Shields Jerry A, Shields Carol L, Lally Sara E, Milman Tatyana, Eagle Ralph C
Department of Ocular Oncology, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, PA, USA.
Department of Pathology, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, PA, USA.
Middle East Afr J Ophthalmol. 2018 Apr-Jun;25(2):115-117. doi: 10.4103/meajo.MEAJO_7_18.
An 8-year-old girl was referred for an amelanotic iris tumor believed to have enlarged slightly over 3 months, suspicious for juvenile xanthogranuloma (JXG). The affected right eye had a lightly pigmented, vascular iris mass measuring 6 mm in basal dimension and 2 mm in thickness. There were no feeder vessels, seeding, inflammatory cells, or cutaneous abnormalities. Diagnostic fine needle aspiration biopsy (FNAB) was performed, revealing spindle B melanoma cells that were immunoreactive for melanocytic markers HMB45 and Melan-A. Complete tumor resection by basal sector iridectomy was performed. Histopathology confirmed spindle B melanoma. At 14-years follow up, there has been no recurrence or metastasis and visual acuity remains 20/25. Iris melanoma can develop in children and clinically resemble nodular JXG.
一名8岁女孩因患无色素性虹膜肿瘤前来就诊,该肿瘤在3个月内似乎略有增大,怀疑为幼年性黄色肉芽肿(JXG)。患侧右眼虹膜有一色素沉着浅、有血管的肿物,基底径为6mm,厚度为2mm。未见供血血管、播散、炎性细胞或皮肤异常。进行了诊断性细针穿刺活检(FNAB),结果显示梭形B黑色素瘤细胞,对黑素细胞标志物HMB45和Melan-A呈免疫反应阳性。通过基底节段虹膜切除术进行了肿瘤全切。组织病理学证实为梭形B黑色素瘤。随访14年,无复发或转移,视力仍为20/25。虹膜黑色素瘤可发生于儿童,临床上与结节性JXG相似。