LOCALIZATION AND HISTOLOGICAL STRUCTURE OF SPINAL CORD TUMORS IN PATIENTS IN SUMY REGION

O. Potapov, O. Kmyta, O. Tsyndrenko, N. Dmytrenko, E. Kolomiets, V. V. Pokhmura, M. P. Khavro, T. V. Bereznyi
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Spinal tumors partially contain pathological genes, but in many cases, researchers don't know what causes these genetic changes.\n\nTumors of the central nervous system (CNS) make up 12% of all tumors, tumors of the spinal cord – 3% of nervous system disorders, in the structure of malignant lesions of the CNS – 1,4-5%, occur mainly at the age of 20-60 years. In children, as well as in elderly and senile persons, these tumors are rare. Most often, they develop not from the brain matter, but from the surrounding tissue, and when they increase in size, they compress the spinal cord.\n\nSpinal tumors are usually divided into primary and secondary. The group of primary tumors include tumors, originating from the brain matter (intramedullar tumors), and those that grow from the membranes of the brain, roots, vessels (extramedullar tumors). Extramedullar tumors are much more common (in 80% of all spinal tumors) than intramedullar tumors.\n\nExtramedullar tumors can be both subdural and epidural. The majority of extramedullar tumors are subdural. Occasionally there are tumors, some of which are located inside the dural sac, and some – outside the dura mater, they are subdural-epidural tumors, as well as epidural-extrovertebral tumors.\nAmong extramedullar tumors the most commonly diagnosed are meningiomas and neurinomas, among intramedullar the most common are ependymomas, less common are astrocytomas and oligodendroglioma. Glioblastomas of the spinal cord is extremely rare; the most common metastases from the posterior fossa are medulloblastomas.\nIntracerebral tumors of the spinal cord are characterized by greater biological benignity, than similar brain tumors. Extracerebral spinal cord tumors have no such differences in their biological properties.\nIn general, spinal cord tumors are more common in elderly patients. Neurinomas and meningiomas predominate in adults, and ependymomas and dysgenetic tumors (teratoma, epidermoid cysts) – in children.\nPeculiarities of etiopathogenetic aspects, clinical course, influence on socio-economic factors encourage further improvement of diagnosis and more detailed study of this type of tumors.\n\nMaterials and methods. The analysis of medical records of patients with spinal cord tumors, who were hospitalized in neurological departments of the Sumy Regional and 4th City Clinical Hospitals in 2015-2018 was carried out. 69 clinical cases were processed in order to investigate the prevalence of spinal cord tumors in the Sumy region, the characteristics of the disease in this group of patients, the leading symptoms, methods of diagnosis and treatment.\nThe analysis of statistical data, obtained after processing of the research materials, was carried out using the licensed version of the IBM SPSS Statistics 17 software.\n Our study significantly established that, according to the histological structure, in 46 patients (28 women and 18 men) meningiomas were predominant and that in 31 patients they were located at the level of Th6-Th12. Mainly in 42 patients (33 women and 9 men, p<0.05) spinal cord neoplasms were localized at the level of Th6-Th12, with extramedular-intradural tumor location – 57 patients (38 women and 19 men).\nAccording to our study, pain syndrome significantly prevailed in 42 patients (35 with extramedular-intradural tumor localization).\nThe study of the histological structure of tumors depending on their localization is an integral part of both diagnosis and treatment, and an important component of predicting the quality of life of the patient.","PeriodicalId":315243,"journal":{"name":"Eastern Ukrainian Medical Journal","volume":"11 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Eastern Ukrainian Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21272/eumj.2019;7(4):372-376","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Spinal cord tumors include tumors developing from its parenchyma, vessels, roots and membranes. The main theory of the formation of spinal cord tumors is the polyetiological dysontogenetic theory. According to this theory, hereditary factors, dysembriogenesis, trauma, carcinogenic effects, viral infection, intoxication, radiation, etc. play an important role in the development of tumors. Although scientists keep finding out more about genetic and environmental factors influencing the development of many types of tumors, spinal tumors are still a relatively unknown subject. Spinal tumors partially contain pathological