Kosmidou Aikaterini, Gavriilaki Eleni, Tragiannidis Athanasios
2nd Department of Internal Medicine, General Hospital of Kavala, 65500 Kavala, Greece.
2nd Propedeutic Department of Internal Medicine, Hippocration Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.
Cancers (Basel). 2024 Apr 11;16(8):1462. doi: 10.3390/cancers16081462.
Immune thrombocytopenia (ITP) is an autoimmune disease characterized by isolated thrombocytopenia. It is diagnosed in patients with a platelet count below 100,000 per cubic millimeter in whom other causes of thrombocytopenia have been ruled out, and its diagnosis is generally one of exclusion. Clinical manifestations of patients may vary from asymptomatic disease to mild mucocutaneous or life-threatening bleeding. Glucocorticoids are used as first-line treatment for ITP, while other second-line medications, mainly thrombopoietin-receptor agonists (TPO-RA) and rituximab, are given to patients in whom ITP does not remit, or relapses soon after glucocorticoid treatment. Refractoriness of ITP strongly questions its diagnosis and necessitates a thorough clinical and laboratory work-up to decide whether that is the case of refractory ITP or a misdiagnosis. The aim of this review is to summarize the conditions associated with isolated thrombocytopenia and highlight the characteristics of confusing cases. Even though the case of a myelodysplastic syndrome presented with isolated thrombocytopenia (MDS-IT) is relatively rare and not well-established in the literature, it constitutes one of the most predominant misdiagnoses of refractory ITP. MDS-IT patients are thought to present with multilineage dysplasia, normal karyotype and low risk prognostic score, based on IPSS-R. It has been shown that a significant proportion of MDS-IT patients are misdiagnosed as having the more common ITP. Therefore, it is crucial that in confusing cases of persistent thrombocytopenia a detailed diagnostic work-up is applied-including evaluation of peripheral-blood smear, bone marrow examination and cytogenetic testing-to avoid unnecessary therapy delay.
免疫性血小板减少症(ITP)是一种以孤立性血小板减少为特征的自身免疫性疾病。对于血小板计数低于每立方毫米100,000且已排除其他血小板减少原因的患者可诊断为此病,其诊断通常是排除性诊断。患者的临床表现可能从无症状疾病到轻度黏膜皮肤出血或危及生命的出血不等。糖皮质激素用作ITP的一线治疗药物,而其他二线药物,主要是血小板生成素受体激动剂(TPO-RA)和利妥昔单抗,则用于ITP未缓解或在糖皮质激素治疗后很快复发的患者。ITP的难治性强烈质疑其诊断,因此有必要进行全面的临床和实验室检查,以确定是难治性ITP还是误诊。本综述的目的是总结与孤立性血小板减少相关的情况,并突出混淆病例的特征。尽管以孤立性血小板减少为表现的骨髓增生异常综合征(MDS-IT)病例相对少见且在文献中尚未充分确立,但它是难治性ITP最主要的误诊之一。基于国际预后评分系统(IPSS-R),MDS-IT患者被认为存在多系发育异常、核型正常且预后风险评分低。研究表明,相当一部分MDS-IT患者被误诊为更常见的ITP。因此,在持续性血小板减少的混淆病例中,应用详细的诊断检查(包括外周血涂片评估、骨髓检查和细胞遗传学检测)至关重要,以避免不必要的治疗延误。