Cytogenetic, Clinical, Hematologic, Demographic, Immunohistochemical, and Flow Cytometry Characteristics of Patients with Plasma Cell Neoplasm in Five Years: A First Report from Iran.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Iranian Journal of Medical Sciences Pub Date : 2024-02-01 DOI:10.30476/IJMS.2023.96892.2855
Mansoureh Shokripour, Seyed Ehsan Hosseini, Navid Omidifar, Maral Mokhtari, Akbar Safaei
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引用次数: 0

Abstract

Background: The aggregation of clonal plasma cells causes plasma cell neoplasms, which vary in severity and clinical outcomes. The present research focused on the epidemiological, clinical, immunologic, and cytogenetic characteristics of plasma cell neoplasms.

Methods: In this five-year retrospective cross-sectional study, demographic information such as age and sex, calcium elevation, renal insufficiency, anemia, and bone lesion (CRAB) characteristics, as well as laboratory data including bone marrow and peripheral blood film results, immunohistochemistry, flow cytometry, and cytogenetic study outcomes were collected at Shiraz University of Medical Sciences, Shiraz, Iran. The collected data were analyzed using SPSS Statistics software (version 20.0). Descriptive statistics were reported as numbers, percentages, and mean±SD.

Results: 417 newly diagnosed plasma cell neoplasm patients were confirmed by bone marrow or other tissue biopsy tests. 279 patients were men (66.9%). The most prevalent age group was 60-64 years old (18.46%). Plasma cell myeloma (PCM) affected 355 (85.13%) patients, while monoclonal gammopathy of undetermined significance (MGUS) affected 6 (1.43%) patients. Solitary plasmacytoma was seen in 56 (13.42%) patients. At the time of diagnosis, 119 (33.52%) of 355 PCM patients were asymptomatic, whereas 236 (66.47%) patients had at least one CRAB symptom, 55 (15.49%) had two or more, and 14 (3.94%) had three or more. There were 7 (1.97%) cases of amyloidosis. Cytogenetic abnormalities were found in 51.28% (40/78) of the patients. Twenty-one individuals (52.5%) were hyperdiploid with multiple trisomy, while 19 (47.50%) were not.

Conclusion: When diagnosed, Iranian PCM patients might have more advanced disease. PCM was more prevalent in young adults, and hyperdiploid was the most common cytogenetic finding in this investigation.

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五年来浆细胞肿瘤患者的细胞遗传学、临床、血液学、人口统计学、免疫组化和流式细胞术特征:伊朗首次报告
背景:克隆浆细胞的聚集会导致浆细胞肿瘤,其严重程度和临床结果各不相同。本研究重点关注浆细胞肿瘤的流行病学、临床、免疫学和细胞遗传学特征:在这项为期五年的回顾性横断面研究中,伊朗设拉子市设拉子医科大学收集了年龄和性别、血钙升高、肾功能不全、贫血和骨病(CRAB)特征等人口统计学信息,以及骨髓和外周血片结果、免疫组化、流式细胞术和细胞遗传学研究结果等实验室数据。收集的数据使用 SPSS 统计软件(20.0 版)进行分析。描述性统计以数字、百分比和均数±SD的形式报告:结果:417 名新诊断的浆细胞肿瘤患者通过骨髓或其他组织活检得到确诊。279名患者为男性(66.9%)。高发年龄段为 60-64 岁(18.46%)。浆细胞骨髓瘤(PCM)患者有 355 名(85.13%),而意义未定的单克隆丙种球蛋白病(MGUS)患者有 6 名(1.43%)。56例(13.42%)患者为单发浆细胞瘤。确诊时,355 名多发性骨髓瘤患者中有 119 人(33.52%)无症状,236 人(66.47%)至少有一种 CRAB 症状,55 人(15.49%)有两种或两种以上症状,14 人(3.94%)有三种或三种以上症状。淀粉样变性病例有 7 例(1.97%)。51.28%的患者(40/78)发现细胞遗传学异常。21例(52.5%)为多三体高二倍体,19例(47.50%)为非多三体高二倍体:结论:伊朗多发性骨髓瘤患者在确诊时可能已是晚期。结论:伊朗多发性骨髓瘤患者在确诊时可能已是晚期,多发性骨髓瘤多发于青壮年,高二倍体是本次调查中最常见的细胞遗传学结果。
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来源期刊
Iranian Journal of Medical Sciences
Iranian Journal of Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
3.20
自引率
0.00%
发文量
84
审稿时长
12 weeks
期刊介绍: The Iranian Journal of Medical Sciences (IJMS) is an international quarterly biomedical publication, which is sponsored by Shiraz University of Medical Sciences. The IJMS intends to provide a scientific medium of com­muni­cation for researchers throughout the globe. The journal welcomes original clinical articles as well as clinically oriented basic science re­search experiences on prevalent diseases in the region and analysis of various regional problems.
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