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Spinal tumor

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53:. Intradural tumors are located inside the dura mater lining and are further subdivided into intramedullary and extramedullary tumors. Intradural-intramedullary tumors are located within the dura and spinal cord parenchyma, while intradural-extramedullary tumors are located within the dura but outside the spinal cord parenchyma. The most common presenting symptom of spinal tumors is nocturnal back pain. Other common symptoms include 365:
amenable to resection than intramedullary tumours, and even possible to be operated through microendoscopic or pure endoscopic approaches. In patients with metastatic tumors, treatment is palliative with the goal of improving the patient's quality of life. In these cases, indications for surgery include pain, stabilization, and spinal cord decompression.
332:(STIR) is also commonly added to the MRI protocol for detecting spinal cord tumors. Myelography may be used as a substitute when the patient cannot undergo an MRI or it is unavailable. X-rays and CT are more commonly used to view the bony structures. They are less frequently used for spinal cord tumors, however, since they cannot reliably detect them. 1333:
Patchell, Dr. Roy A.; Tibbs, Phillip A.; Regine, William F.; Payne, Richard; Saris, Stephen; Kryscio, Richard J.; Mohiuddin, Mohammed; Young, Byron (20 August 2005). "Direct decompressive surgical resection in the treatment of spinal cord compression caused by metastatic cancer: a randomised trial".
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The diagnosis of spinal tumors is challenging, as the symptoms can be non-specific and often mimic more common and benign degenerative spinal diseases. A comprehensive medical examination is necessary to look for signs or symptoms that may point towards a more serious condition. This includes a
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Surgery has several indications depending on the type of tumor, which includes complete resection, decompression of the nerves, and stabilization. An attempt at total gross resection for a possible cure is an option for patients with primary spinal cord tumors. Extramedullary tumours are more
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Treatment often involves some combination of surgery, radiation, and chemotherapy. Observation with follow-up imaging may be an option for small, benign lesions. Steroids may also be given before surgery in cases of significant cord compression. Outcomes depend on a number of factors including
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are possible options as an adjunct to surgery or for tumors not amenable to surgery. Intradural-extramedullary tumors are often benign, so observation with follow-up imaging is an option in cases where the lesions are small and the patient is asymptomatic. Radiotherapy and chemotherapy may be
405:, either metastatic or primary. Some suggest that direct decompressive surgery combined with postoperative radiotherapy, provide better outcomes than treatment with radiotherapy alone for patients with spinal cord compression due to metastatic cancer. 109:
The symptoms of spinal tumors are often non-specific, resulting in a delay in diagnosis. Spinal nerve compression and weakening of the vertebral structure cause the symptoms. Pain is the most common symptom at presentation. Other common symptoms of
386:, type of tumor, and amount of surgical resection achieved. In cases where radiotherapy is chosen, radiation is usually delivered to the involved segment in the spinal cord and the uninvolved segment above and below the involved segment. 217:
Intradural tumors are located within the dura mater. These are further broken down into intramedullary and extramedullary tumors. Intradural-intramedullary tumors are located within the spinal cord itself, with the most common being
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Common primary cancers in metastatic spinal tumors includes breast, prostate, lung, and kidney cancer. It is important to diagnose and promptly treat metastatic tumors as they can lead to long-term neurologic deficit from epidural
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Hamamoto, Yasushi; Kataoka, M.; Senba, T.; Uwatsu, K.; Sugawara, Y.; Inoue, T.; Sakai, S.; Aono, S.; Takahashi, T.; Oda, S. (9 May 2009). "Vertebral Metastases with High Risk of Symptomatic Malignant Spinal Cord Compression".
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at the lumbar spine. Most symptoms from spinal tumors occur due to compression of the spinal cord as it plays a primary role in motor and sensory function. The spinal cord is surrounded by three layers known as the spinal
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The cause of spinal tumors is unknown. Most extradural tumors are metastatic commonly from breast, prostate, lung, and kidney cancer. There are many genetic factors associated with intradural tumors, most commonly
1536: 1976: 1961: 45:. There are three main types of spinal tumors classified based on their location: extradural and intradural (intradural-intramedullary and intradural-extramedullary). Extradural tumors are located outside the 1477: 300:
Imaging is often the next step when the diagnosis is unclear or there is greater suspicion for a serious condition that may need immediate intervention. Common types of medical imaging include
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Treatment greatly varies depending on the type of spinal cord tumors, goals of care, and prognosis. The primary forms of treatment include surgical resection, radiotherapy, and chemotherapy.
