Laryngeal stenosis in a patient with severe congenital neutropenia

BandoH.; NagaoH.; NishioT.; HirotaR.; SakaguchiH.; ImamuraT.; HisaY.

首页> 外文期刊>The Laryngoscope: A Medical Journal for Clinical and Research Contributions in Otolaryngology, Head and Neck Medicine and Surgery, Facial Plastic and Reconstructive Surgery .. >Laryngeal stenosis in a patient with severe congenital neutropenia

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Laryngeal stenosis in a patient with severe congenital neutropenia

机译：严重先天性中性粒细胞减少症患者的喉管狭窄

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Objectives/Hypothesis: We report the first case of laryngeal stenosis with granuloma in a patient with severe congenital neutropenia (SCN). Study Design: Case report and retrospective review. Methods: Review of medical records. Results: A 6-year-old female who was diagnosed with SCN presented with a cough and wheezing. An endoscopic study revealed laryngeal stenosis with granuloma. Tracheotomy and direct laryngoscopy were performed under general anesthesia, and administration of granulocyte colony-stimulating factor was started. The laryngeal granuloma disappeared 3 weeks later, and the tracheal stoma was closed. Conclusions: Presence of a laryngeal lesion should be considered in SCN patients with persistent airway symptoms.

机译：目的/假设：我们报告了重度先天性中性粒细胞减少症（SCN）患者的首例喉狭窄合并肉芽肿。研究设计：病例报告和回顾性审查。方法：检查病历。结果：一名诊断为SCN的6岁女性出现咳嗽和喘息。内窥镜检查显示喉部狭窄伴肉芽肿。在全身麻醉下进行气管切开和直接喉镜检查，并开始给予粒细胞集落刺激因子。 3周后，喉肉芽肿消失，气管造口关闭。结论：伴有持续气道症状的SCN患者应考虑存在喉部病变。

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《The Laryngoscope: A Medical Journal for Clinical and Research Contributions in Otolaryngology, Head and Neck Medicine and Surgery, Facial Plastic and Reconstructive Surgery ..》 |2013年第2期|共3页
作者
BandoH.; NagaoH.; NishioT.; HirotaR.; SakaguchiH.; ImamuraT.; HisaY.;
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正文语种 eng
中图分类耳鼻咽喉科学;
关键词
Kostmann; Larynx; severe congenital neutropenia; stenosis;

机译：Kostmann;Larynx;重度先天性中性粒细胞减少症;狭窄;

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1. Laryngeal stenosis in a patient with severe congenital neutropenia [J] . BandoH., NagaoH., NishioT., The Laryngoscope: A Medical Journal for Clinical and Research Contributions in Otolaryngology, Head and Neck Medicine and Surgery, Facial Plastic and Reconstructive Surgery .. . 2013,第2期

机译：严重先天性中性粒细胞减少症患者的喉管狭窄
2. Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes. [J] . Newburger PE, Pindyck TN, Zhu Z, Pediatric blood & cancer . 2010,第2期

机译：共有ELANE突变和父亲单倍型的患者出现周期性中性粒细胞减少和严重的先天性中性粒细胞减少：通过修饰基因确定表型的证据。
3. Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group | Haematologica [J] . J Donadieu, T Leblanc, B Bader Meunier, Haematologica . 2005,第1期

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4. PATIENT-SPECIFIC THREE-DIMENSIONAL COMPUTATIONAL HEART MODELING AND PRINTING TO ENHANCE CLINICAL UNDERSTANDINGS AND TREATMENT PLANNING: CONGENITAL RECURRENT PULMONARY ARTERY STENOSIS AND TRANSCATHETER PULMONARY VALVE REPLACEMENT [C] . Amanda C. Tenhoff, Varun Aggarwal, Rebecca Ameduri, Design of Medical Devices Conference . 2021

机译：患者特异性三维计算心脏建模和印刷，增强临床谅解和治疗计划：先天性复发性肺动脉狭窄和经导管肺瓣膜置换
5. Aberrant subcellular targeting of the G185R neutrophil elastase mutant associated with severe congenital neutropenia induces premature apoptosis of differentiating promyelocytes, and, Expression and function of the transient receptor potential 2 (TRPM2) ion channel in dendritic cells. [D] . Massullo, Pam. 2007

机译：与严重的先天性中性粒细胞减少症相关的G185R中性粒细胞弹性蛋白酶突变体的异常亚细胞靶向诱导分化的早幼粒细胞的过早凋亡，以及树突状细胞中瞬时受体电位2（TRPM2）离子通道的表达和功能。
6. Cyclic Neutropenia and Severe Congenital Neutropenia in Patients with a Shared ELANE Mutation and Paternal Haplotype: Evidence for Phenotype Determination by Modifying Genes [O] . Peter E. Newburger, Talia N. Pindyck, Zhiqing Zhu, -1

机译：循环中性蛋白和严重先天性缺口患者共用Elane突变和Paternal单倍型：通过修饰基因的表型测定的证据
7. Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: Evidence for phenotype determination by modifying genes Conflict of interest: Nothing to declare. [O] . Newburger, Peter E., Pindyck, Talia N., Zhu, Zhiqing, 2010

机译：共有ELaNE突变和父本单倍型患者的循环中性粒细胞减少症和严重的先天性中性粒细胞减少症：通过修饰基因确定表型的证据感兴趣的冲突：无需申报。

Laryngeal stenosis in a patient with severe congenital neutropenia

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