Meyer D R, Wobig J L
Department of Ophthalmology, Albany Medical College, NY 12203.
Ophthalmology. 1992 Aug;99(8):1313-7. doi: 10.1016/s0161-6420(92)31831-7.
The authors report on a 30-year-old man who presented with progressive bilateral exophthalmos over a 2-year period.
Computed tomography showed large heterogeneous masses in the superior aspect of both orbits. Excisional biopsy via bilateral lateral orbitotomies showed the tumors to be well-circumscribed, relatively avascular, localized neurofibromas. The patient had several features suggestive of multiple endocrine neoplasia type IIB, including Marfanoid habitus, enlarged corneal nerves, thickened lips, and mucosal neuromas.
Localized neurofibromas are rare in the orbit and, unlike plexiform neurofibromas, are not typically associated with von Recklinghausen's neurofibromatosis. Bilaterality of such localized neurofibromas has not been previously reported. Recognition of ophthalmic lesions suggestive of multiple endocrine neoplasia IIB should prompt evaluation for systemic manifestations of this disorder.
作者报告了一名30岁男性,其在2年时间里出现进行性双侧眼球突出。
计算机断层扫描显示双侧眼眶上部有巨大的异质性肿块。通过双侧外侧眶切开术进行的切除活检显示肿瘤边界清晰,相对无血管,为局限性神经纤维瘤。该患者有几个提示IIB型多发性内分泌肿瘤的特征,包括类马凡体型、角膜神经增粗、嘴唇增厚和黏膜神经瘤。
局限性神经纤维瘤在眼眶中很少见,与丛状神经纤维瘤不同,通常不与冯雷克林霍增氏神经纤维瘤病相关。此前尚未报道过这种局限性神经纤维瘤的双侧性。认识到提示IIB型多发性内分泌肿瘤的眼科病变应促使对该疾病的全身表现进行评估。