Reticular erythematous mucinosis syndrome. Report of two cases.
Reticular erythematous mucinosis syndrome. Report of two cases.
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网状红斑性粘蛋白沉着症综合征。
DOI：
10.1001/archderm.115.11.1340
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发表时间：
1979
影响因子：
--
通讯作者：
J. Parrish
中科院分区：
文献类型：
--
作者：
W. Morison;C. Shea;J. Parrish
两名女性患者的皮疹具有网状红斑性粘蛋白沉着症综合征的形态和组织学特征。然而，这两个案例都有与之前描述不同的特征。在一个案例中，在一次导致红斑的阳光照射后三到四个星期，皮疹开始出现，并在两到三周后消退。暴露于紫外线 B (UVB) 或 UVC 辐射可能会再现皮疹。在另一名患者中，皮疹累及手臂和面部，但躯干未受累，这是一个更具特征性的受累部位；它与阳光照射后病情加重的病史有关，但在照片测试中无法重现皮疹。
Two female patients had eruptions with the morphologic and histologic features of reticular erythematous mucinosis syndrome. However, both cases had features that differed from previous descriptions. In one case the eruption developed three to four weeks after a single erythemogenic sun exposure and faded after two to three weeks. The rash could be reproduced by exposure to ultraviolet B (UVB) or UVC radiation. In the other patient, the eruption involved the arms and face and spared the trunk, which is a more characteristic site of involvement; it was associated with a history of exacerbation following sun exposure, but the rash could not be reproduced on phototesting.