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肢端持久性丘疹性黏蛋白沉积症
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作者 harris j.e. Purcell S.M. +1 位作者 Griffin T.D. 党倩丽 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第8期7-7,共1页
Acral persistent papular mucinosis is a rare subtype of localized lichen myxedematosus. For half a century, this disease has endured a controversial and constantly evolving classification. We describe a patient who pr... Acral persistent papular mucinosis is a rare subtype of localized lichen myxedematosus. For half a century, this disease has endured a controversial and constantly evolving classification. We describe a patient who presented with discrete,flesh- colored papules on the hands, wrists, and forearms in a distribution consistent with acral persistent papular mucinosis. Histology was also constant with this disease, showing a well- circumscribed deposition of mucin in the upper and mid dermis that spared a small grenzzone. The changing nomenclature and diagnostic requirements of acral persistent papular mucinosis that have allowed it to remain a topic of debate are examined through a comprehensive review of the literature. All reported cases are reviewed. 展开更多
关键词 肢端 持久性 局部黏液性水肿 诊断需要 黏蛋白 腕部
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