otitis externa

外耳炎
  • 文章类型: Case Reports
    背景:外耳炎(EEO)是最难以治疗的外耳炎,并以外耳道皮肤过敏的炎症症状为特征。它被认为是主要由皮肤病和过敏反应引起的慢性皮肤炎症。食物过敏原也被认为是诱发炎症的原因。然而,食物特异性IgG4在该疾病中的作用尚不清楚.
    方法:一名54岁女性主诉外耳道反复瘙痒3年,手指甲龟裂2年。
    方法:她被诊断为EEO,并接受了消除鸡蛋食物的治疗策略,牛奶和小麦,在先前症状控制治疗的基础上,以食物特异性IgG4和益生菌的结果为指导。
    结果:治疗17个月后,她最终没有所有症状,所有食物的血清IgG4特异性均在正常范围内。
    结论:据我们所知,这是第一份揭示食物特异性IgG4在EEO中的临床意义的报告,以食物特异性IgG4为指导的饮食消除的成功治疗为难治性EEO的临床管理提供了新的思路。
    BACKGROUND: Eczematous external otitis (EEO) is the most difficult-to-treat otitis externa, and characterized by the symptoms of inflammation with hypersensitivity of the external ear canal skin. It is acknowledged as a chronic skin inflammation primarily caused by dermatological and allergic reactions. Food allergens are also considered a cause to induce the inflammation. However, the role of food specific IgG4 in this disease is unclear yet.
    METHODS: A 54-year-old woman complained of recurrent itching of the external auditory meatus for 3 years and nails chapping of hands for 2 years.
    METHODS: She was diagnosed with EEO and underwent the therapeutic strategy as food elimination of egg, milk and wheat, guided by the result of food specific IgG4 together with probiotics on the basis of previous symptom controlling therapy.
    RESULTS: After 17 months\' treatment, she was finally free of all the symptoms and the serum IgG4 specific to all foods are under normal limit.
    CONCLUSIONS: To the best of our knowledge, it is the first report revealing the clinical significance of food specific IgG4 in EEO, and the successful treatment with diet elimination guided by food specific IgG4 threw a new light on the clinical management of refractory EEO.
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  • 文章类型: Case Reports
    坏死性外耳炎(NOE)是一种严重的感染,主要影响外耳道,主要见于糖尿病(DM)患者等免疫功能低下的个体。此病例报告重点介绍了NOE的异常并发症:颞骨和鼻咽脓肿。这些并发症强调了NOE的严重程度,特别是由稀有病原体如克雷伯菌引起的。我们详细介绍了一名70岁男性,患有不受控制的DM,他表现出严重的右耳疼痛,脓性分泌物,和显著的耳后肿胀。实验室调查显示炎症标志物升高和糖尿病控制不佳。培养证实肺炎克雷伯菌,影像学显示颞骨和鼻咽部弥漫性水肿和脓肿形成。患者静脉注射头孢他啶和环丙沙星治疗6周,其次是口服环丙沙星。有效管理NOE需要全面、多学科方法。早期干预,定期监测,和影像学检查对于及时发现和管理并发症至关重要.
    Necrotizing otitis externa (NOE) is a severe infection primarily affecting the external auditory canal, seen mainly in immunocompromised individuals as patients with diabetes mellitus (DM). This case report highlights unusual complications of NOE: temporal bone and nasopharyngeal abscesses. These complications underscore the severity of NOE, particularly when caused by rare pathogens such as Klebsiella species. We detail the case of a 70-year-old male with uncontrolled DM who presented with severe right ear pain, purulent discharge, and significant postauricular swelling. Laboratory investigations revealed elevated inflammatory markers and poorly controlled diabetes. Cultures confirmed Klebsiella pneumoniae, and imaging showed diffuse edema and abscess formation in the temporal bone and nasopharynx. The patient was treated with intravenous Ceftazidime and ciprofloxacin for 6 weeks, followed by oral ciprofloxacin. Effective management of NOE necessitates a comprehensive, multidisciplinary approach. Early intervention, regular monitoring, and imaging are critical for promptly detecting and managing complications.
