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Essential thrombocythemia

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JAK/STAT pathway. The JAK2 protein controls the production of blood cells from hematopoietic stem cells which are located in the bone marrow and can eventually become platelets, red blood cells or white blood cells. Specifically in ET, a JAK2 mutation is acquired rather than inherited. The most common JAK2 mutation is V617F which is the replacement of a valine amino acid with phenylalanine amino acid at the 617 position, hence the name V617F. This mutation results in the JAK2 protein constantly being turned on, which leads to the overproduction of abnormal blood cells, in ET it is platelets or megakaryocytes. There is also another JAK2 mutation found in exon 12, however much less common.
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amino acid domain, a proline rich P-domain, and a carboxyl domain. All of these parts facilitate the function of CALR. CALR mutation is caused by insertions or deletions of amino acids in exon 9 that cause a reading shift, which then leads to the formation of a novel C terminus. There are two common types of CALR mutations, type 1 and type 2. Type 1 mutations are a 52-bp deletion and type 2 mutations are a 5-bp insertion. In type 1 mutations, the negativle charged amino acids in the CALR C terminus are completely eliminated, and in the type 2 mutations, roughly half are eliminated. There are other mutations involving CALR, however these two are the most common.
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Klampfl T, Gisslinger H, Harutyunyan AS, Nivarthi H, Rumi E, Milosevic JD, Them NC, Berg T, Gisslinger B, Pietra D, Chen D, Vladimer GI, Bagienski K, Milanesi C, Casetti IC, Sant'Antonio E, Ferretti V, Elena C, Schischlik F, Cleary C, Six M, Schalling M, Schönegger A, Bock C, Malcovati L, Pascutto C,
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There is also a small number of people who have a different mutation called CALR, which is abbreviated from calreticulin. CALR is a protein found in the endoplasmic reticulum (ER). Its purpose is to maintain calcium homeostasis and control protein folding. There are three parts to CALR including an
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Nangalia J, Massie CE, Baxter EJ, Nice FL, Gundem G, Wedge DC, Avezov E, Li J, Kollmann K, Kent DG, Aziz A, Godfrey AL, Hinton J, Martincorena I, Van Loo P, Jones AV, Guglielmelli P, Tarpey P, Harding HP, Fitzpatrick JD, Goudie CT, Ortmann CA, Loughran SJ, Raine K, Jones DR, Butler AP, Teague JW,
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Essential thrombocythemia is sometimes described as a slowly progressive disorder with long asymptomatic periods punctuated by thrombotic or hemorrhagic events. However, well-documented medical regimens can reduce and control the number of platelets, which reduces the risk of these thrombotic or
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Lastly, the least common mutation found in patients with ET are MPL mutations. The MPL gene is responsible for making thrombopoeitin receptor proteins which promote the growth and division of cells. This receptor protein is vital in producing platelets. There are various MPL mutations, but most
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There are three known genetic mutations that cause ET. The most common genetic mutation is a JAK2 mutation. Roughly 50% of the population of ET patients have this mutation. The JAK 2 gene signals a protein that promotes the growth of cells. The protein is part of a signaling pathway called the
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The PT1 study compared hydroxyurea plus aspirin to anagrelide plus aspirin as initial therapy for ET. Hydroxyurea treated patients had a lower incidence of arterial thrombosis, lower incidence of severe bleeding and lower incidence of transformation to myelofibrosis, but the risk of venous
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can lower the platelet count. Low-dose aspirin is used to reduce the risk of blood clot formation unless the platelet count is very high, where there is a risk of bleeding from the disease, and hence this measure would be counter-productive as aspirin-use increases the risk of bleeding.
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O'Meara S, McLaren S, Bianchi M, Silber Y, Dimitropoulou D, Bloxham D, Mudie L, Maddison M, Robinson B, Keohane C, Maclean C, Hill K, Orchard K, Tauro S, Du MQ, Greaves M, Bowen D, Huntly BJ, Harrison CN, Cross NC, Ron D, Vannucchi AM, Papaemmanuil E, Campbell PJ, Green AR (Dec 2013).
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Not all those affected will require treatment at presentation. Patients are usually designated as having a low or high risk of bleeding or developing blood clots based on their age, medical history, blood counts and their lifestyles. Low risk individuals are usually treated with
337:. Platelets derived from the abnormal megakaryocytes are activated, which, along with the elevated platelet count, contributes to the likelihood of forming blood clots. The increased possibility of bleeding when the platelet count is over 1 million is due to 415:
The following revised diagnostic criteria for essential thrombocythemia were proposed in 2005. The diagnosis requires the presence of both A criteria together with B3 to B6, or of criterion A1 together with B1 to B6. The criteria are as follows:
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Tefferi, A (March 2011). "Annual Clinical Updates in Hematological Malignancies: a continuing medical education series: polycythemia vera and essential thrombocythemia: 2011 update on diagnosis, risk-stratification, and management".
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hemorrhagic events. The lifespan of a well-controlled ET person is well within the expected range for a person of similar age but without ET. ET is the myeloproliferative neoplasm least likely to progress to acute myeloid leukemia.
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thrombosis was higher with hydroxycarbamide than with anagrelide. It is unknown whether the results are applicable to all ET patients. In people with symptomatic ET and extremely high platelet counts (exceeding 1 million),
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typical are point mutations that cause amino acid changes. The MPL mutation activates the thrombopoeitin receptor despite the absence of the ligand. This causes the constant proliferation of cells.
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Vardiman, JW; Thiele, J; Arber, DA; Brunning, RD; Borowitz, MJ; Porwit, A; Harris, NL; Le Beau, MM; Hellström-Lindberg, E; Tefferi, A; Bloomfield, CD (July 2009).
