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Craniopharyngioma physical examination

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Overview

Overview

The diagnosis of craniopharyngioma is often made late after the initial appearance of symptoms. The clinical picture at the time of diagnosis often dominated by nonspecific manifestations of intracranial pressure like headache, nausea and vomiting. Primary manifestations are visual impairment and endocrine deficits.

Physical examination

Physical examination

General exam

Hypothyroidism

Cortisol deficiency

Changes in volume and sodium control

Neurologic examination

References

References

  1. 1.0 1.1 Mortini P (August 2017). “Craniopharyngiomas: a life-changing tumor”. Endocrine. 57 (2): 191–192. doi:10.1007/s12020-016-1192-2. PMID 27981519.
  2. Müller HL (February 2016). “Craniopharyngioma and hypothalamic injury: latest insights into consequent eating disorders and obesity”. Curr Opin Endocrinol Diabetes Obes. 23 (1): 81–9. doi:10.1097/MED.0000000000000214. PMC 4700877. PMID 26574645.
  3. 3.0 3.1 Cohen LE (August 2016). “Update on childhood craniopharyngiomas”. Curr Opin Endocrinol Diabetes Obes. 23 (4): 339–44. doi:10.1097/MED.0000000000000264. PMID 27258775.
  4. 4.0 4.1 Qi ST (May 2017). “[The status and prospects of craniopharyngioma]”. Zhonghua Yi Xue Za Zhi (in Chinese). 97 (17): 1281–1282. doi:10.3760/cma.j.issn.0376-2491.2017.17.001. PMID 28482426.
  5. 5.0 5.1 Müller HL (June 2014). “Craniopharyngioma”. Endocr. Rev. 35 (3): 513–43. doi:10.1210/er.2013-1115. PMID 24467716.


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