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  • 文章类型: Case Reports
    复发性多软骨炎(RPC)是一种罕见的自身免疫性疾病,通常模仿复发性外耳炎。这种多系统疾病主要影响体内的软骨结构,耳廓是最常见的影响。RPC与炎症标志物和抗核抗体(ANA)升高有关,会导致软骨破坏.我们的病例是一名74岁的白人男性,有外周血管疾病(PVD)的病史,他在临床上反复发作,尽管使用了多种抗生素和非甾体抗炎药(NSAIDs),但右上耳疼痛肿胀14天。他在同一只耳朵患有慢性感觉神经性听力损失。在过去的七个月中,他多次出现相同的症状,并被诊断出患有外耳炎。他否认关节炎,疲劳,皮疹,磨损,过敏,创伤,或发烧。他开了抗菌药物,交替NSAIDs,和甲基强的松龙暂时缓解。他只服用他汀类药物,家族史平淡无奇。他发热,生命体征正常。在体检时,他没有急性痛苦,声音正常,但有弥漫性红斑,tender,肿胀的右耳耳廓和外管保留肺叶。其余的体检并不显著。实验室结果显示,C反应蛋白(CRP)升高100mg/L(正常范围:<3mg/L),红细胞沉降率(ESR)200mm/小时(正常范围:<20mm/小时)。ANA滴度为1:160,具有均匀的模式,但其他自身抗体呈阴性。在全血细胞计数(CBC)或综合代谢面板(CMP)上没有注意到危险信号,他的快速血浆反应素(RPR)试验为阴性。在这个病人身上,泼尼松每天60毫克开始作为单一疗法,和风湿病也被咨询。尽管进行了抗生素治疗,但由于反复和持续的上耳感染,患者仍寻求咨询,最终被诊断出患有罕见的疾病,称为复发性多软骨炎。经过这种治疗,耳廓软骨炎迅速好转。然后将类固醇剂量缓慢减少并维持在每天10mg以防止突然发作。随后,开始使用皮质类固醇后,炎症标志物下降到正常水平。
    Relapsing polychondritis (RPC) is a rare autoimmune condition that often mimics recurrent external otitis. This multisystemic disease primarily affects cartilaginous structures in the body, with the ear pinna being the most commonly impacted. RPC is associated with elevated inflammatory markers and antinuclear antibodies (ANA), and it can lead to chondral destruction. Our case is a 74-year-old Caucasian male with a history of peripheral vascular disease (PVD) who presented to the clinic with recurrent, painful swelling of the right upper ear for 14 days despite multiple antibiotics and nonsteroidal anti-inflammatory drugs (NSAIDs). He had chronic sensorineural hearing loss in the same ear. He was seen multiple times with identical symptoms in the last seven months and was diagnosed with otitis externa. He denied arthritis, fatigue, rash, abrasion, allergies, trauma, or fever. He was prescribed antimicrobials, alternating NSAIDs, and methylprednisolone with temporary relief. He is only on statins and has an unremarkable family history. He was afebrile with normal vital signs. On physical examination, he was not in acute distress and had a normal voice but had a diffusely erythematous, tender, swollen right ear pinna and external canal sparing the lobe. The rest of the physical examination was unremarkable. Laboratory results showed elevated C-reactive protein (CRP) of 100 mg/L (normal range: <3 mg/L) and erythrocyte sedimentation rate (ESR) of 200 mm/hour (normal range: <20 mm/hour). ANA titer is 1:160 with a homogenous pattern, but other autoantibodies were negative. No red flags were noted on the complete blood count (CBC) or comprehensive metabolic panel (CMP), and his rapid plasma reagin (RPR) test was negative. In this patient, prednisone 60 mg daily was initiated as monotherapy, and rheumatology was also consulted. The patient sought consultation due to recurrent and persistent upper ear infections despite antibiotic treatment and was ultimately diagnosed with a rare medical condition called relapsing polychondritis. Following this treatment, the auricular chondritis improved promptly. The steroid dosage was then slowly tapered and maintained at 10 mg daily to prevent flare-ups. Subsequently, after the initiation of corticosteroids, inflammatory markers trended down to normal levels.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    在10岁的雄性博洛尼亚犬中,怀疑原因不明的耳廓软骨炎,有五个月的双侧结节性疼痛性和溃疡性脓性肉芽肿性皮炎的病史,并有推定的耳廓软骨破坏。用免疫抑制剂量的泼尼松龙解决疼痛和病变,然而,这种情况导致耳廓和外部运河畸形。
    Auricular chondritis of unknown cause was suspected in a 10-year-old male Bolognese dog with a five-month history of painful bilateral nodular and ulcerative pyogranulomatous dermatitis of the pinnae with putative auricular cartilage destruction. Pain and lesions resolved with immunosuppressive doses of prednisolone, yet the condition resulted in deformity of both pinnae and external canals.
