Case Report Diagnosis and Management of Essential Trombositosis in RSUD Sanjiwani Gianyar and RSUP Sanglah

  • Ni Wayan Sri Wardani RSUD Sanjiwani
  • I Ketut Ery Purnama Warsana Putra RSUD Sanjiwani
  • Ni Made Renny A Rena RSUP Sanglah Denpasar
Kata Kunci: Essential thrombocytosis, haemorrhagic, thrombosis

Abstrak

Essential thrombocytosis (ET) is a very rare disorder with 1-2 / 100,000 incidents in the world. In Indonesia there is still no concrete data regarding the incidence of ET. Essential thrombocytosis can affect all ages but most at age> 60 years, with median age diagnosed ET about 65-70 years. Women are more often affected than men with a 2: 1 ratio. Patients can have hemorrhagic tendencies in the form of bleeding in the gums, epistaxis and microvascular thrombus. The diagnosis of ET can be established by WHO criteria of platelet increase> 450, in bone marrow biopsy obtained megakariocyte cells, no WHO criteria for PV, CML, MDS, or other myeloid neoplasm diseases, and clonal marker. Management of ET is done based on the consideration of the risk level of the occurrence of thrombosis complications. Risk factors for thrombosis are age, thrombosis risk, cardiovascular risk, and the presence of a JAK2 V617F mutation. Treatment of ET can use antiplatelet and cytoreductive drugs with an age-based use of indication. The results of this case report show a matching between the theory and the situation in the patient.

##submission.authorBiographies##

##submission.authorWithAffiliation##
Internal Medicine
##submission.authorWithAffiliation##
Internal Medicine

Referensi

LJ Spiyak. Harrison’s Principal of Internal Medicine. 19th Ed. Mc Graw Hill Educ. 2015;676–8.

I Alwi, S. Salim, R Hidayat, J Kurniawan DLT. Penatalaksanaan di Bidang Ilmu Penyakit Dalam Panduan Praktik Klinis. 2015. 551-4 p.

M A Papadakis SJM. Current Medical Diagnosis and Treatment. In: Mc Graw Hill lMedical. 2013. p. 513–5.

Institutet K. Clinical and Epidemiological Studies in Malin Hultcrantz Stockholm 2013. 2013.

Moulard O, Mehta J, Fryzek J, Olivares R, Iqbal U, Mesa RA. Epidemiology of myelofibrosis, essential thrombocythemia, and polycythemia vera in the European Union. Eur J Haematol. 2014;92(4):289–97.

Briére JB. Essential thrombocythemia. Orphanet J Rare Dis. 2007;2(1):1–17.

Mehta J, Wang H, Iqbal SU, Mesa R. Epidemiology of myeloproliferative neoplasms in the United States. Leuk Lymphoma. 2014;55(3):595–600.

Oehadian A. Aspek Hematologi Tuberkulosis. 2003;

Bakta IM. Hematologi Klinik Ringkas. In: Buku Kedokteran EGC. 2011. p. 1472–82.

Hernández-Boluda JC, Gómez M. Target hematologic values in the management of essential thrombocythemia and polycythemia vera. Eur J Haematol. 2015;94(1):4–11.

Arber DA, Orazi A, Hasserjian R, Borowitz MJ, Beau MM Le, Bloomfield CD, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016;127(20):2391–406.

Rumi E, Cazzola M. How I treat How I treat essential thrombocythemia. Blood. 2016;128(20):2403–14.

Diterbitkan
2018-06-01
Bagian
Articles
Abstrak viewed = 1067 times
PDF (English) downloaded = 500 times