Thyparampil Preeti J, Yen Michael T, Dhingra Sadhna, Shetlar Debra J, Zarrin-Khameh Neda, Musher Benjamin L
Department of Ophthalmology, Northwestern University, Evanston, Illinois, and Departments of Ophthalmology, Pathology, and Medicine, Baylor College of Medicine, Houstan, Texas, U.S.A.
Ophthalmic Plast Reconstr Surg. 2018 Jan-Feb;34(1):e17-e19. doi: 10.1097/IOP.0000000000000968.
Primary neuroendocrine tumors of the orbit are exceedingly rare and typically present with gradual, progressive exophthalmos. In this report, an otherwise healthy 64-year-old woman undergoes resection of a well-differentiated neuroendocrine tumor after presenting with acute proptosis. An extensive clinical and radiographic evaluation reveals no other evidence of disease, establishing the diagnosis of a primary neuroendocrine tumor. The case presentation is followed by a brief review of the classification, presentation, and evaluation of orbital neuroendocrine tumors.
眼眶原发性神经内分泌肿瘤极为罕见,通常表现为逐渐进展的眼球突出。在本报告中,一名64岁身体健康的女性在出现急性眼球突出后接受了高分化神经内分泌肿瘤切除术。广泛的临床和影像学评估未发现其他疾病证据,确诊为原发性神经内分泌肿瘤。病例报告之后是对眼眶神经内分泌肿瘤的分类、表现及评估的简要综述。