山东大学耳鼻喉眼学报 ›› 2020, Vol. 34 ›› Issue (6): 99-103.doi: 10.6040/j.issn.1673-3770.0.2020.237

• • 上一篇    下一篇

原发局限性扁桃体淀粉样变1例并文献复习

冯晨,金霄雪,韩莹莹,邹娟娟,李延忠, 王岩   

  1. 山东大学), 山东 济南 250012
  • 发布日期:2021-01-11
  • 通讯作者: 王岩. E-mail:wangyan66@sdu.edu.cn
  • 基金资助:
    山东省重点研发计划项目(2018GSF118001);山东省自然科学基金项目(ZR2018MH017)

Primary localized tonsil amyloidosis: a case report and literature review

FENG Chen, JIN Xiaoxue, HAN Yingying, ZOU Juanjuan, LI Yanzhong, WANG Yan   

  1. Department of Otorhinolaryngology, Qilu Hospital, Cheeloo College of Medicine, Shandong University / NHC Key Laboratory of Otorhinolaryngology (Shandong University), Jinan 250012, Shandong, China
  • Published:2021-01-11

摘要: 目的 探讨原发局限性扁桃体淀粉样变的临床表现、诊断思维、治疗方法及预后,以便对其进行早期诊断。 方法 回顾性分析1例原发局限性扁桃体淀粉样变患者的临床资料并复习相关文献进行总结。 结果 原发局限性扁桃体淀粉样变早期缺乏特异性症状,疾病进展常较快,临床表现常为双侧扁桃体不对称增长或双侧迅速增大导致的咽部异物感为主,其余包括扁桃体赘生物、溃疡、咽干、咽痒、咽痛、吞咽困难等非特异性表现。对无痛性扁桃体肥大且无炎症症状患者,如若病程较短、双侧扁桃体明显不对称、表面溃疡和质地硬等,都应先行病理活检。 结论 原发局限性扁桃体淀粉样变临床及影像表现无特异性,因而详细病史采集、全身系统检查、病理活检等有效手段对于早期诊断疾病非常重要。

关键词: 原发局限性, 淀粉样变, 扁桃体, 临床表现, 病理活检

Abstract: Objective To investigate the clinical characteristics, diagnosis, treatment, and prognosis of primary localized tonsil amyloidosis, to enable its early diagnosis. Methods A patient with primary localized tonsil amyloidosis was retrospectively reviewed, along with previous cases of primary localized tonsil amyloidosis found in the literature. Results The clinical manifestations of primary localized tonsil amyloidosis lack specificity, and its early manifestations are often atypical. Besides, the disease often rapidly progresses. The clinical manifestations are mainly a pharyngeal foreign body sensation caused by the asymmetric growth or rapid enlargement of the bilateral tonsil. Other non-specific manifestations include tonsil growth, an ulcer, dry pharynx, pharynx itch, pharynx pain, and dysphagia. For patients with painless hypertrophy of the tonsil and no inflammatory symptoms, a pathological biopsy should be performed if bilateral tonsil asymmetry is apparent, there is a surface ulcer, the texture is hard, or the history is short. Conclusion The clinical and imaging manifestations of primary localized tonsil amyloidosis are non-specific. Therefore, it is imperative to carefully consider the patient's medical history, systemic examination findings, and pathological biopsy findings to diagnose primary localized tonsil amyloidosis at an early stage.

Key words: Primary limitations, Amyloidosis, Tonsils, Clinical manifestations, Pathological biopsy

中图分类号: 

