MRI Diagnosis of Ovarian Mucinous Cystic Fibroadenoma: Clinical Case Study
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摘要:
卵巢囊性腺纤维瘤(OCAF)是一种卵巢上皮来源少见的卵巢肿瘤,由卵巢表面的苗勒上皮和纤维间质细胞组成。临床发病少见,又以浆液性最为多见。本文报告1例浆黏液性囊性腺纤维瘤病例,76岁女性,以腹痛2年余,触及下腹包块8个月而就诊,MRI检查发现病变呈大小不等、信号不均的囊腔及实性成分T2WI明显低信号改变,影像诊断囊性腺纤维瘤;患者术后病理结果为浆黏液性囊性腺纤维瘤,术后随访良好。本文旨在对该疾病进行影像描述与总结,提高诊断的准确性。
Abstract:Ovarian cystic adenofibroma is a rare ovarian tumor of epithelial origin and is composed of Mullerian epithelium and fibrostromal cells on the surface of the ovary. Its clinical incidence is rare, and serous is the most common. This article reports a case of mucinous cystic fibroadenoma in a 76-year-old female who presented abdominal pain for more than two years and a palpable mass in the lower abdomen for eight months. MRI resonance imaging revealed lesions of varying sizes, an uneven signal in the cystic cavity, and significantly low signal changes in the solid components on T2WI. Imaging diagnosis of cystic adenofibroma is performed. The post-operative pathological result of the patient indicates mucinous cystic fibroadenoma, and the post-operative follow-up is favorable. This article aims to provide an imaging description and summary of the disease to improve its diagnosis accuracy.
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Keywords:
- magnetic resonance imaging /
- tumor ovarii /
- mucoplasmic /
- cystadenofibroma
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