A 36-year-old man with a history of juvenile pilocytic astrocytoma of the optic pathway,
which was diagnosed at age 13 and treated with surgical resection followed by chemotherapy
and radiation for progression in his mid-20s with resultant panhypopituitarism, presented
to the hospital in early spring with progressive but intermittent muscle aches and
weakness of 2 months’ duration. He denied vomiting or excessive diarrhea. The panhypopituitarism
had been well-managed on supplemental hormone therapy.
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to The American Journal of MedicineAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Frameworks for Internal Medicine.Wolters Kluwer, Philadelphia, PA2018
- Periodic paralysis and voltage-gated ion channels.Kidney Int. 1996; 49: 9-18
- The impact of hypothermia on serum potassium concentration: a systematic review.Resuscitation. 2017; 118: 35-42
- Thermoregulation: recent concepts and remaining questions.Neurology. 2007; 69: 1293-1297
Article Info
Publication History
Published online: November 08, 2020
Footnotes
Funding: None.
Conflicts of Interest: None.
Authorship: All authors had access to the data and a role in writing this manuscript.
Identification
Copyright
© 2020 Elsevier Inc. All rights reserved.