为多个小叶,轮廓光滑,有时呈分叶状,与周围器官分界清楚。

结论

对于 20-30 岁的女性,超声发现高度血管化、大的、实性、分叶状、边界不规则的附件肿块,内部回声不均匀时,应怀疑为卵巢未成熟畸胎瘤。

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