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Branehog I, Ridell B, Swolin B, Weinfeld A (1975). "Megakaryocyte quantifications in relation to thrombokinetics in primary thrombocythaemia and allied diseases".
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may be present in up to 10% of cases. Patients with the Philadelphia chromosome have a potential for the development of acute leukemia, especially
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Vannucchi, AM (June 2010). "Insights into the pathogenesis and management of thrombosis in polycythemia vera and essential thrombocythemia".
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Fu, R; Zhang, L; Yang, R (November 2013). "Paediatric essential thrombocythaemia: clinical and molecular features, diagnosis and treatment".
1501:"The role of thrombocytapheresis in the contemporary management of hyperthrombocytosis in myeloproliferative neoplasms: A case-based review" 3081: 2931: 2089: 2072: 1701: 589:
age at onset is 65–70 years and it is more frequent in females than in males. The incidence in children is 0.09/100,000 per year.
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Valera, MC; Parant, O; Vayssiere, C; Arnal, JF; Payrastre, B (October 2011). "Essential thrombocythemia and pregnancy".
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Boddu, Prajwal; Falchi, Lorenzo; Hosing, Chitra; Newberry, Kate; Bose, Prithviraj; Verstovsek, Srdan (2017-07-01).
472: 384: 2716: 2355: 1926: 128: 536:). Currently unapproved but in late-stage clinical trials (NCT04254978) are agents that lower platelets such as 136: 2901: 2867: 2567: 2437: 2325: 2068: 1897: 1712: 492: 462: 191: 179: 2108: 1127:
Prins, Daniel; González Arias, Carlos; Klampfl, Thorsten; Grinfeld, Jacob; Green, Anthony R. (February 2020).
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of the resulting protein, that creates a novel terminal peptide and causes a loss of endoplasmic reticulum
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at the time of diagnosis, which is usually made after noting an elevated platelet level on a routine
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hematocrit < midpoint of normal range or normal red cell mass in presence of normal iron stores
2975: 2345: 2027: 1832: 1425: 1375: 1315: 1185: 1109: 1009: 924: 831: 729: 641: 306: 302: 90: 1985: 1959: 50: 1556: 3025: 2980: 2889: 2234: 2010: 1919: 1752: 1723: 1605: 1538: 1520: 1481: 1417: 1367: 1307: 1262: 1215: 1205: 1166: 1148: 1101: 1059: 1001: 959: 916: 880: 823: 785: 721: 679: 632:, a procedure that removes platelets from the blood and returns the remainder to the patient. 451: 183: 160: 70: 2060: 2000: 1995: 1855: 1597: 1528: 1512: 1471: 1463: 1409: 1357: 1299: 1254: 1197: 1156: 1140: 1091: 1049: 1041: 993: 951: 908: 870: 862: 815: 775: 713: 629: 597: 565: 548: 525: 270: 202: 2402: 3086: 2340: 2174: 1880: 274: 246: 17: 2015: 552: 529: 305:), fatigue, headache, nausea, vomiting, abdominal pain, visual disturbances, dizziness, 2365: 2077: 2020: 1902: 1695: 1684: 1533: 1500: 1476: 1451: 1161: 1128: 1054: 1029: 955: 875: 850: 501: 421: 387:. All mutations (insertions or deletions) affected the last exon, generating a reading 368: 334: 148: 58: 1623: 3132: 2681: 2613: 2375: 2197: 2192: 2187: 1944: 1775: 1400:
BirgegĂĄrd, G (July 2013). "Pharmacological management of essential thrombocythemia".
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Fabris, F; Randi, ML (October 2009). "Essential thrombocythemia: past and present".
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can be used to remove platelets from the blood to reduce the risk of thrombosis.
2965: 2451: 2182: 1990: 1822: 1811: 1747: 613: 612:. Essential thrombocythemia can be linked with a three-fold increase in risk of 537: 258: 673: 293:(CBC). The most common symptoms are bleeding (due to dysfunctional platelets), 2370: 2335: 2310: 1954: 1936: 1728: 1669: 1665: 997: 717: 625: 601: 556: 533: 294: 230: 124: 75: 1524: 1152: 1030:"Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2" 2469: 2360: 2305: 1892: 1758: 605: 445:
stainable iron in the bone marrow or normal red cell mean corpuscular volume
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Essential thrombocythaemia, essential thrombocytosis, primary thrombocytosis
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no collagen fibrosis and ≤ grade 2 reticulin fibrosis (using 0–4 scale)
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European Journal of Obstetrics, Gynecology, and Reproductive Biology
352:(V617F) is present in 40–50% of cases and is diagnostic if present. 1080:"Somatic mutations of calreticulin in myeloproliferative neoplasms" 2846: 617: 1706: 428: 346: 2406: 1779: 1240:"Management of Polycythemia Vera and Essential Thrombocythemia" 309:, and numbness in the extremities; the most common signs are 3016:
Adult type of generalized eruption of cutaneous mastocytosis
616:. Throughout pregnancy, close monitoring of the mother and 764:"Pathogenesis and management of essential thrombocythemia" 644:
comic strip was diagnosed with essential thrombocythemia.
1129:"Mutant Calreticulin in the Myeloproliferative Neoplasms" 375:-negative patients with essential thrombocythemia and 672:
Ashorobi, Damilola; Gohari, Pouyan (August 6, 2023).
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The incidence of ET is 0.6-2.5/100,000 per year, the
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Superti-Furga G, Cazzola M, Kralovics R (Dec 2013).
