Simpson G T, Strong M S, Skinner M, Cohen A S
Ann Otol Rhinol Laryngol. 1984 Jul-Aug;93(4 Pt 1):374-9. doi: 10.1177/000348948409300418.
Seven cases of localized amyloidosis limited to structures of the head and neck and upper aerodigestive and lower respiratory tracts evaluated and treated at Boston University Hospitals in a recent 7-year period were reviewed. Negative Congo red staining of abdominal adipose aspiration biopsy or rectal biopsy specimens established that the amyloidosis was not systemic. Localized amyloidosis occurred in discrete masses in a variety of sites in the aerodigestive tract including the orbit, nasopharynx, lips, floor of mouth, tongue, larynx, and tracheobronchial tree. Five patients required surgical excision because of significant airway obstruction or organic dysfunction. Amyloid deposits completely excised with the carbon dioxide laser have not recurred, though other amyloid masses may appear elsewhere within the same organ or region. Amyloidosis may occur primarily or secondarily to other disease states. Localized amyloidosis has not been chemically identified but is usually defined by the absence of systemic features. While rare, amyloidosis must be recognized and understood by the otolaryngologist/head and neck surgeon to allow appropriate diagnostic and therapeutic planning.
回顾了最近7年在波士顿大学医院评估和治疗的7例局限于头颈部结构以及上气道消化道和下呼吸道的局限性淀粉样变性病例。腹部脂肪抽吸活检或直肠活检标本刚果红染色阴性,证实淀粉样变性并非全身性。局限性淀粉样变性以离散肿块的形式出现在上气道消化道的多个部位,包括眼眶、鼻咽、嘴唇、口腔底部、舌头、喉部和气管支气管树。5例患者因严重气道阻塞或器官功能障碍需要手术切除。用二氧化碳激光完全切除的淀粉样沉积物未复发,不过其他淀粉样肿块可能出现在同一器官或区域的其他部位。淀粉样变性可能原发,也可能继发于其他疾病状态。局限性淀粉样变性尚未通过化学方法鉴定,但通常通过缺乏全身性特征来定义。虽然罕见,但耳鼻喉科医生/头颈外科医生必须认识和了解淀粉样变性,以便进行适当的诊断和治疗规划。