93:. Diagnosis involves a complete medical evaluation followed by imaging with a CT or MRI. A biopsy may be obtained in certain cases to categorize the lesion if the diagnosis is uncertain. 919:
Holt, T.; Hoskin, P.; Maranzano, E.; Sahgal, A.; Schild, S.E.; Ryu, S.; Loblaw, A. (6 March 2012). "Malignant epidural spinal cord compression: the role of external beam radiotherapy".
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are commonly seen in patients with suppressed immune systems. The majority of extradural tumors are due to metastasis, most commonly from breast, prostate, lung, and kidney cancer.
1918: 356:. These do not affect the tumor mass itself, but tend to reduce the inflammatory reaction around it and decrease the overall volume of the mass impinging on the spinal cord. 1319: 145:
to confirm or exclude spinal metastasis. Rapid identification and intervention of metastatic spinal cord compression is necessary to preserve neurologic function.
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focusing on any motor or sensory deficits. Patients with either benign degenerative spinal disease or spinal tumors often present with back pain. A patient with
1299: 214:. Spinal cord tumors are classified based on their location within the spinal cord: intradural (intradmedullary and extramedullary) and extradural tumors. 1379:"The combined use of surgery and radiotherapy to treat patients with epidural cord compression due to metastatic disease: a cost-utility analysis" 1449: 382:
administered alone or in conjunction with surgery. The choice of chemotherapy or radiotherapy is a multidisciplinary process and depends on the
499: 1781: 230:. Intradural-extramedullary tumors are located within the dura but outside of the spinal cord parenchyma, with the most common being 1902: 1826: 1750: 1080: 475: 1377:
Furlan, J.C.; Chan, K.K.; Sandoval, G.A.; Lam, K.C.; Klinger, C.A.; Patchell, R.A.; Laporte, A.; Fehlings, M.G. (May 2012).
134:. The diagnosis is challenging, primarily because symptoms often mimic more common and benign degenerative spinal diseases. 1588: 1442: 1254:""Microendoscopic" versus "pure endoscopic" surgery for spinal intradural mass lesions: a comparative study and review" 769:
Nambiar, Mithun; Kavar, B (2012). "Clinical presentation and outcome of patients with intradural spinal cord tumours".
246:). Extradural tumors are located outside the dura mater most commonly in the vertebral bodies from metastatic disease. 2071: 1776: 153:
The cause of the majority of spinal tumors is currently not known. Primary spinal tumors are associated with a few
254:. Primary extradural tumors are rare and most arise from surrounding bony and soft tissue structures, including 1435: 1099:
Chamberlain, Marc C.; Tredway, Trent L. (2011-06-01). "Adult Primary Intradural Spinal Cord Tumors: A Review".
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whether the tumor is benign or malignant, primary or metastatic, and location of the tumor. Treatment is often
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is a new technique for treating spinal tumors. This treatment can be tailored to the particular tumor of the
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Mechtler, Laszlo L.; Nandigam, Kaveer (2013-02-01). "Spinal Cord Tumors: New Views and Future Directions".
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Note: Not all brain tumors are of nervous tissue, and not all nervous tissue tumors are in the brain (see
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is a primary symptom of spinal cord compression in patients with known malignancy. Back pain may prompt a
320:. MRI is the imaging of choice for spinal tumors. The MRI protocol that is most frequently used includes 503: 390: 329: 309: 1059: 1840: 130:
often occur in the later stages of the disease. Children may present with spinal deformities such as
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may be used as a supplementary imaging modality for tumors involving bony structures of the spine.
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Jennelle, Richard L. S.; Vijayakumar, Vani; Vijayakumar, Srinivasan (2 August 2011).
