Kiruthiga Kala Gnanasekaran, Younes Sheren, Natkunam Yasodha
Department of Pathology, King Edward Memorial Hospital, Pune, India.
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Am J Clin Pathol. 2022 Dec 1;158(6):672-677. doi: 10.1093/ajcp/aqac119.
Rosai-Dorfman disease (RDD) is a rare disorder characterized by the accumulation of large S100 protein-positive histiocytes that typically exhibit emperipolesis. The recently reported expression of Oct-2 in RDD histiocytes led us to explore whether PU.1, a transcription factor that is required for monocyte and B-cell development, could similarly function as a diagnostic marker in RDD.
We evaluated the expression of PU.1 and Oct-2 using immunohistochemistry in 19 patients diagnosed with RDD involving nodal, extranodal, and cutaneous sites.
Both PU.1 and Oct-2 were positive in all cases studied, with a strong intensity of staining in 84% of cases in which more than 50% of the lesional cells were positive. In three patients, both markers showed weak to moderate intensity of staining. Two patients had concomitant RDD and Langerhans cell histiocytosis in which PU.1 stained both types of histiocytes while Oct-2 stained only the RDD component.
PU.1 emerged as a robust marker with crisp nuclear staining in RDD histiocytes as well as in engulfed inflammatory cells. Strong coexpression of PU.1 and Oct-2 is a useful diagnostic marker in differentiating histiocytic/dendritic cell proliferations.
罗萨伊 - 多夫曼病(RDD)是一种罕见疾病,其特征为大量S100蛋白阳性组织细胞积聚,这些组织细胞通常表现出血细胞吞噬现象。最近报道RDD组织细胞中Oct - 2的表达促使我们探究PU.1(一种单核细胞和B细胞发育所需的转录因子)是否同样可作为RDD的诊断标志物。
我们采用免疫组织化学方法评估了19例诊断为RDD的患者(病变累及淋巴结、结外和皮肤部位)中PU.1和Oct - 2的表达情况。
在所研究的所有病例中,PU.1和Oct - 2均呈阳性,在超过50%的病变细胞为阳性的病例中,84%表现为强染色强度。在3例患者中,两种标志物均显示弱至中等强度染色。2例患者同时患有RDD和朗格汉斯细胞组织细胞增生症,其中PU.1对两种类型的组织细胞均染色,而Oct - 2仅对RDD成分染色。
PU.1在RDD组织细胞以及被吞噬的炎性细胞中呈现出清晰的核染色,是一种可靠的标志物。PU.1和Oct - 2的强共表达是鉴别组织细胞/树突状细胞增殖的有用诊断标志物。