Unusual sellar lesions mimicking a pituitary neuroendocrine tumour (PitNET)

Autores/as

  • Cristina Pizzimenti Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina
  • Mariausilia Franchina Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Anatomic Pathology, University of Messina
  • Vincenzo Fiorentino Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Anatomic Pathology, University of Messina
  • Salvatore Cannavò Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Endocrinology, University of Messina
  • Francesco Ferraù Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Endocrinology, University of Messina
  • Antonio Ieni Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Anatomic Pathology, University of Messina
  • Guido Fadda Department of Human Pathology in Adult and Developmental Age “Gaetano Barresi”, Section of Anatomic Pathology, University of Messina
  • Giovanni Tuccari

DOI:

https://doi.org/10.13129/1828-6550/APMB.110.2.2022.CCS2

Palabras clave:

PitNET, sellar lesions, hypophysitis, meningioma

Resumen

Sellar region hosts a wide range of different types of lesions. Most of these lesions present with mass effect symptoms and, often, with symptoms related to hormonal disturbances, mimicking a pituitary neuroendocrine tumour (PitNET). We report two cases of sellar lesions with clinical and radiological features suggestive for PitNET. Histological and immunohistochemical analysis led to a diagnosis respectively for lymphocytic hypophysitis (LH) and meningioma.

Referencias

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Zada, G., Lopes, M.B., Mukundan, S., Laws, E. (2016). Atlas of Sellar and Parasellar Lesions, Springer, doi:10.1007/978-3-319-22855-6

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Publicado

2022-12-22

Número

Vol. 110 Núm. 2 (2022)

Sección

CLINICAL CASE SEMINAR

Licencia

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