    怀疑一只10岁的雄性波伦亚犬患有不明原因的耳廓软骨炎,该犬有5个月的双侧耳廓结节性和溃疡性脓性肉芽肿性皮炎病史,并假定耳廓软骨破坏。使用免疫抑制剂量的泼尼松缓解疼痛和病变,但病因导致耳廓和外耳道畸形。.
    Une chondrite auriculaire d’étiologie inconnue est suspectée chez un bichon bolonais mâle de 10 ans qui présente depuis 5 mois une dermatite pyogranulomateuse nodulaire et ulcéreuse bilatérale douloureuse du pavillon de l\'oreille avec une destruction présumée du cartilage auriculaire. La douleur et les lésions disparaissent avec des doses immunosuppressives de prednisolone, mais l\'affection entraîne une déformation des deux pavillons et des conduits auriculaires externes.
    Bei einem 10 Jahre alten männlichen Bologneser mit einer 5 Monate lang andauernden Anamnese einer schmerzhaften bilateralen nodulären und ulzerativen pyogranulomatösen Dermatitis der Pinnae mit vermeintlicher aurikulärer Knorpeldestruktion unbekannter Ursache wurde eine aurikuläre Chondritis vermutet. Die Schmerzen und die Veränderungen verschwanden mit immunsuppressiven Dosen von Prednisolon, aber die Ätiologie verursachte dennoch eine Deformierung beider Pinnae und der äußeren Gehörkanäle.
    耳介軟骨の破壊を伴う有痛性の両側結節性および潰瘍性肉芽腫性皮膚炎を5ヵ月間認めた10歳の雄のボロニーズ犬において、原因不明の耳介軟骨炎が疑われた。痛みや病変は免疫抑制量のプレドニゾロン投与で消失したが、病因は両側耳介および外耳道の変形であった。.
    Suspeitou‐se de condrite auricular de causa desconhecida em um cão macho Bolonhês de 10 anos de idade com um histórico de cinco meses de dermatite piogranulomatosa ulcerativa e nodular bilateral no pavilhão auricular com suposta destruição de cartilagem auricular. A dor e as lesões resolveram com doses imunossupressoras de prednisolona apesar de a etiologia ter resultado na deformidade de ambas as orelhas e condutos auditivos.
    Se sospechó la existencia de una condritis auricular de causa desconocida en un perro boloñés de 10 años con historia de 5 meses de duración de una dermatitis nodular ulcerativa piogramulomatosa y bilateral en las orejas con posible destrucción del cartílago auricular. El dolor y las lesiones se resolvieron con dosis inmunosupresoras de prednisolona pero la enfermedad produjo deformación de ambas orejas y de los canales auriculares externos.
