两个独特的病例嗜酸性肉芽肿病多血管炎的儿童治疗与抗白细胞介素-5治疗:婴儿起病和下颌唾液腺累及。

IF 2.8 3区 医学 Q1 PEDIATRICS
Evangelia Constantine, Adam M Bartholomeo, Inna Powers, Jerimiah L Lysinger, Pia J Hauk, Jordan Abbott, Heather H de Keyser, Nicholas J Gilman, Csaba Galambos, Angus Toland, Nicholas Willard, Jason Weinman, David Mong, Clara Lin, Jessica L Bloom
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引用次数: 0

摘要

背景:anca相关性血管炎是一种累及中小血管的全身性自身免疫性疾病。嗜酸性肉芽肿病合并多血管炎(EGPA,以前的Churg Strauss综合征)是儿童最不常见的形式,很少有病例报道。我们提出两个独特的儿科病例,这两个治疗与抗白细胞介素-5治疗。病例介绍:病例1是一名患有哮喘和过敏的13岁男性,表现为咳嗽和眶周水肿一个月,随后出现下颌下肿胀。评估发现慢性鼻窦炎,体重减轻,c-ANCA和抗mpo IgG抗体阳性,外周血嗜酸性粒细胞增多,肺嗜酸性粒细胞增多,气管和肺结节,下颌下涎腺嗜酸性粒细胞浸润,肉芽肿和纤维化符合EGPA的诊断。他在使用糖皮质激素和美polizumab治疗后病情好转,出现了显著的部分缓解,最终改用贝纳利珠单抗和霉酚酸酯治疗,出现了完全缓解。病例2于19个月大时出现急性呼吸窘迫并有反应性气道疾病史。在抗mpo和p-ANCA阳性的情况下,肺活检证实EGPA诊断(嗜酸性毛细血管炎和嗜酸性粒细胞间质扩张)。三年来,他服用美polizumab的效果非常好。结论:据我们所知,这是第一例报道的儿童EGPA的下颌下唾液腺浸润,也是文献中报道的最年轻的成功治疗的EGPA患者。这些病例显示了EGPA患儿年龄和疾病表现的差异,以及对抗白细胞介素-5治疗的阳性反应。患有EGPA的儿童可能会出现常见或不寻常的症状,需要敏锐的识别,以避免诊断延误和长期损害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two unique cases of eosinophilic granulomatosis with polyangiitis in childhood treated with anti-interleukin-5 therapy: infantile-onset and submandibular salivary gland involvement.

Background: ANCA-associated vasculitis is a systemic autoimmune disease involving small- and medium-sized blood vessels. Eosinophilic granulomatosis with polyangiitis (EGPA, previously Churg Strauss Syndrome) is the least common form in childhood with few cases reported. We present two unique pediatric cases, both of which were treated with anti-interleukin-5 therapy.

Case presentation: Case one is a 13-year-old male with asthma and allergies who presented with one month of cough and periorbital edema and subsequently developed submandibular swelling. Evaluation identified chronic sinusitis, weight loss, positive c-ANCA and anti-MPO IgG antibodies, peripheral blood eosinophilia, pulmonary eosinophilia, tracheal and pulmonary nodules, and eosinophilic infiltration of the submandibular salivary gland with granulomas and fibrosis fitting a diagnosis of EGPA. He improved with glucocorticoids and mepolizumab with a significant partial response, and eventually switched to benralizumab and mycophenolate mofetil with complete response. Case two presented at 19-months-old in acute respiratory distress with a history of reactive airway disease. EGPA diagnosis was confirmed on lung biopsy (eosinophilic capillaritis and interstitial expansion of eosinophils) in the setting of anti-MPO and p-ANCA positivity. He has done very well on mepolizumab for three years.

Conclusions: To our knowledge, this is the first reported case of submandibular salivary gland infiltrate in a child with EGPA and the youngest successfully treated patient with EGPA reported in the literature. These cases demonstrate the variation in age and disease manifestations seen in children with EGPA as well as positive responses to anti-interleukin-5 therapy. Children with EGPA may present with common or unusual complaints and require astute recognition to avoid delays in diagnosis and long-term damage.

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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