Department of Dermatology, Eberhard Karls University, Liebermeisterstr. 25, DE-72076 Tübingen, Germany.
Acta Derm Venereol. 2010;90(1):65-7. doi: 10.2340/00015555-0763.
Progressive mucinous histiocytosis is a very rare, benign, non-Langerhans' cell histiocytosis limited to the skin. In total ten patients (all women) in four families and three sporadic cases have been reported. We report here the first published case of a male patient with progressive mucinous histiocytosis. The multiple red papules on the scalp and forearms were asymptomatic and had slowly increased over approximately the past 20 years. The patient's mother had similar lesions. Histological examination revealed nodules in the dermis with histiocytes and mucin deposition. The histiocytes stained positively with CD31 and negative with CD34, CAM 5.2, PGM-1 and factor XIIIa. Ultrastructurally, the histiocytes showed numerous circular myelin bodies and zebra bodies reminiscent of those seen in lysosomal storage diseases. The genetic transmission of hereditary progressive mucinous histiocytosis remains unclear; we assume an autosomal dominant transmission with some hormonal factor that makes hereditary progressive mucinous histiocytosis more likely in women.
进行性黏蛋白组织细胞增生症是一种非常罕见的良性非朗格汉斯细胞组织细胞增生症,局限于皮肤。总共报道了 10 例(均为女性)患者来自 4 个家系和 3 例散发病例。我们在此报告首例男性进行性黏蛋白组织细胞增生症患者。头皮和前臂多发性红色丘疹无症状,大约 20 年来缓慢增多。患者的母亲也有类似皮损。组织学检查显示真皮内有结节,其内有组织细胞和黏蛋白沉积。组织细胞 CD31 染色阳性,CD34、CAM5.2、PGM-1 和因子 XIIIa 染色阴性。电镜下,组织细胞显示大量圆形髓磷脂体和斑马体,类似于溶酶体贮积病中所见。遗传性进行性黏蛋白组织细胞增生症的遗传传递方式尚不清楚;我们假设为常染色体显性遗传,伴有某种激素因素,使女性更易患遗传性进行性黏蛋白组织细胞增生症。