Kalayci Tugce Ozlem, Akatlı Ayşe Nur, Sönmezgöz Fitnet, Türkmen Şamdancı Emine
Department of Radiology, Malatya Beydagi Government Hospital, Malatya, Turkey.
Department of Pathology, School of Medicine, Malatya, Turkey.
Acta Med Iran. 2015;53(4):246-9.
Giant uterine leiomyomas are extremely rare neoplasms and are challenging both diagnostically and therapeutically. A 49-year-old premenopausal female presented at our Department complaining of abdominal pain and distention for several years. Ultrasound (US), color Doppler US, abdominal computed tomography imaging after administration of contrast material, and abdominal magnetic resonance imaging were performed. Histopathologic examination revealed a pedunculated subserosal uterine leiomyoma. In this case report, we present abdominopelvic multimodal radiologic imaging findings of our patient with a giant subserosal uterine leiomyoma, in conjunction with histopathological findings.
巨大子宫平滑肌瘤是极其罕见的肿瘤，在诊断和治疗方面都具有挑战性。一名49岁的绝经前女性因多年来的腹痛和腹胀前来我院就诊。进行了超声（US）、彩色多普勒超声、注射造影剂后的腹部计算机断层扫描成像以及腹部磁共振成像检查。组织病理学检查显示为带蒂浆膜下子宫平滑肌瘤。在本病例报告中，我们展示了该巨大浆膜下子宫平滑肌瘤患者的腹盆腔多模态放射学成像结果，并结合组织病理学结果。
