Yataco-Vicente J A, Araujo-Castillo R V, López Fuentes M H
Departamento de Investigación, Escuela de Medicina, Universidad Peruana de Ciencias Aplicadas, Lima, Perú; Sociedad Científica de Estudiantes de Medicina de la Universidad Peruana de Ciencias Aplicadas (SOCIEMUPC), Lima, Perú.
Departamento de Investigación, Escuela de Medicina, Universidad Peruana de Ciencias Aplicadas, Lima, Perú.
Arch Soc Esp Oftalmol (Engl Ed). 2018 Oct;93(10):515-518. doi: 10.1016/j.oftal.2018.05.006. Epub 2018 Jun 21.
To report a case of orbital mass and proptosis, diagnosed as Rosai-Dorfman disease (RDD).
Clinical case report based on the review of clinical charts, radiological images, and histopathology.
A 42-year-old male with orbital mass and proptosis of the right eye. A surgical biopsy was performed, and the diagnosis of RDD was established using microscopy and immunohistochemistry. Definitive management included open tumour cytoreduction, with good response.
The RDD is a rare, benign, proliferative condition of unknown origin. It rarely affects the cranial cavities, with the orbital presentation being very unusual. Diagnostic confirmation is essential for the best surgical management.
报告一例眼眶肿物伴眼球突出病例，诊断为罗萨伊-多夫曼病（RDD）。
基于临床病历、影像学图像和组织病理学检查进行临床病例报告。
一名42岁男性，右眼有眼眶肿物伴眼球突出。进行了手术活检，通过显微镜检查和免疫组织化学确诊为RDD。最终治疗包括开放性肿瘤细胞减灭术，效果良好。
RDD是一种罕见的、良性的、起源不明的增殖性疾病。它很少累及颅腔，眼眶表现非常罕见。明确诊断对于最佳手术治疗至关重要。
