Cravero John Corbyn, Ibrahim Samar
Baylor Scott & White Medical Center - Temple, Texas.
Fed Pract. 2024 May;41(Suppl 2):S20-S23. doi: 10.12788/fp.0475. Epub 2024 May 15.
Rosai Dorfman disease is a rare non-Langerhans cell histiocytosis that affects lymph nodes, soft tissues, and other organs. The etiology of Rosai Dorfman disease is poorly understood, though it may involve an immunologic processes or infection. Treatment varies according to the disease presentation.
A male aged 56 years was evaluated for a cutaneous mass on his right medial thigh. Initially, the patient received surgical debulking with subsequent observation and no systemic therapy. However, the mass recurred, prompting another surgical removal 9 years after the initial surgery. A mass biopsy showed infiltration of plasma cells, lymphocytes, histiocytes, and occasional neutrophils with noted reactivity of S-100 protein and CD163, but not CD1a. No systemic therapy was initiated, and the patient agreed to a period of watchful waiting.
Rosai Dorfman disease of soft tissue occurs in older adults and is often associated with soft tissue abnormalities, and more rarely, in lipomas. Multidisciplinary management of the disease and research for mutations and microenvironment of RDD is needed to better understand its clinicopathological nature and improve novel therapies.
罗萨伊 - 多夫曼病是一种罕见的非朗格汉斯细胞组织细胞增多症,可累及淋巴结、软组织及其他器官。尽管罗萨伊 - 多夫曼病的病因尚不清楚,但可能涉及免疫过程或感染。治疗方法因疾病表现而异。
一名56岁男性因右大腿内侧皮肤肿物接受评估。最初,患者接受了手术减瘤,随后进行观察,未接受全身治疗。然而,肿物复发,促使在初次手术后9年再次进行手术切除。肿物活检显示浆细胞、淋巴细胞、组织细胞浸润,偶见中性粒细胞,S - 100蛋白和CD163呈阳性反应,但CD1a阴性。未启动全身治疗,患者同意进行一段时间的观察等待。
软组织罗萨伊 - 多夫曼病发生于老年人,常与软组织异常相关,较少与脂肪瘤相关。需要对该疾病进行多学科管理,并研究罗萨伊 - 多夫曼病的突变和微环境,以更好地了解其临床病理性质并改进新的治疗方法。