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Disseminated punctate keratoderma: a rare case report and review of the literature

机译:播散性点状角化病:罕见病例报告和文献复习

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We report a rare case of a 53-year-old womanpresenting with diffuse, late-onset disseminatedhyperkeratotic papules. Biopsy showed massivehyperkeratosis overlying a crateriform epidermaldepression and hypergranulosis with mild epidermalhyperplasia. There was no parakeratosis, cornoidlamella, or dyskeratosis. Based on the clinical findingsand histopathological features, a diagnosis ofdisseminated punctate keratoderma was made. Thisis a rare subtype of palmoplantar keratoderma, whichhas a putative increased risk of malignancy. This casereport emphasizes the importance of identifyingthe clinical and histological presentation of this rarecondition; referral of the patient for age-appropriatemalignancy screening is appropriate. We also presenta concise review of treatment options.
机译:我们报告了一个罕见的病例,该病例为53岁的女性,表现为弥漫性,迟发性弥漫性角化性丘疹。活检显示大片角化过度症覆盖在颅状表皮凹陷和肉芽过多伴轻度表皮增生。没有角化不全,角质层或角化不全。根据临床表现和组织病理学特征,诊断为弥散性点状角化病。这是掌o角化病的一种罕见亚型,可能会增加恶性肿瘤的风险。该病例报告强调了识别这种罕见病的临床和组织学表现的重要性。推荐将患者转诊以进行年龄-适应症对齐检查。我们还介绍了治疗方案的简明概述。

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