Literature DB >> 6427938

Neurofibromatosis and primary hyperparathyroidism.

M G Freimanis, R W Rodgers, N A Samaan.   

Abstract

Patients who have cutaneous and osseous neurofibromatosis, especially those with pathologic fractures, bone pain, roentgenographic evidence of cystic lesions, or hypercalcemia, should be evaluated carefully for the presence of a hormonally active parathyroid adenoma. They may have a reversible cause of osteitis fibrosa cystica. Palpation of the neck, serum and urine collections for measuring calcium and phosphorus levels, PTH determinations, bone roentgenograms, and bone biopsy help to establish the diagnosis.

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Year:  1984        PMID: 6427938     DOI: 10.1097/00007611-198406000-00039

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  2 in total

1.  Hypercalcemic hyperparathyroidism and hypophosphatemic osteomalacia complicating neurofibromatosis.

Authors:  R S Weinstein; R L Harris
Journal:  Calcif Tissue Int       Date:  1990-06       Impact factor: 4.333

2.  Parathyroid adenoma and bilateral pheochromocytoma in a patient with neurofibromatosis.

Authors:  Basmah Al-Wahhabi
Journal:  Ann Saudi Med       Date:  2005 May-Jun       Impact factor: 1.526

  2 in total

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