3095: 3068: 3061: 3039: 2994: 2962: 2953: 2898: 2876: 2854: 2845: 2812: 2803: 2794: 2760: 2738: 2729: 2703: 2694: 2674: 2643: 2621: 2612: 2581: 2554: 2545: 2519: 2477: 2468: 2459: 2444: 2295: 2252: 2173: 2117: 2059: 2052: 2045: 1973: 1935: 1848: 1841: 1738: 1642: 219: 209: 198: 169: 159: 143: 118: 89: 69: 40: 35: 1190:International Review of Cell and Molecular Biology 2937:Refractory cytopenia with multilineage dysplasia 678:. Treasure Island (FL): StatPearls Publishing. 285:Most people with essential thrombocythemia are 2600:Accelerated phase chronic myelogenous leukemia 1184:Guglielmelli, Paola; Calabresi, Laura (2021), 524:, whereas those at high risk are treated with 27:Overproduction of platelets in the bone marrow 2418: 1791: 8: 667: 665: 663: 661: 659: 657: 65:in a patient with essential thrombocythemia. 500:no cytogenetic abnormalities suggestive of 434:B1. No cause for a reactive thrombocytosis 3065: 2959: 2851: 2809: 2800: 2735: 2700: 2618: 2551: 2474: 2465: 2456: 2425: 2411: 2403: 2056: 2049: 1845: 1798: 1784: 1776: 1639: 855:International Journal of Clinical Practice 205:, plateletpheresis, cytoreductive therapy. 80: 49: 32: 1532: 1475: 1361: 1346:"Management of Essential Thrombocythemia" 1160: 1095: 1053: 874: 779: 851:"Headache in essential thrombocythaemia" 2917:Refractory anemia with excess of blasts 1583: 1581: 1579: 1577: 1445: 1443: 1441: 1439: 1395: 1393: 1391: 1389: 1339: 1337: 1335: 1333: 1331: 1329: 979: 977: 975: 973: 699: 697: 695: 693: 653: 640:Jill Kaplan, the female protagonist of 424:> 400 Ă— 10/ÎĽL for at least 2 months. 1278: 1276: 801: 799: 757: 755: 753: 751: 749: 747: 745: 743: 261:. It may, albeit rarely, develop into 1450:Tefferi, A; Barbui, T (August 2013). 849:Frewin, R; Dowson, A (October 2012). 7: 3082:Acute panmyelosis with myelofibrosis 1561:The Lecturio Medical Concept Library 383:mutations the second most common in 2932:Paroxysmal nocturnal hemoglobinuria 1084:The New England Journal of Medicine 1034:The New England Journal of Medicine 442:B2. No evidence of iron deficiency 956:10.1111/j.1600-0609.1975.tb01087.x 241:) is a rare chronic blood cancer ( 25: 1402:Expert Opinion on Pharmacotherapy 2657:Juvenile myelomonocytic leukemia 2152:platelet storage pool deficiency 2104:Heparin-induced thrombocytopenia 867:10.1111/j.1742-1241.2012.02986.x 311:increased white blood cell count 2922:Chromosome 5q deletion syndrome 2833:Acute megakaryoblastic leukemia 2662:Chronic myelomonocytic leukemia 2573:Myeloid dendritic cell leukemia 1363:10.1182/asheducation-2011.1.215 1259:10.1182/asheducation-2005.1.201 986:Internal and Emergency Medicine 781:10.1182/asheducation-2009.1.621 706:Internal and Emergency Medicine 223:0.6-2.5/100,000 cases per year. 3006:Diffuse cutaneous mastocytosis 1871:Activated protein C resistance 1238:Campbell PJ, Green AR (2005). 901:American Journal of Hematology 808:British Journal of Haematology 1: 2774:Chronic eosinophilic leukemia 2533:Chronic neutrophilic leukemia 1517:10.1016/j.leukres.2017.03.008 363:In 2013, two groups detected 3114:Biphenotypic acute leukaemia 3049:Xanthelasmoidal mastocytosis 1965:Trousseau sign of malignancy 1602:10.1016/j.ejogrb.2011.04.040 1414:10.1517/14656566.2013.797408 1304:10.1182/blood-2009-03-209262 1202:10.1016/bs.ircmb.2021.09.003 1145:10.1097/HS9.0000000000000333 762:Beer, PA; Green, AR (2009). 622:low molecular weight heparin 385:myeloproliferative neoplasms 345:adhesion. A mutation in the 315:reduced red blood cell count 215:Median survival is 18 years. 