This report aims to identify a rare occurrence of craniopharyngioma in the pituitary stalk region and its similarities with lymphocytic hypophysitis.
Case presentation detailing imaging and clinical findings of the tumor.
Comparison with typical symptoms of lymphocytic hypophysitis.
Diagnostic review based on imaging techniques and histopathology.
The tumor exhibited characteristics atypical for lymphocytic hypophysitis.
Histological analysis confirmed the diagnosis of craniopharyngioma.
Patient underwent successful treatment with no recurrence noted in follow-ups.
Abstract
DOI: 10.20452/pamw.17289, Published online: May 04, 2026, Authors: Adrian Czechowski, Ewelina Rzepka, Edyta Tkacz, Grzegorz Zieliński, Aleksandra Gilis-Januszewska, Alicja Hubalewska-Dydejczyk