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Olfactory neurocytoma as a unique cause of chronic SIADH
  1. Mohammad Farwana,
  2. Chrysostomos Tornari,
  3. Ann Sandison and
  4. Pavol Surda
  1. Ear, Nose and Throat / Head and Neck Department, Guy's and St Thomas' Hospitals NHS Trust, London, UK
  1. Correspondence to Dr Mohammad Farwana; farwana94{at}gmail.com

Abstract

A 32-year-old man was found to have a nasal mass on DOTATATE positron emission tomography (PET) scan to investigate the cause of his syndrome of inappropriate antidiuretic hormone secretion (SIADH). The patient presented 6 years earlier with malignant hypertension followed by a second emergency admission for hyponatraemia. Multiple scans and blood tests over 6 years yielded no cause for his SIADH. Nasendoscopy was unremarkable. A PET scan prompted endoscopic sinus surgery which resulted in the resection of a mass in the anterior hiatus semilunaris. The histological findings were fitting with a diagnosis of a neurocytic-type tumour favouring an olfactory neurocytoma. Following resection, the patient remains well and is cured of his SIADH. An olfactory neurocytoma although rare should be considered as a benign differential for a mass in the nasal space. This case demonstrates how an olfactory neurocytoma can present as a cause of SIADH.

  • ear
  • nose and throat/otolaryngology
  • head and neck cancer
  • endocrine cancer
  • neurooncology
  • adrenal disorders

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Footnotes

  • Contributors MF, CT and AS conceived the idea of publishing this unique case. Histopathology expertise was provided by PS. The case report was written and submitted by MF.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.