Shindo Daisuke, Shimono Taro, Takami Toshihiro, Tanaka Sayaka, Tsukamoto Taro, Miki Yukio
Department of Diagnostic and Interventional Radiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, 545-8585, Japan.
Department of Neurosurgery, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, Japan.
Jpn J Radiol. 2015 Nov;33(11):706-9. doi: 10.1007/s11604-015-0475-5. Epub 2015 Aug 28.
Spinal hamartoma is a very rare, benign spinal lesion, usually occurring in children with either spinal dysraphism or neurofibromatosis type 1. We report a case of thoracic spinal hamartoma in a 75-year-old male without associated lesions. This patient represents the oldest of 19 patients whose cases we found reported in detail and one of only nine reported cases without associated lesions. On magnetic resonance imaging, the current patient showed a well-defined exophytic appearance arising from the dorsal midline surface of the spinal cord. We discuss the radiological and pathological features of spinal hamartoma and review the literature, focusing on magnetic resonance imaging features for diagnosing spinal hamartoma.
脊髓错构瘤是一种非常罕见的良性脊髓病变,通常发生于患有脊髓发育异常或1型神经纤维瘤病的儿童。我们报告一例75岁男性的胸段脊髓错构瘤,该患者无相关合并病变。该患者是我们发现详细报道的19例患者中年龄最大的,也是仅有的9例无相关合并病变的报道病例之一。在磁共振成像上,该患者显示出一个边界清晰的外生性肿物,起源于脊髓背侧中线表面。我们讨论了脊髓错构瘤的影像学和病理学特征,并回顾了文献,重点关注诊断脊髓错构瘤的磁共振成像特征。