Grussendorf-Conen E I, Köhnen M, Klingmüller G
Hautarzt. 1984 Aug;35(8):408-14.
We studied a case of idiopathic mucinosis follicularis which persisted for 7 months. Histologically, the strong pathological changes began within the sebaceous glands and secondarily occurred in other parts of the pilosebaceous unit. We could demonstrate by electron microscopy that all the follicular cells in this process were undifferentiated sebaceous cells. Therefore, we think that the pathogenesis of mucinosis follicularis originates from a disturbance in the differentiation process of sebaceous cells.
我们研究了一例持续7个月的特发性毛囊黏蛋白病病例。组织学上，强烈的病理变化始于皮脂腺，继发于毛囊皮脂腺单位的其他部位。通过电子显微镜我们能够证明，在此过程中所有的毛囊细胞均为未分化的皮脂腺细胞。因此，我们认为毛囊黏蛋白病的发病机制源于皮脂腺细胞分化过程的紊乱。
