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Published on: September 20, 2018
Castleman's disease in the orbit of a 17-year-old girl: a case report
Nicholas W Jones1, Tamara R Fountain, Beenu Thakral
1*Princeton University, Princeton, New Jersey; †Department of Surgery and §Department of Pathology, NorthShore University HealthSystem, Evanston, Illinois; ‡Department of Ophthalmology, Rush University Medical Center, Chicago, Illinois, U.S.A.
Abstract:
Castleman's disease is an atypical lympho proliferative disorder comprising hyaline vascular elements, plasma cells, or a mixture of both, which can present in unicentric or multicentric fashion. Resection of unicentric lesions is typically curative, but multicentric disease, also characterized by constitutional symptoms and a poorer prognosis, often requires treatment with chemotherapy, radiation, steroids, or immune modulators. Castleman's disease is rarely diagnosed in the orbit. The authors present the clinical and histopathological findings of a 17-year-old who was found to have a focal lesion in her orbit. She was successfully treated with surgical resection and was free of disease recurrence or other sequelae at 10-months follow up.