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你能诊断出骨髓瘤中的免疫性血小板减少症吗?一例多发性骨髓瘤患者的血小板减少症病例。

Can you Diagnose Immune Thrombocytopenia in Myeloma? A Case of Thrombocytopenia in a Patient with Multiple Myeloma.

作者信息

Diogo Cláudia, Fernandes Carolina, Cunha Sandra, Luz Luís, Santos João Gaião, Monteiro Joana Raquel

机构信息

Department of Internal Medicine, Unidade Local de Saúde da Região de Leiria, Leiria, Portugal.

Blood Department, Unidade Local de Saúde da Região de Leiria, Leiria, Portugal.

出版信息

Eur J Case Rep Intern Med. 2024 Nov 11;11(12):004981. doi: 10.12890/2024_004981. eCollection 2024.

Abstract

UNLABELLED

Multiple myeloma (MM) is the second most common haematological malignancy, the diagnosis of which has doubled in recent years. Immune thrombocytopenia consists of isolated thrombocytopenia secondary to antibody mediated peripheral platelet destruction. In most cases, there is no identifiable cause (primary immune thrombocytopenia). Its association with multiple myeloma is rare. Early recognition of this association is essential for raising awareness among clinicians, allowing for a rapid differential diagnosis and therapeutic optimization, reducing side effects and improving prognosis. Thus, we present a clinical case of concomitant immune thrombocytopenia and MM, whose initial presentation was thrombocytopenia. This clinical case is the first case among thirteen described in the literature in which chemotherapy was the initial treatment for both pathologies, as seen in this review.

LEARNING POINTS

Multiple myeloma is the second most common haematological malignancy and is associated with a broad group of pathologies, including, in some cases, autoimmune manifestations. Thrombocytopenia in multiple myeloma is common due to therapy or bone marrow plasmacytosis, but the association of immune thrombocytopenia with multiple myeloma is rare.Raising clinicians' awareness of the association of multiple myeloma with immune thrombocytopenia is essential for a rapid differential diagnosis. This can alter therapeutic possibilities and consequent patient prognoses.

摘要

未标注

多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤,近年来其诊断率翻了一番。免疫性血小板减少症是由抗体介导的外周血小板破坏继发的孤立性血小板减少症。在大多数情况下,没有可识别的病因(原发性免疫性血小板减少症)。它与多发性骨髓瘤的关联很少见。早期识别这种关联对于提高临床医生的认识、实现快速鉴别诊断和优化治疗、减少副作用以及改善预后至关重要。因此,我们呈现一例同时患有免疫性血小板减少症和MM的临床病例,其最初表现为血小板减少症。本临床病例是文献中描述的13例病例中的首例,如本综述所见,两种病症的初始治疗均为化疗。

学习要点

多发性骨髓瘤是第二常见的血液系统恶性肿瘤,与多种病症相关,在某些情况下包括自身免疫表现。多发性骨髓瘤中的血小板减少症因治疗或骨髓浆细胞增多症而常见,但免疫性血小板减少症与多发性骨髓瘤的关联很少见。提高临床医生对多发性骨髓瘤与免疫性血小板减少症关联的认识对于快速鉴别诊断至关重要。这可以改变治疗可能性以及随之而来的患者预后。

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