A rare case of isolated IgG4-related hypophysitis with Rathke’s cleft cyst presenting as panhypopituitarism

SUMMARY: We report a rare case of biopsy-proven isolated immunoglobulin G4 (IgG4)-related hypophysitis and Rathke’s cleft cyst (RCC) presenting as panhypopituitarism. A 54-year-old Caucasian female presented with symptoms of slurred speech, altered mental status, polyuria and polydipsia and was foun...

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Detalles Bibliográficos
Autores principales: Hashmi, Hiba Z, Rupakula, Dinkar, Magar, Rekha, Clark, H Brent, Moheet, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2023
Materias:
New Disease or Syndrome: Presentations/Diagnosis/Management
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241233/
https://www.ncbi.nlm.nih.gov/pubmed/37067235
http://dx.doi.org/10.1530/EDM-22-0359

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