Vázquez García J, Almagro Sánchez M, Fonseca Capdevila E
Department of Dermatology, Juan Canalejo Hospital, La Coruña. Spain.
Clin Exp Dermatol. 2001 Jul;26(5):398-401. doi: 10.1046/j.1365-2230.2001.00844.x.
A 72-year-old woman developed three consecutive processes that showed characteristics of different neutrophilic dermatoses. First, she developed a picture resembling granuloma faciale, followed by a Sweet's syndrome-like eruption, and then by a superficial pyoderma gangrenosum. She was later diagnosed with myelodysplastic syndrome. This case demonstrates that neutrophilic dermatoses form a spectrum of entities that do not necessarily occur in isolation.
一名72岁女性先后出现了三个具有不同嗜中性皮病特征的病程。首先,她出现了类似面部肉芽肿的表现,接着是类Sweet综合征样皮疹,然后是浅表性坏疽性脓皮病。她后来被诊断为骨髓增生异常综合征。该病例表明,嗜中性皮病构成了一系列不一定单独发生的疾病。