  • R766
[1] Wechalekar AD, Gillmore JD, Hawkins PN. Systemic amyloidosis[J]. Lancet, 2016, 387(10038): 2641-2654. doi:10.1016/s0140-6736(15)01274-x.
[2] Merchionne F, Procaccio P, Dammacco F. Waldenström's macroglobulinemia. An overview of its clinical, biochemical, immunological and therapeutic features and our series of 121 patients collected in a single center[J]. Crit Rev Oncol Hematol, 2011, 80(1): 87-99. doi:10.1016/j.critrevonc.2010.09.007.
[3] Nuvolone M, Merlini G. Systemic amyloidosis: novel therapies and role of biomarkers[J]. Nephrol Dial Transplant, 2017, 32(5): 770-780. doi:10.1093/ndt/gfw305.
[4] Ben Salah R, Marzouk S, Kaddour N, et al. Tonsil amyloidosis revealing a Waldenström macroglobulinemia[J]. Eur Arch Otorhinolaryngol, 2012, 269(4): 1301-1304. doi:10.1007/s00405-011-1886-2.
[5] Weidner T, Illing T, Elsner P. Primary localized cutaneous amyloidosis: a systematic treatment review[J]. Am J Clin Dermatol, 2017, 18(5): 629-642. doi:10.1007/s40257-017-0278-9.
[6] 仲济龙,张剑. 扁桃体淀粉样变性1例[J]. 江西医药, 1994(2): 115.
[7] Real de Asúa D, Costa R, Galván JM, et al. Systemic AA amyloidosis: epidemiology, diagnosis, and management[J]. Clin Epidemiol, 2014, 6: 369-377. doi:10.2147/CLEP.S39981.
[8] 中国系统性淀粉样变性协作组, 国家肾脏疾病临床医学研究中心. 系统性轻链型淀粉样变性诊断和治疗指南[J]. 中华医学杂志, 2016, 96(44): 3540-3548. doi:10.3760/cma.j.issn.0376-2491.2016.44.002.
[9] 吉晓滨, 梁赐芳. 喉淀粉样变性病的临床报告并文献复习[J]. 临床耳鼻咽喉科杂志, 2004, 18(9): 521-523. doi:10.3969/j.issn.1001-1781.2004.09.004. JI Xiaobin, LIANG Cifang. Cases report and literature review of laryngeal amyloidosis[J]. Journal of Clinical Otorhinolaryngology, 2004, 18(9): 521-523. doi:10.3969/j.issn.1001-1781.2004.09.004.
[10] 王成刚, 牛雅琪, 马亮, 等. 舌淀粉样变性1例报告并文献复习[J]. 全科口腔医学杂志(电子版), 2019, 6(25): 2-4. WANG Chenggang, NIU Yaqi, MA Liang, et al. Amyloidosis of tongue: a case report and literature review[J]. Electronic Journal of General Stomatology, 2019, 6(25): 2-4.
[11] Green KM, Morris DP, Pitt M, et al. Amyloidosis of Waldeyer's ring and larynx[J]. J Laryngol Otol, 2000, 114(4): 296-298. doi:10.1258/0022215001905391.
[12] Kyle KA, Bayed KD. Amyloidosis: review op 236 cases[J]. Medicine, 1975, 54(4): 271-299. doi:10.1097/00005792-197507000-00001.
[13] 王新花, 张蕴莉. 1例多发性骨髓瘤舌淀粉样变误诊病例分析[J]. 军医进修学院学报, 2011, 32(5): 526-528.
