Cetin Okan, Yetisir Sertac, Akpinar Timur Selcuk, Yegen Gülcin, Altinkaynak Mustafa
Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, 34093, Istanbul, Turkey.
Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Wien Med Wochenschr. 2025 Sep 9. doi: 10.1007/s10354-025-01110-x.
Rosai-Dorfman disease (RDD) is a rare histiocytic disorder that may clinically and histologically resemble IgG4-related disease (IgG4-RD), especially in the presence of IgG4-positive plasma cell infiltration. In this case, a 69-year-old woman with generalized lymphadenopathy, constitutional symptoms, and elevated IgG4 levels was initially suspected to have IgG4-RD based on core needle biopsy. However, further evaluation with excisional lymph node biopsy revealed emperipolesis and S100-positive histiocytes, confirming the diagnosis of RDD. This case illustrates the diagnostic challenge of differentiating RDD from IgG4-RD, given the overlap in both clinical presentation and histopathological features, and highlights the importance of excisional biopsy combined with careful clinical evaluation to ensure an accurate diagnosis and appropriate management.
罗萨伊-多夫曼病(RDD)是一种罕见的组织细胞疾病,在临床和组织学上可能类似于IgG4相关性疾病(IgG4-RD),尤其是在存在IgG4阳性浆细胞浸润的情况下。在本病例中,一名69岁女性出现全身淋巴结肿大、全身症状和IgG4水平升高,最初基于粗针活检怀疑患有IgG4-RD。然而,通过切除性淋巴结活检进一步评估发现了血细胞吞噬现象和S100阳性组织细胞,确诊为RDD。鉴于临床表现和组织病理学特征存在重叠,该病例说明了鉴别RDD与IgG4-RD的诊断挑战,并强调了切除活检结合仔细的临床评估对于确保准确诊断和恰当治疗的重要性。