Gawkrodger D J, Stavropoulos P G, McLaren K M, Buxton P K
Clin Exp Dermatol. 1989 Mar;14(2):150-3. doi: 10.1111/j.1365-2230.1989.tb00914.x.
Two patients with lichen planus pemphigoides and two with bullous lichen planus were compared. Lichen planus pemphigoides was clinically distinguished by a more generalized lichen planus, more extensive blistering, the need for systemic corticosteroids and by a longer course. The blister of bullous lichen planus was a subepidermal bulla showing degeneration of the epidermal basal layer and other features of lichen planus, whereas in lichen planus pemphigoides the bulla was similar to that of bullous pemphigoid albeit with rather more neutrophils than are usually seen. Direct immunofluorescence was positive in lichen planus pemphigoides and negative in bullous lichen planus. Lichen planus pemphigoides and bullous lichen planus are separate entities: the former is an auto-immune disease precipitated by lichen planus and not related to bullous pemphigoid, the latter is probably not auto-immune but represents the extreme consequence of the lymphoid infiltrate at the dermo-epidermal junction.
对两名类天疱疮样扁平苔藓患者和两名大疱性扁平苔藓患者进行了比较。类天疱疮样扁平苔藓在临床上的特征为更广泛的扁平苔藓、更广泛的水疱形成、需要使用全身性皮质类固醇且病程更长。大疱性扁平苔藓的水疱为表皮下大疱,表现为表皮基底层变性及其他扁平苔藓特征,而类天疱疮样扁平苔藓的水疱与大疱性类天疱疮的水疱相似,尽管中性粒细胞比通常所见的更多。直接免疫荧光在类天疱疮样扁平苔藓中呈阳性,在大疱性扁平苔藓中呈阴性。类天疱疮样扁平苔藓和大疱性扁平苔藓是不同的疾病实体:前者是由扁平苔藓引发的自身免疫性疾病,与大疱性类天疱疮无关,后者可能不是自身免疫性疾病,而是真皮-表皮交界处淋巴浸润的极端结果。