Immunohistopathological analyses of a case of pemphigus vegetans with antibodies against desmoglein 1 and desmocollins 1-3.

Anri Kimura, Teruhiko Makino, Shohei Kitayama, Megumi Mizawa, Norito Ishii, Takashi Hashimoto, Tadamichi Shimizu
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Abstract

Pemphigus vegetans is a rare type of pemphigus characterized by vegetative lesions primarily localized to the intertriginous area. Despite its unique clinical presentation, the underlying pathomechanism remains unclear owing to the rarity of the disease. We report a case of pemphigus vegetans with antibodies against desmoglein 1 and desmocollins 1-3. Furthermore, immunohistochemical analyses were performed to address the pathogenesis of this disease. A 73-year-old man presented with multiple vegetative plaques with erythema on the trunk, groins, and extremities. Mucosal lesions were not observed. Laboratory examinations revealed mild leukocytosis with eosinophilia. A histopathological examination of the skin lesion showed epidermal hyperplasia and intraepidermal abscesses with marked infiltration of neutrophils and eosinophils, and infiltration of lymphocytes and eosinophils into the upper derms. Bacterial culture of the skin tissue was positive for Staphylococcus aureus. Direct immunofluorescence showed deposits of IgG and C3 on keratinocyte surfaces in the epidermis. Autoantibodies against desmoglein 1 and autoantibodies against desmocollin 1, desmocollin 2, and desmocollin 3 were detected by enzyme-linked immunosorbent assays. The diagnosis of pemphigus vegetans was made. Initiation of prednisolone (1.0 mg/kg/day) gradually improved his skin symptoms. We performed immunohistochemical analyses of the lesional skin, which revealed infiltration of CD3-positive, CD4-positive, and CD68-positive cells in the upper dermis, but CD20- or CD56-positive cells were negative. In addition, the present case showed more prominent infiltration of IL-17A- and IL-22-positive cells in the upper dermis than in pemphigus foliaceus, a type of pemphigus with autoantibodies against desmoglein 1. Furthermore, these cells co-expressed CD3 and CD68. We hypothesized that IL-22 and IL-17A produced by T cells and macrophages and their dysregulation might be involved in the pathogenesis of pemphigus vegetans. Additionally, skin colonization and/or infection with Staphylococcus aureus could potentially contribute to the pathogenesis of the disease.

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对一例带有去疱疹素 1 和去疱疹素 1-3 抗体的植物性天疱疮病例的免疫组织病理学分析。
植物性丘疹痤疮是一种罕见的丘疹性痤疮,其特征是植物性皮损主要发生在三叉神经间区。尽管其临床表现独特,但由于该病罕见,其潜在的病理机制仍不清楚。我们报告了一例带有去疱疹素 1 和去疱疹素 1-3 抗体的植物性丘疹病例。此外,我们还进行了免疫组化分析,以探讨该病的发病机制。一名 73 岁的男子出现多发性植物性斑块,躯干、腹股沟和四肢出现红斑。未发现粘膜病变。实验室检查显示白细胞轻度增高,伴有嗜酸性粒细胞增多。皮损的组织病理学检查显示表皮增生和表皮内脓肿,中性粒细胞和嗜酸性粒细胞明显浸润,淋巴细胞和嗜酸性粒细胞浸润到真皮上部。皮肤组织的细菌培养呈金黄色葡萄球菌阳性。直接免疫荧光显示,IgG 和 C3 沉积在表皮的角质细胞表面。通过酶联免疫吸附试验检测到了去疣素 1 自身抗体和去疣素 1、去疣素 2 和去疣素 3 自身抗体。诊断结果为植物性天疱疮。泼尼松龙(1.0 毫克/千克/天)逐渐改善了他的皮肤症状。我们对病变皮肤进行了免疫组化分析,结果显示真皮上层有 CD3 阳性、CD4 阳性和 CD68 阳性细胞浸润,但 CD20 或 CD56 阳性细胞呈阴性。此外,本病例真皮上层出现的 IL-17A- 和 IL-22 阳性细胞浸润比叶状天疱疮更为显著,叶状天疱疮是一种具有去疱疹素 1 自身抗体的天疱疮类型。我们推测,T细胞和巨噬细胞产生的IL-22和IL-17A及其失调可能参与了植物性丘疹脓疱病的发病机制。此外,皮肤定植和/或感染金黄色葡萄球菌也可能是该病的发病机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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