Linear IgA bullous dermatosis and elevated bullous interleukin‐6 levels: Responsive to treatment with Anti‐IL‐6 receptor monoclonals

Author:

Jordan Stanley C.12ORCID,Balzer Bonnie3,Nast Cynthia3,Atienza Janet1,Lim Katherine1,Kumar Sanjeev1,Nissen Nicholas1,Shin Bongha12

Affiliation:

1. Comprehensive Transplant Center Cedars‐Sinai Medical Center Los Angeles California USA

2. Transplantation & Immunology Laboratory Cedars‐Sinai Medical Center Los Angeles California USA

3. Department of Pathology & Laboratory Medicine Cedars‐Sinai Medical Center Los Angeles California USA

Abstract

AbstractLinear IgA bullous dermatosis (LABD) is  a rare autoimmune/inflammatory skin condition. Here, we report on a patient who developed treatment resistant LABD. At diagnosis, elevations of IL‐6 and C‐reactive protein in the blood and extreme elevations of IL‐6 in LABD bullous fluid were seen. The patient responded well to tocilizumab (anti‐IL‐6 receptor) treatment.

Publisher

Wiley

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Tofacitinib for the treatment of severe rare skin diseases: a narrative review;European Journal of Clinical Pharmacology;2024-01-17

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