176:Chronic myelogenous leukemia 2491:Acute myeloblastic leukemia 2285:Nonthrombocytopenic purpura 1861:Antithrombin III deficiency 1557:"Essential Thrombocythemia" 604:are contraindicated during 437:normal inflammatory indices 367:mutations in a majority of 243:myeloproliferative neoplasm 3160: 3011:Erythrodermic mastocytosis 2778:Hypereosinophilic syndrome 2240:Congenital afibrinogenemia 2144:Glanzmann's thrombasthenia 473:acute lymphocytic leukemia 18:Essential thrombocythaemia 2826:Essential thrombocythemia 2356:Gastrointestinal bleeding 2158:Hermansky–Pudlak syndrome 1927:Antiphospholipid syndrome 1908:Essential thrombocythemia 1818: 998:10.1007/s11739-009-0319-3 718:10.1007/s11739-009-0284-x 620:is recommended. Low-dose 235:essential thrombocythemia 129:transient ischemic attack 57: 48: 36:Essential thrombocythemia 2438:hematological malignancy 2326:Subconjunctival bleeding 2132:Bernard–Soulier syndrome 2095:Upshaw–Schulman syndrome 2069:Thrombocytopenic purpura 1898:Sticky platelet syndrome 675:Essential Thrombocytosis 497:no significant dysplasia 493:myelodysplastic syndrome 463:chronic myeloid leukemia 192:secondary thrombocytosis 180:myelodysplastic syndrome 2595:Philadelphia chromosome 2316:Intracranial hemorrhage 469:Philadelphia chromosome 245:) characterised by the 133:acute coronary syndrome 2230:Factor XIII deficiency 2210:Hypoprothrombinemia/II 2205:von Willebrand disease 2163:Gray platelet syndrome 333:are more sensitive to 263:acute myeloid leukemia 171:Differential diagnosis 3109:Primary myelofibrosis 3041:Systemic mastocytosis 2986:Systemic mastocytosis 2225:Factor XII deficiency 2215:Factor VII deficiency 2033:Renal vein thrombosis 1344:Cervantes, F (2011). 1196:, Elsevier: 163–178, 1097:10.1056/NEJMoa1311347 1046:10.1056/NEJMoa1312542 491:B6. No evidence of a 393:KDEL retention signal 377:primary myelofibrosis 339:von Willebrand factor 188:primary myelofibrosis 61:image representing a 3031:Solitary mastocytoma 3021:Urticaria pigmentosa 2927:Sideroblastic anemia 1981:Deep vein thrombosis 1876:Protein S deficiency 1866:Protein C deficiency 1624:"The Pajama Diaries" 299:deep vein thrombosis 291:complete blood count 137:Budd-Chiari syndrome 63:bone marrow aspirate 2220:Factor X deficiency 2109:May–Hegglin anomaly 1886:Prothrombin G20210A 1468:10.1038/leu.2013.99 686:– via PubMed. 480:B5. No evidence of 461:B4. No evidence of 450:B3. No evidence of 427:A2. Acquired V617F 356:is a member of the 149:hematopoietic cells 2976:Mast cell leukemia 2868:Erythroleukemia/M6 2752:Acute eosinophilic 2346:Pulmonary hematoma 2253:Signs and symptoms 2028:Pulmonary embolism 1833:Bleeding diathesis 1739:External resources 1186:"The MPL mutation" 944:Scand. J. Haematol 642:The Pajama Diaries 636:In popular culture 303:pulmonary embolism 281:Signs and symptoms 253:(thrombocytes) by 165:Clinical criteria. 147:Overproduction of 3139:Myeloid neoplasia 3126: 3125: 3122: 3121: 3057: 3056: 3026:Mast cell sarcoma 2981:Mast cell sarcoma 2949: 2948: 2945: 2944: 2912:Refractory anemia 2890:Polycythemia vera 2841: 2840: 2790: 2789: 2786: 2785: 2725: 2724: 2690: 2689: 2670: 2669: 2608: 2607: 2541: 2540: 2400: 2399: 2396: 2395: 2248: 2247: 2235:Dysfibrinogenemia 2119:Platelet function 2041: 2040: 1920:Purpura fulminans 1773: 1772: 1505:Leukemia Research 1211:978-0-323-89939-0 913:10.1002/ajh.21946 820:10.1111/bjh.12530 452:polycythemia vera 227: 226: 184:polycythemia vera 161:Diagnostic method 153:genetic mutations 59:Histopathological 30:Medical condition 16:(Redirected from 3151: 3102: 3075: 3066: 3062:Multiple/unknown 3042: 2999: 2969: 2960: 2905: 2883: 2861: 2852: 2819: 2810: 2801: 2767: 2745: 2736: 2717:Acute basophilic 2710: 2701: 2650: 2628: 2619: 2588: 2561: 2552: 2526: 2484: 2475: 2466: 2457: 2427: 2420: 2413: 2404: 2061:Thrombocytopenia 2057: 2050: 2006:Lowenberg's sign 1856:Clotting factors 1846: 1800: 1793: 1786: 1777: 1640: 1628: 1627: 1620: 1614: 1613: 1585: 1572: 1571: 1569: 1567: 1553: 1547: 1546: 1536: 1496: 1490: 1489: 1479: 1447: 1434: 1433: 1408:(10): 1295–306. 1397: 1384: 1383: 1365: 1341: 1324: 1323: 1289: 1280: 1271: 1270: 1244: 1235: 1229: 1228: 1227: 1226: 1181: 1175: 1174: 1164: 1124: 1118: 1117: 1099: 1074: 1068: 1067: 1057: 1040:(25): 2391–405. 