Lo strano caso di un paziente affetto da acromegalia con osteoporomalacia senza ipogonadismo

Translated title of the contribution: The strange case of a patient affected by acromegaly with osteoporomalacia without hypogonadism

Massimo D'Amore, G. Minenna, S. D'Amore, P. Scagliusi, S. Caprio

Research output: Contribution to journalArticlepeer-review

Abstract

Acromegaly is a rare disease that, in the majority of cases, is due to the presence of a benign growth hormone (GH)-producing tumor of the pituitary. Growth hormone has profound effects on linear bone growth, bone metabolism, and bone mass. In acromegaly, the skeletal effects of chronic GH excess have been mainly addressed by evaluating bone mineral density (BMD). Most data were obtained in patients with active acromegaly, and apparently high or normal BMD was observed in the absence of hypogonadism. The Autors describe a case of patient affected by acromegaly without hypogonadism with serious osteoporosis and biological signs of osteomalacia.

Translated title of the contributionThe strange case of a patient affected by acromegaly with osteoporomalacia without hypogonadism
Original languageItalian
Pages (from-to)291-294
Number of pages4
JournalReumatismo
Volume57
Issue number4
Publication statusPublished - 2005

ASJC Scopus subject areas

  • Rheumatology

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