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Paraneoplastic plaque-like cutaneous mucinosis: a case report

机译:副肿瘤样斑块状皮肤粘液病:一例报告

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Plaque-like cutaneous mucinosis (PCM) is a rare disorder of dermal mucin deposition.? Some patients with PCM will be found to have an associated malignancy. We report the case of a 72-year-old man presenting with new onset pruritic, waxy-appearing erythematous and skin-colored papules and nodules coalescing into plaques on his shoulder, scalp, and forehead. Skin biopsy revealed cutaneous mucinosis. Despite conservative treatment, his skin lesions progressed, and he was found to have an occult malignancy of pancreatobiliary origin. After several months of chemotherapy, his skin lesions showed progressive improvement. To our knowledge, this is the third reported case of paraneoplastic PCM and the first reported to occur in association with underlying adenocarcinoma of pancreatobiliary origin. PCM may occasionally represent a paraneoplastic dermatosis. This case highlights the importance of a search for occult malignancy in such patients.
机译:斑块样皮肤粘液病(PCM)是一种罕见的皮肤粘蛋白沉积疾病。将发现一些PCM患者伴有恶性肿瘤。我们报道了一例72岁的男子,他的新发性瘙痒性,蜡质外观的红斑和皮肤色丘疹和结节在他的肩膀,头皮和额头上结成斑块。皮肤活检显示皮肤粘液病。尽管采取了保守治疗,他的皮肤病变仍在发展,并且发现他患有胰腺胆源性隐匿性恶性肿瘤。经过几个月的化疗后,他的皮肤病变逐渐改善。据我们所知,这是第三例报告的副肿瘤性PCM病例,也是第一例报告的与胰腺胆源性基础腺癌有关的病例。 PCM有时可能代表副肿瘤性皮肤病。这种情况强调了在这类患者中寻找隐匿性恶性肿瘤的重要性。

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