| International Journal of Clinical and Experimental Pathology | |
| Subcorneal pustular dermatosis an immnohisto-pathological perspective | |
| Ana Maria Abreu-Velez1  | |
| 关键词: Subcorneal pustular dermatosis; anti-ribosomal protein S6-pS240; mast cell tryptase; HLA-DPDQDR; ZAP-70; | |
| DOI : | |
| 学科分类:生理学与病理学 | |
| 来源: e-Century Publishing Corporation | |
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【 摘 要 】
Subcorneal pustular dermatosis (SPD) represents a chronic, relapsing sterile pustular eruption, involving the trunk and flexoral proximal extremities. A 54-year-old female presented with recurrent, flaccid pustules measuring several millimeters in diameter, on normal and mildly erythematous skin of the groin and submammary areas. Biopsies for hematoxylin and eosin (H&E) examination, direct immunofluorescence (DIF) and immunohistochemistry (IHC) analysis were performed. The H&E staining demonstrated typical features of SPD, including some damage within dermal pilosebaceous units subjacent to the subcorneal blistering process. DIF revealed strong deposits of immunoreactants IgG, IgM, fibrinogen and complement/C3, present in a shaggy pattern within the subcorneal disease areas; in focal, areas of the basement membrane junction and in focal pericytoplasmic areas of epidermal keratinocytes. IHC revealed strong positivity to HLA-DPDQDR, mast cell tryptase, CD68, and ZAP-70 in the subcorneal inflammatory infiltrate, and surrounding dermal blood vessels. Myeloperoxidase was also positive. Positive staining with the anti-ribosomal protein S6-pS240 at the edges of hair follicles and sebaceous glands subjacent to the subcorneal blisters was also noted. Conclusions: We conclude that this disorder may have several components in its etiopathology, including a possible restricted immune response and a possible genetic component; these possibilities warrant further investigation.
【 授权许可】
CC BY-NC
【 预 览 】
| Files | Size | Format | View |
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| RO201901230338590ZK.pdf | 582KB |
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