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7例青灰火焰型色素血管性母斑病患者:眼部色素沉着(黑素细胞增多症或黑变病)与鲜红斑痣合并存在,有发生黑色素瘤的风险。

Phacomatosis pigmentovascularis of cesioflammea type in 7 patients: combination of ocular pigmentation (melanocytosis or melanosis) and nevus flammeus with risk for melanoma.

作者信息

Shields Carol L, Kligman Brad E, Suriano Mayerling, Viloria Vanessa, Iturralde Juan C, Shields Margaret V, Say Emil A T, Shields Jerry A

机构信息

Ocular Oncology Service, Wills Eye Institute, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Arch Ophthalmol. 2011 Jun;129(6):746-50. doi: 10.1001/archophthalmol.2011.135.

Abstract

OBJECTIVE

To describe the features of phacomatosis pigmentovascularis (cesioflammea type).

DESIGN

Noninterventional retrospective case series composed of 7 patients.

RESULTS

Nevus flammeus combined with ipsilateral ocular melanocytosis or melanosis was seen in all 7 patients. Additional contralateral nevus flammeus was observed in 3 patients. Nevus flammeus (unilateral in 4 patients and bilateral in 3 patients) was distributed in trigeminal nerves V1 (n = 3), V2 (n = 7), and V3 (n = 5). Related findings included diffuse choroidal hemangioma (n = 1) and glaucoma (n = 1), with no patients having brain hemangioma or seizures. Ocular pigmentary abnormalities (unilateral in all 7 patients) included congenital ocular melanocytosis (n = 6) and conjunctival acquired melanosis (n = 1). Pigmentation was sectorial (partial) in 5 patients and complete in 2 patients. Melanocytosis involved the periocular skin in 1 patient, sclera in 2 patients, iris in 2 patients, and choroid in 4 patients. In 3 of 6 patients, melanocytosis was visible in the choroid only on dilated fundus evaluation. Related tumors included choroidal melanoma (n = 3), optic disc melanocytoma (n = 1), and conjunctival melanoma in situ (primary acquired melanosis) (n = 1). Melanoma metastasis developed in 1 patient.

CONCLUSIONS

Phacomatosis pigmentovascularis shows features of nevus flammeus and more serious ocular pigmentary abnormalities (uveoscleral melanocytosis and conjunctival melanosis). Melanocytosis may be detected only by dilated ocular fundus examination, as found in 3 of 6 patients. Furthermore, choroidal melanoma can develop from melanocytosis, as noted in 3 of our 6 patients (50%). All patients with nevus flammeus should be examined for phacomatosis pigmentovascularis by an ophthalmologist because ocular melanocytosis and uveal melanoma may remain hidden within the eye.

摘要

目的

描述色素血管性斑痣性错构瘤病(火焰色型)的特征。

设计

由7例患者组成的非干预性回顾性病例系列。

结果

7例患者均可见火焰状痣合并同侧眼黑变病或黑变病。3例患者观察到对侧额外的火焰状痣。火焰状痣(4例单侧,3例双侧)分布于三叉神经V1(n = 3)、V2(n = 7)和V3(n = 5)。相关发现包括弥漫性脉络膜血管瘤(n = 1)和青光眼(n = 1),无患者有脑血管瘤或癫痫发作。眼部色素沉着异常(7例患者均为单侧)包括先天性眼黑变病(n = 6)和结膜后天性黑变病(n = 1)。5例患者色素沉着为扇形(部分),2例患者为完全性。黑变病累及1例患者的眼周皮肤、2例患者的巩膜、2例患者的虹膜和4例患者的脉络膜。6例患者中有3例仅在散瞳眼底检查时脉络膜可见黑变病。相关肿瘤包括脉络膜黑色素瘤(n = 3)、视盘黑素细胞瘤(n = 1)和结膜原位黑色素瘤(原发性后天性黑变病)(n = 1)。1例患者发生黑色素瘤转移。

结论

色素血管性斑痣性错构瘤病表现为火焰状痣和更严重的眼部色素沉着异常(葡萄膜巩膜黑变病和结膜黑变病)的特征。如6例患者中有3例所示,黑变病可能仅通过散瞳眼底检查才能发现。此外,如我们6例患者中有3例(50%)所示,脉络膜黑色素瘤可由黑变病发展而来。所有火焰状痣患者均应由眼科医生检查是否患有色素血管性斑痣性错构瘤病,因为眼部黑变病和葡萄膜黑色素瘤可能隐藏于眼内。

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