Ocular perivascular epithelioid cell tumor: report of 2 cases with distinct clinical presentations

被引:20
作者
Furusato, Emiko [1 ]
Cameron, J. Douglas [1 ]
Newsom, Roger W. [2 ]
Fujishiro, Takashi [3 ]
Kojima, Takayoshi [3 ]
Specht, Charles S. [4 ]
Fetsch, John F. [5 ]
Furusato, Bungo [6 ]
Sesterhenn, Isabell A. [6 ]
Rushing, Elisabeth J. [1 ]
机构
[1] Armed Forces Inst Pathol, Dept Neuropathol & Ophthalm Pathol, Washington, DC 20306 USA
[2] Tidewater Eye Ctr, Portsmouth, VA 23707 USA
[3] Saitama Red Cross Hosp, Dept Ophthalmol, Saitama 3388553, Japan
[4] Penn State Hershey, Dept Pathol Ophthalmol & Neurosurg, Hershey, PA 17033 USA
[5] Armed Forces Inst Pathol, Dept Soft Tissue Pathol, Washington, DC 20306 USA
[6] Armed Forces Inst Pathol, Dept Genitourinary Pathol, Washington, DC 20306 USA
关键词
Ciliary body; Eyelid; Immunohistochemistry; Perivascular epithelioid cell tumor; OF-THE-LITERATURE; NEOPLASMS; ORBIT;
D O I
10.1016/j.humpath.2009.12.006
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Perivascular epithelioid cell tumors comprise a rare and recently described family of neoplasms that characteristically coexpress melanocytic and myoid markers. We describe the clinicopathologic features of 2 ocular cases. Case 1 occurred in a 26-year-old woman with a recurrent left upper eyelid tumor, and case 2 was diagnosed in a 7-year-old boy with a left ciliary body mass. This is the first report of perivascular epithelioid cell tumor arising in the ciliary body or eyelid. Neither patient in our series had documented evidence of the tuberous sclerosis complex. Despite its rarity, perivascular epithelioid cell tumor should be considered in the differential diagnosis of ocular melanocytic lesions. Although most examples appear cytologically bland, experience is limited regarding their malignant potential; and therefore, complete surgical resection and close follow-up are recommended. Published by Elsevier Inc.
引用
收藏
页码:768 / 772
页数:5
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