1024: 1018: 1017: 981: 968: 967: 939: 933: 932: 895: 889: 888: 878: 846: 840: 839: 803: 794: 793: 783: 759: 738: 737: 701: 688: 687: 669: 630:plateletpheresis 598:Hydroxycarbamide 566:plateletpheresis 549:Hydroxycarbamide 526:hydroxycarbamide 431:mutation present 287:without symptoms 277:, or platelets. 203:Low-dose aspirin 85: 84: 53: 33: 21: 3159: 3158: 3154: 3153: 3152: 3150: 3149: 3148: 3129: 3128: 3127: 3118: 3096: 3091: 3087:Myeloid sarcoma 3069: 3053: 3040: 3035: 2995: 2990: 2963: 2941: 2899: 2894: 2877: 2872: 2855: 2837: 2813: 2782: 2761: 2756: 2739: 2721: 2704: 2686: 2666: 2644: 2639: 2622: 2604: 2582: 2577: 2555: 2537: 2520: 2515: 2478: 2449: 2440: 2431: 2401: 2392: 2341:Hemopericardium 2291: 2244: 2175:Clotting factor 2169: 2113: 2037: 1986:Bancroft's sign 1969: 1960:Virchow's triad 1931: 1881:Factor V Leiden 1837: 1814: 1804: 1774: 1769: 1768: 1734: 1733: 1651: 1637: 1632: 1631: 1622: 1621: 1617: 1587: 1586: 1575: 1565: 1563: 1555: 1554: 1550: 1498: 1497: 1493: 1449: 1448: 1437: 1399: 1398: 1387: 1343: 1342: 1327: 1287: 1282: 1281: 1274: 1242: 1237: 1236: 1232: 1224: 1222: 1212: 1183: 1182: 1178: 1126: 1125: 1121: 1090:(25): 2379–90. 1076: 1075: 1071: 1026: 1025: 1021: 983: 982: 971: 941: 940: 936: 897: 896: 892: 861:(10): 976–983. 848: 847: 843: 805: 804: 797: 761: 760: 741: 703: 702: 691: 671: 670: 655: 650: 638: 595: 583: 574: 546: 517: 512: 413: 327: 319:enlarged spleen 283: 275:red blood cells 79: 31: 28: 23: 22: 15: 12: 11: 5: 3157: 3155: 3147: 3146: 3144:Coagulopathies 3141: 3131: 3130: 3124: 3123: 3120: 3119: 3117: 3116: 3111: 3105: 3103: 3093: 3092: 3090: 3089: 3084: 3078: 3076: 3063: 3059: 3058: 3055: 3054: 3052: 3051: 3045: 3043: 3037: 3036: 3034: 3033: 3028: 3023: 3018: 3013: 3008: 3002: 3000: 2992: 2991: 2989: 2988: 2983: 2978: 2972: 2970: 2957: 2951: 2950: 2947: 2946: 2943: 2942: 2940: 2939: 2934: 2929: 2924: 2919: 2914: 2908: 2906: 2896: 2895: 2893: 2892: 2886: 2884: 2874: 2873: 2871: 2870: 2864: 2862: 2849: 2843: 2842: 2839: 2838: 2836: 2835: 2829: 2828: 2822: 2820: 2807: 2798: 2792: 2791: 2788: 2787: 2784: 2783: 2781: 2780: 2770: 2768: 2758: 2757: 2755: 2754: 2748: 2746: 2733: 2727: 2726: 2723: 2722: 2720: 2719: 2713: 2711: 2698: 2692: 2691: 2688: 2687: 2685: 2684: 2678: 2676: 2672: 2671: 2668: 2667: 2665: 2664: 2659: 2653: 2651: 2641: 2640: 2638: 2637: 2631: 2629: 2616: 2610: 2609: 2606: 2605: 2603: 2602: 2597: 2591: 2589: 2579: 2578: 2576: 2575: 2570: 2564: 2562: 2549: 2543: 2542: 2539: 2538: 2536: 2535: 2529: 2527: 2517: 2516: 2514: 2513: 2508: 2503: 2498: 2493: 2487: 2485: 2472: 2463: 2454: 2442: 2441: 2432: 2430: 2429: 2422: 2415: 2407: 2398: 2397: 2394: 2393: 2391: 2390: 2389: 2388: 2380: 2379: 2378: 2373: 2368: 2366:Hemoperitoneum 2363: 2358: 2350: 2349: 2348: 2343: 2338: 2330: 2329: 2328: 2323: 2318: 2313: 2308: 2299: 2297: 2293: 2292: 2290: 2289: 2288: 2287: 2277: 2272: 2267: 2262: 2256: 2254: 2250: 2249: 2246: 2245: 2243: 2242: 2237: 2232: 2227: 2222: 2217: 2212: 2207: 2202: 2201: 2200: 2195: 2190: 2179: 2177: 2171: 2170: 2168: 2167: 2166: 2165: 2160: 2148: 2147: 2146: 2136: 2135: 2134: 2123: 2121: 2115: 2114: 2112: 2111: 2106: 2100: 2099: 2098: 2097: 2092: 2082: 2081: 2080: 2078:Evans syndrome 2065: 2063: 2054: 2047: 2043: 2042: 2039: 2038: 2036: 2035: 2030: 2025: 2024: 2023: 2018: 2013: 2011:Peabody's sign 2008: 2003: 1998: 1993: 1988: 1977: 1975: 1971: 1970: 1968: 1967: 1962: 1957: 1952: 1947: 1941: 1939: 1933: 1932: 1930: 1929: 1924: 1923: 1922: 1912: 1911: 1910: 1905: 1903:Thrombocytosis 1900: 1890: 1889: 1888: 1883: 1878: 1873: 1868: 1863: 1852: 1850: 1843: 1839: 1838: 1836: 1835: 1830: 1825: 1819: 1816: 1815: 1805: 1803: 1802: 1795: 1788: 1780: 1771: 1770: 1767: 1766: 1755: 1743: 1742: 1740: 1736: 1735: 1732: 1731: 1720: 1709: 1698: 1687: 1672: 1652: 1647: 1646: 1644: 1643:Classification 1636: 1635:External links 1633: 1630: 1629: 1615: 1573: 1548: 1491: 1462:(8): 1617–20. 1435: 1385: 1325: 1272: 1230: 1210: 1176: 1119: 1069: 1019: 969: 934: 907:(3): 292–301. 890: 841: 814:(3): 295–302. 