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The etiology, clinical features and medical treatment of somatotroph adenomas |
Hua Gao1, Jianhua Li2, Yazhuo Zhang1,3,4* |
1.Key Laboratory of Central Nervous System Injury Research, Beijing Neurosurgical Institute, Capital Medical University, Beijing 100050, China
2.Department of Neurosurgery, Binzhou People’s Hospital, Binzhou, Shandong 256610, China
3.Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China
4.Beijing Neurosurgical Institute, Center of Brain Tumor, Beijing Institute for Brain Disorder, Capital Medical University, Beijing 100050, China |
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Abstract Somatotroph adenomas lead to hypersecretion of growth hormones (GH) and may cause mass effects. Patients with somatotroph adenomas may present with acral and soft tissue enlargement, joint pain, heart and respiratory failure, diabetes mellitus and hypertension, resulting in increased morbidity and mortality. Early diagnosis and treatment are therefore important in prolonging life and improving quality of life. Recent studies depicted the landscape of genetic and epigenetic changes in sporadic somatotroph adenomas. New approaches are being developed for genetic testing, diagnosis and surveillance, which are helpful in early diagnosis, treatment and disease control of somatotroph adenomas. Data suggest that patients with somatotroph adenomas are best treated with multidisciplinary teams composed of neuro-endocrinologists, neurosurgeons, radiation oncologists and other specialists. This mini-review summarizes in a concise way the up-to-date discussion on the etiology, new diagnostic techniques and novel treatments of somatotroph adenomas.
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Keywords
somatotroph adenomas
growth hormone (GH)
somatic mutation
apparent genetics
treatment
management
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Issue Date: 01 September 2018
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