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同时诊断慢性淋巴细胞白血病和浆细胞骨髓瘤:2 例报告及鉴别诊断要点。

Concurrent Diagnosis of Chronic Lymphocytic Leukemia and Plasma Cell Myeloma: Report of 2 Cases and Differential Diagnostic Considerations.

机构信息

Department of Pathology and Laboratory Medicine, Nuvance Health, Danbury Hospital, Danbury, CT, USA.

Washington and Lee University, Lexington, VA, USA.

出版信息

Am J Case Rep. 2024 Oct 5;25:e944707. doi: 10.12659/AJCR.944707.

DOI:10.12659/AJCR.944707
PMID:39367591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11460407/
Abstract

BACKGROUND Simultaneous occurrence of chronic lymphocytic leukemia (CLL) and plasma cell myeloma (PCM) is an uncommon hematological condition, with most patients presenting in late adult life. When these diagnoses occur concurrently, it often poses diagnostic challenges to the pathologist, with other important differential diagnoses including lymphoplasmacytic lymphoma, marginal-zone lymphoma, and chronic lymphocytic leukemia with plasmacytoid differentiation. Ancillary studies are indispensable in arriving at a reliable diagnosis in this clinical scenario. CASE REPORT We present 2 cases of simultaneous CLL and PCM that were diagnosed in our facility. The bone marrow in these patients showed increased plasma cells with a separate population of neoplastic lymphoid cells. Bone marrow examination and ancillary studies (immunohistochemistry, fluorescence in situ hybridization, and molecular studies) were performed in both cases to arrive at the diagnosis and rule out other important differential diagnoses. While the first patient was still being observed at the time of writing this report, and found to be clinically stable during his last clinic visit, the second patient succumbed to the disease as a result of gram-negative sepsis. CONCLUSIONS CLL and PCM can occasionally co-exist, posing diagnostic challenges to the pathologist. Ancillary diagnostic techniques are important in making a correct diagnosis. Making an accurate diagnosis is vital as this will guide appropriate treatment strategies. Whenever these 2 conditions occur simultaneously, patients often succumb as a result of progression of PCM.

摘要

背景

慢性淋巴细胞白血病(CLL)和浆细胞骨髓瘤(PCM)同时发生是一种罕见的血液学情况,大多数患者在成年后期出现。当这些诊断同时发生时,常给病理学家带来诊断挑战,其他重要的鉴别诊断包括淋巴浆细胞淋巴瘤、边缘区淋巴瘤和浆细胞分化的慢性淋巴细胞白血病。辅助研究在这种临床情况下对做出可靠的诊断是不可或缺的。

病例报告

我们介绍了在我们机构诊断的 2 例同时发生的 CLL 和 PCM。这些患者的骨髓中显示浆细胞增多,并有单独的肿瘤性淋巴样细胞群。对这两例患者均进行了骨髓检查和辅助研究(免疫组化、荧光原位杂交和分子研究)以做出诊断并排除其他重要的鉴别诊断。虽然在撰写本报告时,第一例患者仍在观察中,在最近的一次就诊时发现其临床稳定,但第二例患者因革兰氏阴性菌败血症而死亡。

结论

CLL 和 PCM 偶尔可以共存,给病理学家带来诊断挑战。辅助诊断技术对做出正确诊断很重要。做出准确的诊断至关重要,因为这将指导适当的治疗策略。每当这两种情况同时发生时,患者通常会因 PCM 的进展而死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/98a1731ad849/amjcaserep-25-e944707-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/30fd3f819cc1/amjcaserep-25-e944707-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/e533a8b7ec49/amjcaserep-25-e944707-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/a1a2c4ed6e03/amjcaserep-25-e944707-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/061e8e5a0b3c/amjcaserep-25-e944707-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/18a21a92401c/amjcaserep-25-e944707-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/98a1731ad849/amjcaserep-25-e944707-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/30fd3f819cc1/amjcaserep-25-e944707-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/e533a8b7ec49/amjcaserep-25-e944707-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/a1a2c4ed6e03/amjcaserep-25-e944707-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/061e8e5a0b3c/amjcaserep-25-e944707-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/18a21a92401c/amjcaserep-25-e944707-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/11460407/98a1731ad849/amjcaserep-25-e944707-g006.jpg

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Plasma cell myeloma following a prior diagnosis of chronic lymphocytic leukemia/small lymphocytic lymphoma.先前诊断为慢性淋巴细胞白血病/小淋巴细胞淋巴瘤后发生的浆细胞骨髓瘤。
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血液系统恶性肿瘤中的继发性免疫缺陷:以多发性骨髓瘤和慢性淋巴细胞白血病为例。
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