1."Step-up"surgical treatment strategy for patulous Eustachian tube.
Huiwen YANG ; Le XIE ; Yu SUN
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2023;37(6):494-498
Patients with patulous Eustachian tubes(PET) usually suffer from annoying symptoms, such as tinnitus, autophony and aural fullness, due to the excessive opening of the Eustachian tube. There is no uniform standard of treatment, and conservative therapy combined with"Stepup"surgical intervention strategy is the main treatment. In this article, we reviewed various surgical treatments of patulous Eustachian tube in recent years, including key points of surgical operation, effectiveness, safety and complications. Full communication and evaluation are needed to establish appropriate patients' expectations preoperatively. A "Stepup" treatment strategy will be carried out, including conservative treatment, tympanic membrane surgery, Eustachian tube pharyngeal orifice constriction surgery, Eustachian tube tympanic orifice plug surgery and Eustachian tube muscle surgery, which aims to maintain normal Eustachian tube function and good middle ear ventilation.
Humans
;
Eustachian Tube/surgery*
;
Ear Diseases/diagnosis*
;
Ear, Middle
;
Tympanic Membrane/surgery*
;
Tinnitus
;
Otitis Media
2.A case report of middle ear cholesteatoma complicated with labyrinthine fistulaand delayed endolymphatic hydrops.
Feng LIN ; Qianru WU ; Yibo ZHANG ; Chunfu DAI
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2023;37(8):670-672
Delayed endolymphatic hydrops (DEH) is a rare disease that causes vertigo and is often misdiagnosed as other vertigo diseases. This article reports on a patient with vertigo who was easily misdiagnosed. The patient was a middle ear cholesteatoma complicated by labyrinthine fistula (LF); however, his vertigo was episodic vertigo, which could not be explained solely by LF causing labyrinthitis. The possibility of endolymphatic hydrops was suspected, which was confirmed by inner ear magnetic resonance gadolinium imaging. This is the first reported case of middle ear cholesteatoma complicated by LF and DEH. The patient underwent surgical resection of the cholesteatoma and three semicircular canal obstructions at the same time. During two years postoperative follow-up, the patient did not experience a recurrence of vertigo. When diagnosing vertigo diseases, a careful history of vertigo is of utmost importance.
Humans
;
Endolymphatic Hydrops/diagnosis*
;
Cholesteatoma, Middle Ear/complications*
;
Vertigo/complications*
;
Labyrinth Diseases/complications*
;
Magnetic Resonance Imaging/adverse effects*
;
Semicircular Canals
4.A Case of Middle Ear Neuroendocrine Adenoma in a Patient with Hearing Loss and Facial Palsy
Woojoo NAM ; Tae Hwan KIM ; Min Beom KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 2019;62(3):182-187
Middle ear adenoma is a very rare disease which is benign and originates from the middle ear mucosa. Patients of middle ear adenoma usually come to the clinic for unilateral hearing loss or tinnitus, but rarely for accompanied facial palsy. It is non-gender specific and occurs over a wide range of ages. The recurrence rate is known to be very low, but few authors argue that neuroendocrine adenoma should be considered as a low grade carcinoma due to some cases of recurrence. A 18 years-old male who had a left side facial palsy about 3 years ago but has currently improved as compared with the initial onset, visited our clinic for the left side hearing loss. Pure tone audiogram showed about 30 dB of conductive hearing loss and a pinkish polypoid mass involving the left tympanic membrane. We removed a tumor via transmastoid approach. The final diagnosis was middle ear adenoma with neuroendocrine differentiation. Neither signs of complication nor recurrence were observed after six months of the surgery.
Adenoma
;
Diagnosis
;
Ear, Middle
;
Facial Paralysis
;
Hearing Loss
;
Hearing Loss, Conductive
;
Hearing Loss, Unilateral
;
Hearing
;
Humans
;
Male
;
Mucous Membrane
;
Rare Diseases
;
Recurrence
;
Tinnitus
;
Tympanic Membrane
5.Submucosal injection of pharyngeal ostium of Eustachian tube for diagnosis of patulous Eustachian tube.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2018;32(2):106-108
To evaluate the clinical value of submucosal injection of pharyngeal ostium of Eustachian tube in diagnosing patulous Eustachian tube(PET).Twenty-six patients(32 sides),whose the symptoms were consistent with PET,were enrolled from March 2014 to May 2016.The symptoms and signs of all patients were evaluated after submucosal injection of saline into the Eustachian tube.Immediately after submucosal injection of saline into the Eustachian tube,the symptoms and signs disappeared in 24 cases(29 sides),and improved in 2 cases(3 sides).The resolution and/or improvement of symptoms and signs lasted for less than 24 hours in 12 patients,for more than 24 hours in 9 patients,and for more than 48 hours in 4 patients.No adverse reactions were observed.Submucosal injection may be a simple and practical method for auxiliary diagnosis of PET,and may be used in preoperative evaluation of Eustachian tuboplasty.
