Trombocitemia esencial, una rara causa de compromiso cerebrovascular.

Autores/as

Palabras clave:

Trombocitopenia esencial, Janus quinasa 2, Calreticulina, Accidente cerebrovascular, Trombosis intracraneal

Resumen

La trombocitemia esencial hace parte de un grupo de neoplasias mieloproliferativas crónicas caracterizadas por presentar cromosoma de filadelfia negativo, entre las cuales se encuentran también la policitemia vera y la mielofibrosis primaria. El objetivo de esta revisión de tema fue esclarecer la relación entre la trombocitemia esencial y el compromiso cerebrovascular. Se realizó una búsqueda en las bases de datos PubMed, Scielo, Google Scholar, empleando los descriptores: “Neoplasias mieloprofeliferativias”, “Trombocitemia esencial”, “Accidente cerebrovascular”, “trombosis intracranelal”, “janus quinasa 2”, “calreticulina”; se encontró un total de 70 artículos de los cuales se seleccionaron 50 artículos que se encontraban publicados en los último 5 años. El accidente cerebrovascular isquémico, el accidente cerebrovascular hemorrágico, la trombosis del seno dural y la trombosis venosa cerebral, pueden ser complicaciones de la trombocitemia esencial, que, aunque es una rara etiología deben tenerse en cuenta, pues son las complicaciones la principal causa de mortalidad en los pacientes con esta enfermedad.

Descargas

Los datos de descargas todavía no están disponibles.

Biografía del autor/a

Mariana Muñoz-Ríos, Universidad Pontificia Bolivariana Medellín (Colombia)

Estudiante de medicina.

Citas

Stefanou MI, Richter H, Härtig F, Wang Y, Örgel A, Bender B, et al. Recurrent ischaemic cerebrovascular events as presenting manifestations of myeloproliferative neoplasms. Eur J Neurol. 2019; 26(6):90310. DOI: 10.1111/ene.13907

Szuber N, Mudireddy M, Nicolosi M, Penna D, Vallapureddy RR, Lasho TL, et al. 3023 Mayo Clinic Patients With Myeloproliferative Neoplasms: Risk-Stratified Comparison of Survival and Outcomes Data Among Disease Subgroups. Mayo Clin Proc. 2019; 94(4):599-610. DOI: 10.1016/j.mayocp.2018.08.022

Srour SA, Devesa SS, Morton LM, Check DP, Curtis RE, Linet MS, et al. Incidence and patient survival of myeloproliferative neoplasms and myelodysplastic/myeloproliferative neoplasms in the United States, 2001-12. Br J Haematol. 2016; 174(3):382-96. DOI: 10.1111/bjh.14061

Ajebo G, Patel SJ, Kota V, Guddati AK. A nationwide analysis of outcomes of stroke in hospitalized patients with essential thrombocythemia: 2006 to 2014. Am J Blood Res. 2020; 10(4):76-81

Momozaki A, Masuoka J, Furukawa T, Koguchi M, Ito H,Yoshioka F, et al. Hemorrhagic stroke associated with essential hrombocythemia: Case report and literature review. J Stroke Cerebrovasc Dis. 2020; 29(10):1050-69. DOI: 10.1016/j.jstrokecerebrovasdis.2020.105069

Kamiunten A, Shide K, Kameda T, Sekine M, Kubuki Y,Ito M, et al. Thrombohemorrhagic events, disease progression, and survival in polycythemia vera and essential thrombocythemia: a retrospective survey in Miyazaki prefecture, Japan. Int J Hematol. 2018; 107(6):681-88. DOI: 10.1007/s12185-018-2428-0

Xie J, Geng L, Yuan B, Guo Y,Zhang Z. Complex intracranial vascular complications caused by essential thrombocythemia: a critical case report. BMC Neurology.2020; 20(407). DOI: 10.1186/s12883-020-01986-9

Tefferi A, Pardanani A. Essential Thrombocythemia. N Engl J Med. 2019; 381(22):2135-44. DOI: 10.1056/NEJMcp1816082

Ianotto JC, Curto-Garcia N, Lauermanova M, Radia D, Kiladjian JJ, Harrison CN. Characteristics and outcomes of patients with essential thrombocythemia or polycythemia vera diagnosed before 20 years of age: a systematic review. Haematologica. 2019; 104(8):1580-1588. DOI: 10.3324/haematol.2018.200832

Cattaneo D, Croci GA, Bucelli C, Tabano S, Cannone M, Gaudioso G. Triple-Negative Essential Thrombocythemia: Clinical-Pathological and Molecular Features. A Single-Center Cohort Study. Front Oncol. 2021; 11(637116). DOI: 10.3389/fonc.2021.637116

Cijanes EA, Sarmiento M. Factores pronósticos en trombocitopenia. Hematología. 2020; 24 (2):44-54.

