Zheng Xingxing, Tian Hongzhe, Li Wei, Yang Meihong, Jin Chenwang, Pang Yuhui
Department of Medical Imaging, Baoji Central Hospital, Baoji, China.
Department of Medical Imaging, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Front Oncol. 2025 Apr 7;15:1484820. doi: 10.3389/fonc.2025.1484820. eCollection 2025.
Rosai Dorfman disease (RDD), also known as sinus histiocytosis with extensive lymph node involvement, is a rare histiocytosis with unknown etiology. Liver RDD is relatively rare and is often reported in individual cases. Exploring the imaging and pathological features of extrahepatic Rosai Dorfman disease (RDD) and conducting a comprehensive analysis of reported cases in domestic and foreign literature to enhance understanding of this rare disease.
We collected data from a patient diagnosed with liver RDD in our hospital. In addition, we searched for liver RDD cases through PubMed and conducted a literature review.
Of the patient data used in this study, 1 patient's data was obtained from our hospital records and 16 were retrieved from literature. There were 6 males and 11 females aged between 2-72 years, with an average age of 33.55 ± 19.38 years. Four patients presented with isolated liver nodules without the involvement of lymph nodes or extranodal organs, two patients presented with a case that involved extranodal organs but not lymph nodes, two patients presented with a case involving lymph nodes but not extranodal organs, eight patients presented with a case involving both lymph nodes and extranodal organs and lastly one patient presented with a case that did not involve either lymph nodes or extranodal organs. Four of the patients underwent enhanced scanning. The results revealed that 2 of them showed low enhancement, and the other 2 showed no significant enhancement. Only 1 case underwent PET-CT, and the results indicated a high uptake. Immunohistochemistry was performed on all 17 cases of liver RDD, and the results were positive for CD1a (-), CD68 (+), and S-100 (+).
Liver RDD can manifest at any age. It presents with nonspecific imaging findings and a challenging preoperative diagnosis. Patients with extranodal hepatic RDD present with typical RDD characteristic immunohistochemistry features such as, high uptake on PET-CT, and no to mild enhancement on contrast-enhanced scans. For an early diagnosis, it is beneficial to fully comprehend these traits.
罗萨伊-多夫曼病(RDD),也称为伴有广泛淋巴结受累的窦性组织细胞增多症,是一种病因不明的罕见组织细胞增多症。肝脏RDD相对罕见,常以个案形式报道。探讨肝外罗萨伊-多夫曼病(RDD)的影像学和病理特征,并对国内外文献报道的病例进行综合分析,以加深对这种罕见疾病的认识。
我们收集了我院一名诊断为肝脏RDD患者的数据。此外,我们通过PubMed搜索肝脏RDD病例并进行文献综述。
本研究使用的患者数据中,1例患者的数据来自我院记录,16例从文献中检索到。有6名男性和11名女性,年龄在2至72岁之间,平均年龄为33.55±19.38岁。4例患者表现为孤立性肝结节,无淋巴结或结外器官受累;2例患者表现为累及结外器官但未累及淋巴结;2例患者表现为累及淋巴结但未累及结外器官;8例患者表现为累及淋巴结和结外器官;最后1例患者表现为既未累及淋巴结也未累及结外器官。4例患者接受了增强扫描。结果显示,其中2例表现为低增强,另外2例无明显增强。仅1例患者接受了PET-CT检查,结果显示摄取增高。对所有17例肝脏RDD病例进行了免疫组织化学检查,结果显示CD1a(-)呈阳性、CD68(+)呈阳性、S-100(+)呈阳性。
肝脏RDD可在任何年龄出现。它表现出非特异性的影像学表现,术前诊断具有挑战性。结外肝RDD患者表现出典型的RDD特征性免疫组织化学特征,如PET-CT摄取增高,增强扫描无至轻度增强。为了早期诊断,充分了解这些特征是有益的。