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Spinal cord compression is commonly found in patients with metastatic malignancy.
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Ribas, Eduardo S. C.; Schiff, David (1 May 2012). "Spinal Cord Compression".
740: 578: 285: 186: 77:(VHL) syndrome. The most common type of intradural-extramedullary tumors are 1394: 1219: 1886: 1874: 1603: 1412: 1355: 1277: 1238: 1179: 1128: 1042: 983: 940: 897: 847: 790: 748: 640: 586: 533: 398: 374: 259: 243: 158: 115: 1023: 839: 570: 2026: 1745: 1707: 1573: 1541: 1493: 313: 223: 182: 90: 42: 1953: 1890: 1803: 1646: 1376: 289: 239: 231: 219: 203: 185:
is a long, cylindrical anatomical structure that is located within the
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Bilsky, Mark H. (2005-11-01). "New therapeutics in spine metastases".
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can be seen in patients with von Hippel-Lindau disease. Spinal cord
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Neoplasms located in either the vertebral column or the spinal cord
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weakness, sensory loss, and difficulty walking. Loss of bowel and
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are associated with neurofibromatosis 1 (NF1). Meningiomas and
85:. The most common type of intradural-intramedullary tumors are 54: 1919:
WHO classification of the tumors of the central nervous system
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sequences, including contrast enhanced T1-weighted sequences.
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are associated with neurofibromatosis 2 (NF2). Intramedullary
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Gossman, William; Hoang, Stanley; Mesfin, Fassil B. (2019),
693:"Spinal Tumors – Types, Symptoms, Diagnosis and Treatment" 61:
control may occur during the later stages of the disease.
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Balériaux, D. L. F. (1999-08-01). "Spinal cord tumors".
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Segal D, Constantini S. C.; Korn, Lidar (14 May 2012).
1251: 1943: 1200: 1098: 865: 519: 1457: 921:Current Opinion in Supportive and Palliative Care 2063: 718: 961: 768: 292:raises suspicion for a more serious condition. 627:Burton, Matthew R.; Mesfin, Fassil B. (2019), 352:) may be administered if there is evidence of 118:, numbness in hands and legs, and rapid onset 1443: 1320:"Spinal Tumors | Mount Sinai - New York" 626: 101:for the vast majority of metastatic tumors. 1782:Embryonal tumour with multilayered rosettes 962:Reith, W.; Yilmaz, U. (December 2011). "". 522:"Cancer, Intramedullary Spinal Cord Tumors" 1450: 1436: 1252:Dhandapani, S; Karthigeyan, M (Sep 2018). 