Abstract
A 29-year-old Ethiopian man presented with marked bilateral visual loss, headache, hypopituitarism and significant hyponatraemia (115 mmol/L). A brain MRI scan demonstrated a large, lobulated, sellar and suprasellar mass, elevating the floor of the 3rd ventricle and compressing the optic chiasm. The patient underwent a transphenoidal resection of the mass followed by a craniotomy 10 days later. Histological examination demonstrated a Hyams’ grade III neuroblastoma with ectopic expression of vasopressin. He underwent fractionated radiotherapy at a dose of 60 Gy in 30 fractions. Fourteen months after the onset, he is well with no neuroimaging evidence of tumour recurrence. His serum and urine sodium are completely normalised.
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Acknowledgements
The authors are extremely grateful to Mr. Bob Chapman, Department of Histopathology, Chairing Cross Hospital, London, for his assistance in photography and Mrs. Poonam Singh for technical work.
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Radotra, B., Apostolopoulos, V., Sandison, A. et al. Primary Sellar Neuroblastoma Presenting with Syndrome of Inappropriate Secretion of Anti-diuretic Hormone. Endocr Pathol 21, 266–273 (2010). https://doi.org/10.1007/s12022-010-9140-9
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DOI: https://doi.org/10.1007/s12022-010-9140-9