Leukemia/BMT Program of British Columbia, Vancouver General Hospital, Vancouver, Canada.
Department of Internal Medicine, University of British Columbia, Vancouver, Canada.
Eur J Haematol. 2023 Jun;110(6):633-638. doi: 10.1111/ejh.13944. Epub 2023 Feb 22.
Myeloid and erythroid precursor vacuolation is a common dysplastic finding associated with myeloid malignancies, toxins, drug, and nutritional deficiencies. It has been described as a core morphologic feature in VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. We sought to determine the number of cases attributable to VEXAS syndrome in bone marrow biopsies and aspirates (BAMB) reporting myeloid precursor vacuolation. We reviewed 1318 individual BAMB reports from January 2020 to July 2021 where "vacuole(s)," "vacuolation," or "vacuolated" was reported. Bone marrow biopsies with vacuolation confined to blasts or those completed as routine workup prior to stem cell transplant or post induction chemotherapy for AML (acute myeloid leukemia) were excluded. Myeloid and erythroid precursor vacuolation was noted in 219 reports representing 210 patients. The most common etiology was myelodysplastic syndrome (MDS) (38.6%), AML (16.7%), lymphoproliferative disorders and multiple myeloma (7.6%), drug or toxin exposure (5.2%) myeloproliferative neoplasm (MPN) or MPN/MDS overlap syndrome (4.3%). VEXAS syndrome was determined to be the etiology in 2.9% of patients. Two additional cases of VEXAS syndrome with bone marrow biopsies reported in the specified time frame did not explicitly report myeloid or erythroid precursor vacuolation but were identified based on clinical suspicion and repeat BAMB review. Myeloid and erythroid precursor vacuolation is a dysplastic feature attributable to VEXAS syndrome in at least 2.9% of cases. Standardized reporting of vacuolization, triaging of molecular sequencing and optimal treatment of this disorder are critical issues facing those seeing patients with suspected VEXAS syndrome.
骨髓和红系前体细胞空泡化为骨髓恶性肿瘤、毒素、药物和营养缺乏相关的常见发育不良表现。它已被描述为 VEXAS(空泡、E1 酶、X 连锁、自身炎症、体细胞)综合征的核心形态学特征。我们旨在确定骨髓活检和抽吸(BAMB)报告中骨髓前体细胞空泡化为 VEXAS 综合征的归因病例数。我们回顾了 2020 年 1 月至 2021 年 7 月期间的 1318 份单独的 BAMB 报告,其中报告了“空泡(s)”、“空泡化”或“空泡化”。排除了空泡仅限于原始细胞或完成于干细胞移植前常规检查或 AML(急性髓系白血病)诱导化疗后的骨髓活检。219 份报告中观察到骨髓和红系前体细胞空泡化,代表 210 例患者。最常见的病因是骨髓增生异常综合征(MDS)(38.6%)、AML(16.7%)、淋巴增生性疾病和多发性骨髓瘤(7.6%)、药物或毒素暴露(5.2%)、骨髓增生性肿瘤(MPN)或 MPN/MDS 重叠综合征(4.3%)。确定 VEXAS 综合征为病因的患者占 2.9%。在指定时间范围内报告的另外两例 VEXAS 综合征的骨髓活检并未明确报告骨髓或红系前体细胞空泡化,但基于临床怀疑和重复 BAMB 检查而被识别。骨髓和红系前体细胞空泡化为至少 2.9%的 VEXAS 综合征相关发育不良特征。对空泡化进行标准化报告、对分子测序进行分类和对该疾病进行最佳治疗是那些怀疑 VEXAS 综合征患者的关键问题。