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一名患有X连锁无丙种球蛋白血症患者的坏疽性脓皮病

Pyoderma Gangrenosum in a Patient with X-Linked Agammaglobulinemia.

作者信息

Tan Qi, Ren Fa-Liang, Wang Hua

机构信息

Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing, China.

Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Chongqing, China.

出版信息

Ann Dermatol. 2017 Aug;29(4):476-478. doi: 10.5021/ad.2017.29.4.476. Epub 2017 Jun 21.

Abstract

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by germline mutations of B-cell tyrosine kinase (BTK) gene. It is characterized by decreased serum immunoglobulins levels and circulating mature B cells. This defect in humoral immunity leads to increased susceptibility to infection. Pyoderma gangrenosum (PG) is an uncommon, ulcerating, neutrophilic dermatosis. Here we report PG in an 8-year-old patient with XLA. The patient received intravenous immunoglobulin treatment in conjunction with prednisone and topical application of 0.03% tacrolimus ointment and the ulcer was almost completely healed in the 2 weeks of follow-up. The coexistence has been rarely reported. XLA may be a possible cofactor in the pathogenesis of PG.

摘要

X连锁无丙种球蛋白血症(XLA)是一种由B细胞酪氨酸激酶(BTK)基因种系突变引起的原发性免疫缺陷疾病。其特征为血清免疫球蛋白水平降低和循环成熟B细胞减少。这种体液免疫缺陷导致感染易感性增加。坏疽性脓皮病(PG)是一种罕见的溃疡性嗜中性皮病。在此,我们报告一名8岁XLA患者发生PG。该患者接受了静脉注射免疫球蛋白治疗,联合泼尼松及外用0.03%他克莫司软膏,随访2周溃疡几乎完全愈合。这种共存情况鲜有报道。XLA可能是PG发病机制中的一个潜在辅助因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e735/5500714/5fc355517a92/ad-29-476-g001.jpg

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