The etiologies and management of spinal cord compression in childhood cancers: Are we aware of the emergency of cord compression?

Arzu Okur, Özge Vural, Faruk Güçlü Pınarlı
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Abstract

Background: The spinal cord compression causes irreversible long-term permanent neurological sequelae. This study aims to increase awareness of childhood cancers that cause cord compression by comparing histopathological diagnosis, treatments, and survival rates to the literature.

Methods: Seventy-three patients (38 male, 35 female) with spinal cord compression, among 1085 patients diagnosed with solid tumors at Gazi University Department of Pediatric Oncology between 1991 and 2021 were retrospectively evaluated.

Results: The mean time between the onset of complaints and diagnosis was 27.5± 24.9 (2-150) days. The first three most common tumors that caused cord compression; were central nervous system tumors in 22 (30%), neuroblastoma in 17 (23%), and malignant germ cell tumors in 8 (10%) cases. Of the patients, 46 (63%) had compression due to extradural masses, and 27 (37%) patients had an intradural compression. The most common symptoms were pain in 60 (82%), weakness in 57 (78%), and pins and needles in 28 (38%) patients, respectively. The clinical physical neurological examination findings were motor deficit in 62 (84%), and deep tendon reflex changes in 54 patients (73.9%). Compression findings were detected in 58 (79.5%) patients at diagnosis, and in 15 (20.5%) of them during follow-up. The most common level of compression was seen in the thoracolumbar region in 19 (26%) cases. In 65 (89%) patients with cord compression, corticosteroids were given as anti-edema treatment. Surgical excision was performed in 39 (53%) patients. Spinal radiotherapy was given to 35 patients (48%) with radiosensitive tumors. Chemotherapy protocols were started in 52 (71.2%) cases according to their diagnoses. Complete neurological recovery was achieved in 33 (45%) patients. The 5-year overall survival rates for solid tumors with extradural compression and intradural compression were 62% and 22%, respectively (p=0.002).

Conclusions: Neurological sequela-free recovery is possible with early diagnosis and urgent treatment. Spinal compression must be detected by detailed systemic and neurological examination and imaging methods. Patients should be rapidly transferred to pediatric oncology units after starting anti-edema treatment.

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儿童癌症脊髓压迫的病因和处理:我们知道脊髓压迫的紧急情况吗?
背景:脊髓压迫会导致不可逆转的长期永久性神经后遗症。本研究旨在通过将组织病理学诊断、治疗和存活率与文献进行比较,提高人们对导致脊髓压迫的儿童癌症的认识。方法:回顾性评估1991年至2021年间在加孜大学儿科肿瘤系诊断为实体瘤的1085名患者中的73名脊髓压迫患者(38名男性,35名女性)。结果:从发病到确诊的平均时间为27.5±24.9(2-150)天。导致脊髓压迫的前三种最常见的肿瘤;中枢神经系统肿瘤22例(30%),神经母细胞瘤17例(23%),恶性生殖细胞肿瘤8例(10%)。在这些患者中,46名(63%)患者因硬膜外肿块而受到压迫,27名(37%)患者受到硬膜内压迫。最常见的症状分别是疼痛60例(82%)、虚弱57例(78%)和针扎28例(38%)。临床物理神经检查结果为62例(84%)运动功能障碍,54例(73.9%)深肌腱反射改变。58例(79.5%)患者在诊断时发现压迫,15例(20.5%)患者在随访中发现压迫。19例(26%)胸腰椎受压最常见。在65例(89%)脊髓压迫患者中,给予皮质类固醇作为抗水肿治疗。手术切除39例(53%)患者。35例(48%)放射敏感肿瘤患者接受了脊髓放射治疗。52例(71.2%)患者根据诊断开始了化疗方案。33名(45%)患者的神经系统完全恢复。硬膜外压迫和硬膜内压迫的实体瘤的5年总生存率分别为62%和22%(p=0.002)。脊椎压迫必须通过详细的系统和神经检查以及成像方法进行检测。在开始抗水肿治疗后,患者应迅速转移到儿科肿瘤科。
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