PHOX2B -associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-beta.

IF 0.8 4区 医学 Q4 HEMATOLOGY Journal of Pediatric Hematology/Oncology Pub Date : 2025-04-01 Epub Date: 2025-02-17 DOI:10.1097/MPH.0000000000003005
Alix Chupin, Benjamin Dudoignon, Nathalie Couque, Plamen Bokov, Sophie Mayer, Fatoumata Simaga, Marion Gauthier-Villars, Caroline Masserot, Sakina Benkaddouss, Pascale Philippe-Chomette, Emmanuel Jouglar, Julien Masliah-Planchon, Isabelle Aerts, Dominique Valteau-Couanet, Franck Bourdeaut, Gudrun Schleiermacher, Yassine Bouchoucha
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Abstract

Alterations of PHOX2B function is associated with a wide range of diseases, including congenital central hypoventilation syndrome (CCHS) and neural crest-derived tumors, from low-grade (ganglioneuromas) to malignant forms (neuroblastomas). We report a case bearing a novel nonpolyalanine repeat PHOX2B pathogenic variant presenting both as high-risk neuroblastoma and late-onset CCHS. CCHS was revealed upon severe respiratory decompensation while the patient was administered the anti-GD2 antibody dinutuximab-beta, as part of neuroblastoma treatment. From this experience, we make propositions for the management of patients with high-risk neuroblastoma and a constitutional pathogenic variant of PHOX2B .

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用地努妥昔单抗治疗后发现phox2b相关的先天性中枢性低通气综合征。
PHOX2B 功能的改变与多种疾病相关,包括先天性中枢通气不足综合征(CCHS)和神经嵴衍生肿瘤,从低级别(神经节细胞瘤)到恶性形式(神经母细胞瘤)。我们报告了一例患有新型非多丙氨酸重复PHOX2B致病变体的病例,该变体同时表现为高危神经母细胞瘤和晚发CCHS。作为神经母细胞瘤治疗的一部分,患者在服用抗 GD2 抗体地纽昔单抗-beta 时出现严重的呼吸衰竭,从而引发了 CCHS。根据这一经验,我们提出了治疗高危神经母细胞瘤患者和 PHOX2B 体系致病变异体的建议。
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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
期刊最新文献
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