Ma Shirley P, Hardy Thomas G
Department of Ophthalmology, The Royal Melbourne Hospital, Parkville, Australia.
Ophthalmic Plast Reconstr Surg. 2017 Jan/Feb;33(1):e10-e13. doi: 10.1097/IOP.0000000000000376.
Prolidase deficiency and solitary mastocytoma of the eyelid are both exceedingly rare. Prolidase deficiency is an inherited connective tissue disorder that has systemic sequelae, such as intractable skin ulceration, poor wound healing, recurrent infections, and intellectual impairment. Cutaneous mastocytoma is an isolated, aberrant cutaneous aggregation of mast cells. A case of an adult with severe prolidase deficiency who developed cutaneous mastocytoma of the eyelid was presented. To the authors' knowledge, adult-onset solitary mastocytoma of the eyelid has never been reported previously.
脯氨酰肽酶缺乏症和眼睑孤立性肥大细胞瘤都极为罕见。脯氨酰肽酶缺乏症是一种遗传性结缔组织疾病,会引发全身性后果,如顽固性皮肤溃疡、伤口愈合不良、反复感染以及智力障碍。皮肤肥大细胞瘤是肥大细胞的一种孤立性、异常性皮肤聚集。本文报告了一例患有严重脯氨酰肽酶缺乏症的成年人发生眼睑皮肤肥大细胞瘤的病例。据作者所知,此前从未有过成人期眼睑孤立性肥大细胞瘤的报道。