呼吸器アデノマトイドハマルトーマ 嗅覚外裂け病の特徴
Jakob L Fischer1, Eugene Oh2, Dipti P Sajed3
1Department of Otolaryngology-Head and Neck Surgery, University of California Los Angeles, Los Angeles, California, USA.
The Laryngoscope
|August 26, 2025
まとめ
呼吸器上皮アデノマトイドハマルトーマ (REAH) は良性な鼻腔疾患である. 嗅覚裂けのREAHは,嗅覚外裂けのREAH患者よりもアレルギーや喘息の高齢患者で発生します.
科学分野:
- 耳鼻喉科
- 病理学について
- 鼻腔疾患
背景:
- 呼吸器上皮アデノマトイドハマルトーマ (REAH) は認識されていない非新生体である.
- 病因は不明で,単独または慢性鼻炎 (CRS) と併発することがあります.
研究 の 目的:
- REAHに関する1つの機関の15年間の経験を評価する.
- 嗅覚裂け (OC) REAHとOC外REAHを特徴づけ,比較する.
主な方法:
- 病理学的に確認された88例のREAH (2009年−2024年) の遡及レビュー
- プレゼンテーションとアウトカムを特徴付けるために,患者チャートとイメージングのレビュー.
- OC-REAHとOC-REAH以外の患者の人口統計,併発症,および表現の比較
主要な成果:
- REAHは88人の患者 (58. 6 ± 15. 6歳; 58% 男性; 75% 白人) で発生した.
- OC-REAH (55. 7%) は,OC以外のREAH (44. 3%) と比較して,アレルギー性鼻炎,喘息,および以前の内視鼻腔外科手術の頻度が高い高齢患者で診断されました.
- エクストラOCREAHは稀にシノナサルの塊として現れ,時には他の病理を模倣し,再発は観察されなかった.
結論:
- REAHは,表情が変化し,病因が完全に理解されていない良性である.
- REAHにおけるOCの関与は,高齢化とアレルギー性鼻炎と喘息の発生率の上昇と関連しています.
- REAHは別々の質量として現れ,潜在的に他の鼻腔疾患を模倣する可能性があります.
関連する概念動画
Olfactory Receptors: Location and Structure
9.6K
The process of olfaction, also known as the sense of smell, is a sophisticated chemical response system. The specialized sensory neurons that facilitate this process, known as olfactory receptor neurons, are situated in an upper segment of the nasal cavity, known as the olfactory epithelium. Olfactory sensory neurons are bipolar, with their dendrites extending from the epithelium's apex into the mucus that lines the nasal cavity. Airborne molecules, when inhaled, traverse the olfactory...
9.6K
Cystic Fibrosis: Pathogenesis
360
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
360
Classification of Epithelial Tissues: Simple Epithelium
10.2K
Simple epithelium consists of a single layer of cells that lines body cavities and blood vessels. The shape of the cells in the epithelium reflects the function of the tissue. Cells in simple squamous epithelium appear as thin scales with flat, elliptical nuclei that mirror the form of the cell.
Because of the thinness of the cells, simple squamous epithelium is present where the rapid passage of chemical compounds is observed. For example, the endothelium that lines the capillaries and vessels...
Because of the thinness of the cells, simple squamous epithelium is present where the rapid passage of chemical compounds is observed. For example, the endothelium that lines the capillaries and vessels...
10.2K