1101:Current Neurology and Neuroscience Reports 810: 808: 498:: CS1 maint: location missing publisher ( 1402: 1228: 1218: 1032: 1022: 879: 829: 764: 762: 760: 758: 556: 368: 1326: 998: 1903:Malignant peripheral nerve sheath tumor 1827:Primary central nervous system lymphoma 1751:Dysembryoplastic neuroepithelial tumour 861: 859: 857: 805: 629:"Cancer, Conus And Cauda Equina Tumors" 14: 2064: 1370: 1149: 868:Current Treatment Options in Neurology 755: 274: 1431: 1194: 1094: 1092: 1054: 1052: 955: 818:Japanese Journal of Clinical Oncology 687: 685: 683: 681: 679: 677: 675: 462: 460: 458: 456: 454: 452: 450: 448: 446: 444: 442: 440: 438: 104: 912: 854: 714: 712: 673: 671: 669: 667: 665: 663: 661: 659: 657: 655: 622: 620: 618: 616: 614: 612: 610: 608: 606: 604: 552: 550: 548: 515: 513: 436: 434: 432: 430: 428: 426: 424: 422: 420: 418: 1589:Subependymal giant cell astrocytoma 24: 1152:Expert Review of Neurotherapeutics 1089: 1049: 176: 25: 2083: 1423: 709: 652: 601: 545: 510: 415: 1777:Atypical teratoid rhabdoid tumor 771:Journal of Clinical Neuroscience 1312: 1292: 1245: 1143: 1871:Cranial and paraspinal nerves 13: 1: 1584:Pleomorphic xanthoastrocytoma 1459:Tumours of the nervous system 1348:10.1016/S0140-6736(05)66954-1 408: 49:lining and are most commonly 1629:Anaplastic oligodendroglioma 1270:10.1016/j.spinee.2018.02.002 933:10.1097/spc.0b013e32834de701 339: 269: 7: 330:Short-TI Inversion Recovery 10: 2088: 783:10.1016/j.jocn.2011.05.021 391:minimally invasive surgery 359: 310:Magnetic resonance imaging 295: 2017: 1947: 1927: 1911: 1839: 1817: 1794: 1764: 1720: 1690: 1660: 1637: 1614: 1564: 1555: 1535: 1526: 1502: 1474: 1465: 1113:10.1007/s11910-011-0190-2 1073:10.1007/978-3-540-44715-3 976:10.1007/s00117-011-2152-8 890:10.1007/s11940-012-0176-7 733:10.1016/j.ncl.2012.09.011 635:, StatPearls Publishing, 528:, StatPearls Publishing, 148: 114:include muscle weakness, 2072:Nervous system neoplasia 1756:Lhermitte–Duclos disease 1680:Choroid plexus carcinoma 1675:Choroid plexus papilloma 1164:10.1586/14737175.5.6.831 1061:Surgery of Spinal Tumors 723:. Spinal Cord Diseases. 306:computer tomography scan 1220:10.4103/2152-7806.96075 354:spinal cord compression 252:spinal cord compression 112:spinal cord compression 1599:Anaplastic astrocytoma 1594:Fibrillary astrocytoma 369:Non-Surgical Treatment 37:located in either the 1855:Esthesioneuroblastoma 1579:Pilocytic astrocytoma 1395:10.1093/neuonc/nos062 571:10.1007/s003300050831 502:) CS1 maint: others ( 1860:Ganglioneuroblastoma 1765:CNS embryonal tumors 1670:Choroid plexus tumor 193:of the skull to the 128:bladder incontinence 1703:Gliomatosis cerebri 1305:New York Daily News 1024:10.5402/2011/719715 840:10.1093/jjco/hyp039 389:The combination of 275:Medical Examination 236:nerve sheath tumors 189:. It runs from the 83:nerve-sheath tumors 71:neurofibromatosis 2 67:neurofibromatosis 1 2018:External resources 1867:Nerve sheath tumor 1809:Hemangiopericytoma 721:Neurologic Clinics 559:European Radiology 468:Spinal cord tumors 384:histological grade 105:Signs and symptoms 2059: 2058: 1941: 1940: 1880:Neurofibromatosis 1835: 1834: 1790: 1789: 1716: 1715: 1624:Oligodendroglioma 1522: 1521: 1489:Craniopharyngioma 1342:(9486): 643–648. 1082:978-3-540-44714-6 970:(12): 1018–1024. 