Perifollicular concentric granulomas: A clue to IgG4-related lymphadenopathy.

IF 0.6 4区 医学 Q4 HEMATOLOGY
Journal of Hematopathology Pub Date : 2024-12-01 Epub Date: 2024-12-04 DOI:10.1007/s12308-024-00615-5
Joanna L Conant, Sean S M Bullis, Clayton Wilburn
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引用次数: 0

Abstract

A 69-year-old with well-controlled HIV was evaluated for persistent cough, in the context of years of fatigue and influenza A infection 6 months prior. Chest CT and PET scans were notable for adenopathy concerning for a lymphoproliferative disorder. Radiologic studies also showed diffuse FDG uptake in the prostate, consistent with prostatitis. Axillary lymph node biopsy showed follicular and paracortical hyperplasia, and few germinal centers showed perifollicular non-necrotizing granulomas. Immunohistochemical staining demonstrated a predominance of IgG4 positive plasma cells. Serum protein electrophoresis (SPEP) and immunosubtraction showed a board-domed peak pattern suggestive of possible monoclonality. Serum IgG4 levels were elevated, and the patient was diagnosed with IgG4-related disease (IgG4-RD). This case highlights morphologic and SPEP patterns that can aid in supporting a diagnosis of IgG4-RD.

滤泡周围同心肉芽肿:igg4相关淋巴结病的线索。
我们对一名69岁的艾滋病病毒控制良好的患者进行了持续咳嗽的评估,该患者在6个月前出现了多年的疲劳和甲型流感感染。胸部CT和PET扫描显示与淋巴增生性疾病有关的腺病。放射学研究也显示前列腺弥漫性氟脱氧葡萄糖摄取,与前列腺炎一致。腋窝淋巴结活检显示滤泡和皮质旁增生,少数生发中心显示滤泡周围非坏死性肉芽肿。免疫组化染色显示IgG4阳性浆细胞居多。血清蛋白电泳(SPEP)和免疫减影显示板状圆顶峰模式,提示可能是单克隆。血清IgG4水平升高,诊断为IgG4相关疾病(IgG4- rd)。本病例强调形态和SPEP模式可以帮助支持IgG4-RD的诊断。
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来源期刊
Journal of Hematopathology
Journal of Hematopathology HEMATOLOGYPATHOLOGY-PATHOLOGY
CiteScore
0.80
自引率
0.00%
发文量
45
期刊介绍: The Journal of Hematopathology aims at providing pathologists with a special interest in hematopathology with all the information needed to perform modern pathology in evaluating lymphoid tissues and bone marrow. To this end the journal publishes reviews, editorials, comments, original papers, guidelines and protocols, papers on ancillary techniques, and occasional case reports in the fields of the pathology, molecular biology, and clinical features of diseases of the hematopoietic system. The journal is the unique reference point for all pathologists with an interest in hematopathology. Molecular biologists involved in the expanding field of molecular diagnostics and research on lymphomas and leukemia benefit from the journal, too. Furthermore, the journal is of major interest for hematologists dealing with patients suffering from lymphomas, leukemias, and other diseases. The journal is unique in its true international character. Especially in the field of hematopathology it is clear that there are huge geographical variations in incidence of diseases. This is not only locally relevant, but due to globalization, relevant for all those involved in the management of patients.
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