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不典型浆细胞白血病误诊为急性白血病:1 例报告。

Atypical Plasma Cell Leukemia Mistaken for Acute Leukemia: A Case Report.

机构信息

Department of Cytology, Faculty of Medicine, University of Rijeka, Clinical Hospital Center Rijeka, 51000 Rijeka, Croatia.

Department of Pathology and Laboratory Medicine, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 5A2, Canada.

出版信息

Medicina (Kaunas). 2024 Aug 20;60(8):1351. doi: 10.3390/medicina60081351.

Abstract

The patient we present here had many clinical, morphological, and laboratory findings characteristic of acute leukemia. During the course of the disease, the diagnosis changed from acute leukemia to chronic small B-cell lymphoproliferative disease, a blastoid variant of mantle cell lymphoma, and finally to atypical plasma cell leukemia. Atypical plasma cell leukemia is a rare condition with aggressive biological behavior. Our patient relapsed a short time after achieving complete remission, in spite of aggressive therapy and autologous stem cell transplantation. During relapse, it was possible to morphologically identify malignant cells as being of plasma cell origin, although immature and atypical. Atypical plasma cell leukemia presents a diagnostic challenge as it may mimic other neoplasms both morphologically and clinically. It is also recognized that plasma cell neoplasm immunophenotype may not be entirely specific for its lineage where common diagnostic biomarkers are applied by immunohistochemistry or flow cytometry. Where this is the case, only focused investigation for plasma cell lineage will be more informative. This patient has unusual clinical presentation, a nondescript morphology of the circulating plasma cells, as well as an immunophenotype, detected by the initial panels used for flow cytometry and immunohistochemistry, that was not entirely specific for plasma cells. Such cases present a good reminder of the diagnostic complexity of atypical plasma cell leukemia and emphasize that plasma cell differentiation needs to be interrogated in cases where the initial work-up shows unusual results.

摘要

我们在此介绍的患者具有许多急性白血病的临床、形态学和实验室特征。在疾病过程中,诊断从急性白血病转变为慢性小 B 细胞淋巴增生性疾病、套细胞淋巴瘤的 blastoid 变体,最后变为不典型浆细胞白血病。不典型浆细胞白血病是一种具有侵袭性生物学行为的罕见疾病。尽管进行了积极的治疗和自体干细胞移植,我们的患者在完全缓解后不久就复发了。在复发期间,虽然幼稚和不典型,但可以从形态学上识别出恶性细胞起源于浆细胞。不典型浆细胞白血病具有诊断挑战,因为它在形态学和临床上可能模仿其他肿瘤。人们还认识到,在应用免疫组织化学或流式细胞术检测常见诊断生物标志物时,浆细胞肿瘤免疫表型可能不完全特异于其谱系。在这种情况下,仅针对浆细胞谱系进行有针对性的调查将更具信息性。该患者具有不寻常的临床表现、循环浆细胞的形态不典型以及免疫表型,最初的流式细胞术和免疫组织化学检测面板并非完全特异于浆细胞。这种情况很好地提醒了人们不典型浆细胞白血病的诊断复杂性,并强调在初始检查结果异常的情况下,浆细胞分化需要进行探究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/995f/11356772/af3442a3e518/medicina-60-01351-g001.jpg

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