Department of Gynecology, Shinsuma General Hospital, 4-1-6 Isonare-cho, Suma-ku, Kobe 654-0047, Japan.
Jpn J Radiol. 2011 May;29(4):272-5. doi: 10.1007/s11604-010-0538-6. Epub 2011 May 24.
We report a case of multicystic adenomyosis, which is an exceedingly rare benign tumor. The patient complained of an irregular menstrual cycle and abnormal genital bleeding that gradually increased in amount and frequency. The patient finally became severely anemic, and a hysterectomy was therefore performed. T2-weighted magnetic resonance imaging (MRI) indicated hyperplasia of the endometrium, with a myometrial lesion, where a high signal intensity multicystic mass was observed. The preoperative diagnosis was complicated by confusing MRI results. Postoperative macroscopic examination revealed a villous endometrium and a myometrium thickened with multiple small cysts containing serous transparent fluid. The final diagnosis, based on the hysterectomy specimen, was adenomyosis coexisting with simple endometrial hyperplasia. The MRI and positron emission tomography images are presented.
我们报告一例罕见的良性多房性子宫腺肌病。患者因月经周期不规则和异常阴道出血逐渐增多且频繁就诊,最终因严重贫血而行子宫切除术。T2 加权磁共振成像(MRI)显示子宫内膜增生,伴子宫肌层病变,可见高信号多囊性肿块。术前诊断因 MRI 结果混淆而变得复杂。术后大体检查显示绒毛状子宫内膜和子宫肌层增厚,有多个小囊,内含浆液性透明液体。根据子宫切除标本的最终诊断为腺肌病合并单纯性子宫内膜增生。现报告该病例并附上 MRI 和正电子发射断层扫描图像。