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费城阴性骨髓增殖性肿瘤中的降钙素原。

Serum procalcitonin in Philadelphia-negative myeloproliferative neoplasms.

机构信息

Department of Internal Medicine, General Hospital of Šibenik-Knin County, Stjepana Radića 83, 22000, Šibenik, Croatia.

Department of Laboratory Diagnostics, General Hospital of Šibenik-Knin County, Šibenik, Croatia.

出版信息

Wien Klin Wochenschr. 2021 Jan;133(1-2):62-64. doi: 10.1007/s00508-020-01651-8. Epub 2020 Apr 16.

Abstract

Philadelphia-negative myeloproliferative neoplasms (MPNs), essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), are rare clonal hematopoietic stem cell disorders accompanied by a strong inflammatory milieu, which is directly responsible for constitutional symptoms associated with the disease, such as fever, weight loss or night sweats. Non-hematologists sometimes (and often wrongly) consider the fever in MPN patients to be a symptom of an underlying disease, which may have devastating consequences. Serum procalcitonin (PCT) is a circulating biomarker commonly used to improve the diagnostic accuracy of bacterial infections and to guide antibiotic therapy. The aim of this study was to test whether PCT could aid the clinician in the early diagnosis of bacterial infections in MPNs. This study investigated PCT in 41 ambulatory MPN patients (13 ET, 13 PV and 15 MF) who had no signs of infection and compared it to 10 MPN patients with microbiologically and/or serologically documented bacterial infections. Median PCT in MPN patients was 0.02 ng/mL (range 0.01-0.09 ng/mL). No difference in PCT was found between ET, PV and MF patients (p = 0.993), whereas MPN patients with documented bacterial infections had significantly higher PCT (median PCT 2.45, range 0.90-5.40 ng/mL) when compared to MPN patients with (median PCT 0.03 ng/mL) or without constitutional symptoms (median PCT 0.02 ng/mL; p < 0.001 for both analyses). These results clearly show that PCT should not be considered as a disease biomarker in MPNs and careful clinical assessment for the signs of infection is needed when MPN patients present with fever and high PCT.

摘要

费城阴性骨髓增殖性肿瘤(MPN)、特发性血小板增多症(ET)、真性红细胞增多症(PV)和骨髓纤维化(MF)是罕见的克隆性造血干细胞疾病,伴有强烈的炎症环境,这直接导致与疾病相关的全身症状,如发热、体重减轻或盗汗。非血液科医生有时(而且经常错误地)认为 MPN 患者的发热是潜在疾病的症状,这可能会产生毁灭性的后果。血清降钙素原(PCT)是一种常用的循环生物标志物,用于提高细菌感染的诊断准确性,并指导抗生素治疗。本研究旨在测试 PCT 是否有助于临床医生早期诊断 MPN 中的细菌感染。本研究调查了 41 名无感染迹象的门诊 MPN 患者(13 名 ET、13 名 PV 和 15 名 MF)的 PCT,并将其与 10 名经微生物学和/或血清学证实有细菌感染的 MPN 患者进行了比较。MPN 患者的 PCT 中位数为 0.02ng/mL(范围 0.01-0.09ng/mL)。ET、PV 和 MF 患者的 PCT 无差异(p=0.993),而有细菌感染记录的 MPN 患者的 PCT 明显高于无(中位数 PCT 0.03ng/mL)或无全身症状的 MPN 患者(中位数 PCT 0.02ng/mL;p<0.001)。这些结果清楚地表明,PCT 不应被视为 MPN 的疾病生物标志物,当 MPN 患者出现发热和高 PCT 时,需要仔细的临床评估以确定感染迹象。

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