Онкопедиатрия. 2016; 3: 228-239
Особенности нейрогенных опухолей у пациентов с синдромом опсоклонус-миоклонус
Качанов Д. Ю., Шаманская Т. В., Ильина Е. С., Терещенко Г. В., Ликарь Ю. Н., Андреев Е. С., Малевич О. Б., Хомякова С. П., Щербаков А. П., Рощин В. Ю., Коновалов Д. М., Ольшанская Ю. В., Казакова А. Н., Островская М. А., Варфоломеева С. Р.
https://doi.org/10.15690/onco.v3i3.1602Аннотация
Синдром опсоклонус-миоклонус (ОМС) — редкое неврологическое заболевание, которое в большинстве случаев является паранеопластическим процессом. У детей с ОМС более чем в половине случаев выявляются нейрогенные опухоли, чаще нейробластома (НБ). НБ, ассоциированная с ОМС, имеет анатомические и биологические особенности, которые оказывают влияние на выбор методов диагностики для выявления опухоли и тактики ведения этой группы больных. В данной статье представлены основные характеристики НБ при ОМС, которые легли в основу разработки диагностического алгоритма, направленного на выявление нейрогенных опухолей у пациентов, страдающих ОМС.
Список литературы
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19. Takama Y, Yoneda A, Nakamura T, Nakaoka T, Higashio A, Santo K, et al. Early Detection and Treatment of Neuroblastic Tumor with Opsoclonus-Myoclonus Syndrome Improve Neurological Outcome: A Review of Five Cases at a Single Institution in Japan. Eur J Pediatr Surg. 2016;26(1):54–9.
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21. Shulkin BL, Shapiro B. Current concepts on the diagnostic use of MIBG in children. J Nucl Med. 1998;39(4):679–88.
22. Parisi MT, Hattner RS, Matthay KK, Berg BO, Sandler ED. Optimized diagnostic strategy for neuroblastoma in opsoclonus- myoclonus. J Nucl Med. 1993;34(11):1922–6.
23. Fendler WP, Melzer HI, Walz C, von Schweinitz D, Coppenrath E, Schmid I, et al. High 123I-MIBG uptake in neuroblastic tumours indicates unfavourable histopathology. Eur J Nucl Med Mol Imaging. 2013 Oct;40(11):1701–10.
24. Georger B, Hero B, Harms D, Grebe J, Scheidhauer K, Bertold F. Metabolic activity and clinical features of primary ganglioneuromas. Cancer. 2001;91(10):1905–13.
25. Качанов Д.Ю., Шаманская Т.В., Коновалов Д.М., Ликарь Ю.Н., Рощин В.Ю., Муфтахова Г.М., Терещенко Г.В., Андреев Е.С., Сухов М.Н., Новичкова Г.А., Варфоломеева С.Р. Ганглионейрома у детей. Вопросы гематологии/онкологии и иммунопатологии в педиатрии. 2014;13(3):33–41.
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27. Schilling FH, Bihl H, Jacobsson H, Ambros PF, Martinsson T, Borgstrom P, et al. Combined (111)In- pentetreotide scintigraphy and (123)I-mIBG scintigraphy in neuroblastoma provides prognostic information. Med Pediatr Oncol. 2000;35:688–91.
28. Kroiss A, Putzer D, Uprimny C, Decristoforo C, Gabriel M, Santner W, et al. Functional imaging in phaeochromocytoma and neuroblastoma with 68Ga-DOTATyr3- octreotide positron emission tomography and 123I-metaiodobenzylguanidine. Eur J Nucl Med Mol Imaging. 2011;38:865–73.
29. Prathamesh J, Vikram L. Somatostatin receptor positron emission tomography/computed tomography (PET/CT) in the evaluation of opsoclonus-myoclonus ataxia syndrome. Indian J Nucl Med. 2013;28(2):108–111.
30. Pranzatelli МR, Tate E. Inflammatory and autoimmune disorders of the nervous system in children. Clinics in Developmental Medicine. 2010;184–185:152–173.
31. Wolff M, Schöning M, Niemann G, Krägeloh-Mann I. Late detection of neuroblastoma in a patient with prolonged cerebellar ataxia without opsoclonus. Neuropediatrics. 2001 Apr;32(2):101–3.
Oncopediatrics. 2016; 3: 228-239
Sympathetic nervous system tumors in children with opsoclonus myoclonus syndrome
Kachanov D. Y., Shamanskaya T. V., Il’ina E. S., Tereschenko G. V., Likar Y. N., Andreev E. S., Malevich O. B., Homyakova S. P., Shcherbakov A. P., Roschin V. Y., Konovalov D. M., Olshanskaya Y. V., Kazakova A. N., Ostrovskaya M. A., Varfolomeeva S. R.
https://doi.org/10.15690/onco.v3i3.1602Abstract
References
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5. De Grandis E. Pediatric Neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome: early diagnosis. In book Neuroblastoma. Pediatric Cancer 1. Hayat MA. (ed.). Springer Science. 2012. P. 21– 29.
6. Pranzatelli MR, Tate ED, Galvan I,Wheeler A. A controlled pilot study of piracetamfor pediatric opsoclonusmyoclonus. Clin Neuropharmacol. 2001;24:352–7.
7. Shimada H. The International Neuroblastoma Pathology Classification. Pathologica. 2003 Oct;95(5):240–1.
8. Brodeur GM, Pritchard J, Berthold F, Carlsen NL, Castel V, Castelberry RP, et al. Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol. 1993 Aug;11(8):1466–77.
