Spine Research Group, Monefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA; Department of Neurological Surgery, Monefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA.
Spine Research Group, Monefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA; Department of Neurological Surgery, Monefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA.
World Neurosurg. 2019 Nov;131:47-51. doi: 10.1016/j.wneu.2019.07.173. Epub 2019 Jul 29.
Spinal tuberculosis has been listed as a rare cause of neuroforaminal widening with only 2 previous reports in the literature. Here, we report the third case of an extradural tuberculoma extending through and expanding the neural foramen closely masquerading as a nerve sheath tumor including, to the best of our knowledge, the first description of magnetic resonance imaging, operative, and histopathology findings.
A 65-year-old Nigerian man presented with signs and symptoms of worsening thoracic myeloradiculopathy for the past month. Imaging found an extradural dumbbell-shaped lesion involving the spinal canal, neural foramen, and paraspinal area with a combination of solid and cystic components causing bony remodeling of the pedicle and vertebral body, as well as enlargement of the neural foramen. Surgery was performed to resect the mass, and pathology postoperatively demonstrated caseating granulomas, rare thin elongated organisms on Ziehl-Neelsen staining, and involvement of nerve fascicles.
This case illustrates that a tuberculoma can have many of the features of a benign neoplasm, such as encapsulation, appearance of a slow rate of growth, and development of necrosis or even cystic degeneration. With the specific findings of entrapped nerve fascicles, we postulate that the lesion represents a nerve sheath tuberculoma rather than spinal tuberculosis of the pedicle or posterior elements. Furthermore, only a lesion of the nerve sheath would have the characteristic dumbbell appearance as it extends through the foramen.
脊柱结核已被列为神经孔扩大的罕见原因,文献中仅有 2 例既往报道。在此,我们报告第 3 例硬膜外结核瘤通过并扩大神经孔的病例,其表现极为类似神经鞘瘤,包括我们所知的首例磁共振成像、手术和组织病理学发现。
一名 65 岁的尼日利亚男性,过去一个月出现进行性加重的胸髓神经根病症状和体征。影像学发现椎管、神经孔和椎旁区存在哑铃形硬膜外病变,具有实性和囊性成分的组合,导致椎弓根和椎体的骨重塑,以及神经孔的扩大。进行了手术切除肿块,术后病理显示干酪样肉芽肿,在齐-尼染色上罕见的细长薄体,以及神经束的受累。
本病例表明,结核瘤可能具有许多良性肿瘤的特征,如包膜、生长速度缓慢、出现坏死甚至囊性变性。结合受累神经束的特定发现,我们推测该病变代表神经鞘结核瘤,而不是椎弓根或后柱的脊柱结核。此外,只有神经鞘的病变才会有特征性的哑铃状外观,因为它通过神经孔延伸。