Stoebner P, Lavabre-Bertrand T, Raison-Peyron N, Barnéon G, Meynadier J, Meunier L
Service de Dermatologie-Allergologie-Photobiologie, Hôpital Saint-Eloi, 2, avenue Bertin-Sans, 34295 Montpellier Cedex 05, France.
Ann Dermatol Venereol. 2000 Feb;127(2):201-4.
We describe an original case of a primary cutaneous mucinosis, associated with a refractory anemia with excess of blast.
A 65 year-old female consulted for erythematous-purple blush reticulated and large plaques that progressively developed on the trunk and limbs. Biopsies showed abundant dermis mucin deposits with a perivascular lymphocytic infiltrate. The epidermis was normal. Laboratory evaluation showed refractory anemia with excess of blast, associated with cytogenetic abnormalities. After two years course, the progressive aggravation of the myelodysplastic syndrome was associated with a progressive extension of the cutaneous mucinosis.
This is the first report of an atypical primary diffuse and extensive cutaneous mucinosis. Primary cutaneous mucinosis may be associated with systemic diseases. To our knowledge, the association with refractory anemia with excess of blast has not been described previously. Mucine deposits may be considered as a consequence of neutrophilic dysfunction that are observed in myelodysplastic syndromes.
我们描述了一例原发性皮肤黏蛋白病的原始病例,该病例与伴有原始细胞增多的难治性贫血相关。
一名65岁女性因躯干和四肢逐渐出现的红斑性紫色网状和大片斑块前来就诊。活检显示真皮有大量黏蛋白沉积,并伴有血管周围淋巴细胞浸润。表皮正常。实验室评估显示伴有原始细胞增多的难治性贫血,并伴有细胞遗传学异常。经过两年病程,骨髓增生异常综合征的逐渐加重与皮肤黏蛋白病的逐渐扩展相关。
这是首例非典型原发性弥漫性广泛性皮肤黏蛋白病的报告。原发性皮肤黏蛋白病可能与全身性疾病相关。据我们所知,此前尚未描述过其与伴有原始细胞增多的难治性贫血的关联。黏蛋白沉积可能被认为是骨髓增生异常综合征中观察到的中性粒细胞功能障碍的结果。