9. NB2004 protocol. http://www.kinderkrebsinfo.de/dlja_specialistov/protokoly_gpoh/pohkinderkrebsinfotherapiestudien/nb2004/index_rus.html
10. Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457–481.
11. Pang KK, de Sousa C, Lang B, Pike MG. A prospective study of the presentation and management of dancing eye syndrome/opsoclonus-myoclonus syndrome in the United Kingdom. Eur J Paediatr Neurol. 2010 Mar;14(2):156–61.
12. Cushing H, Wolbach SB. The transformation of a malignant paravertebral sympathicoblastoma into a benign ganglioneuroma. Am J Pathol. 1927 May;3(3):203–216.
13. Hero B, Schleiermacher G. Update onpediatric opsoclonus myoclonus syndrome. Neuropediatrics. 2013;44:324–9.
14. Krug P, Schleiermacher G, Michon J, Valteau-Couanet D, Brisse H, Peuchmaur M, et al. Opsoclonus-myoclonus in children associated or not with neuroblastoma. Eur J Paediatr Neurol. 2010 Sep;14(5):400–9.
15. Rudnick E, Khakoo Y, Antunes NL, Seeger RC, Brodeur GM, Shimada H, et al. Opsoclonus- myoclonus-ataxia syndrome in neuroblastoma: clinical outcome and antineuronal antibodies- a report from the Children’s Cancer Group Study. Med Pediatr Oncol. 2001 Jun;36(6):612–22.
16. Gambini C, Conte M, Bernini G, Angelini P, Pession A, Paolucci P, et al. Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochemical and molecular features of 15 Italian cases. Virchows Arch. 2003 Jun;442(6):555–62.
17. Hiyama E, Yokoyama T, Ichikawa T, Hiyama K, Kobayashi M, Tanaka Y, et al. Poor outcome in patients with advanced stage neuroblastoma and coincident opsomyoclonus syndrome. Cancer. 1994;74(6):1821–6.
18. Boltshauser E, Deonna T, Hirt HR. Myoclonic encephalopathy of infantsor «dancing eyes syndrome». Report of 7 cases with long-term follow-up and review of the literature (cases with and without neuroblastoma). Helv Paediatr Acta. 1979 May;34(2):119–33.
19. Takama Y, Yoneda A, Nakamura T, Nakaoka T, Higashio A, Santo K, et al. Early Detection and Treatment of Neuroblastic Tumor with Opsoclonus-Myoclonus Syndrome Improve Neurological Outcome: A Review of Five Cases at a Single Institution in Japan. Eur J Pediatr Surg. 2016;26(1):54–9.
20. Brunklaus A, Pohl K, Zuberi SM, de Sousa C. Investigating neuroblastoma in childhood opsoclonus-myoclonus syndrome. Arch Dis Child. 2012 May;97(5):461–3.
21. Shulkin BL, Shapiro B. Current concepts on the diagnostic use of MIBG in children. J Nucl Med. 1998;39(4):679–88.
22. Parisi MT, Hattner RS, Matthay KK, Berg BO, Sandler ED. Optimized diagnostic strategy for neuroblastoma in opsoclonus- myoclonus. J Nucl Med. 1993;34(11):1922–6.
23. Fendler WP, Melzer HI, Walz C, von Schweinitz D, Coppenrath E, Schmid I, et al. High 123I-MIBG uptake in neuroblastic tumours indicates unfavourable histopathology. Eur J Nucl Med Mol Imaging. 2013 Oct;40(11):1701–10.
24. Georger B, Hero B, Harms D, Grebe J, Scheidhauer K, Bertold F. Metabolic activity and clinical features of primary ganglioneuromas. Cancer. 2001;91(10):1905–13.
25. Kachanov D.Yu., Shamanskaya T.V., Konovalov D.M., Likar' Yu.N., Roshchin V.Yu., Muftakhova G.M., Tereshchenko G.V., Andreev E.S., Sukhov M.N., Novichkova G.A., Varfolomeeva S.R. Ganglioneiroma u detei. Voprosy gematologii/onkologii i immunopatologii v pediatrii. 2014;13(3):33–41.
26. Reubi JC. Peptide receptors as molecular targets for cancer diagnosis and therapy. Endocr rev. 2003;24:389–427.
27. Schilling FH, Bihl H, Jacobsson H, Ambros PF, Martinsson T, Borgstrom P, et al. Combined (111)In- pentetreotide scintigraphy and (123)I-mIBG scintigraphy in neuroblastoma provides prognostic information. Med Pediatr Oncol. 2000;35:688–91.
28. Kroiss A, Putzer D, Uprimny C, Decristoforo C, Gabriel M, Santner W, et al. Functional imaging in phaeochromocytoma and neuroblastoma with 68Ga-DOTATyr3- octreotide positron emission tomography and 123I-metaiodobenzylguanidine. Eur J Nucl Med Mol Imaging. 2011;38:865–73.
29. Prathamesh J, Vikram L. Somatostatin receptor positron emission tomography/computed tomography (PET/CT) in the evaluation of opsoclonus-myoclonus ataxia syndrome. Indian J Nucl Med. 2013;28(2):108–111.
30. Pranzatelli MR, Tate E. Inflammatory and autoimmune disorders of the nervous system in children. Clinics in Developmental Medicine. 2010;184–185:152–173.
31. Wolff M, Schöning M, Niemann G, Krägeloh-Mann I. Late detection of neuroblastoma in a patient with prolonged cerebellar ataxia without opsoclonus. Neuropediatrics. 2001 Apr;32(2):101–3.
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