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首页> 外文期刊>The Journal of dermatology >Hereditary lactate dehydrogenase M-subunit deficiency with late-developing pustular psoriasis-like lesions
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Hereditary lactate dehydrogenase M-subunit deficiency with late-developing pustular psoriasis-like lesions

机译:遗传性乳酸脱氢酶M亚基缺乏伴晚期脓疱型银屑病样病变

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摘要

Hereditary lactate dehydrogenase (LDH) M-subunit deficiency is very rare and we have found reports of close to a dozen cases in the published work, two of which were associated with pustular psoriasis-like lesions. We report a third case of pustular psoriasis-like eruptions associated with LDH M-subunit deficiency, which occurred 24 years after the diagnosis of LDH M-subunit deficiency. These cases indicate that abnormal activity of LDH can induce pustular psoriatic lesions in the long term. Some patients with symptoms of hereditary LDH M-subunit deficiency have antecedent annular scaly plaque lesions, that resemble psoriatic lesions. We discuss a hypothesis to explain this scenario.
机译:遗传性乳酸脱氢酶(LDH)M亚基缺乏非常罕见,我们在已发表的著作中发现了近十例病例的报告,其中两例与脓疱型牛皮癣样病变有关。我们报告了第三例与LDH M亚基缺乏相关的脓疱型牛皮癣样爆发,该病例在诊断LDH M亚基缺乏后24年发生。这些情况表明,LDH的异常活性可长期诱发脓疱型银屑病病变。一些具有遗传性LDH M亚基缺乏症状的患者具有先前的环形鳞状斑块病变,类似于牛皮癣性病变。我们讨论一个假设来解释这种情况。

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