Coexistence of pituitary incidentaloma and primary hyperparathyroidism mimicking multiple endocrine neoplasia Type 1: A case report

dc.contributor.authorGorgel, Ahmet
dc.contributor.authorTecellioglu, Mehmet
dc.contributor.authorCankaya, Cem
dc.date.accessioned2022-03-16T09:53:54Z
dc.date.available2022-03-16T09:53:54Z
dc.date.issued2021
dc.departmentİnönü Üniversitesien_US
dc.description.abstractThe widespread use of imaging procedures has led to an increased discovery of incidental masses in the pituitary gland. Although the majority of pituitary incidentalomas are non-functioning benign adenomas but their increased prevalence poses a diagnostic and therapeutic challenge. These masses may cause various hormonal disturbances as well as they might also be a component of multiple endocrine neoplasia syndromes type 1 (MEN-1) or type 4 (MEN-4). In both syndromes, primary hyperparathyroidism frequently accompanies with pituitary adenomas. Herein we present a 56-year-old man with pituitary incidentaloma who is also detected primary hyperparathyroidism. Contrary to our expectations, any gene defects could be found related with neither MEN-1 nor MEN-4 in the genetic examination.en_US
dc.identifier.citationGorgel, A., Tecellioglu, M., & Cankaya, C. (2021). Coexistence of pituitary incidentaloma and primary hyperparathyroidism mimicking multiple endocrine neoplasia Type 1: A case report . Annals of Medical Researchen_US
dc.identifier.urihttps://hdl.handle.net/11616/55970
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCoexistence of pituitary incidentaloma and primary hyperparathyroidism mimicking multiple endocrine neoplasia Type 1: A case reporten_US
dc.typeArticleen_US

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