Mendonca Teena Mariet, Lashkari Harsha Prasada, Suresh Pooja K, Kondaveti Rahul, Ali Faraz, Rodrigues Gladys R
Department of Ophthalmology, Kasturba Medical College, Mangalore Manipal Academy of Higher Education Manipal, Kozhikode, Kerala, India.
Division of Pediatric Hematology/Oncology, Department of Pediatrics, Kasturba Medical College, Mangalore Manipal Academy of Higher Education Manipal, Kozhikode, Kerala, India.
Oman J Ophthalmol. 2022 Jun 29;15(2):228-230. doi: 10.4103/ojo.ojo_180_21. eCollection 2022 May-Aug.
Ewing sarcoma is one of the rare, highly malignant neuroectodermal tumors frequently involving bones. Primary orbital Ewing sarcoma is extremely uncommon. We report a rare case of a 5-year-old boy who presented to us with a painless, slow-growing mass above the medial canthus of the left eye, the clinical appearance of which was masquerading as an internal angular dermoid. The child was subsequently diagnosed to have primary orbital Ewing sarcoma. Primary orbital Ewing sarcoma is a rare tumor with poor prognosis, poses diagnostic challenges, and demands a high index of clinical suspicion.
尤因肉瘤是一种罕见的、高度恶性的神经外胚层肿瘤,常累及骨骼。原发性眼眶尤因肉瘤极为罕见。我们报告一例罕见病例,一名5岁男孩因左眼内眦上方出现无痛性、生长缓慢的肿块前来就诊,其临床表现易被误诊为内眦皮样囊肿。该患儿随后被诊断为原发性眼眶尤因肉瘤。原发性眼眶尤因肉瘤是一种预后较差的罕见肿瘤,诊断具有挑战性,需要高度的临床怀疑指数。