Reticular Erythematous Mucinosis Syndrome
Reticular Erythematous Mucinosis Syndrome
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网状红斑性粘蛋白沉积症综合征
DOI：
10.1111/j.1346-8138.1986.tb02929.x
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发表时间：
1986
期刊：
影响因子：
--
通讯作者：
T. Aoki
中科院分区：
文献类型：
--
作者：
T. Funai;T. Aoki
一位71岁男性患者，在胸骨和右肋弓部位出现两年的无症状红斑块。在组织学上，毛囊漏斗周围和真皮毛细血管周围有大量的淋巴细胞浸润，但在淋巴细胞周围和胶原束之间可见少量胶体铁阳性物质沉积，程度较轻。网状红斑性粘蛋白沉着症(REM)综合征是有争议的，其本质是粘蛋白沉着症？此病例似乎是REM综合征的极端，其中粘蛋白沉积最少。
A 71‐year‐old man visited us with asymptomatic erythematous patches of two years' duration on the sternum and right costal arch areas. Histologically there was an appreciable amount of lymphocytic infiltration around the infundibulum of the hair follicle and the dermal capillaries, but the deposition of a colloidal iron positive material was observed around the lymphocytic infiltration and between the collagen bundles to only a mild degree. Reticular erythematous mucinosis (REM) syndrome is controversial; what is its nature as a mucinosis? This case seems to be the extreme of REM syndrome in which mucin deposition was minimal.