European Journal of Case Reports in Internal Medicine (May 2021)

A Rare Case of Hypophosphataemic Osteomalacia in von Recklinghausen Neurofibromatosis

  • Yasmine Makhlouf,
  • Soumaya Boussaid,
  • Houda Ajlani,
  • Samia Jemmali,
  • Sonia Rekik,
  • Hela Sehli,
  • Mouhamed Eleuch

DOI
https://doi.org/10.12890/2021_002618

Abstract

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Background: Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is a one of the more common hereditary autosomal disorders. However, osteomalacia in neurofibromatosis type 1 is very rare tumour-induced osteomalacia; fibroblast growth factor-23 is usually implicated. Patients and methods: We report the case of a patient with a history of von Recklinghausen neurofibromatosis who presented with hypophosphataemic osteomalacia. Results: The patient was treated with high-dose calcitriol and oral phosphate with clinical improvement. Conclusion: Even though it is a rare entity, we must consider the diagnosis of hypophosphataemic osteomalacia in patients with neurofibromatosis in order to deliver appropriate treatment.

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