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Spiny keratoderma

机译:刺性角化病

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摘要

We present a case of a 48-year-old man with an approximately 30-year history of spiny projections on the palms, which were histopathologically consistent with spiny keratoderma. Spiny keratoderma is a rare entity of unknown etiology that has been described with both hereditary and acquired variants. The hereditary form, which is most likely the diagnosis in our patient, manifests at a younger age and is benign. The acquired variant, which presents in older adults, has been associated with a variety of systemic diseases and malignant conditions. In patients suspected of having acquired spiny keratoderma, an evaluation for malignant conditions may be warranted.
机译:我们介绍了一个48岁的男人的案例,该男人的手掌上有多刺的突起已有30年的历史,这在组织病理学上与多刺的角质层一致。多刺性角化皮病是一种罕见的病因不明的实体,已被遗传和获得性变体描述。遗传形式最有可能在我们的患者中得到诊断,表现为年龄较小且良性。获得的变异体存在于老年人中,已与多种系统疾病和恶性疾病相关。对于怀疑患有多发性角化皮病的患者,可能需要对恶性疾病进行评估。

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