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Neuromyelitis Optica Spectrum Disorder Manifested by Persistent Hiccups and Severe Esophagitis in an Adolescent
Priya Singh1, Reinaldo Garcia1,2, Madhura Y Phadke3
1From the Northeast Ohio Medical University, Rootstown, OH.
Insights
Persistent hiccups in an 18-year-old male were initially attributed to esophagitis but were ultimately diagnosed as a symptom of neuromyelitis optica spectrum disorder, a rare autoimmune condition.
Area of Science:
- Neurology
- Gastroenterology
- Immunology
Background:
- Persistent hiccups are often evaluated by gastroenterologists, with causes spanning multiple organ systems.
- Hiccups exceeding 48 hours are classified as persistent, and those over 2 months as intractable.
Observation:
- An 18-year-old male presented with persistent hiccups, nausea, and emesis, initially diagnosed with severe esophagitis.
- Despite gastrointestinal treatment, hiccups worsened, prompting a neurological consultation.
- Brain MRI revealed a dorsal medullary lesion, leading to the diagnosis of neuromyelitis optica spectrum disorder.
Findings:
- Neuromyelitis optica spectrum disorder is a rare, severe autoimmune central nervous system condition.
- Early diagnosis and treatment are crucial for managing relapses in neuromyelitis optica spectrum disorder.
- The patient experienced rapid symptom improvement with high-dose intravenous steroids.
Implications:
- This case highlights the importance of considering neurological etiologies for hiccups, especially when gastrointestinal causes are unresponsive to treatment.
- It underscores the need for a multidisciplinary approach, integrating neurology and gastroenterology, for complex cases.
- Prompt neurological evaluation can lead to timely diagnosis and management of rare autoimmune disorders presenting with atypical symptoms.
Abstract:
Patients with persistent hiccups are often referred to gastrointestinal services. Hiccups lasting greater than 48 hours are classified as persistent, while those lasting longer than 2 months are termed intractable. The etiology of hiccups is broad and can include many organ systems. Here, we present the case of an 18-year-old male patient who presented to the emergency department with an 8-day history of nausea, emesis, and intermittent hiccups. The patient was admitted to the gastroenterology service and underwent workup including esophagogastroduodenoscopy and imaging. Esophagogastroduodenoscopy revealed severe distal esophagitis. He was started on high-dose proton pump inhibitor and sucralfate. During the course of hospital admission, the patient's intermittent hiccups worsened to become constant. Several medical therapies led to little improvement. We initially felt that the esophagitis was the etiology of the patient's symptoms, however, due to ongoing symptoms unresponsive to typical therapy, we obtained a neurological consult. Brain MRI revealed a dorsal medullary lesion. Subsequent work up confirmed the diagnosis of neuromyelitis optica spectrum disorder. Neuromyelitis optica spectrum disorder is a rare, serious, sometimes fatal autoimmune condition of the central nervous system. Early diagnosis and treatment are important predictors of future relapses. Our patient was started on high-dose intravenous steroids with rapid improvement in symptoms. He was discharged home on steroids, proton pump inhibitor and close neurology and gastroenterology follow up. This case outlines the importance of consideration of neurological causes of hiccups or other centrally mediated conditions with gastrointestinal manifestations, even when a concomitant gastrointestinal condition is present.
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