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  • 文章类型: Case Reports
    外耳炎是一种影响外耳道的炎症性和感染性疾病。术语耳漏是指排出物从耳朵流出,这是外耳炎连同炎症的主要症状之一。外耳道病变或中耳疾病伴鼓膜穿孔是耳漏的病因。耳漏是感染的指征。抗菌药物是各种细菌和真菌感染的常规治疗,但是他们有阻力发展等障碍,副作用,患者负担能力,等。阿育吠陀文本中提到的GandhakRasayana制剂可以是治疗各种传染病的良好选择。Karnasrava是一种耳部疾病,称为Vata主导的Tridoshaja病,是可以治愈的。Karnasrava一词表示从耳朵排出,是不言而喻的。Karnasrava由广泛的疾病组成,根据体征和症状,可以与外耳炎密切相关。GandhakRasayana表现出显著的抗菌作用,外耳炎的抗真菌和抗炎活性。通过本病例报告评价其抗菌和抗真菌活性可为研究提供科学依据。一名31岁的男性患者在SaneGuruji医院的OPD注册,Hadapsar,浦那在临床上被诊断为Karnasrava(外耳炎),脓液培养对克雷伯菌属呈阳性。我们开始使用GandhakRasayana-一种阿育吠陀配方,在早晨和晚上用温水治疗两片,持续21天。观察到治疗结果为Karnashula(耳痛)减少,Karnasrava(耳朵放电),Karnakandu(瘙痒),耳塞和炎症变化。处理后培养物对于生物体是阴性的。在从III级到I级的Brighton分级量表中注意到了改善。GandhakRasayana在当前情况下显示出明显的抗菌活性。评估它的抗菌作用,抗真菌和抗炎活性可为研究提供科学依据。
    Otitis externa is an inflammatory and infectious disease that affects the external auditory canal. The term otorrhea refers to the outflow of discharge from the ear which is one of the main symptoms of otitis externa along with inflammation. External ear canal pathology or middle ear illness with tympanic membrane perforation is the etiological factor of otorrhea. Otorrhea is an indication of infection. Antimicrobial agents are the conventional treatment of various bacterial and fungal infections, but they have impediments such as resistance development, side effects, patient affordability, etc. The Gandhak Rasayana formulation mentioned in the Ayurvedic text can be a good option for the treatment of various infectious diseases. Karnasrava is a type of ear disease referred to as Vata predominant Tridoshaja disease and it is curable. The term Karnasrava signifies discharge from ear and is self-explanatory. Karnasrava consists of a wide spectrum of diseases and can have a near correlation with otitis externa as per signs and symptoms. Gandhak Rasayana exhibited significant antibacterial, antifungal and anti-inflammatory activity in otitis externa. Evaluating its antibacterial and antifungal activity can provide scientific evidence for the study through the present case report. A 31-year-old male patient registered in OPD at Sane Guruji Hospital, Hadapsar, Pune was clinically diagnosed as Karnasrava (Otitis externa) and pus culture positive for Klebsiella species. We started the treatment with Gandhak Rasayana-an Ayurvedic formulation of 250mg two tablets in the morning and evening with lukewarm water for 21 days. The outcome of the treatment was observed as a reduction in Karnashula (otalgia), Karnasrava (ear discharge), Karnakandu (itching), ear blockage and inflammatory changes. Post-treatment culture was negative for the organism. The improvement was noted in Brighton grading scale from grade III to grade I. Gandhak Rasayana showed significant antibacterial activity in the present case. Evaluating its antibacterial, antifungal and anti-inflammatory activity can provide scientific evidence for the study.
