Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. It is related to high levels of growth hormone (GH) and insulin-like growth factor-I ([[IGF-1]]). ===MRI=== The enhancement was significantly lower in [[GH secreting pituitary neuroendocrine tumor]] than in non-secreting ones. ((Lundin P, Bergström K. Gd-DTPA-enhanced MR imaging of pituitary macroadenomas. Acta Radiol. 1992 Jul;33(4):323-32. PubMed PMID: 1633042.)). [[T2 weighted image]] differentiates [[GH secreting pituitary neuroendocrine tumor]]s into subgroups with particular behaviors. This raises the question of whether T2-weighted signal could represent a factor in the classification of [[acromegaly]] in future studies ((Potorac I, Petrossians P, Daly AF, Schillo F, Ben Slama C, Nagi S, Sahnoun Fathallah M, Brue T, Girard N, Chanson P, Nasser G, Caron P, Bonneville F, Ravérot G, Lapras V, Cotton F, Delemer B, Higel B, Boulin A, Gaillard S, Luca F, Goichot B, Dietemann J, Beckers A, Bonneville J. Pituitary MRI characteristics in 297 acromegaly patients based on T2-weighted sequences. Endocr Relat Cancer. 2015 Jan 2. pii: ERC-14-0305. [Epub ahead of print] PubMed PMID: 25556181.)). In patients with [[acromegaly]], [[T2 weighted image]] signal intensity at diagnosis correlates with histological features and predicts biochemical outcome of first-line somatostatin analogues (SA) treatment ((Heck A, Ringstad G, Fougner SL, Casar-Borota O, Nome T, Ramm-Pettersen J, Bollerslev J. Intensity of pituitary neuroendocrine tumor on T2-weighted magnetic resonance imaging predicts the response to octreotide treatment in newly diagnosed acromegaly. Clin Endocrinol (Oxf). 2012 Jul;77(1):72-8. doi: 10.1111/j.1365-2265.2011.04286.x. PubMed PMID: 22066905.)). ===Biomarkers=== Each of the biomarkers, Ki-67 and p53, along with patient's age and mixed GH-prolactin secretion showed a kind of correlation with each of aspects of the clinical, hormonal and radiologic outcome of GH-secreting pituitary neuroendocrine tumors ((Alimohamadi M, Ownagh V, Mahouzi L, Ostovar A, Abbassioun K, Amirjmshidi A. The impact of immunohistochemical markers of Ki-67 and p53 on the long-term outcome of growth hormone-secreting pituitary neuroendocrine tumors: A cohort study. Asian J Neurosurg. 2014 Jul-Sep;9(3):130-6. doi: 10.4103/1793-5482.142732. PubMed PMID: 25685203; PubMed Central PMCID: PMC4323896. )). ===== Best Practices ===== D1-rGH could be a highly specific test for the early diagnosis of long-term acromegaly persistence, which is predicted by a value > 2.5 ng/mL with a great degree of certainty. The diagnostic performance of D2-rGH was insufficient. Further research is required to validate these preliminary results prior to modifying the postoperative management of acromegaly ((Cambria V, Beccuti G, Prencipe N, Penner F, Gasco V, Gatti F, Romanisio M, Caputo M, Ghigo E, Zenga F, Grottoli S. First but not second postoperative day growth hormone assessments as early predictive tests for long-term acromegaly persistence. J Endocrinol Invest. 2021 Apr 10. doi: 10.1007/s40618-021-01553-0. Epub ahead of print. PMID: 33837920.)). somatotroph_adenoma_diagnosis.txt Last modified: 2024/06/07 02:51by 127.0.0.1