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:: دوره 9، شماره 2 - ( 10-1396 ) ::
جلد 9 شماره 2 صفحات 189-193 برگشت به فهرست نسخه ها
Jak-2 mutation frequency in patients with thrombocytosis
چکیده:   (1028 مشاهده)
Background: We aimed to investigate the etiologic causes and the existence of Janus kinase 2  mutation (JAK2) in cases with thrombocytosis.
Methods: In this retrospective study, patients, who were admitted to hematology clinic with thrombocytosis between 2013 and 2015, were investigated in terms of the etiological causes of thrombocytosis and the existence of JAK2 mutation.
Results: We retrospectively evaluated 136 cases that underwent JAK2 mutation analysis due to ET preliminary diagnosis in our hematology clinic. The mean age of the patients was 56.7±15.3 years (range: 22-86 years) and 71 (52%) were males. JAK2 mutation was found to be positive in 58 (42%) of cases. The mean platelet counts of the cases were 860.25×109 / L (range: 455-1,105 109 /L) and the mean spleen vertical length was 135.1±21.6 mm (range: 110-220 mm).
Conclusions: JAK2 mutation analysis and bone marrow biopsy are the two main procedures to diagnose primary thrombocytosis in adults with persistent thrombocytosis after excluding the causes of secondary thrombocytosis. Myeloproliferative neoplasms and essential thrombocytosis are the common causes of primary thrombocytosis in adults with persistent thrombocytosis, as myelodysplastic syndrome rarely causes primary thrombocytosis.

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نوع مطالعه: Original Article | موضوع مقاله: Hematology
دریافت: ۱۳۹۵/۳/۳۱ | پذیرش: ۱۳۹۶/۷/۳۰ | انتشار: ۱۳۹۶/۱۰/۲۰
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Yokus O, Gedik H. Jak-2 mutation frequency in patients with thrombocytosis . Caspian J Intern Med. 2018; 9 (2) :189-193
URL: http://caspjim.com/article-1-787-fa.html

Jak-2 mutation frequency in patients with thrombocytosis . 1. 1396; 9 (2) :189-193

URL: http://caspjim.com/article-1-787-fa.html



دوره 9، شماره 2 - ( 10-1396 ) برگشت به فهرست نسخه ها
Caspian Journal of Internal Medicine
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