795: 739: 689: 652: 651: 649: 646: 637: 634: 594: 591: 582: 579: 573: 570: 545: 542: 516: 513: 511: 508: 507: 506: 505: 504: 502:myelodysplasia 498: 489: 488: 487: 478: 477: 476: 459: 458: 457: 448: 447: 446: 440: 439: 438: 432: 425: 422:Platelet count 412: 409: 379:, which makes 335:growth factors 331:megakaryocytes 326: 323: 282: 279: 255:megakaryocytes 247:overproduction 225: 224: 221: 217: 216: 213: 207: 206: 200: 196: 195: 173: 167: 166: 163: 157: 156: 145: 141: 140: 122: 116: 115: 93: 87: 86: 73: 67: 66: 55: 54: 46: 45: 42: 38: 37: 29: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 3156: 3145: 3142: 3140: 3137: 3136: 3134: 3115: 3112: 3110: 3107: 3106: 3104: 3101: 3100: 3094: 3088: 3085: 3083: 3080: 3079: 3077: 3074: 3073: 3067: 3064: 3060: 3050: 3047: 3046: 3044: 3038: 3032: 3029: 3027: 3024: 3022: 3019: 3017: 3014: 3012: 3009: 3007: 3004: 3003: 3001: 2998: 2993: 2987: 2984: 2982: 2979: 2977: 2974: 2973: 2971: 2968: 2967: 2961: 2958: 2956: 2952: 2938: 2935: 2933: 2930: 2928: 2925: 2923: 2920: 2918: 2915: 2913: 2910: 2909: 2907: 2904: 2903: 2897: 2891: 2888: 2887: 2885: 2882: 2881: 2875: 2869: 2866: 2865: 2863: 2860: 2859: 2853: 2850: 2848: 2844: 2834: 2831: 2830: 2827: 2824: 2823: 2821: 2818: 2817: 2811: 2808: 2806: 2802: 2799: 2797: 2793: 2779: 2775: 2772: 2771: 2769: 2766: 2765: 2759: 2753: 2750: 2749: 2747: 2744: 2743: 2737: 2734: 2732: 2728: 2718: 2715: 2714: 2712: 2709: 2708: 2702: 2699: 2697: 2693: 2683: 2682:Histiocytosis 2680: 2679: 2677: 2673: 2663: 2660: 2658: 2655: 2654: 2652: 2649: 2648: 2642: 2636: 2633: 2632: 2630: 2627: 2626: 2620: 2617: 2615: 2614:Myelomonocyte 2611: 2601: 2598: 2596: 2593: 2592: 2590: 2587: 2586: 2580: 2574: 2571: 2569: 2566: 2565: 2563: 2560: 2559: 2553: 2550: 2548: 2544: 2534: 2531: 2530: 2528: 2525: 2524: 2518: 2512: 2509: 2507: 2504: 2502: 2499: 2497: 2494: 2492: 2489: 2488: 2486: 2483: 2482: 2476: 2473: 2471: 2467: 2464: 2462: 2458: 2455: 2453: 2447: 2443: 2439: 2435: 2428: 2423: 2421: 2416: 2414: 2409: 2408: 2405: 2387: 2384: 2383: 2381: 2377: 2376:Hematosalpinx 2374: 2372: 2369: 2367: 2364: 2362: 2359: 2357: 2354: 2353: 2351: 2347: 2344: 2342: 2339: 2337: 2334: 2333: 2331: 2327: 2324: 2322: 2319: 2317: 2314: 2312: 2309: 2307: 2304: 2303: 2301: 2300: 2298: 2294: 2286: 2283: 2282: 2281: 2278: 2276: 2273: 2271: 2268: 2266: 2263: 2261: 2258: 2257: 2255: 2251: 2241: 2238: 2236: 2233: 2231: 2228: 2226: 2223: 2221: 2218: 2216: 2213: 2211: 2208: 2206: 2203: 2199: 2196: 2194: 2191: 2189: 2186: 2185: 2184: 2181: 2180: 2178: 2176: 2172: 2164: 2161: 2159: 2156: 2155: 2154: 2153: 2149: 2145: 2142: 2141: 2140: 2137: 2133: 2130: 2129: 2128: 2125: 2124: 2122: 2120: 2116: 2110: 2107: 2105: 2102: 2101: 2096: 2093: 2091: 2088: 2087: 2086: 2083: 2079: 2076: 2075: 2074: 2070: 2067: 2066: 2064: 2062: 2058: 2055: 2051: 2048: 2044: 2034: 2031: 2029: 2026: 2022: 2019: 2017: 2014: 2012: 2009: 2007: 2004: 2002: 2001:Louvel's sign 1999: 1997: 1996:Lisker's sign 1994: 1992: 1989: 1987: 1984: 1983: 1982: 1979: 1978: 1976: 1972: 1966: 1963: 1961: 1958: 1956: 1953: 1951: 1948: 1946: 1945:Thrombophilia 1943: 1942: 1940: 1938: 1934: 1928: 1925: 1921: 1918: 1917: 1916: 1913: 1909: 1906: 1904: 1901: 1899: 1896: 1895: 1894: 1891: 1887: 1884: 1882: 1879: 1877: 1874: 1872: 1869: 1867: 1864: 1862: 1859: 1858: 1857: 1854: 1853: 1851: 1847: 1844: 1840: 1834: 1831: 1829: 1826: 1824: 1821: 1820: 1817: 1813: 1809: 1806:Disorders of 1801: 1796: 1794: 1789: 1787: 1782: 1781: 1778: 1765: 1761: 1760: 1756: 1754: 1750: 1749: 1745: 1744: 1741: 1737: 1730: 1726: 1725: 1721: 1719: 1715: 1714: 1710: 1708: 1704: 1703: 1699: 1697: 1693: 1692: 1688: 1686: 1682: 1681: 1677: 1673: 1671: 1667: 1663: 1662: 1658: 1654: 1653: 1650: 1645: 1641: 1634: 1625: 1619: 1616: 1611: 1607: 1603: 1599: 1595: 1591: 1584: 1582: 1580: 1578: 1574: 1562: 1558: 1552: 1549: 1544: 1540: 1535: 1530: 1526: 1522: 1518: 1514: 1510: 1506: 1502: 1495: 1492: 1487: 1483: 1478: 1473: 1469: 1465: 1461: 1457: 1453: 1446: 1444: 1442: 1440: 1436: 1431: 1427: 1423: 1419: 1415: 1411: 1407: 1403: 1396: 1394: 1392: 1390: 1386: 1381: 1377: 1373: 1369: 1364: 1359: 1355: 1351: 1347: 1340: 1338: 1336: 1334: 1332: 1330: 1326: 1321: 1317: 1313: 1309: 1305: 1301: 1298:(5): 937–51. 