Neurosarcoidosis manifesting as panhypopituitarism
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.
Main Authors: | Monique Oye, Michael Chahin, Nithya Krishnan, Pramod Reddy |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2019-12-01
|
Series: | Clinical Case Reports |
Subjects: | |
Online Access: | https://doi.org/10.1002/ccr3.2521 |
Similar Items
-
A rare cause of respiratory distress and edema in neonate: Panhypopituitarism
by: Fatma Dursun, et al.
Published: (2017-08-01) -
Pituitary Abscess Causing Panhypopituitarism in a Patient With Neurobrucellosis: Case Report
by: Gustavo De la Peña-Sosa, MD, et al.
Published: (2024-01-01) -
Postpartum psychosis as a presentation of panhypopituitarism
by: Jananee Muralidharan, et al.
Published: (2024-01-01) -
Unusual Clinical Course of Neurosarcoidosis Manifested with Acute Hydrocephalus
by: Dragana Jovanović, et al.
Published: (2021-01-01) -
Neurosarcoidosis and Partial Motor Seizure
by: Ayşegül Gündüz, et al.
Published: (2007-08-01)