Rizvi Syed Wajahat Ali, Rizvi Syed Ali Raza, Qadri Shagufta, Khalid Saifullah, Siddiqui Mohammed Azfar, Khan Adeeb Alam, Akhter Afeefa
Department of Ophthalmology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India.
Department of Ophthalmology, Al Nahdha Hospital, MOH, Muscat, Oman.
Oman J Ophthalmol. 2024 Jun 27;17(2):254-260. doi: 10.4103/ojo.ojo_299_23. eCollection 2024 May-Aug.
Malignant peripheral nerve sheath tumor of the orbit is an exceedingly rare entity. These tumors exhibit locally aggressive behavior, recurrences, distant metastasis, and poor response to existing treatment protocols. Orbital nerve sheath tumors are often associated with neurofibromatosis 1, and malignant transformation of neurofibroma into malignant nerve sheath tumor has also been seen. The recommended treatment for localized disease is radical or wide surgical excision to achieve negative margins followed by chemoradiation. For extensive disease, chemotherapy and radiotherapy can be utilized to stabilize the disease. Due to poor response and outcomes with current regimens, the focus has been shifted to approaches utilizing molecular targets and immunological agents. Despite all the advancements, the outcomes still remain discouraging for moderate- to high-grade lesions and thus necessitate studies to design promising treatment modalities.
眼眶恶性外周神经鞘瘤是一种极其罕见的疾病。这些肿瘤表现出局部侵袭性行为、复发、远处转移,并且对现有治疗方案反应不佳。眼眶神经鞘瘤常与1型神经纤维瘤病相关,也可见神经纤维瘤恶变为恶性神经鞘瘤。对于局限性疾病,推荐的治疗方法是根治性或广泛手术切除以达到切缘阴性,随后进行放化疗。对于广泛性疾病,可采用化疗和放疗来稳定病情。由于目前治疗方案的反应和效果不佳,重点已转向利用分子靶点和免疫制剂的方法。尽管取得了所有这些进展,但中高级别病变的治疗结果仍然令人沮丧,因此有必要开展研究以设计出有前景的治疗方式。