1297: 1293: 1286: 1279: 1277: 1273: 1268: 1264: 1260: 1256: 1252: 1248: 1241: 1234: 1231: 1221: 1217: 1213: 1207: 1203: 1199: 1195: 1191: 1187: 1180: 1177: 1172: 1168: 1163: 1158: 1154: 1150: 1146: 1142: 1138: 1134: 1130: 1123: 1120: 1115: 1111: 1107: 1103: 1098: 1093: 1089: 1085: 1081: 1073: 1070: 1065: 1061: 1056: 1051: 1047: 1043: 1039: 1035: 1031: 1023: 1020: 1015: 1011: 1007: 1003: 999: 995: 992:(3): 177–84. 991: 987: 980: 978: 976: 974: 970: 965: 961: 957: 953: 950:(5): 321–32. 949: 945: 938: 935: 930: 926: 922: 918: 914: 910: 906: 902: 894: 891: 886: 882: 877: 872: 868: 864: 860: 856: 852: 845: 842: 837: 833: 829: 825: 821: 817: 813: 809: 802: 800: 796: 791: 787: 782: 777: 773: 769: 765: 758: 756: 754: 752: 750: 748: 746: 744: 740: 735: 731: 727: 723: 719: 715: 711: 707: 700: 698: 696: 694: 690: 685: 681: 677: 676: 668: 666: 664: 662: 660: 658: 654: 647: 645: 643: 635: 633: 631: 627: 623: 619: 615: 611: 607: 603: 599: 592: 590: 588: 580: 578: 571: 569: 567: 561: 558: 554: 550: 543: 541: 539: 535: 531: 527: 523: 514: 509: 503: 499: 496: 495: 494: 490: 485: 484: 483: 482:myelofibrosis 479: 474: 470: 466: 465: 464: 460: 455: 454: 453: 449: 444: 443: 441: 436: 435: 433: 430: 426: 423: 419: 418: 417: 410: 408: 404: 400: 396: 394: 390: 386: 382: 378: 374: 370: 366: 361: 359: 355: 351: 348: 344: 340: 336: 332: 324: 322: 320: 316: 312: 308: 304: 300: 296: 292: 288: 280: 278: 276: 272: 268: 267:myelofibrosis 264: 260: 256: 252: 248: 244: 240: 236: 232: 222: 218: 214: 212: 208: 204: 201: 197: 193: 189: 185: 181: 177: 174: 172: 168: 164: 162: 158: 154: 150: 146: 142: 138: 134: 130: 126: 123: 121: 120:Complications 117: 113: 109: 105: 101: 97: 94: 92: 88: 83: 77: 74: 72: 68: 64: 60: 56: 52: 47: 43: 39: 34: 19: 3097: 3070: 2997:Mastocytosis 2964: 2900: 2878: 2856: 2825: 2814: 2762: 2740: 2705: 2645: 2623: 2583: 2556: 2521: 2479: 2452:granulocytes 2386:Hemarthrosis 2150: 2138: 2126: 2016:Pratt's sign 1907: 1828:coagulopathy 1757: 1746: 1722: 1711: 1700: 1689: 1674: 1655: 1618: 1596:(2): 141–7. 1593: 1589: 1564:. Retrieved 1560: 1551: 1508: 1504: 1494: 1459: 1455: 1405: 1401: 1353: 1349: 1295: 1291: 1250: 1246: 1233: 1223:, retrieved 1193: 1189: 1179: 1136: 1132: 1122: 1087: 1083: 1072: 1037: 1033: 1022: 989: 985: 947: 943: 937: 904: 900: 893: 858: 854: 844: 811: 807: 771: 767: 712:(5): 381–8. 709: 705: 674: 639: 596: 584: 581:Epidemiology 575: 562: 553:interferon-α 547: 530:interferon-α 518: 414: 405: 401: 397: 380: 365:calreticulin 362: 358:Janus kinase 353: 328: 284: 238: 234: 228: 2966:Mastocytoma 2139:aggregation 2021:Rose's sign 1991:Homans sign 1823:Coagulation 1748:MedlinePlus 1139:(1): e333. 774:: 621–628. 614:miscarriage 538:bomedemstat 515:Indications 389:frame shift 295:blood clots 259:bone marrow 41:Other names 3133:Categories 2450:and other 2371:Hematocele 2336:Hemothorax 2311:Hemoptysis 2183:Hemophilia 1955:Thrombosis 1724:DiseasesDB 1356:: 215–21. 1350:Hematology 1247:Hematology 1225:2024-05-07 1133:HemaSphere 768:Hematology 648:References 626:enoxaparin 602:anagrelide 557:anagrelide 534:anagrelide 371:-negative/ 231:hematology 125:Thrombosis 76:Hematology 2470:Myelocyte 2436:-related 2361:Hemobilia 2306:Epistaxis 1893:Platelets 1759:eMedicine 1525:0145-2126 1511:: 14–22. 1253:: 201–8. 1153:2572-9241 929:205293800 606:pregnancy 593:Pregnancy 572:Prognosis 510:Treatment 411:Diagnosis 317:, and an 251:platelets 220:Frequency 211:Prognosis 199:Treatment 112:dizziness 104:migraines 71:Specialty 2955:CFU-Mast 2696:CFU-Baso 2547:Monocyte 2352:abdomen 2275:Petechia 2270:Hematoma 2260:Bleeding 2127:adhesion 2053:By cause 2046:Bleeding 1950:Thrombus 1849:By cause 1842:Clotting 1812:clotting 1808:bleeding 1764:med/2266 1610:21640467 1543:28380402 1486:23558521 1456:Leukemia 1430:11357000 1422:23668666 1380:18862829 1372:22160037 1312:19357394 1267:16304381 1220:34756243 1171:32382708 1114:14787432 1106:24325356 1064:24325359 1006:19789961 921:21351120 885:22889110 836:10880402 828:24032343 790:20008247 734:43185338 726:19636672 684:30969531 467:But the 360:family. 