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骨髓增生异常综合征转化为急性髓系白血病并同时并发坏死性嗜酸性粒细胞增多综合征。

Transformation of a myelodysplastic syndrome to acute myeloid leukemia and concurrent necrotizing sweet syndrome.

作者信息

Vera-Lastra Olga, Olvera-Acevedo Arturo, Pulido-Díaz Nancy, Quintal-Ramírez Marissa de Jesús, Ordoñez-González Irvin, Cimé-Aké Erik, Cruz-Domínguez María Pilar, Medina Gabriela

机构信息

Internal Medicine Department, Hospital de Especialidades Centro Médico Nacional La Raza, IMSS, Mexico City.

Universidad Nacional Autónoma de México, Mexico City.

出版信息

Dermatol Reports. 2021 Mar 17;13(1):9017. doi: 10.4081/dr.2021.9017. eCollection 2021 Mar 18.

Abstract

The Sweet's syndrome, is an inflammatory skin disorder characterized by extensive infiltration of neutrophils in the dermis with extension to the subcutis, known as acute febrile neutrophilic dermatosis. It may occur as a paraneoplastic syndrome. To our knowledge, there are currently few reports about transformation of a myelodysplastic syndrome to acute myeloid leukemia and concurrent necrotizing Sweet syndrome in the literature. Herein we describe an unusual case in a young patient with these characteristics that evolved to a fatal outcome.

摘要

斯威特综合征是一种炎症性皮肤病,其特征是真皮内有大量中性粒细胞浸润并延伸至皮下组织,也被称为急性发热性嗜中性皮病。它可能作为一种副肿瘤综合征出现。据我们所知,目前文献中关于骨髓增生异常综合征转化为急性髓系白血病并同时并发坏死性斯威特综合征的报道很少。在此,我们描述了一名具有这些特征的年轻患者的罕见病例,该病例最终发展为致命结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3142/8018258/b924d985493d/dr-13-1-9017-g001.jpg

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