Department of Dermatology and Venereology, Soroka Medical Center, Faculty of Health Sciences, Ben-Gurion University of Negev, Beer-Sheva, Israel.
Br J Dermatol. 2010 Dec;163(6):1245-52. doi: 10.1111/j.1365-2133.2010.09967.x.
Acute generalized exanthematous pustulosis (AGEP) is a rare severe pustular reaction pattern with a typical clinical picture.
To characterize the histopathological features of AGEP in a large series of cases with a validated diagnosis. METHODS; A multinational retrospective histopathological study was conducted. It included 102 hospitalized patients (recruited within the EuroSCAR and RegiSCAR studies) with a validated diagnosis of probable or definite AGEP. A systematic description of the histopathological features in AGEP was done based on a standardized grading system.
Sub/intracorneal pustules (41%), intraepidermal pustules (20%) or combinations of them (38%) were observed in 102 cases. The pustules were usually large (> 15 keratinocytes) (82% and 89%, respectively) and regularly contained eosinophils (36% and 32%, respectively). Spongiform features were less prominent in the sub/intracorneal pustules compared with the intraepidermal pustules (44% and 95%, respectively). The main epidermal features were necrotic keratinocytes (67%), including incidental segmental necrosis (7%), and spongiosis (80%) with neutrophil exocytosis (77%). The main dermal features were papillary oedema (88%) and mixed superficial (100%), interstitial (93%), and mid/deep-dermal infiltrates (95%) containing neutrophils (100%) and eosinophils (81%). Follicular pustules were also seen (23%), but vasculitis generally was absent. Classical features of plaque-type psoriasis were infrequent and usually mild. No significant differences were observed between a subgroup of 16 cases with and 86 cases without psoriasis.
The present histopathological study concerns a large series of cases with a validated diagnosis of AGEP. It provides diagnostic clues in favour of AGEP in patients with a pustular eruption.
急性泛发性发疹性脓疱病(AGEP)是一种罕见的严重脓疱性反应模式,具有典型的临床特征。
在经过验证的诊断中,描述大系列 AGEP 的组织病理学特征。
进行了一项多国回顾性组织病理学研究。它包括在 EuroSCAR 和 RegiSCAR 研究中招募的 102 名住院患者(确诊为可能或明确的 AGEP)。基于标准化分级系统,对 AGEP 的组织病理学特征进行了系统描述。
在 102 例病例中观察到亚/表皮内脓疱(41%)、表皮内脓疱(20%)或两者的组合(38%)。脓疱通常较大(>15 个角质形成细胞)(分别为 82%和 89%),并且通常含有嗜酸性粒细胞(分别为 36%和 32%)。与表皮内脓疱相比,亚/表皮内脓疱的海绵状特征不太明显(分别为 44%和 95%)。主要的表皮特征是坏死的角质形成细胞(67%),包括偶然的节段性坏死(7%)和海绵状(80%)伴中性粒细胞外渗(77%)。主要的真皮特征是乳头水肿(88%)和混合浅表(100%)、间质(93%)和中/深部真皮浸润(95%),其中含有中性粒细胞(100%)和嗜酸性粒细胞(81%)。也可见滤泡性脓疱(23%),但通常不存在血管炎。斑块型银屑病的经典特征很少见且通常较轻。在有和没有银屑病的 16 例病例亚组和 86 例病例之间未观察到显著差异。
本组织病理学研究涉及经过验证的 AGEP 诊断的大系列病例。它为患有脓疱性皮疹的患者提供了支持 AGEP 的诊断线索。