DOI: 10.12890/2020_001950

Pseudoacromegaly Associated with Non-Functioning Pituitary Adenoma

Authors

  • Awatef Alotaibi Department of Endocrinology, King Fahad Military Medical Complex, Dhahran, Saudi Arabia
  • Ahmad Habib Department of Endocrinology, King Fahad Military Medical Complex, Dhahran, Saudi Arabia
  • Moutaz Osman Department of Endocrinology, King Fahad Military Medical Complex, Dhahran, Saudi Arabia
  • Khaled Alzahrani Department of Neurosurgery, King Fahad Military Medical Complex, Dhahran, Saudi Arabia
  • Faisal Alzahrani Department of Radiology, King Fahad Military Medical Complex, Dhahran, Saudi Arabia

aotaibi@live.com

Keywords

Pituitary, growth factors, acromegaly, pseudoacromegaly, adenoma

Abstract

Acromegaly is characterized by excess skin and soft tissue growth due to increased growth hormone (GH) levels. Patients with similar physical findings but without somatotroph axis abnormalities are considered to have pseudoacromegaly. The list of pseudoacromegaly differential diagnoses is long. It may be caused by several congenital and acquired conditions and diagnosis can be challenging due to its rarity and occasional overlapping of some of these conditions. The presence of a pituitary tumour in such cases may lead to a misdiagnosis of acromegaly, and thus, biochemical evaluation is key. Here, we present a case of pseudoacromegaly with an acromegaloid phenotype, normal IGF levels, a supressed GH response to an oral glucose tolerance test, moderate insulin resistance and non-functioning pituitary microadenoma.

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References

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Published

2020-10-09

Issue

Vol. 7 No. 12 (2020)

How to Cite

1.
Alotaibi A, Habib A, Osman M, Alzahrani K, Alzahrani F. Pseudoacromegaly Associated with Non-Functioning Pituitary Adenoma . EJCRIM [Internet]. 2020 Oct. 9 [cited 2026 Nov. 3];7(12). Available from: https://ejcrim.com/index.php/ejcrim/article/view/1950