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Suspected silent pituitary somatotroph neuroendocrine tumor associated with acromegaly-like bone disorders: a case report.

Tongxin XiaoXinxin MaoOu WangYong YaoKan DengHuijuan ZhuLian Duan
Published in: BMC endocrine disorders (2024)
GH-positive pituitary neuroendocrine tumors with hormonal tests that do not meet the diagnostic criteria for acromegaly may also cause GH hypersecretion presentations. Patients with pituitary tumors and suspicious acromegaly symptoms may require more proactive treatment than non-functioning tumors of similar size and invasiveness.
Keyphrases
  • growth hormone
  • neuroendocrine tumors
  • type diabetes
  • polycystic ovary syndrome
  • soft tissue
  • adipose tissue
  • skeletal muscle
  • metabolic syndrome