A rare case of essential thrombocythemia with pseudo-hyperkalemia.

IF 1.2 4区 医学 Q4 HEMATOLOGY
Blood Coagulation & Fibrinolysis Pub Date : 2024-06-01 Epub Date: 2024-03-13 DOI:10.1097/MBC.0000000000001295
Ugur Kalan, Jale Vardi, Selin Kucukyurt Kaya, Ahmet Kursad Gunes
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引用次数: 0

Abstract

Essential thrombocythemia (ET) is a rare clonal stem cell disorder that affects the production of platelets in the bone marrow. This condition causes an overproduction of platelets, which can lead to blood clots and other complications. Potassium, on the other hand, is an essential mineral that plays a vital role in various bodily functions, including nerve impulses and muscle contractions. Here, in this case report, we investigated a case of pseudo-hyperkalemia caused by essential thrombocythemia in a 77-year-old woman with very high platelet counts. Moreover, this case report, which has no similar examples in the literature review, is important for clinicians.

一例罕见的伴有假性高钾血症的原发性血小板增多症。
原发性血小板增多症(ET)是一种罕见的克隆性干细胞疾病,会影响骨髓中血小板的生成。这种疾病会导致血小板过度生成,从而引发血栓和其他并发症。另一方面,钾是人体必需的矿物质,在包括神经冲动和肌肉收缩在内的各种身体机能中发挥着重要作用。在本病例报告中,我们研究了一例由血小板计数极高的 77 岁女性原发性血小板增多症引起的假性高钾血症。此外,本病例报告在文献综述中没有类似的例子,因此对临床医生具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
111
审稿时长
4-8 weeks
期刊介绍: Blood Coagulation & Fibrinolysis is an international fully refereed journal that features review and original research articles on all clinical, laboratory and experimental aspects of haemostasis and thrombosis. The journal is devoted to publishing significant developments worldwide in the field of blood coagulation, fibrinolysis, thrombosis, platelets and the kininogen-kinin system, as well as dealing with those aspects of blood rheology relevant to haemostasis and the effects of drugs on haemostatic components
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