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Journals / Annals of Medical Research / 2021 / Cilt: 28 - Sayı: 5

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

Ahmet Gorgel
Mehmet Tecellioglu
Cem Cankaya
Pages
1078–1081
Publication Date
2022-10-12
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Contrary to our expectations, any gene defects could be found related with neither MEN-1 nor MEN-4 in the genetic examinatio

📌 3 Key Takeaways

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Objective & Hypothesis:The widespread use of imaging procedures has led to an increased discovery of incidental masses in the pituitary gland.
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Key Findings & Data:Although the majority of pituitary incidentalomas are non-functioning benign adenomas but their increased prevalence poses a diagnostic and therapeutic challenge.
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Conclusion & Impact:Contrary to our expectations, any gene defects could be found related with neither MEN-1 nor MEN-4 in the genetic examinatio
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The 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 examinatio

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Cite This Article

Gorgel, A., Tecellioglu, M., Cankaya, C. (2022). Coexistence of pituitary incidentaloma and primary hyperparathyroidism mimicking multiple endocrine neoplasia Type 1: A case report. Annals of Medical Research, Cilt: 28 - Sayı: 5, 1078–1081. https://ajindex.com/articles/446022

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