Skoda R, Duekb A,Grisouard J. Pathogenesis of myeloproliferative neoplasms. Experimental Hematology. 2015; 43:599-608. DOI: 10.1016/j.exphem.2015.06.007

Vainchenker W, Kralovics R. Genetic basis and molecular pathophysiology of classical myeloproliferative neoplasms. Blood. 2017; 129 (6):667-679. DOI: 10.1182/blood-2016-10-695940

Chuzi S, Stein B. Essential thrombocythemia: a review of the clinical features, diagnostic challenges, and treatment modalities in the era of molecular Discovery. Leuk Lymphoma. 2017; 58(12):2786-2798. DOIi: 10.1080/10428194.2017.1312371

Sieza Y, Di C, Mazziotta L, Archuby ML, Riva ME, Orellano L. Distribución de mutaciones en JAK2, MPL y CARL en pacientes con sospecha de neoplasias mieloproliferativas crónicas Phi negativas proveniente e hospitales públicos de la providencia de Buenos Aires. Hematología.2018; 22(2):151-156.

Nagai K,Shimoyama T,Yamaguchi H,Sakamoto Y, Suda S, Wakita S, et al. Clinical characteristics and brain MRI findings in myeloproliferative Neoplasms. J Neurol Sci. 2020; 416(15):116990. DOI: 10.1016/j.jns.2020.116990

Guevara M, Pérez J, Vera J, Saldierna E. Plaquetoféresis terapéutica para el manejo de trombocitosis esencial, reporte de caso y revisión del método. Rev Mex Patol Clin Med Lab. 2020; 67(2):81-84.

Yuan J, Wu Y, Hao J, Hu W. The comorbidity of acute ischemic stroke and splenic infarction resulting from essential thrombocythemia. Neurol Sci. 2018; 39(10):1787-1790. DOI: 10.1007/s10072-018-3462-7

Frederiksen H, Szépligeti S, Bak M, Ghanima W, Hasselbalch HC, Christiansen CF. Vascular Diseases In Patients With Chronic Myeloproliferative Neoplasms - Impact Of Comorbidity. Clin Epidemiol. 2019; 11:955-967. DOI: 10.2147/CLEP.S216787

Stankowska K, Gadomska G, Boinska J, Michalska M, Bartoszewska-Kubiak A, Rość D. Extrinsic blood coagulation pathway and risk factors for thrombotic events in patients with essential thrombocythemia. Pol Arch Med Wewn. 2016; 126(5):340-6. DOI: 10.20452/pamw.3429

Lussana F, Carobbio A, Salmoiraghi S, Guglielmelli P, Vannucchi AM, Bottazzi B et al. Driver mutations (JAK2V617F, MPLW515L/K or CALR), pentraxin-3 and C-reactive protein in essential thrombocythemia and polycythemia vera. J Hematol Oncol. 2017; 10(1):54. DOI: 10.1186/s13045-017-0425-z

Košťá M, Schwarz J, Ovesná P, Penka M, Dulíček P. Ph− myeloproliferative neoplasms and the related risk factors for stroke occurrence: Results from a registry of patients treated with Anagrelide. J Thromb Thrombolysis. 2021; 51(1):112-119. DOI: 10.1007/s11239-020-02175-8

Yacoub A, Lyons R, Verstovsek S, Shao R, Chu DT, Agrawal A, et al. Disease and Clinical Characteristics of Patients With a Clinical Diagnosis of Essential Thrombocythemia Enrolled in the MOST Study. Clin Lymphoma Myeloma Leuk. 2021; (21):2152-2650. DOI: 10.1016/j.clml.2021.02.011

Trifan G, Shafi N, Testai FD. Implications of Janus Kinase 2 Mutation in Embolic Stroke of Unknown Source. J Stroke Cerebrovasc Dis. 2018; 27(10):2572-2578. DOI: 10.1016/j.jstrokecerebrovasdis.2018.05.052

Okabe M, Yamaguchi H, Usuki K, Kobayashi Y, Kawata E, Kuroda J, et al. Clinical features of Japanese polycythemia vera and essentialthrombocythemia patients harboring CALR, JAK2V617F, JAK2Ex12del,and MPLW515L/K mutations. Leukemia Research. 2016; 40:68-76. DOI: 10.1016/j.leukres.2015.11.002

Cerquozzi S, Barraco D, Lasho T, Finke C, Hanson CA, Ketterling RP, et al. Risk factors for arterial versus venous thrombosis in polycythemia vera: a single center experience in 587 patients. Blood Cancer J. 2017; 7(12):662. DOI: 10.1038/s41408-017-0035-6

Ball S, Thein KZ, Maiti A, Nugent K. Thrombosis in Philadelphia negative classical myeloproliferative neoplasms: a narrative review on epidemiology, risk assessment, and pathophysiologic mechanisms. J Thromb Thrombolysis. 2018; 45(4):516-528. DOI: 10.1007/s11239-018-1623-4

Merkler AE. Blood Cell Disorders and the Nervous System. Continuum (Minneap Minn). 2020; 26(3):659-674. DOI: 10.1212/CON.0000000000000858

Ferro JM, Infante J. Cerebrovascular manifestations in hematological diseases: an update. J Neurol.2021. DOI: 10.1007/s00415-021-10441-9

Arboix A, Jiménez C, Massons J, Parra O, Besses C. Hematological disorders: a commonly unrecognized cause of acute stroke. Expert Rev Hematol. 2016; 9(9):891-901. DOI: 10.1080/17474086.2016.1208555

Ong E, Barraco F, Nighoghossian N, Praire A, Desestret V, Derex L, et al. Cerebrovascular events as presenting manifestations of Myeloproliferative Neoplasm. Rev Neurol (Paris). 2016; 172(11):703-708. DOI: 10.1016/j.neurol.2016.09.010

Campbell BCV, De Silva DA, Macleod MR, Coutts SB, Schwamm LH, Davis SM,et al. Ischaemic stroke. Nat Rev Dis Primers. 2019; 5(1):70.

