Geerts M L, Overbeke J, Kint A, Cormane R H
Br J Dermatol. 1978 May;98(5):529-36. doi: 10.1111/j.1365-2133.1978.tb01938.x.
An electron microscopic study of Mendes da Costa's disease (MCD) has been undertaken to determine whether this disease is a variant of epidermolysis bullosa dystrophica, or should be classified as a separate disease entity. It was shown that in MCD lacunae occur in the lower layers of the epidermis, in the presence of normal anchoring fibrils. In the recessive form of epidermolysis bullosa dystrophica (EBD), however, no lacunae were found in the epidermis, and anchoring fibrils were absent. These findings support the concept that MCD should not be considered as a special form of epidermolysis bullosa dystrophica.
已对门德斯·达·科斯塔病(MCD)进行了电子显微镜研究,以确定该疾病是否为营养不良性大疱性表皮松解症的一种变体,或者是否应归类为一种独立的疾病实体。结果表明,在MCD中,表皮下层出现腔隙,同时存在正常的锚定原纤维。然而,在隐性营养不良性大疱性表皮松解症(EBD)中,表皮中未发现腔隙,且不存在锚定原纤维。这些发现支持了MCD不应被视为营养不良性大疱性表皮松解症特殊形式的观点。