抄録
Objective: Essential thrombocythaemia is a rare disease. Design: A clinical study. Materials and Methods: An 86-year-old man had marked thrombocytosis, increased leukocyte count and anemia. Analysis of the Janus Activating Kinase 2 (JAK2) V617F (GTC→TTC) gene from his leukocytes demonstrated the JAK2 mutation (V617F GTC→TTC, G1849T, exon 14). Results: A diagnosis of essential Thrombocythaemia was made. Conclusions: He has been good in health without chemotherapy since then.
本文言語 | English |
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ページ(範囲) | 438-439 |
ページ数 | 2 |
ジャーナル | International Medical Journal |
巻 | 26 |
号 | 5 |
出版ステータス | Published - 2019 |
ASJC Scopus subject areas
- 医学(全般)