Reticulate acropigmentation of Kitamura and Dowling-Degos disease overlap: a rare case report

Anukriti Yadav, Rashmi Sarkar, Surabhi Sinha, V. Mendiratta, Kiran Agarwal
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引用次数: 0

Abstract

Reticulate acropigmentation of Kitamura (RAK) and Dowling-Degos disease (DDD) belong to the rare heterogeneous group of reticulate pigmentary disorders. They are inherited as an autosomal dominant trait with variable penetrance and are characterized by the presence of hyperpigmented macules coalescing in a reticular fashion. We hereby describe a 29-year-old male patient having hyperpigmented macules on the neck, axillae, dorsum of the hands and feet, along with palmar pitting. A clinicopathological overlap of both these entities (RAK and DDD) was seen in this patient, which is a rare occurrence, indicating that they are two different phenotypic presentations of a single disease.
北村网状色素沉着与道林-德戈斯病重叠:一例罕见病例报告
北村网状色素沉着病(RAK)和道林-德戈斯病(DDD)属于罕见的异质性网状色素沉着病。它们是常染色体显性遗传,具有不同的渗透性,其特征是色素沉着斑呈网状聚集。我们在此描述一名 29 岁的男性患者,他的颈部、腋窝、手背和足背有色素沉着斑,同时伴有手掌点状出血。在该患者身上,这两种疾病(RAK 和 DDD)的临床病理表现出现了重叠,这种情况非常罕见,表明它们是一种疾病的两种不同表型表现。
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27 weeks
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