Shah Mohit Veerkumar, Pisat Sanket, Jain Mukul, Chatterjee Mrinalini, Nadkarni Sanaa, Bijlani Suman
Abhipraay-Centre for Advanced Ultrasound/Guided Interventions & Genetic Clinic, Mumbai, India.
Akansha Maternity and Surgical Hospital, Andheri Mumbai, India.
J Obstet Gynaecol India. 2021 Dec;71(6):633-636. doi: 10.1007/s13224-021-01474-1. Epub 2021 May 2.
Accessory and cavitated uterine mass is rare developmental Mullerian anomaly. There is a non-communicating uterus-like mass that occurs contiguously along wall of uterus often underdiagnosed and needs expertise to identify. To raise awareness, provide information about this pathology and emphasize role of coronal 3D ultrasound in its diagnosis. A 28-year-old married female presented with dysmenorrhea and chronic pelvic pain. On ultrasound, a homogeneously isoechoic mass was noted in right lateral wall of uterus with central echogenicity. On 3D reconstruction, the main uterine cavity was normal and both cornu were visualized without any recognized Mullerian anomaly. No communication with the main endometrial cavity seen. On laparoscopy, mass was located under right round ligament insertion. Sectioning revealed chocolate colored fluid. ACUM is non-communicating uterus-like mass. It resembles uterus both macroscopically and microscopically. It represents a cavitated mass lined by endometrial glands and stroma surrounded by irregular smooth muscle cells. Criterias for diagnosing ACUM are (1) accessory cavitated mass located under round ligament; (2) normal uterus, fallopian tubes, and ovaries (3) surgical case with excised mass and pathological examination; (4) accessory cavity lined by endometrium with glands and stroma; (5) chocolate-brown fluid contents. On ultrasound, they appear solid isoechoic masses with central cystic areas separate from ovaries. 3D reconstruction can be used to rule out Mullerian anomaly. ACUM is a rare surgically treatable cause of dysmenorrhea, often underdiagnosed due to lack of knowledge about entity. 3D ultrasound can be highly accurate in making the diagnosis.
附件性子宫空洞性肿块是一种罕见的苗勒管发育异常。存在一个与子宫壁相邻的不与外界相通的子宫样肿块,常常被漏诊,需要专业知识来识别。为提高认识,提供有关这种病理情况的信息,并强调冠状面三维超声在其诊断中的作用。一名28岁已婚女性因痛经和慢性盆腔疼痛就诊。超声检查发现子宫右侧壁有一个均匀等回声肿块,中央有回声。三维重建显示主子宫腔正常,双侧宫角可见,未发现任何公认的苗勒管异常。未见与主子宫内膜腔相通。腹腔镜检查发现肿块位于右圆韧带附着处下方。切开后可见巧克力色液体。附件性子宫空洞性肿块是不与外界相通的子宫样肿块。它在宏观和微观上都类似于子宫。它表现为一个由子宫内膜腺体和间质衬里、被不规则平滑肌细胞包围的空洞性肿块。诊断附件性子宫空洞性肿块的标准为:(1)位于圆韧带下方的附件性空洞性肿块;(2)子宫、输卵管和卵巢正常;(3)手术切除肿块并进行病理检查的病例;(4)由带有腺体和间质的子宫内膜衬里的附件腔;(5)巧克力棕色液体内容物。在超声检查中,它们表现为实性等回声肿块,中央有囊性区域,与卵巢分开。三维重建可用于排除苗勒管异常。附件性子宫空洞性肿块是一种罕见的可手术治疗导致痛经的病因,常因对该疾病缺乏了解而被漏诊。三维超声在做出诊断方面可以非常准确。