{"title":"Early-onset ROHHAD-NET syndrome with severe sleep-related respiratory distress: A case report","authors":"Yudai Hirakawa , Masanori Nishi , Naoya Higuchi , Hiroi Eguchi , Takuji Nakamura , Yuya Ito , Takaharu Yamada , Masafumi Sanefuji , Akari Nakamura-Utsunomiya , Muneaki Matsuo","doi":"10.1016/j.bdcasr.2025.100118","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>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.</div></div><div><h3>Case presentation</h3><div>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.</div></div><div><h3>Conclusion</h3><div>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.</div></div>","PeriodicalId":100196,"journal":{"name":"Brain and Development Case Reports","volume":"4 1","pages":"Article 100118"},"PeriodicalIF":0.0000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain and Development Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950221725000571","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/3 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.