[14] Gilad R, Milillo P, Som PM. Severe diffuse systemic amyloidosis with involvement of the pharynx, larynx, and Trachea: CT and MR findings[J]. AJNR Am J Neuroradiol, 2007, 28(8): 1557-1558. doi:10.3174/ajnr.A0604.
[15] 曹广亚. 单纯性扁桃体淀粉样变性二例[J]. 临床耳鼻咽喉科杂志, 1995(3): 185.
[16] 王萍, 江刚. 扁桃体淀粉样变1例[J]. 临床耳鼻咽喉科杂志, 2001(4): 184. doi: 10.3969/j.issn.1001-1781.2001.04.029.
[17] 宋玉芬, 杨存礼, 韩冰, 等. 双侧扁桃体淀粉样变1例[J]. 临床耳鼻咽喉科杂志, 2003(1): 13. doi: CNKI:SUN:LCEH.0.2003-01-007.
[18] 冯勇, 奚玲, 余晓旭, 等. 鼻、咽及喉部淀粉样变12例临床分析[J]. 临床耳鼻咽喉头颈外科杂志, 2011, 25(24): 1115-1117. doi:10.3969/j.issn.1001-1781.2011.24.004. FENG Yong, XI Ling, YU Xiaoxu, et al. Analysis of clinical manifestations of rhinal and pharyngeal and laryngeal amyloidosis by 12 cases[J]. Journal of Clinical Otorhinolaryngology, 2011, 25(24): 1115-1117. doi:10.3969/j.issn.1001-1781.2011.24.004.
[19] López Amado M, Lorenzo Pati(~overn)o MJ, López Blanco G, et al. Giant primary amyloidoma of the tonsil[J]. J Laryngol Otol, 1996, 110(6): 613-615. doi:10.1017/s0022215100134413.
[20] Eriksen HE. A case of primary localized amyloidosis in both tonsils[J]. J Laryngol Otol, 1970, 84(5): 525-531. doi:10.1017/s0022215100072182.
[21] Beiser M, Messer G, Samuel J, et al. Amyloidosis of Waldeyer's ring. A clinical and ultrastructural report[J]. Acta Otolaryngol, 1980, 89(5/6): 562-569. doi:10.3109/00016488009127175.
[22] Röcken C, Hegenbarth V, Schmitz M, et al. Plasmacytoma of the tonsil with AL amyloidosis: evidence of post-fibrillogenic proteolysis of the fibril protein[J]. Virchows Arch, 2000, 436(4): 336-344. doi:10.1007/s0042800-50456.
[23] Chiesa Estomba CM, Araujo Da Costa AS, Rivera Schmitz T. A rare cause of tonsillar asymmetry[J]. Eur Ann Otorhinolaryngol Head Neck Dis, 2015, 132(6): 361-362. doi:10.1016/j.anorl.2015.06.002.
[24] Takahashi M, Matsuda H, Ito K, et al. Pediatric localized amyloidosis in mesopharynx[J]. Int J Pediatr Otorhinolaryngol, 2002, 66(2): 181-184. doi:10.1016/s0165-5876(02)00215-x.
[25] Falk RH, Alexander K M, Liao R, et al. Al(light-chain)cardiac amyloidosis: a review of diagnosis and therapy[J]. J Am Coll Cardiol, 2016, 68(12): 1323-1341. doi:10.1016/j.jacc.2016.06.053.
[1] 张钰曲毅. 眼弓形体病的发病机制及防治研究进展[J]. 山东大学耳鼻喉眼学报, 2022, 36(5): 70-76.
[2] 张丰珍, 王桂香, 魏沄沄, 张亚梅, 赵靖, 王华, 李宏彬, 李晓丹, 张杰. 合并轻度出血性疾病的扁桃体和(或)腺样体切除术患儿围手术期管理[J]. 山东大学耳鼻喉眼学报, 2022, 36(4): 66-72.
