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April 10, 2026Reports — Medical Cases Images and Videos0 citationsOpen Access

Hypopituitarism Revealing Probable Neurosarcoidosis: A Case Report and Diagnostic Challenges

MSMichał SzklarzMMMikołaj MadekszaKWKatarzyna Wołos-Kłosowicz

Key Points

  • To highlight the diagnostic challenges of neurosarcoidosis when presenting with pituitary dysfunction.
  • Case report of a 37-year-old woman with secondary amenorrhea and suspected pituitary microadenoma.
  • Initial and follow-up magnetic resonance imaging to evaluate pituitary changes.
  • Clinical management involving high-dose corticosteroids and later methotrexate.
  • Diagnosis of probable neurosarcoidosis with multiaxial anterior pituitary insufficiency.
  • Early MRI showed a small pituitary lesion and thickening of the pituitary stalk.
  • Partial improvement in symptoms and imaging following corticosteroid therapy, with persistent hypopituitarism requiring long-term management.

Abstract

Background and Clinical Significance: Neurosarcoidosis (NS) is a rare manifestation of systemic sarcoidosis involving the central nervous system, with highly variable neurological and endocrine presentations. Among these, anterior pituitary dysfunction is particularly uncommon and diagnostically challenging. Case Presentation: We report the case of a 37-year-old woman with a 4-year history of secondary amenorrhoea and an initially suspected pituitary microadenoma, who was ultimately diagnosed with probable NS presenting with multiaxial anterior pituitary insufficiency. Early magnetic resonance imaging (MRI) revealed a small pituitary lesion and isolated pituitary stalk thickening, without other central nervous system abnormalities. Subsequent imaging demonstrated contrast-enhancing lesions involving the meninges and cranial nerves, along with progression of pituitary stalk involvement and loss of the posterior pituitary bright spot. Further evaluation confirmed systemic sarcoidosis. High-dose corticosteroid therapy led to partial clinical and radiological improvement; however, relapse necessitated methotrexate, and persistent pituitary hormone deficiencies required long-term hormonal replacement. Conclusions: This case highlights the diagnostic complexity of NS presenting with isolated endocrine dysfunction and subtle imaging findings. It underscores the need to consider systemic sarcoidosis in patients with unexplained hypopituitarism.

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Cite This Study

Szklarz et al. (2026) studied this question.

synapsesocial.com/papers/69d893eb6c1944d70ce04e59https://doi.org/10.3390/reports9020113
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