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腰椎脊髓成熟性畸胎瘤:一例报告及文献复习

Mature Teratoma at the Lumbar Spinal Cord: A Case Report and Literature Review.

作者信息

Zavala-Romero Lilian, Villanueva-Castro Eliezer, Datta-Banik Rudradeep, Ortiz-Altamirano Alexis Genaro, Rodriguez-Esquivel María Magdalena, Cienfuegos-Meza Jesús, Arriada-Mendicoa Juan Nicasio

机构信息

Department of Neurosurgery, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City, MEX.

Department of Neuropathology, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City, MEX.

出版信息

Cureus. 2024 Jan 15;16(1):e52307. doi: 10.7759/cureus.52307. eCollection 2024 Jan.

Abstract

Mature spinal teratoma is a rare type of germ cell tumor that arises from any of the three germ cell layers (ectoderm, mesoderm, and endoderm) and consists of differentiated tissues and structures that reflect the cellular organization and morphology of normal adult tissues. It has the ability to grow independently and cause compressive symptoms when found in this rare location. In this article, we present the case of a 29-year-old male patient with the onset of neurological symptoms beginning with pelvic limb paresthesias and progressing to back pain. Magnetic resonance imaging (MRI) revealed a tumor at L1-L4, which was resected by laminotomy, and histopathology revealed a mature intradural teratoma. Fortunately, this histologic type had a good prognosis for our patient, who had a significant clinical improvement. A systematic review was performed using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) methodology with PubMed and Google Scholar to find similar case reports and to summarize the main features of this disease, which contributes to the understanding of its diagnostic presentation, treatment, and prognosis, improving clinical practice in the management of similar cases. The rarity of this condition, together with its wide clinical heterogeneity and prognosis, underscores the importance of a thorough evaluation of cases of intramedullary lesions, where the consideration of uncommon diseases in the differential diagnosis should be highlighted.

摘要

成熟性脊髓畸胎瘤是一种罕见的生殖细胞肿瘤,起源于三个胚层(外胚层、中胚层和内胚层)中的任何一个,由分化的组织和结构组成,反映了正常成人组织的细胞组织和形态。当在这个罕见部位发现时,它有能力独立生长并引起压迫症状。在本文中,我们介绍了一例29岁男性患者,其神经系统症状始于盆腔肢体感觉异常,随后发展为背痛。磁共振成像(MRI)显示L1-L4水平有一个肿瘤,通过椎板切开术将其切除,组织病理学检查显示为成熟的硬脊膜内畸胎瘤。幸运的是,这种组织学类型对我们的患者预后良好,其临床症状有显著改善。我们使用系统评价和Meta分析的首选报告项目(PRISMA)方法,在PubMed和谷歌学术上进行了系统评价,以查找类似病例报告并总结该疾病的主要特征,这有助于了解其诊断表现、治疗和预后,改善类似病例管理中的临床实践。这种疾病的罕见性,连同其广泛的临床异质性和预后,凸显了对髓内病变病例进行全面评估的重要性,其中应强调在鉴别诊断中考虑罕见疾病。

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