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冷球蛋白血症肺部受累的临床特征、影像学表现及预后

Clinical characteristics, radiological features and outcomes in pulmonary involvement of cryoglobulinemia.

作者信息

Han Hong-Xiao, Su Wei, Tian Xinlun, Zhou Dao-Bin, Li Jian, Cao Xin-Xin

机构信息

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1 Shuaifuyuan, 100730, Beijing, China.

Department of Laboratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Orphanet J Rare Dis. 2024 May 2;19(1):185. doi: 10.1186/s13023-024-03159-0.

Abstract

BACKGROUND

Cryoglobulinemia with pulmonary involvement is rare, and its characteristics, radiological findings, and outcomes are still poorly understood.

METHODS

Ten patients with pulmonary involvement of 491 cryoglobulinemia patients at Peking Union Medical College Hospital were enrolled in this retrospective study. We analyzed the characteristics, radiological features and management of pulmonary involvement patients, and compared with those of non-pulmonary involvement with cryoglobulinemia.

RESULTS

The 10 patients with pulmonary involvement (2 males; median age, 53 years) included three patients with type I cryoglobulinemia and seven patients with mixed cryoglobulinemia. All of 10 patients were IgM isotype cryoglobulinemia. All type I patients were secondary to B-cell non-Hodgkin lymphoma. Four mixed patients were essential, and the remaining patients were secondary to infections (n = 2) and systemic lupus erythematosus (n = 1), respectively. Six patients had additional affected organs, including skin (60%), kidney (50%), peripheral nerves (30%), joints (20%), and heart (20%). The pulmonary symptoms included dyspnea (50%), dry cough (30%), chest tightness (30%), and hemoptysis (10%). Chest computed tomography (CT) showed diffuse ground-glass opacity (80%), nodules (40%), pleural effusions (30%), and reticulation (20%). Two patients experienced life-threatening diffuse alveolar hemorrhage. Five patients received corticosteroid-based regimens, and four received rituximab-based regimens. All patients on rituximab-based regimens achieved clinical remission. The estimated two-year overall survival (OS) was 40%. Patients with pulmonary involvement had significantly worse OS and progression-free survival than non-pulmonary involvement patients of cryoglobulinemia (P < 0.0001).

CONCLUSIONS

A diagnosis of pulmonary involvement should be highly suspected for patients with cryoglobulinemia and chest CT-indicated infiltrates without other explanations. Patients with pulmonary involvement had a poor prognosis. Rituximab-based treatment may improve the outcome.

摘要

背景

合并肺部受累的冷球蛋白血症较为罕见,其特征、影像学表现及预后仍知之甚少。

方法

北京协和医院491例冷球蛋白血症患者中,10例合并肺部受累患者纳入本回顾性研究。我们分析了肺部受累患者的特征、影像学特点及治疗情况,并与未合并肺部受累的冷球蛋白血症患者进行比较。

结果

10例肺部受累患者(2例男性;中位年龄53岁)包括3例I型冷球蛋白血症患者和7例混合型冷球蛋白血症患者。10例患者均为IgM同型冷球蛋白血症。所有I型患者均继发于B细胞非霍奇金淋巴瘤。4例混合型患者为原发性,其余患者分别继发于感染(2例)和系统性红斑狼疮(1例)。6例患者有其他受累器官,包括皮肤(60%)、肾脏(50%)、周围神经(30%)、关节(20%)和心脏(20%)。肺部症状包括呼吸困难(50%)、干咳(30%)、胸闷(30%)和咯血(10%)。胸部计算机断层扫描(CT)显示弥漫性磨玻璃影(80%)、结节(40%)、胸腔积液(30%)和网状影(20%)。2例患者发生危及生命的弥漫性肺泡出血。5例患者接受了以皮质类固醇为基础的治疗方案,4例接受了以利妥昔单抗为基础的治疗方案。所有接受以利妥昔单抗为基础治疗方案的患者均实现临床缓解。估计两年总生存率(OS)为40%。合并肺部受累的冷球蛋白血症患者的OS和无进展生存率明显低于未合并肺部受累的患者(P<0.0001)。

结论

对于冷球蛋白血症且胸部CT显示有浸润但无其他解释的患者,应高度怀疑合并肺部受累。合并肺部受累的患者预后较差。以利妥昔单抗为基础的治疗可能改善预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba16/11067141/541bb965c3ea/13023_2024_3159_Fig1_HTML.jpg

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