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Rare disease
‘Tumour-induced osteomalacia’
  1. Javier Munoz1,
  2. Rosa Michel Ortega2,
  3. Florence Celzo3,
  4. Vijayalakshmi Donthireddy1
  1. 1Department of Hematology and Oncology, Henry Ford Hospital, Detroit, Michigan, USA
  2. 2Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan, USA
  3. 3Department of Endocrinology, Henry Ford Hospital, Detroit, Michigan, USA
  1. Correspondence to Dr. Javier Munoz, Javier.munoz{at}me.com

Summary

A 60-year-old man presented 2 years before his diagnosis with long-standing muscle cramping, progressive generalised weakness and chronic hip pain. The patient was found to have bilateral femoral neck pathologic fractures therefore, underwent reamed intramedullary nailing of both femurs. Laboratory studies showed hypophosphataemia. Bone marrow biopsy was negative for malignancy. Positron emission tomography demonstrated fludeoxyglucose uptake only in the posterior neck. Bone scan showed innumerable foci of increased activity throughout the skeleton consistent with pseudofractures seen in osteomalacia. Fine needle aspiration from the mass in the neck revealed a phosphaturic mesenchymal tumour of mixed connective tissue type. Resection of the mass in the neck resulted in resolution of generalised complaints with no evidence of recurrence with a follow-up of 12 months.

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Footnotes

  • Competing interests None.

  • Patient consent Obtained.