477:978-3-319-99438-3 282:neurological exam 264:hemangioblastomas 228:hemangioblastomas 167:hemangioblastomas 155:genetic syndromes 75:Von-Hippel Lindau 16:(Redirected from 2079: 1945: 1944: 1932:brain metastasis 1896:Acoustic neuroma 1698:Oligoastrocytoma 1691:Multiple/unknown 1562: 1561: 1553: 1552: 1533: 1532: 1507: 1482: 1472: 1471: 1452: 1445: 1438: 1429: 1428: 1417: 1416: 1406: 1374: 1368: 1367: 1330: 1324: 1323: 1316: 1310: 1309: 1308:. 13 April 2010. 1296: 1290: 1289: 1264:(9): 1592–1602. 1249: 1243: 1242: 1232: 1222: 1198: 1192: 1191: 1147: 1141: 1140: 1096: 1087: 1086: 1066: 1056: 1047: 1046: 1036: 1026: 1002: 996: 995: 959: 953: 952: 916: 910: 909: 883: 863: 852: 851: 833: 812: 803: 802: 766: 753: 752: 716: 707: 706: 704: 703: 689: 650: 649: 648: 647: 624: 599: 598: 565:(7): 1252–1258. 554: 543: 542: 541: 540: 517: 508: 507: 497: 489: 464: 262:, and vertebral 202:. These are the 195:conus medullaris 187:vertebral cavity 39:vertebral column 21: 2087: 2086: 2082: 2081: 2080: 2078: 2077: 2076: 2062: 2061: 2060: 2055: 2054: 2013: 2012: 1956: 1942: 1937: 1936: 1923: 1907: 1831: 1813: 1786: 1772:Medulloblastoma 1760: 1722: 1712: 1686: 1656: 1633: 1616:Oligodendrocyte 1610: 1545: 1539: 1537:Neuroepithelial 1518: 1503: 1498: 1475: 1461: 1456: 1426: 1421: 1420: 1375: 1371: 1331: 1327: 1318: 1317: 1313: 1298: 1297: 1293: 1250: 1246: 1207:Surg Neurol Int 1199: 1195: 1148: 1144: 1097: 1090: 1083: 1064: 1058: 1057: 1050: 1003: 999: 960: 956: 917: 913: 881:10.1.1.613.5814 864: 855: 831:10.1.1.624.6511 813: 806: 767: 756: 717: 710: 701: 699: 691: 690: 653: 645: 643: 625: 602: 555: 546: 538: 536: 518: 511: 491: 490: 478: 466: 465: 416: 411: 371: 362: 350:corticosteroids 342: 298: 277: 272: 256:Ewing's sarcoma 208:arachnoid mater 179: 177:Pathophysiology 151: 107: 28: 23: 22: 15: 12: 11: 5: 2085: 2075: 2074: 2057: 2056: 2053: 2052: 2034: 2022: 2021: 2019: 2015: 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Retrieved 697:www.aans.org 696: 644:, retrieved 632: 562: 558: 537:, retrieved 525: 467: 399:chemotherapy 388: 379:radiotherapy 375:chemotherapy 372: 363: 343: 299: 278: 260:osteosarcoma 248: 224:astrocytomas 216: 180: 152: 136: 116:sensory loss 108: 95: 91:astrocytomas 63: 30: 29: 2043:orthoped/49 2027:MedlinePlus 1746:Neurocytoma 1708:Gliosarcoma 1574:Astrocytoma 1494:Pituicytoma 326:T2-weighted 322:T1-weighted 314:myelography 240:schwannomas 232:meningiomas 220:ependymomas 183:spinal cord 163:schwannomas 87:ependymomas 79:meningiomas 73:(NF2), and 43:spinal cord 2003:DiseasesDB 1891:Schwannoma 1804:Meningioma 1647:Ependymoma 1336:The Lancet 1017:: 719715. 702:2019-12-03 646:2019-12-03 633:StatPearls 539:2019-12-03 526:StatPearls 486:1084270205 409:References 318:bone scans 290:myelopathy 204:dura mater 99:palliative 51:metastatic 47:dura mater 2050:radio/169 2038:eMedicine 1566:Astrocyte 1514:Pinealoma 1467:Endocrine 1172:1473-7175 1121:1534-6293 876:CiteSeerX 826:CiteSeerX 741:0733-8619 579:1432-1084 494:cite book 395:radiation 340:Treatment 280:complete 270:Diagnosis 212:pia mater 171:lymphomas 143:bone scan 139:Back pain 132:scoliosis 120:paralysis 35:neoplasms 2066:Category 2046:med/2993 1796:Meninges 1639:Ependyma 1413:22505658 1356:16112300 1278:29452284 1239:22629489 1188:32071879 1180:16274340 1137:14866999 1129:21327734 1067:. 