Shome Debraj, Honavar Santosh G, Reddy Vijay Anand P, Vemuganti Geeta K
Department of Ophthalmic Plastic Surgery, Orbit and Ocular Oncology, L.V. Prasad Eye Institute, Hyderabad, India.
Ophthalmic Plast Reconstr Surg. 2007 Mar-Apr;23(2):147-8. doi: 10.1097/IOP.0b013e318032af94.
A 20-month-old child with systemic features of neurofibromatosis type 1 presented with sudden-onset proptosis. Biopsy and histopathology confirmed the diagnosis of an embryonal rhabdomyosarcoma. The tumor regressed completely with chemotherapy and external beam radiotherapy. This case highlights the association of rhabdomyosarcoma with neurofibromatosis type 1.
一名患有1型神经纤维瘤病全身症状的20个月大儿童出现突发眼球突出。活检及组织病理学检查确诊为胚胎性横纹肌肉瘤。经化疗和外照射放疗后，肿瘤完全消退。该病例突出了横纹肌肉瘤与1型神经纤维瘤病之间的关联。
