[Clinical characteristics analysis of patients with immune-related pancytopenia complicated by connective tissue diseases].

Q3 Medicine
Y Y Sun, C Y Liu, Z H Shao
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引用次数: 0

Abstract

A retrospective collection of clinical data was conducted on patients with connective tissue diseases (CTD) complicated by cytopenia (which could not be attributed to any currently named hematological diseases) who were hospitalized and treated in the Department of Hematology, Tianjin Medical University General Hospital from May 2022 to May 2024. Based on the prognosis, the patients were divided into the remission group (including complete remission and partial remission) and the non-remission group (clinically non-remission). Follow-up was conducted until December 2024 or until the patient's death, with an analysis of their clinical manifestations, laboratory findings, and prognosis, etc. A total of 45 patients were included, comprising 2 males and 43 females, with an age of (57±15) years. The follow-up duration [M (Q1, Q3)] was 9 (6, 18) months. Thirty-seven patients (82.2%) had other organ involvement, with 23 patients (51.1%) experiencing infections, 7 patients (15.6%) having thrombosis, 7 patients (15.6%) having neoplastic diseases. Forty-two patients (93.3%) exhibited bicytopenia or pancytopenia, with a median neutrophil-to-lymphocyte ratio of 2.4 (1.0, 6.6). In 91% (41/45) of the patients, reticulocyte counts were not low, and all patients demonstrated active bone marrow in the iliac crest and/or sternum. Among the 37 patients (82.2%) with positive antinuclear antibodies, a negative correlation was observed between antinuclear antibody titers and red blood cell levels (r=-0.40,P=0.015). There were 30 cases in the remission group and 15 cases in the non-remission group. The ferritin levels in the non-remission group were higher than those in the remission group [838 (61, 1 695) vs 123 (30, 279)μg/L, P=0.035]. Patients with immune-related pancytopenia complicated by CTD exhibited no inversion of the neutrophil-to-lymphocyte ratio, no low reticulocyte counts, and active bone marrow proliferation. Their antinuclear antibody titers were negatively correlated with the degree of red blood cell reduction, and the ferritin levels were higher in the non-remission group.

[免疫相关性全血细胞减少症合并结缔组织病的临床特点分析]。
回顾性收集2022年5月至2024年5月在天津医科大学总医院血液科住院治疗的结缔组织病(CTD)合并细胞减少症(不能归因于任何目前已命名的血液病)患者的临床资料。根据预后将患者分为缓解组(包括完全缓解和部分缓解)和非缓解组(临床无缓解)。随访至2024年12月或患者死亡,分析其临床表现、实验室结果和预后等。共纳入45例患者,其中男性2例,女性43例,平均年龄(57±15)岁。随访时间[M (Q1, Q3)]为9(6,18)个月。其他脏器受累37例(82.2%),感染23例(51.1%),血栓形成7例(15.6%),肿瘤病变7例(15.6%)。42例(93.3%)患者表现为双细胞减少或全细胞减少,中性粒细胞与淋巴细胞比值中位数为2.4(1.0,6.6)。91%(41/45)的患者网织网细胞计数不低,所有患者在髂骨和/或胸骨表现出活跃的骨髓。37例(82.2%)抗核抗体阳性患者中,抗核抗体滴度与红细胞水平呈负相关(r=-0.40,P=0.015)。缓解组30例,非缓解组15例。非缓解组铁蛋白水平高于缓解组[838 (61,1 695)vs 123 (30, 279)μg/L, P=0.035]。免疫相关性全血细胞减少合并CTD的患者没有中性粒细胞与淋巴细胞比例的逆转,没有低网织细胞计数和活跃的骨髓增殖。他们的抗核抗体滴度与红细胞减少程度呈负相关,非缓解组的铁蛋白水平更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
400
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