Zhang Xianchen, Liu Luping
Department of Radiology, The Second Affiliated Hospital of Shandong First Medical University, No. 366 Taishan Street, Taian City 271000, Shandong, China.
Department of Oncology, Tai'an City Cancer Prevention Hospital, Taian City Shandong, China.
Radiol Case Rep. 2021 Apr 10;16(6):1428-1432. doi: 10.1016/j.radcr.2021.03.017. eCollection 2021 Jun.
Angioleiomyoma is a solitary smooth muscle cell tumor that originates from the tunical media of arteries and veins. Its origin in the sacrum is rare, only one case has been recorded in the literature to date, but cases with bone destruction are even rarer. We present a 49-year-old woman with lumbosacral pain, unsteady gait and right lower extremity pain for two years, accompanied by radiation pain. Through plain film, Computerized tomography (CT) and Magnetic resonance imaging (MRI) examination, we diagnosed this case as giant sacral schwannoma(GSS). After an operation, it was pathologically confirmed as angioleiomyoma. The diagnosis of angioleiomyoma should not be based on imaging alone. It requires histopathological examination combined with immunostaining. It should be considered as one of the differential diagnosis of sacral tumors.
血管平滑肌瘤是一种起源于动静脉中膜的孤立性平滑肌细胞肿瘤。其起源于骶骨的情况罕见,迄今为止文献中仅记载了1例,但伴有骨质破坏的病例更为罕见。我们报告1例49岁女性,有腰骶部疼痛、步态不稳及右下肢疼痛2年,并伴有放射性疼痛。通过X线平片、计算机断层扫描(CT)及磁共振成像(MRI)检查,我们将该病例诊断为巨大骶骨神经鞘瘤(GSS)。术后经病理证实为血管平滑肌瘤。血管平滑肌瘤的诊断不应仅基于影像学检查。它需要组织病理学检查并结合免疫染色。它应被视为骶骨肿瘤的鉴别诊断之一。