[3] 金霄雪,韩莹莹,郭瑞祥,倪守洁,邹娟娟,王岩,李延忠. 替牙期扁桃体伴腺样体肥大患儿过敏因素与颌面畸形的相关性[J]. 山东大学耳鼻喉眼学报, 2022, 36(2): 45-50.
[4] 师晓丽, 牟鸿. 多学科联合诊治重度儿童阻塞性睡眠呼吸暂停综合征并发肺动脉高压1例[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 116-119.
[5] 赵兴贺,樊明月,窦训武,贾广彪. 儿童原发扁桃体弥漫大B细胞淋巴瘤1例并文献复习[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 120-124.
[6] 袁晨阳, 刘燕, 房振胜. 儿童阻塞性睡眠呼吸暂停低通气综合征对肺功能的影响[J]. 山东大学耳鼻喉眼学报, 2022, 36(1): 143-148.
[7] 沈倪美,钱茂华,金加欣,秦阳,王军,吴莺,高刚. 超声刀在扁桃体肿瘤切除术中的应用体会[J]. 山东大学耳鼻喉眼学报, 2021, 35(5): 62-66.
[8] 冯世强,姜宪. 可调式支撑喉镜辅助治疗难治性扁桃体术后出血[J]. 山东大学耳鼻喉眼学报, 2021, 35(5): 67-69.
[9] 王学昌, 王涛, 任欣, 赵明俊. 内镜下经口入路保留扁桃体茎突截短术疗效分析[J]. 山东大学耳鼻喉眼学报, 2021, 35(4): 17-21.
[10] 冯晨,郭瑞祥,王岩. 等离子射频消融术在儿童阻塞性睡眠呼吸暂停中的应用和进展[J]. 山东大学耳鼻喉眼学报, 2021, 35(2): 16-21.
[11] 沈瑶,周成勇. 低温等离子辅助下儿童扁桃体全切除与部分切除的比较[J]. 山东大学耳鼻喉眼学报, 2021, 35(2): 22-27.
[12] 刘少锋,黄桂亮,黄振云,孙昌志,罗仁忠. 扁桃体部分切除术治疗儿童阻梗性睡眠呼吸暂停综合征 86例[J]. 山东大学耳鼻喉眼学报, 2021, 35(2): 50-54.
[13] 田天捷,张自雄,杨飞,周意. 缝合腭弓对扁桃体术后出血影响的临床研究[J]. 山东大学耳鼻喉眼学报, 2021, 35(1): 82-85.
[14] Fahad Alkherayf, Hussein Kheshaifati, Abdulhadi Algahtani, Santanu Chakraborty, David Schramm. 上半规管裂综合征[J]. 山东大学耳鼻喉眼学报, 2020, 34(5): 89-96.
[15] 刘雅琴,张立庆,张佳程,董伟达,周涵. 头颈部淀粉样变性23例临床分析[J]. 山东大学耳鼻喉眼学报, 2020, 34(1): 72-77.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
[1] 林彬,王挥戈 . 功能性内镜鼻窦手术后鼻黏膜纤毛转归的研究[J]. 山东大学耳鼻喉眼学报, 2006, 20(6): 481 -487 .
[2] 公 蕾,孙 洁,薛子超,李敬华,薛卫国 . 鼻腔鼻窦恶性肿瘤细胞周期的DNA分析[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 193 -195 .
[3] 陈文文 . 1例T/NK淋巴瘤17年演进[J]. 山东大学耳鼻喉眼学报, 2006, 20(5): 472 -472 .
[4] 栾建刚,梁传余,文艳君,李炯 . 抑制表皮生长因子受体基因表达的pSIREN-ShuttleRNAi表达载体的构建[J]. 山东大学耳鼻喉眼学报, 2006, 20(1): 4 -8 .
[5] 马敬, 钟翠萍 . 手术治疗侵犯翼腭窝的鼻咽纤维血管瘤的方法(附5例报告)[J]. 山东大学耳鼻喉眼学报, 2006, 20(1): 30 -32 .
[6] 刘强和,罗香林,耿宛平,陈 晨,雷 迅,刘芳贤,邓 明 . 快速老化小鼠的听功能和耳蜗螺旋神经元的增龄性变化[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 215 -217 .
[7] 郑鹏凌,陈卫国,易笃友,黄清秀,卢 俊 . 耳内镜下吸引清除耳道耵聍55例并文献复习[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 223 -226 .
[8] 马 敬,钟翠萍,严 星,安 飞 . 耳屏软骨修补无残余软骨的鼻中隔穿孔15例[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 246 -247 .
[9] 崔哲洙,严永峰,崔春莲,金顺吉 . 嗜酸性粒细胞在变应性鼻炎合并慢性鼻窦炎的分布特点[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 250 -252 .
[10] 赵鲁新,翟 洪,潘 洁 . 超声乳化吸除联合晶状体植入治疗急性闭角型青光眼伴白内障23例[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 260 -262 .