School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.
Department of Pathology, Division of Pathological Neuroscience, Tokyo Women's Medical University, Tokyo, Japan.
Neuropathology. 2020 Dec;40(6):632-640. doi: 10.1111/neup.12690. Epub 2020 Sep 3.
Paraganglioma is a neuroendocrine tumor arising from extra-adrenal sites in the peripheral nervous system. Although malignant paraganglioma is known to metastasize to bones, including vertebral bodies, there is little literature on the compressive myelopathy accompanied by sphincter dysfunction; to our knowledge, only 12 cases have been reported. Moreover, neuropathological investigations of the spinal cord in this state have not been well-documented. This autopsy report describes a 55-year-old man with malignant paraganglioma and compression myelopathy caused by vertebral metastasis. The present case showed a gradual numbness and a sudden onset of irreversible paraplegia with sphincter dysfunction, which were not palliated these neurologic dysfunctions despite radiotherapy. Computed tomography (CT) revealed multiple metastases to the bones, lymph nodes, and lungs when he was diagnosed with malignant paraganglioma. At the same time, he had numbness, and magnetic resonance imaging (MRI) showed multiple diffuse metastatic lesions in the vertebral bodies. Following abrupt onset of paralysis, MRI showed fractured third and sixth thoracic vertebral bodies. An autopsy revealed residual vertebral metastases with fractures of the third and sixth thoracic vertebral bodies, resulting in compressive myelopathy at the fourth thoracic segment, which was characterized by complete spinal cord destruction. Destructive spinal cord lesion-induced secondary degeneration was observed in the gracile fasciculus at the rostral side and in the pyramidal tract at the caudal side, which showed Wallerian degeneration. Such pathology was consistent with the presenting neurological symptoms, including paraplegia and somatic sensory loss below the fourth thoracic spinal cord segment. Although it is difficult to identify the pathognomonic morphological changes responsible for the sphincter dysfunction, the present case suggests a supranuclear dysregulation of the somatosensory and central autonomic nervous systems involved in urination and defecation. Based on a review of the literature and the features of the present case, paraganglioma can metastasize aggressively even with a low pathological grading. This case of vertebral metastasis as a result of malignant paraganglioma may not be extraordinary but the autopsy report is rare. This autopsy revealed transverse myelopathy as a result of malignant vertebral metastasis of malignant paraganglioma.
副神经节瘤是一种起源于外周神经系统肾上腺外部位的神经内分泌肿瘤。虽然已知恶性副神经节瘤会转移到骨骼,包括椎体,但很少有文献报道伴有括约肌功能障碍的压迫性脊髓病;据我们所知,只有 12 例报告。此外,这种状态下的脊髓神经病理学研究还没有得到很好的记录。本尸检报告描述了一例 55 岁男性,患有恶性副神经节瘤和椎体转移引起的压迫性脊髓病。本例患者表现为逐渐出现麻木,突然出现不可逆性截瘫伴括约肌功能障碍,尽管进行了放疗,但这些神经功能障碍仍未得到缓解。当他被诊断出患有恶性副神经节瘤时,计算机断层扫描(CT)显示骨骼、淋巴结和肺部有多处转移。同时,他出现麻木,磁共振成像(MRI)显示多个弥漫性转移性病变在椎体。在突然出现瘫痪后,MRI 显示第三和第六胸椎椎体骨折。尸检显示残留的椎体转移瘤伴有第三和第六胸椎椎体骨折,导致第四胸椎段受压性脊髓病,表现为完全性脊髓破坏。在背侧的薄束和腹侧的锥体束中观察到破坏性脊髓病变引起的继发性退行性变,表现为沃勒变性。这种病理学与截瘫和第四胸椎脊髓节段以下的躯体感觉丧失等神经症状一致。虽然难以确定导致括约肌功能障碍的特征性形态改变,但本例提示排尿和排便涉及的感觉和中枢自主神经系统的核上调节障碍。根据文献复习和本病例的特点,即使病理分级较低,副神经节瘤也可能具有侵袭性转移。由于恶性副神经节瘤的椎体转移导致的本病例可能并不特殊,但尸检报告却很少见。本尸检揭示了恶性副神经节瘤恶性椎体转移导致的横贯性脊髓病。