Leonardi Lucia, Testa Alessia, Feleppa Mariavittoria, Paparella Roberto, Conti Francesca, Marzollo Antonio, Spalice Alberto, Giona Fiorina, Gnazzo Maria, Andreoli Gian Marco, Costantino Francesco, Tarani Luigi
Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Pediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Front Pediatr. 2023 Jun 9;11:1087002. doi: 10.3389/fped.2023.1087002. eCollection 2023.
Kabuki syndrome (KS) is a rare multisystemic disease due to mutations in the or genes, which act as epigenetic modulators of different processes, including immune response. The syndrome is characterized by anomalies in multiple organ systems, and it is associated with autoimmune and inflammatory disorders, and an underlying immunological phenotype characterized by immunodeficiency and immune dysregulation. Up to 17% of KS patients present with immune thrombocytopenia characterized by a severe, chronic or relapsing course, and often associated to other hematological autoimmune diseases including autoimmune hemolytic anemia, eventually resulting in Evans syndrome (ES). A 23-year-old woman, clinically diagnosed with KS and presenting from the age of 3 years with ES was referred to the Rare Diseases Centre of our Pediatric Department for corticosteroid-induced hyperglycemia. Several ES relapses and recurrent respiratory infections in the previous years were reported. Severe hypogammaglobulinemia, splenomegaly and signs of chronic lung inflammation were diagnosed only at the time of our observation. Supportive treatment with amoxicillin-clavulanate prophylaxis and recombinant human hyaluronidase-facilitated subcutaneous immunoglobulin replacement were immediately started. In KS patients, the failure of B-cell development and the lack of autoreactive immune cells suppression can lead to immunodeficiency and autoimmunity that may be undiagnosed for a long time. Our patient's case is paradigmatic since she presented with preventable morbidity and severe lung disease years after disease onset. This case emphasizes the importance of suspecting immune dysregulation in KS. Pathogenesis and immunological complications of KS are discussed. Moreover, the need to perform immunologic evaluations is highlighted both at the time of KS diagnosis and during disease follow-up, in order to allow proper treatment while intercepting avoidable morbidity in these patients.
歌舞伎综合征(KS)是一种罕见的多系统疾病,由 或 基因的突变引起,这些基因作为不同过程的表观遗传调节剂,包括免疫反应。该综合征的特征是多个器官系统出现异常,并与自身免疫性和炎症性疾病相关,其潜在的免疫表型以免疫缺陷和免疫失调为特征。高达17%的KS患者出现免疫性血小板减少症,其特征为严重、慢性或复发性病程,且常与其他血液系统自身免疫性疾病相关,包括自身免疫性溶血性贫血,最终导致伊文氏综合征(ES)。一名23岁女性,临床诊断为KS,自3岁起就患有ES,因皮质类固醇诱导的高血糖症被转诊至我们儿科的罕见病中心。据报告,前几年有多次ES复发和反复呼吸道感染。仅在我们观察时才诊断出严重低丙种球蛋白血症、脾肿大和慢性肺部炎症迹象。立即开始使用阿莫西林 - 克拉维酸预防和重组人透明质酸酶促进的皮下免疫球蛋白替代进行支持治疗。在KS患者中,B细胞发育失败和自身反应性免疫细胞抑制缺乏可导致免疫缺陷和自身免疫,可能长期未被诊断。我们患者的病例具有代表性,因为她在疾病发作多年后出现了可预防的发病情况和严重的肺部疾病。这个病例强调了在KS中怀疑免疫失调的重要性。讨论了KS的发病机制和免疫并发症。此外,强调了在KS诊断时和疾病随访期间进行免疫学评估的必要性,以便在这些患者中进行适当治疗的同时,拦截可避免的发病情况。