Malignant melanoma in a Nigerian oculocutaneous albino

O. Awe, Emmanuel Esezobor, Quincy Aigbonorga, C. Owobu
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引用次数: 2

Abstract

Albinism is a rare autosomal recessive disorder occurring as a result of decrease or absence of tyrosinase enzyme resulting in a reduction in melanin synthesis. This is characterized by depigmentation, nystagmus, and photophobia and decrease visual acuity. Malignant melanoma though on the increase worldwide, it is very rare in the albino who have deficient melanocytes that express melanin. We present a case of malignant melanoma in a 26-year-old male undergraduate albino.
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尼日利亚眼皮肤白化患者恶性黑色素瘤
白化病是一种罕见的常染色体隐性遗传病,由于酪氨酸酶减少或缺乏导致黑色素合成减少。其特征是色素沉着、眼球震颤、畏光和视力下降。恶性黑色素瘤虽然在世界范围内呈上升趋势,但在表达黑色素的黑色素细胞缺乏的白化患者中是非常罕见的。我们报告一例恶性黑色素瘤在一个26岁的男性本科白化。
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