脓疱性银屑病
医学
泛发性脓疱性银屑病
皮肤病科
恶化
银屑病
脓疱病
急性全身发疹性脓疱病
鉴别诊断
疾病
病理
外科
内科学
骨髓炎
骨炎
作者
Agnieszka Owczarczyk‐Saczonek,Aleksandra Znajewska-Pander,Witold Owczarek,Agata Maciejewska-Radomska,Waldemar Placek
出处
期刊:Acta dermatovenerologica Alpina, Pannonica et Adriatica (Tiskana izd.)
[Association of Slovenian Dermatovenerologists]
日期:2018-01-01
卷期号:27 (4)
被引量:14
标识
DOI:10.15570/actaapa.2018.44
摘要
Annular pustular psoriasis (APP) is a rare form of pustular psoriasis with a chronic relapsing course and a good prognosis. The clinical picture is characterized by erythematous lesions, usually polycyclic, with the presence of small, sterile pustules on the circumference of the lesions and fine peeling. We present two cases of APP with diagnostic problems: a 65-year-old woman that suffered from intermittent APP with remission and exacerbation for many years, and an 83-year-old man with lesions that developed after atenolol treatment. In both cases, the patients were thought to have drug provocation, and therefore acute generalized exanthematous pustulosis (AGEP) was diagnosed. Only a thorough analysis of the course of the disease and histopathological examination allowed correct diagnosis. The clinical picture of APP is similar to AGEP, generalized pustular psoriasis (GPP), also known as von Zumbusch pustular psoriasis, and subcorneal pustular disease, and it requires accurate differential diagnosis.
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