Schmid Florian, Kerl-French Kerstin, Meier-Schiesser Barbara, Lehmberg Kai, Hoeger Peter H
Department of Pediatrics, Catholic Children's Hospital Wilhelmstift, Hamburg, Germany.
Department of Dermatology, University of Zurich, Zurich, Switzerland.
J Allergy Clin Immunol Glob. 2024 Feb 29;3(2):100233. doi: 10.1016/j.jacig.2024.100233. eCollection 2024 May.
Leukocyte adhesion deficiency type 1 (LAD-1) is a congenital immunodeficiency leading to impaired trafficking of neutrophils to inflammation sites. Solitary or multiple pyoderma gangrenosum (PG)-like skin ulcers (PGLUs) have been reported previously in 13 children (aged 0.5-19 years) with LAD-1.
Our aim was to report the case of a 10-year-old boy presenting with PGLUs as the first manifestation of LAD-1 treated with ustekinumab.
We obtained cytokine profiles.
PGLUs were triggered by cutaneous ringworm infection (). Skin biopsy samples showed increased intralesional expression of IL-17A, Il-23, and IL-1β as compared with their expression in healthy controls. After an unsuccessful attempt at treatment with oral methylprednisolone, ustekinumab induced regression of the ulcerations, associated with complete normalization of the cytokine profile.
PGLUs, triggered by ringworm infection, can be a late harbinger of LAD-1. Ustekinumab is a safe and effective therapeutic option for patients with LAD-1 and PGLUs while bridging the time until stem cell transplantation.
1型白细胞黏附缺陷症(LAD-1)是一种先天性免疫缺陷病,可导致中性粒细胞向炎症部位的转运受损。先前已有报道称,13名年龄在0.5至19岁之间的LAD-1患儿出现了孤立性或多发性坏疽性脓皮病(PG)样皮肤溃疡(PGLU)。
我们旨在报告一名10岁男孩的病例,该男孩以PGLU为LAD-1的首发表现,并接受了乌司奴单抗治疗。
我们获取了细胞因子谱。
PGLU由皮肤癣菌感染引发()。与健康对照相比,皮肤活检样本显示病变内白细胞介素-17A(IL-17A)、白细胞介素-23(Il-23)和白细胞介素-1β(IL-1β)的表达增加。口服甲泼尼龙治疗失败后,乌司奴单抗使溃疡消退,同时细胞因子谱完全恢复正常。
由癣菌感染引发的PGLU可能是LAD-1的晚期预兆。在等待干细胞移植的这段时间里,乌司奴单抗是LAD-1和PGLU患者的一种安全有效的治疗选择。