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弥漫性子宫平滑肌瘤病:一例病例报告及文献综述

Diffuse uterine leiomyomatosis: A case report and review of literature.

作者信息

Ren Hui-Min, Wang Qing-Zhu, Wang Jia-Nan, Hong Gang-Jie, Zhou Shuang, Zhu Jun-Yan, Li Shan-Ji

机构信息

Department of Gynecology, Zhoushan Branch Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Zhoushan 316000, Zhejiang Province, China.

Department of Obstetrics and Gynecology, Ningbo Hangzhou Bay Hospital, Ningbo 315336, Zhejiang Province, China.

出版信息

World J Clin Cases. 2022 Aug 26;10(24):8797-8804. doi: 10.12998/wjcc.v10.i24.8797.

Abstract

BACKGROUND

Diffuse uterine leiomyomatosis (DUL) is a benign uterine smooth muscle neoplasm with unknown etiology. Since DUL is rarely reported, knowledge regarding it is limited. The rate of early diagnosis is low, and DUL is often misdiagnosed as common multiple uterine leiomyomas before surgery.

CASE SUMMARY

A 27-year-old patient with no sexual activity presented to the Emergency Department of our hospital complaining of heavy vaginal bleeding. She had a history of uterine fibroids and menorrhagia. Pelvic examination showed a regularly enlarged uterus, similar in size to that associated with a 4-mo pregnancy. Pelvic magnetic resonance imaging (MRI) revealed numerous multiple uterine fibroids, and a transabdominal myomectomy (TM) was performed. Intraoperative exploration revealed that the myometrium was full of myoma nodules of variable sizes. Over 50 leiomyomas were removed. The pathology report confirmed leiomyoma. The patient was discharged and received a gonadotropin-releasing hormone analog (3.75 mg) for 6 mo. Ten months after surgery, the patient presented to the hospital again for abnormal uterine bleeding. MRI showed an irregular mass with a diameter of 5.2 cm without sharp demarcation in the uterine cavity. Submucosal leiomyoma was considered first, and the patient underwent a hysteroscopic myomectomy plus hymen repair. Intraoperative exploration showed that there were several leiomyomatosis masses in the cavity. Postoperative pathological examination confirmed submucosal leiomyoma and necrotic and generative tissue. Although the menstrual cycle was still irregular, the patient did not have symptoms of menorrhagia for a period of 28 mo after the second surgery.

CONCLUSION

Individuals with DUL are easily misdiagnosed due to the lack of specific manifestations of this disease. MRI is helpful for early identification and preoperative evaluation. There is currently no unified method of diagnosis. For women who want to preserve fertility, conservative surgery should be made an option. When TM is chosen, a modified new myomectomy should be considered to avoid the drawbacks of traditional TM.

摘要

背景

弥漫性子宫平滑肌瘤病(DUL)是一种病因不明的子宫良性平滑肌肿瘤。由于DUL报道较少,对此的了解有限。其早期诊断率低,术前常被误诊为常见的多发性子宫平滑肌瘤。

病例摘要

一名27岁无性活动史的患者因阴道大量出血就诊于我院急诊科。她有子宫肌瘤和月经过多病史。盆腔检查显示子宫规则增大,大小与妊娠4个月时相似。盆腔磁共振成像(MRI)显示有大量多发性子宫肌瘤,遂行经腹子宫肌瘤切除术(TM)。术中探查发现子宫肌层布满大小不一的肌瘤结节。切除了50多个平滑肌瘤。病理报告证实为平滑肌瘤。患者出院后接受了6个月的促性腺激素释放激素类似物(3.75mg)治疗。术后10个月,患者因子宫异常出血再次入院。MRI显示宫腔内有一个直径5.2cm的不规则肿块,边界不清。首先考虑黏膜下平滑肌瘤,患者接受了宫腔镜子宫肌瘤切除术加处女膜修补术。术中探查发现宫腔内有几个平滑肌瘤病肿块。术后病理检查证实为黏膜下平滑肌瘤及坏死和增生组织。虽然月经周期仍不规则,但患者在第二次手术后28个月内没有月经过多的症状。

结论

由于DUL缺乏特异性表现,患者容易被误诊。MRI有助于早期识别和术前评估。目前尚无统一的诊断方法。对于有生育需求的女性,可选择保守手术。当选择TM时,应考虑改良的新型子宫肌瘤切除术以避免传统TM的弊端。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b549/9453368/53ac99542797/WJCC-10-8797-g001.jpg

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