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经核心针活检诊断的非 IgG4 相关纤维性纵隔炎伴类固醇治疗:病例研究及鉴别诊断综述。

Non-IgG4-Related Fibrosing Mediastinitis Diagnosed on Core Needle Biopsy and Treated with Steroids: A Case Study and Review of the Differential Diagnoses.

机构信息

Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.

Department of Pathology, University of Pittsburg Medical Center, Pittsburgh, PA, USA.

出版信息

Int J Surg Pathol. 2024 Sep;32(6):1215-1221. doi: 10.1177/10668969231219646. Epub 2024 Jan 17.

Abstract

OBJECTIVES

This study aimed to investigate the histological characteristics and treatment efficacy of non-immunoglobulin G4-related fibrosing mediastinitis and discuss differential diagnoses for this rare entity.

METHODS

We present a case study of non-immunoglobulin G4-related fibrosing mediastinitis diagnosed on core biopsy and treated with steroids. A total of four 18-gauge core needle biopsy specimens were obtained for surgical pathology. Analysis of the patient's medical history, radiological characteristics of fibrosing mediastinitis, histological features, immunohistochemistry results, the differential diagnosis and treatment efficacy of different types of fibrosing mediastinitis was performed.

RESULTS

This report describes a unique presentation of fibrosing mediastinitis (syncope and weight loss) that was concerning for malignancy. Histological, laboratory and radiographical studies confirmed the diagnosis of non-immunoglobulin G4-related fibrosing mediastinitis. The patient received corticosteroid treatment which showed marked improvement after 1 month of treatment.

CONCLUSIONS

Fibrosing mediastinitis is an extremely uncommon entity with unknown pathogenesis, and it is more important to rule out malignancy and infection than to delineate between fibrosing mediastinitis and IgG4-related disease. In doing this, we may reasonably initiate a trial of corticosteroids which may prove beneficial, as in this patient. More studies on the pathogenesis of fibrosing mediastinitis are necessary to guide better directed treatments.

摘要

目的

本研究旨在探讨非 IgG4 相关纤维性纵隔炎的组织学特征和治疗效果,并讨论该罕见疾病的鉴别诊断。

方法

我们报告了一例经核心活检诊断的非 IgG4 相关纤维性纵隔炎病例,并采用类固醇进行治疗。共获得 4 份 18 号核心针活检标本进行外科病理学分析。对患者的病史、纤维性纵隔炎的影像学特征、组织学特征、免疫组织化学结果、不同类型纤维性纵隔炎的鉴别诊断和治疗效果进行了分析。

结果

本报告描述了一种独特的纤维性纵隔炎表现(晕厥和体重减轻),这令人担忧是否为恶性肿瘤。组织学、实验室和影像学研究证实了非 IgG4 相关纤维性纵隔炎的诊断。患者接受了皮质类固醇治疗,治疗 1 个月后症状明显改善。

结论

纤维性纵隔炎是一种极罕见的疾病,其发病机制尚不清楚。与明确纤维性纵隔炎和 IgG4 相关疾病相比,更重要的是排除恶性肿瘤和感染。通过这样做,我们可以合理地开始皮质类固醇治疗,就像本例患者一样,这可能是有益的。需要更多关于纤维性纵隔炎发病机制的研究,以指导更有针对性的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/764a/11337727/a42f88c34ff9/10.1177_10668969231219646-fig1.jpg

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