Endogenous ochronosis with keratoelastoidosis marginalis

R. Mythreyi, Adikrishnan Swaminathan, A. Priyadarshini, S. Rangarajan, S. Murugan
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引用次数: 1

Abstract

Endogenous ochronosis is a manifestation of alkaptonuria, a rare metabolic disease due to homogentisic acid oxidase deficiency. Darkened urine and arthropathy are the other two components that complete the triad of alkaptonuria. Pigmentation of skin, the presenting feature, is common over the face and ears. A few cases of pigmentation of the palms and soles are reported. Here, we report a case of endogenous ochronosis presenting as keratoelastoidosis marginalis, which is a rare manifestation.
内源性衰老伴边缘角弹性样变性
内源性衰老症是由均质酸氧化酶缺乏症引起的罕见代谢性疾病——尿酸尿症的一种表现。尿变黑和关节病是完成尿黑尿三征的另外两个组成部分。色素沉着的皮肤,呈现特征,是常见的在脸和耳朵。报告了手掌和脚底色素沉着的少数病例。在此,我们报告一例内源性衰老,表现为边缘角弹性样变性,这是一种罕见的表现。
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