Scruggs Ryan T, Black Evan H
*Department of Ophthalmology, Ophthalmic Plastic, Orbital and Reconstructive Surgery, Kresge Eye Institute, Wayne State University School of Medicine, Detroit; and †Department of Ophthalmology, Oakland University, William Beaumont School of Medicine, Royal Oak, Michigan, U.S.A.
Ophthalmic Plast Reconstr Surg. 2015 Jan-Feb;31(1):e6-8. doi: 10.1097/IOP.0000000000000020.
Granular cell tumors were first described in the 1920s and since then have been commonly found throughout the body. They are rarely found in periorbital, orbital, and ocular structures. The authors present a patient with a 2-year history of a lesion that had been previously excised as a presumed chalazion without pathologic analysis. The lesion recurred, and histopathological analysis following complete resection revealed a granular cell tumor. This case is an example of a rare periocular tumor. Although only an isolated case, it provides support for the recommendation that excised lesions be sent to pathologic study, particularly those with an atypical clinical course.
颗粒细胞瘤于20世纪20年代首次被描述,自那时起在全身普遍被发现。它们很少见于眶周、眼眶及眼部结构。作者报告了一名患者,其病变有2年病史,此前被当作睑板腺囊肿切除,未进行病理分析。病变复发,完整切除后组织病理学分析显示为颗粒细胞瘤。该病例是一种罕见的眼周肿瘤的实例。尽管只是个孤立病例,但它支持了这样的建议,即切除的病变应送去做病理研究,尤其是那些临床病程不典型的病变。