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浆细胞(佐恩氏)龟头炎:另一种可能富含IgG4 +浆细胞的炎症性疾病。

Plasma cell (Zoon) balanitis: another inflammatory disorder that can be rich in IgG4+ plasma cells.

作者信息

Aggarwal Nidhi, Parwani Anil V, Ho Jonhan, Cook James R, Swerdlow Steven H

机构信息

*Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA †Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH.

出版信息

Am J Surg Pathol. 2014 Oct;38(10):1437-43. doi: 10.1097/PAS.0000000000000269.

Abstract

Numerous IgG4 plasma cells and a high IgG4/IgG plasma cell ratio are important criteria in the diagnosis of IgG4-related sclerosing disease (IgG4-RSD), a steroid-responsive fibroinflammatory disorder. There is also a growing list of other inflammatory disorders that may mimic IgG4-RSD with many IgG4 plasma cells; however, limited data exist concerning whether plasma cell (Zoon) balanitis (PCB) is among these disorders. We, therefore, reviewed the clinical, histologic, and immunohistochemical features of PCB in 17 patients, including evaluation of CD3, CD20, CD138, κ, λ, IgG, IgG4, IgM, IgA, and IgD. All biopsies showed an infiltrate rich in plasma cells with variable numbers of B and T cells. IgG4 counts in the areas with the greatest density varied from 1/HPF to >200/HPF. Six of 17 (35.3%) cases demonstrated 50 or more IgG4 plasma cells/HPF, with an IgG4/IgG ratio of >40%, at least focally, in 2 of these cases. The plasma cells were clearly polytypic in 12/15 evaluable cases, with an increased proportion of κ-positive plasma cells in 3 (≥4 to 5:1). None of the patients had other clinical evidence of IgG4-RSD or a lymphoproliferative disorder. In conclusion, this study demonstrates that PCB should be added to the growing list of inflammatory disorders that can have significantly increased IgG4 plasma cells but which do not represent IgG4-RSD and which can have increased κ-positive plasma cells in the absence of malignant lymphoma.

摘要

大量IgG4浆细胞和高IgG4/IgG浆细胞比例是IgG4相关硬化性疾病(IgG4-RSD)诊断的重要标准,IgG4-RSD是一种对类固醇有反应的纤维炎性疾病。还有越来越多的其他炎性疾病可能会出现许多IgG4浆细胞而类似IgG4-RSD;然而,关于浆细胞性(佐恩)龟头炎(PCB)是否属于这些疾病的数据有限。因此,我们回顾了17例PCB患者的临床、组织学和免疫组化特征,包括对CD3、CD20、CD138、κ、λ、IgG、IgG4、IgM、IgA和IgD的评估。所有活检均显示富含浆细胞的浸润,伴有数量不等的B细胞和T细胞。密度最大区域的IgG4计数从1/高倍视野到>200/高倍视野不等。17例(35.3%)病例中有6例显示每高倍视野有50个或更多IgG4浆细胞,其中2例至少局部IgG4/IgG比例>40%。在15例可评估病例中的12例中,浆细胞明显为多克隆性,3例κ阳性浆细胞比例增加(≥4比5:1)。所有患者均无IgG4-RSD或淋巴增殖性疾病的其他临床证据。总之,本研究表明,PCB应被列入越来越多的炎性疾病名单中,这些疾病可出现IgG4浆细胞显著增加,但并非IgG4-RSD,且在无恶性淋巴瘤的情况下κ阳性浆细胞可增加。

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