343:platelet 307:fainting 108:headache 100:insomnia 91:Symptoms 2805:CFU-Meg 2731:CFU-Eos 2568:AMoL/M5 2434:Myeloid 2321:Hyphema 2296:By site 2280:Purpura 1974:By site 1718:D013920 1696:M9962/3 1566:22 July 1534:5466892 1477:3740400 1320:3101472 1162:7000472 1055:3966280 964:1060175 876:3469735 610:nursing 522:aspirin 329:In ET, 297:(e.g., 257:in the 96:Fatigue 2511:APL/M3 2461:CFU-GM 2446:CFU-GM 2382:joint 2332:torso 2265:Bruise 2188:A/VIII 1753:000543 1707:187950 1685:238.71 1608:  1541:  1531:  1523:  1484:  1474:  1428:  1420:  1378:  1370:  1318:  1310:  1265:  1218:  1208:  1169:  1159:  1151:  1112:  1104:  1062:  1052:  1014:510829 1012:  1004:  962:  927:  919:  883:  873:  834:  826:  788:  732:  724:  682:  624:(e.g. 587:median 544:Agents 350:kinase 144:Causes 110:, and 78:  2847:CFU-E 2675:Other 2647:MD-MP 2302:head 1937:Clots 1691:ICD-O 1670:D47.3 1666:D75.2 1426:S2CID 1376:S2CID 1316:S2CID 1292:Blood 1288:(PDF) 1243:(PDF) 1110:S2CID 1010:S2CID 925:S2CID 832:S2CID 730:S2CID 618:fetus 325:Cause 271:white 2198:C/XI 2193:B/IX 1810:and 1729:4522 1713:MeSH 1702:OMIM 1680:9-CM 1606:PMID 1568:2021 1539:PMID 1521:ISSN 1482:PMID 1418:PMID 1368:PMID 1354:2011 1308:PMID 1263:PMID 1251:2005 1216:PMID 1206:ISBN 1167:PMID 1149:ISSN 1102:PMID 1060:PMID 1002:PMID 960:PMID 917:PMID 881:PMID 824:PMID 786:PMID 772:2009 722:PMID 680:PMID 608:and 600:and 555:and 429:JAK2 420:A1. 381:CALR 369:JAK2 354:JAK2 347:JAK2 3072:AML 2858:AML 2796:MEP 2742:AML 2707:AML 2625:AML 2585:CML 2558:AML 2481:AML 2090:TTP 2073:ITP 1915:DIC 1676:ICD 1657:ICD 1598:doi 1594:158 1529:PMC 1513:doi 1472:PMC 1464:doi 1410:doi 1358:doi 1300:doi 1296:114 1255:doi 1198:doi 1194:365 1157:PMC 1141:doi 1092:doi 1088:369 1050:PMC 1042:doi 1038:369 994:doi 952:doi 909:doi 871:PMC 863:doi 816:doi 812:163 776:doi 714:doi 532:or 373:MPL 301:or 273:or 265:or 249:of 229:In 3135:: 3099:MP 2902:MD 2880:MP 2816:MP 2764:MP 2635:M4 2523:MP 2506:M2 2501:M1 2496:M0 2085:TM 2071:: 1762:: 1751:: 1727:: 1716:: 1705:: 1694:: 1683:: 1668:, 1664:: 1661:10 1604:. 1592:. 1576:^ 1559:. 1537:. 1527:. 1519:. 1509:58 1507:. 1503:. 1480:. 1470:. 1460:27 1458:. 1454:. 1438:^ 1424:. 1416:. 1406:14 1404:. 1388:^ 1374:. 1366:. 1352:. 1348:. 1328:^ 1314:. 1306:. 1294:. 1290:. 1275:^ 1261:. 1249:. 1245:. 1214:, 1204:, 1192:, 1188:, 1165:. 1155:. 1147:. 1135:. 1131:. 1108:. 1100:. 1086:. 1082:. 1058:. 1048:. 1036:. 1032:. 1008:. 1000:. 988:. 972:^ 958:. 948:15 946:. 923:. 915:. 905:86 903:. 879:. 869:. 859:66 857:. 853:. 830:. 822:. 810:. 798:^ 784:. 770:. 766:. 742:^ 728:. 720:. 708:. 692:^ 656:^ 551:, 540:. 528:, 395:. 321:. 313:, 239:ET 233:, 190:, 186:, 182:, 178:, 151:, 135:, 131:, 127:, 106:, 102:, 98:, 2776:/ 2448:/ 2426:e 2419:t 2412:v 1799:e 1792:t 1785:v 1678:- 1659:- 1649:D 1626:. 1612:. 1600:: 1570:. 1545:. 1515:: 1488:. 1466:: 1432:. 1412:: 1382:. 1360:: 1322:. 1302:: 1269:. 1257:: 1200:: 1173:. 1143:: 1137:4 1116:. 1094:: 1066:. 1044:: 1016:. 996:: 990:5 966:. 954:: 931:. 911:: 887:. 865:: 838:. 818:: 792:. 778:: 736:. 716:: 710:4 475:. 237:( 194:. 155:. 139:. 114:. 20:)

Index

Essential thrombocythaemia

Histopathological
bone marrow aspirate
Specialty
Hematology
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Symptoms
Fatigue
insomnia
migraines
headache
dizziness
Complications
Thrombosis
transient ischemic attack
acute coronary syndrome
Budd-Chiari syndrome
hematopoietic cells
genetic mutations
Diagnostic method
Differential diagnosis
Chronic myelogenous leukemia
myelodysplastic syndrome
polycythemia vera
primary myelofibrosis
secondary thrombocytosis
Low-dose aspirin
Prognosis
hematology

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