2007. 1043:22084772 984:22198141 949:40059786 941:22156794 906:25396373 898:22547256 848:19429929 799:11919425 791:22099075 749:23186903 641:28722908 587:10460357 534:28723060 346:Steroids 200:meninges 1997:D013120 1404:3337309 1364:7761862 1286:3834414 1258:Spine J 1230:3356987 1034:3200210 992:2875418 595:6586168 360:Surgery 312:(MRI), 296:Imaging 69:(NF1), 59:bladder 41:or the 2032:001403 1724:neuron 1721:Mature 1557:Glioma 1505:Other: 1478:Sellar 1411:  1401:  1362:  1354:  1284:  1276:  1237:  1227:  1213:: 52. 1186:  1178:  1170:  1135:  1127:  1119:  1079:  1041:  1031:  990:  982:  947:  939:  904:  896:  878:  846:  828:  797:  789:  747:  739:  639:  593:  585:  577:  532:  484:  474:  377:, and 348:(e.g. 316:, and 308:(CT), 302:X-rays 238:(e.g. 226:, and 210:, and 149:Causes 55:muscle 2008:31483 1986:192.2 1971:C72.0 1912:Other 1360:S2CID 1282:S2CID 1184:S2CID 1133:S2CID 1065:(PDF) 988:S2CID 945:S2CID 902:S2CID 795:S2CID 591:S2CID 403:spine 124:Bowel 1992:MeSH 1981:9-CM 1409:PMID 1352:PMID 1274:PMID 1235:PMID 1176:PMID 1168:ISSN 1125:PMID 1117:ISSN 1077:ISBN 1039:PMID 1015:2011 980:PMID 937:PMID 894:PMID 844:PMID 787:PMID 745:PMID 737:ISSN 637:PMID 583:PMID 575:ISSN 530:PMID 504:link 500:link 482:OCLC 472:ISBN 393:and 324:and 234:and 181:The 89:and 81:and 33:are 1977:ICD 1962:ICD 1841:PNS 1528:CNS 1399:PMC 1391:doi 1344:doi 1340:366 1266:doi 1225:PMC 1215:doi 1160:doi 1109:doi 1069:doi 1029:PMC 1019:doi 972:doi 929:doi 886:doi 836:doi 779:doi 729:doi 567:doi 397:or 288:or 126:or 2068:: 2048:, 2041:: 2030:: 2006:: 1995:: 1984:: 1969:: 1966:10 1934:). 1734:: 1407:. 1397:. 1387:14 1385:. 1381:. 1358:. 1350:. 1338:. 1302:. 1280:. 1272:. 1262:18 1260:. 1256:. 1233:. 1223:. 1209:. 1205:. 1182:. 1174:. 1166:. 1154:. 1131:. 1123:. 1115:. 1105:11 1103:. 1091:^ 1075:. 1051:^ 1037:. 1027:. 1013:. 1009:. 986:. 978:. 968:51 966:. 943:. 935:. 923:. 900:. 892:. 884:. 872:14 870:. 856:^ 842:. 834:. 822:39 820:. 807:^ 793:. 785:. 775:19 773:. 757:^ 743:. 735:. 725:31 711:^ 695:. 654:^ 631:, 603:^ 589:. 581:. 573:. 561:. 547:^ 524:, 512:^ 496:}} 492:{{ 480:. 417:^ 304:, 266:. 258:, 242:, 222:, 206:, 157:. 122:. 1979:- 1964:- 1954:D 1889:/ 1843:: 1549:) 1544:, 1540:( 1480:: 1451:e 1444:t 1437:v 1415:. 1393:: 1366:. 1346:: 1322:. 1288:. 1268:: 1241:. 1217:: 1211:3 1190:. 1162:: 1156:5 1139:. 1111:: 1085:. 1071:: 1045:. 1021:: 994:. 974:: 951:. 931:: 925:6 908:. 888:: 850:. 838:: 801:. 781:: 751:. 731:: 705:. 597:. 569:: 563:9 506:) 488:. 20:)

Index

Spinal cancer
neoplasms
vertebral column
spinal cord
dura mater
metastatic
muscle
bladder
neurofibromatosis 1
neurofibromatosis 2
Von-Hippel Lindau
meningiomas
nerve-sheath tumors
ependymomas
astrocytomas
palliative
spinal cord compression
sensory loss
paralysis
Bowel
bladder incontinence
scoliosis
Back pain
bone scan
genetic syndromes
Neurofibromas
schwannomas
hemangioblastomas
lymphomas
spinal cord

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