まとめ
一件のレビューでは,原発性副甲状腺症患者の17.5%が多発性内分泌アデノマトーシス (M.E.A. ),内分泌系疾患を伴う状態である. ハイパーカルセミアの症状は,これらの患者を他の患者と区別することはありませんでした.
科学分野:
- エンドクリノロジー エンドクリノロジー
- 遺伝学 遺伝学とは
- 腫瘍学 腫瘍学
背景:
- プライマリ・ハイパーパラチロイド症は,常見の内分泌系疾患である.
- 多発性内分泌アデノマトーシス (MEA) とは これは,内分泌腺の腫瘍によって特徴づけられる珍しい遺伝疾患です.
研究 の 目的:
- M.E.A.の有病率を決定する. プライマリ・ハイパーパラチロイド症患者の場合
- M.E.A.を区別するかもしれない臨床的特徴を特定する. 他の副甲状腺腺がん患者からの患者です.
主な方法:
- 原発性パラチロイド性硬化症の119人の患者の遡及的レビュー.
- 臨床データと病理学的発見を分析した.
主要な成果:
- 17.5%の患者がMEAと診断されました.
- M.E.A.間の有意な臨床的差異は観察されなかった. 患者およびその他の副甲状腺腺がん患者.
- M.E.A.M.E.A. について 多発性副甲状腺疾患と最も頻繁に関連していました.
結論:
- 原発性パラチロイド症の症例の有意な割合は,MEAと関連している可能性があります.
- M.E.A.の早期スクリーニング 副甲状腺機能症の患者には必要かもしれません.
- M.E.A.の臨床的影響を理解するためにさらなる研究が必要である. ハイパーパラチロイド症では.
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