Department of Ophthalmology, Wuxi People's Hospital Affiliated of Nanjing Medical University, Qingyang Road 299, Wuxi, 214002, China.
BMC Ophthalmol. 2023 Jun 12;23(1):260. doi: 10.1186/s12886-023-03005-0.
Pure mucosal neuroma syndrome (MNS), an autosomal dominant neurocutaneous disorder, is a rare discrete subgroup in multiple endocrine neoplasia (MEN) type 2B, which present without associated endocrinopathies of MEN2B but with typical physical features such as prominent corneal nerves. Case presentation This report describes a 41-year-old patient with complaint of itchy eyes and irritation, presenting with blocked gland orifices in the upper and lower eyelids, light conjunctival hyperemia, a semitransparent neoplasm measuring 2 mm*2 mm on the nasal limbus suggestive of neuromas, and prominent corneal nerves. In vivo confocal microscopy (IVCM) revealed structural alterations-namely a prominent hyperreflective, thickened nerve plexus and a normal endothelium-in both eyes. Testing for SOS1 mutation was positive. This patient may represent a discrete subgroup termed pure mucosal neuroma syndrome (MNS), which presents with the characteristic appearance of MEN2B but without RET gene mutations.
Prominent corneal nerves have been described in some diseases, such as multiple endocrine neoplasia (MEN) type 1 and type 2A and 2B, congenital ichthyosis, Refsum's disease, leprosy, etc. Ophthalmic assessment including prominent corneal nerves has proven valuable in asymptomatic individuals of MEN2B. Our case illustrates the importance of recognizing the ocular features of MNS, a rare presentation of MEN2B, in order to prevent prophylactic thyroidectomy in these patients for prophylactic thyroidectomy is not mandatory in MNS. However, regular monitoring and genetic counseling are still necessary.
纯黏膜神经瘤综合征(MNS)是一种常染色体显性神经皮肤疾病,是多发性内分泌肿瘤(MEN)2B 型中的一个罕见离散亚群,其没有 MEN2B 的相关内分泌疾病,但具有典型的体格特征,如明显的角膜神经。
本报告描述了一位 41 岁的患者,主诉为眼睛瘙痒和刺激,表现为上、下眼睑腺体开口堵塞,轻度结膜充血,在鼻侧角膜缘有 2mm*2mm 的半透明神经瘤样肿物,角膜神经明显突出。体内共聚焦显微镜(IVCM)显示双眼均存在结构改变,即明显的高反射、增厚的神经丛和正常的内皮。SOS1 突变检测呈阳性。该患者可能代表一个称为纯黏膜神经瘤综合征(MNS)的离散亚群,其表现出 MEN2B 的特征性外观,但没有 RET 基因突变。
在一些疾病中,如多发性内分泌肿瘤(MEN)1 型和 2A、2B 型,先天性鱼鳞病,Refsum 病,麻风病等,已经描述了明显的角膜神经。眼科评估包括明显的角膜神经,在无症状的 MEN2B 个体中具有重要价值。我们的病例说明了认识 MNS 的眼部特征的重要性,这是 MEN2B 的一种罕见表现,以便避免对这些患者进行预防性甲状腺切除术,因为预防性甲状腺切除术在 MNS 中并非强制性。然而,仍需要定期监测和遗传咨询。