Meenakshisundaram Natarajan, Dhandapani Balasubramanian
Department of Neurosurgery, Institute of Neurosurgery, Madras Medical College, Chennai, Tamil Nadu, India.
Asian J Neurosurg. 2019 Jul-Sep;14(3):949-951. doi: 10.4103/ajns.AJNS_65_18.
Giant intradural metastases of nonneurogenic origin involving multiple segments represent an extremely rare manifestation of an unknown primary. The respective literature is very scarce. We present a 45-year-old female with complaints of low back pain for 4 years, involuntary urination for 2 years, and difficulty in using both lower limbs for 1 month. Examination revealed paraparesis with hypotonia. Imaging of lumbosacral spine revealed that expansile lytic destruction of vertebral bodies and posterior elements was noted from D8 to S2 vertebra and a large-sized patchy enhancing heterogeneous intradural extramedullary lesion was noted in D8-S2 level. Decompressive laminectomy from D11 to L4 vertebra and subtotal excision of the lesion were done. There was a marked improvement in the lower limb weakness and low back pain postoperatively. Histopathology revealed metastatic adenocarcinoma. Immunohistochemistry showed epithelial membrane antigen positivity. Accordingly, the aim of the surgery is strictly palliative. The majority of patients benefit with respect to neurological deficit/pain independent of the extent of resection. Thus, decompressive surgery is recommended to increase the quality of life. The occurrence of intradural spinal metastasis is rare. Only few cases of intra dural spinal metastasis involving multiple cord segments and osteolytic bony erosions have been documented. Hence this case is being presented here for its rarity and its uniqueness.
起源于非神经源性的巨大硬膜内转移瘤累及多个节段是一种原发灶不明的极为罕见的表现。相关文献非常稀少。我们报告一例45岁女性,有4年腰痛、2年尿失禁及1个月双下肢活动困难的症状。检查发现双下肢轻瘫伴肌张力减低。腰骶椎影像学检查显示,从胸8至骶2椎体及后部结构有膨胀性溶骨性破坏,在胸8至骶2水平可见一个大的斑片状强化不均匀的硬膜内髓外病变。行胸11至腰4椎体减压性椎板切除术及病变次全切除术。术后下肢无力和腰痛有明显改善。组织病理学显示为转移性腺癌。免疫组化显示上皮膜抗原阳性。因此,手术目的严格来说是姑息性的。大多数患者无论切除范围如何,神经功能缺损/疼痛方面均有改善。因此,建议行减压手术以提高生活质量。硬膜内脊髓转移的发生很罕见。仅有少数累及多个脊髓节段和溶骨性骨质侵蚀的硬膜内脊髓转移病例有文献记载。因此,鉴于该病例的罕见性和独特性,在此予以报道。