Global Burden of Disease Stroke Collaborators. Global, regional, and national burden of stroke, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2019; 18(5):439-458.

World Stroke Organization. WSO global stroke fact sheet. WSO https://www.world-stroke.org/ images/WSO_Global_Stroke_Fact_Sheet_final.pdf (2019).

Kim JM, Jung KH, Park KY. Radiological features and outcomes of essential thrombocythemia-related stroke. J Neurol Sci.2019;398:135-137. DOI: 10.1016/j.jns.2019.01.035

Ferro JM, Aguiar de Sousa D. Cerebral Venous Thrombosis: an Update. Curr Neurol Neurosci Rep. 2019; 19(10):74. DOI: 10.1007/s11910-019-0988-x

Ageno W, Beyer-Westendorf J, Garcia DA, Lazo-Langner A, McBane RD, Paciaroni M. Guidance for the management of venous thrombosis in unusual sites. J Thromb Thrombolysis. 2016; 41(1):129-43. DOI: 10.1007/s11239-015-1308-1

Ferro JM, Canhão P, Aguiar de Sousa D. Cerebral venous thrombosis. Presse Med. 2016; 45(12 Pt 2):429-450.

Devasagayam S, Wyatt B, Leyden J, Kleinig T. Cerebral Venous Sinus Thrombosis Incidence Is Higher Than Previously Thought: A Retrospective Population-Based Study. Stroke. 2016; 47(9):2180-2. DOI: 10.1161/STROKEAHA.116.013617

Pinto MJ, Medeiros PB, Príncipe F, Carvalho M. Cerebral Venous Thrombosis in Hematological Malignancy: Balancing the Risks. J Stroke Cerebrovasc Dis. 2020; 29(4):104683. DOI: 10.1016/j.jstrokecerebrovasdis.2020.104683

Zhang Y, Parikh A, Qian S. Migraine and stroke. Stroke Vasc Neurol. 2017; 2(3):160-167.

Wajngarten M, Silva GS. Hypertension and Stroke: Update on Treatment. Eur Cardiol. 2019; 14(2):111-115.

Sugiyama M, Ueno Y, Kamo H, Edahiro Y, Miyamoto N, Yamashiro K, et al. Specific mechanisms of subarachnoid hemorrhage accompanied by ischemic stroke in essential thrombocythemia: two case reports and a literature review. J Neurol. 2019; 266(8):1869-1878. DOI: 10.1007/s00415-019-09347-4

Raghavan A, Wright CH, Wright JM, Jensen K, Malloy P, Elder T, et al. Outcomes and Clinical Characteristics of Intracranial Hemorrhage in Patients with Hematologic Malignancies: A Systematic Literature Review. World Neurosurg. 2020; 144:15-24.

Owattanapanich W, Auewarakul CU. Intracranial Hemorrhage in Patients with Hematologic Disorders: Prevalence and Predictive Factors. J Med Assoc Thai. 2016; 99(1):15-24.

GBD 2016 Lifetime Risk of Stroke Collaborators, Feigin VL, Nguyen G, Cercy K, Johnson CO, Alam T, et al. Global, Regional, and Country-Specific Lifetime Risks of Stroke, 1990 and 2016. N Engl J Med. 2018; 379(25):2429-2437.

Pavaloiu RM, Mogoanta L. Repeated Events of Acute Ischemic Stroke in a Patient with Essential Thrombocythemia. Curr Health Sci J. 2017; 43(1):95-97. DOI: 10.12865/CHSJ.43.01.16

Amarenco P. Transient Ischemic Attack. N Engl J Med. 2020; 382(20):1933-1941.

Martínez-Sánchez, P., Fuentes, B., Ruiz Ares, G. Ictus isquémico, infarto cerebral y ataque isquémico transitorio. Medicine - Programa de Formación Médica Continuada Acreditado. 2015; 1(71): 4230-4241.

Tanashyan MM, Kuznetsova PI, Shabalina AA, Raskurazhev AA, Lagoda OV, Subortseva IN,et al.Clinical Characteristics of Cerebrovascular Pathology with Patients Suffering from Ph-Negative Myeloproliferative Disease. Cerebrovasc Dis Extra. 2016; 6(3):66-70.

Descargas

Publicado

2022-03-30

Cómo citar

Muñoz-Ríos, M. (2022). Trombocitemia esencial, una rara causa de compromiso cerebrovascular. Salutem Scientia Spiritus, 8(1), 73–78. Recuperado a partir de https://revistas.javerianacali.edu.co/index.php/salutemscientiaspiritus/article/view/696

Número

Sección

Revisión de la literatura