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  • 文章类型: Case Reports
    一名48岁的男子主诉为间歇性右耳耳漏,持续数月,偶发性耳痛和进行性单侧听力障碍。他还报告了鼻窦和上颌骨的头痛和压力频繁发作。先前使用抗生素的全身治疗未能缓解症状。头颈部CT显示乳突完全正常,中耳和外耳道区域没有任何浑浊或骨侵蚀的证据。右耳耳镜检查发现干燥的聚集体,棕色,纤维状物质和碎片阻塞外耳道并阻塞原本完整的鼓膜。外耳道扩张或鼓膜增厚不受重视。将管道清创并将纤维状材料置于福尔马林中。组织病理学检查显示许多分支,分裂的真菌菌丝在密集堆积的簇中组织。在其他领域,真菌菌丝邻接或附着在层状的酮肽上。正如GMS染色所强调的那样,真菌在形态上与曲霉属相容。临床病理结果支持真菌性外耳道炎的诊断,虽然众多无核鳞状细胞与底层细胞的定植相容,可能正在发展,胆脂瘤.从外耳道分离的材料的培养证实了黄曲霉的存在。在这种说明性的情况下,我们介绍了在同步胆脂瘤背景下发展的曲霉相关性耳真菌病的主要临床和微观特征。
    A 48-year-old man presented with a chief complaint of intermittent right ear otorrhea of several-month duration, occasional otalgia and progressive unilateral hearing impairment. He also reported frequent episodes of headache and pressure in the sinuses and maxilla. Previous systemic treatment with antibiotics failed to alleviate the symptoms. A head/neck CT showed completely normal mastoid, middle ear and external auditory canal regions without any evidence of opacification or bone erosion. Otoscopic examination of the right ear disclosed aggregates of dried, brown, fibrillar material and debris occluding the external auditory canal and obstructing the otherwise intact tympanic membrane. Dilation of the external auditory canal or thickening of the tympanic membrane were not appreciated. The canal was debrided and the fibrillar material was placed in formalin. Histopathologic examination revealed numerous branching, septated fungal hyphae organized in densely-packed clusters. In other areas, the fungal hyphae abutted or were attached to lamellated collections of orthokeratin. As highlighted by GMS staining, the fungi were morphologically compatible with Aspergillus species. The clinicopathologic findings supported a diagnosis of fungal otitis externa, while the numerous anucleate squamous cells were compatible with colonization of an underlying, probably developing, cholesteatoma. Culture of material isolated from the external auditory canal confirmed the presence of Aspergillus flavus. In this illustrative case, we present the main clinical and microscopic characteristics of Aspergillus-related otomycosis developing in the setting of a tautochronous cholesteatoma.
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  • 文章类型: Case Reports
    颅底骨髓炎是未经治疗的坏死性外耳炎的不常见但潜在致命的后果。早期识别和适当的治疗对于防止严重的并发症如颅神经麻痹至关重要,脑膜炎,颅内脓肿的形成.本研究中提供的病例报告提供了丰富的临床表现描述,诊断挑战,和采用的干预措施。颅底骨髓炎的早期识别和适当处理对于预防并发症和改善患者预后至关重要。
    Skull base osteomyelitis is a not commonly encountered but potentially fatal consequence of untreated necrotizing otitis externa. Early recognition and appropriate treatment are crucial to prevent serious complications such as cranial nerve palsies, meningitis, and intracranial abscess formation. The case reports presented in this study provide a rich depiction of the clinical presentation, diagnostic challenges, and interventions employed. Early recognition and appropriate management of skull base osteomyelitis are crucial to prevent complications and improve patient outcomes.
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  • 文章类型: Case Reports
    文献报道的大多数恶性外耳炎(MEO)病例归因于铜绿假单胞菌。MEO中的真菌感染也很可能,但极为罕见。而传统的微生物学测试难以诊断。
    两名患者通过宏基因组下一代测序(mNGS)诊断为曲霉菌引起的真菌性恶性外耳炎(FMEO),并在包括手术和伏立康唑在内的综合治疗后康复。由于分泌物反复培养为阴性,病理检查显示肉芽组织增生,中性粒细胞浸润广泛,因此抗真菌治疗被推迟。
    mNGS可能对疑似FMEO患者有帮助,特别是当常规微生物学测试呈阴性时。
    Most of malignant external otitis (MEO) cases reported in the literature are attributed to Pseudomonas aeruginosa. Fungal infections in MEO are also likely but extremely rare. And conventional microbiology tests is difficult to diagnose.
    Two patients were diagnosed with Fungal malignant external otitis (FMEO) due to Aspergillus by metagenomic Next-Generation Sequencing (mNGS) and recovered after comprehensive treatment including operation and voriconazole. The antifungal treatment was delayed due to repeated cultures of secretions being negative and pathological examination showed granulation tissue proliferation with extensive neutrophil infiltration.
    mNGS might be helpful for patients suspected with FMEO, especially when conventional microbiology tests were negative.
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