Abstract
Panhypopituitarism secondary to Neurosarcoidosis is a rare however serious complication. This diagnosis should remain in the differential in patients with hypothalamic-pituitary dysfunction. Biopsy of lesions will give definitive diagnosis.
Author supplied keywords
Cite
CITATION STYLE
APA
Oye, M., Chahin, M., Krishnan, N., & Reddy, P. (2019). Neurosarcoidosis manifesting as panhypopituitarism. Clinical Case Reports, 7(12), 2472–2475. https://doi.org/10.1002/ccr3.2521
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free