genes, but in many cases, researchers don't know what causes these genetic changes. Tumors of the central nervous system (CNS) make up 12% of all tumors, tumors of the spinal cord – 3% of nervous system disorders, in the structure of malignant lesions of the CNS – 1,4-5%, occur mainly at the age of 20-60 years. In children, as well as in elderly and senile persons, these tumors are rare. Most often, they develop not from the brain matter, but from the surrounding tissue, and when they increase in size, they compress the spinal cord. Spinal tumors are usually divided into primary and secondary. The group of primary tumors include tumors, originating from the brain matter (intramedullar tumors), and those that grow from the membranes of the brain, roots, vessels (extramedullar tumors). Extramedullar tumors are much more common (in 80% of all spinal tumors) than intramedullar tumors. Extramedullar tumors can be both subdural and epidural. The majority of extramedullar tumors are subdural. Occasionally there are tumors, some of which are located inside the dural sac, and some – outside the dura mater, they are subdural-epidural tumors, as well as epidural-extrovertebral tumors. Among extramedullar tumors the most commonly diagnosed are meningiomas and neurinomas, among intramedullar the most common are ependymomas, less common are astrocytomas and oligodendroglioma. Glioblastomas of the spinal cord is extremely rare; the most common metastases from the posterior fossa are medulloblastomas. Intracerebral tumors of the spinal cord are characterized by greater biological benignity, than similar brain tumors. Extracerebral spinal cord tumors have no such differences in their biological properties. In general, spinal cord tumors are more common in elderly patients. Neurinomas and meningiomas predominate in adults, and ependymomas and dysgenetic tumors (teratoma, epidermoid cysts) – in children. Peculiarities of etiopathogenetic aspects, clinical course, influence on socio-economic factors encourage further improvement of diagnosis and more detailed study of this type of tumors. Materials and methods. The analysis of medical records of patients with spinal cord tumors, who were hospitalized in neurological departments of the Sumy Regional and 4th City Clinical Hospitals in 2015-2018 was carried out. 69 clinical cases were processed in order to investigate the prevalence of spinal cord tumors in the Sumy region, the characteristics of the disease in this group of patients, the leading symptoms, methods of diagnosis and treatment. The analysis of statistical data, obtained after processing of the research materials, was carried out using the licensed version of the IBM SPSS Statistics 17 software. Our study significantly established that, according to the histological structure, in 46 patients (28 women and 18 men) meningiomas were predominant and that in 31 patients they were located at the level of Th6-Th12. Mainly in 42 patients (33 women and 9 men, p<0.05) spinal cord neoplasms were localized at the level of Th6-Th12, with extramedular-intradural tumor location – 57 patients (38 women and 19 men). According to our study, pain syndrome significantly prevailed in 42 patients (35 with extramedular-intradural tumor localization). The study of the histological structure of tumors depending on their localization is an integral part of both diagnosis and treatment, and an important component of predicting the quality of life of the patient.
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苏梅地区脊髓肿瘤的定位与组织学结构
脊髓肿瘤包括发生于脊髓实质、血管、脊髓根和脊髓膜的肿瘤。脊髓肿瘤形成的主要理论是多器官发育异常理论。根据这一理论,遗传因素、胚胎发育异常、创伤、致癌作用、病毒感染、中毒、辐射等在肿瘤的发生发展中起着重要作用。尽管科学家们不断发现影响多种肿瘤发展的遗传和环境因素,但脊柱肿瘤仍然是一个相对未知的主题。脊柱肿瘤部分包含病理基因,但在许多情况下,研究人员不知道是什么导致了这些基因变化。中枢神经系统(CNS)肿瘤占所有肿瘤的12%,脊髓肿瘤占神经系统疾病的3%,中枢神经系统结构中的恶性病变占1.4% -5%,主要发生在20-60岁。在儿童,以及老年人和老年人中,这些肿瘤是罕见的。大多数情况下,它们不是从大脑物质中发育出来的,而是从周围的组织中发育出来的,当它们的体积增大时,它们会压迫脊髓。脊柱肿瘤通常分为原发性和继发性。原发肿瘤包括起源于脑物质的肿瘤(髓内肿瘤)和生长于脑膜、脑根、血管的肿瘤(髓外肿瘤)。髓外肿瘤比髓内肿瘤更常见(占所有脊髓肿瘤的80%)。髓外肿瘤可以是硬膜下和硬膜外。大多数髓外肿瘤位于硬膜下。偶尔也有肿瘤,有些位于硬脑膜囊内,有些位于硬脑膜外,它们是硬膜下-硬膜外肿瘤,以及硬膜外-椎体肿瘤。髓外肿瘤中最常见的是脑膜瘤和神经鞘瘤,髓内肿瘤中最常见的是室管膜瘤,较少见的是星形细胞瘤和少突胶质细胞瘤。脊髓胶质母细胞瘤极为罕见;最常见的后窝转移瘤是髓母细胞瘤。脊髓脑内肿瘤的特点是比类似的脑肿瘤具有更大的生物良性。脑外脊髓肿瘤在生物学特性上没有这种差异。一般来说,脊髓肿瘤多见于老年患者。成人多见神经瘤和脑膜瘤,儿童多见室管膜瘤和发育不良肿瘤(畸胎瘤、表皮样囊肿)。其发病方面的特点、临床过程、对社会经济因素的影响鼓励进一步提高诊断和更详细地研究这类肿瘤。材料和方法。对2015-2018年苏梅地区和第四市立临床医院神经内科住院的脊髓肿瘤患者病历进行分析。通过对69例临床病例的分析,了解苏梅地区脊髓肿瘤的患病率、本组患者的疾病特点、主要症状、诊断和治疗方法。对研究资料进行处理后得到的统计数据进行分析,使用授权版IBM SPSS Statistics 17软件。我们的研究发现,根据组织学结构,46例患者(女性28例,男性18例)脑膜瘤占主导地位,31例患者位于Th6-Th12水平。42例(女33例,男9例,p<0.05)脊髓肿瘤主要定位于Th6-Th12水平,57例(女38例,男19例)肿瘤位于髓外-硬膜内。根据我们的研究,疼痛综合征在42例患者中明显流行(35例为髓外-硬膜内肿瘤定位)。根据肿瘤的定位来研究肿瘤的组织学结构是诊断和治疗的重要组成部分,也是预测患者生活质量的重要组成部分。
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