Early-onset ROHHAD-NET syndrome with severe sleep-related respiratory distress: A case report

Brain and Development Case Reports Pub Date : 2026-03-01 Epub Date: 2025-12-03 DOI:10.1016/j.bdcasr.2025.100118
Yudai Hirakawa , Masanori Nishi , Naoya Higuchi , Hiroi Eguchi , Takuji Nakamura , Yuya Ito , Takaharu Yamada , Masafumi Sanefuji , Akari Nakamura-Utsunomiya , Muneaki Matsuo
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Abstract

Background

Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, and autonomic dysregulation (ROHHAD) is a rare pediatric disorder often associated with neuroendocrine tumors (ROHHAD-NET). Recent studies have identified serum anti-ZSCAN1 antibodies in most patients, suggesting an autoimmune paraneoplastic neurological syndrome. Respiratory complications, particularly sleep-related hypoventilation, contribute to high mortality rates. Although immunomodulatory therapies have been attempted, their efficacy is limited.

Case presentation

A 2-year-old girl presented with rapid weight gain, hypothalamic dysfunction, autonomic abnormalities, and severe sleep-related hypoventilation. The patient developed intermittent strabismus, hyperphagia, and behavioral changes over 4 months. Imaging revealed a retroperitoneal paravertebral mass, which was pathologically diagnosed as ganglioneuroma. Laboratory findings revealed central hypothyroidism, growth hormone deficiency, hyperprolactinemia, and markedly elevated serum anti-ZSCAN1 antibody levels. Following admission, the patient experienced apnea, airway obstruction, excessive secretions, and wheezing during sleep, requiring mechanical ventilation. Immunotherapies, including plasma exchange, high-dose intravenous immunoglobulin, methylprednisolone pulse, rituximab, mycophenolate mofetil, and intrathecal methotrexate, improve appetite, behavior, and neuropsychiatric symptoms. Cerebrospinal fluid oligoclonal bands were negative, indicating partial immunological remission; however, sleep-related hypoventilation persisted. After discharge, the patient experienced sudden respiratory arrest during sleep and died despite resuscitation.

Conclusion

This case highlights that, ROHHAD-NET, autonomic dysfunction may cause complex sleep-related respiratory failure beyond simple obstructive or central hypoventilation. Elevated anti-ZSCAN1 antibody titers may be correlated with earlier disease onset and severity. Early recognition, aggressive immunomodulation, and consideration of ventilatory support are essential to prevent sudden deaths. Anti-ZSCAN1 antibodies may serve as useful biomarkers for the diagnosis and treatment of ROHHAD-NETs.
早发性ROHHAD-NET综合征伴严重睡眠相关呼吸窘迫1例
快速发作性肥胖伴通气不足、下丘脑功能障碍和自主神经调节失调(ROHHAD)是一种罕见的儿童疾病,常与神经内分泌肿瘤(ROHHAD- net)相关。最近的研究在大多数患者中发现了血清抗zscan1抗体,提示存在自身免疫性副肿瘤神经综合征。呼吸系统并发症,特别是与睡眠有关的低通气,是造成高死亡率的原因之一。虽然免疫调节疗法已经尝试过,但其疗效有限。一名2岁女童表现为体重迅速增加、下丘脑功能障碍、自主神经异常和严重的睡眠相关性低通气。患者在4个月内出现间歇性斜视、吞咽过多和行为改变。影像学显示腹膜后椎旁肿块,病理诊断为神经节神经瘤。实验室结果显示中枢性甲状腺功能减退,生长激素缺乏,高催乳素血症,血清抗zscan1抗体水平明显升高。入院后,患者出现呼吸暂停、气道阻塞、分泌物过多、睡眠时喘息等症状,需要机械通气。免疫疗法,包括血浆置换、大剂量静脉注射免疫球蛋白、甲基强的松龙脉冲、利妥昔单抗、霉酚酸酯和鞘内甲氨蝶呤,可改善食欲、行为和神经精神症状。脑脊液寡克隆带阴性,提示部分免疫缓解;然而,与睡眠相关的低通气仍然存在。出院后,患者在睡眠中出现呼吸骤停,经复苏后死亡。结论本病例强调,ROHHAD-NET、自主神经功能障碍可能导致复杂的睡眠相关呼吸衰竭,而不是单纯的阻塞性或中枢性低通气。抗zscan1抗体滴度升高可能与疾病早期发病和严重程度相关。早期识别、积极免疫调节和考虑通气支持对预防猝死至关重要。抗zscan1抗体可作为诊断和治疗ROHHAD-NETs的有用生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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