Ear Diseases
;
diagnosis
;
Eustachian Tube
;
physiopathology
;
surgery
;
Humans
;
Injections
;
Otitis Media
;
Pharynx
;
Preoperative Care
6.Autoimmune Inner Ear Disease Mimicking Bilateral Ménière's Disease: A Case Report
Hong Ju KIM ; Yoon Gi CHOI ; Hyun Ji KIM ; Kyu Sung KIM
Journal of the Korean Balance Society 2018;17(1):28-35
Autoimmune inner ear disease (AIED) is a rare disease, accounting for < 1% of all cases of hearing impairment or dizziness. It is characterized by sensorineural hearing loss (SNHL) or vestibular dysfunction that results from an immunemediated process. Clinical features of AIED is SNHL that progresses over weeks to month with fluctuating hearing symptoms. Because there are no diagnostic laboratory and clinical feature, response to immunosuppressive therapy were important for diagnosis of AIED. Many diseases such as sudden SNHL and Meniere disease may also mimic AIED, a broad differential must be maintained in patients suspected of having AIED. We report a case of a 46-year-old female who presented with sudden hearing loss and vertigo. We could diagnose her as AIED with systemic lupus erythematous. The symptoms were improved treated with steroids.
Diagnosis
;
Dizziness
;
Ear, Inner
;
Female
;
Hearing
;
Hearing Loss
;
Hearing Loss, Sensorineural
;
Hearing Loss, Sudden
;
Humans
;
Labyrinth Diseases
;
Meniere Disease
;
Middle Aged
;
Rare Diseases
;
Steroids
;
Vertigo
7.Dizziness and orthostatic intolerance in pediatric migraine.
Journal of the Korean Medical Association 2017;60(2):126-133
Pediatric migraine is followed by more frequent episodes of dizziness or vertigo than tension-type headaches. Just as children with migraine show a high sensitivity to light and noise, they are also susceptible to vestibular stimuli, resulting in vertigo or dizziness. Previous studies have found vertigo to be more common among patients with migraine. Vestibular migraine and benign paroxysmal vertigo of childhood have been identified as the most common causes of vertigo in children without ear disease. Benign paroxysmal vertigo of childhood is also thought to be a precursor of later episodes of migraine. The term vestibular migraine was included as a part of the appendix in the International Classification of Headache Disorders 3rd edition beta version, as an increasing number of studies have shown a positive relationship between migraine and vertigo. However, vertigo cannot be easily identified by parents or pediatricians, as young children are unable to explain their vertigo- or migraine-related symptoms. This is also applicable to specialists such as pediatric neurologists and otolaryngologists, as they often do not know the exact definition of vertigo in such patients and cannot make the correct differential diagnosis. Consequently, the inadequate evaluation and treatment of these patients can lead to a high socioeconomic cost. This review article discussing vertigo in pediatric migraine will help more medical doctors to effectively examine, accurately diagnose, and promptly treat young children suffering from migraine or vertigo.
Appendix
;
Child
;
Classification
;
Diagnosis, Differential
;
Dizziness*
;
Ear Diseases
;
Headache Disorders
;
Humans
;
Migraine Disorders*
;
Noise
;
Orthostatic Intolerance*
;
Parents
;
Specialization
;
Tension-Type Headache
;
Vertigo
8.Outcome of Localized Granulomatosis with Polyangiitis: A Case Study.
A Reum CHOE ; In Je KIM ; Jisoo LEE ; Sun Hee SUNG
Journal of Rheumatic Diseases 2016;23(3):174-178
OBJECTIVE: A substantial portion of granulomatosis with polyangiitis (GPA) patients present with localized disease limited to the upper respiratory tract, however; disease spectrum and prognosis of these patients are unclear. The aim of this study is to describe the clinical characteristics and outcome of patients with localized GPA. METHODS: This was a retrospective descriptive case series of patients with a biopsy proven localized GPA presenting to a single tertiary rheumatology service between January 1995 and September 2015. RESULTS: A total of 5 patients, median age 56 years (range 48 to 59 years) at diagnosis and 80% female, were identified. The median follow-up period was 42 months (range 15 to 62 months). Diagnosis was delayed with median time to diagnosis of 12 months (range 3 to 36 months), and patients underwent 1-3 ear, nose, and throat surgeries during the period of diagnostic delay. Sinusitis was the most frequent symptom in all patients, followed by otomastoiditis with cranial nerve palsies (n=2) and orbital mass (n=1). Antineutrophil cytoplasmic antibody (ANCA) was positive initially in 2/5 patients (40%). Two patients with otomastoiditis and cranial nerve palsies progressed to systemic disease with ANCA positive conversion. These two cases along with a case with orbital mass were refractory to standard treatment of cyclophosphamide with glucocorticoids requiring rituximab treatment. CONCLUSION: Patients with localized GPA may progress to systemic disease over the disease course, and may have aggressive disease refractory to standard treatment. Close monitoring for systemic symptoms and repeated ANCA testing is required in patients with localized GPA.
Antibodies, Antineutrophil Cytoplasmic
;
Biopsy
;
Cranial Nerve Diseases
;
Cyclophosphamide
;
Diagnosis
;
Ear
;
Female
;
Follow-Up Studies
;
Glucocorticoids
;
Granulomatosis with Polyangiitis*
;
Humans
;
Nose
;
Orbit
;
Pharynx
;
Prognosis
;
Respiratory System
;
Retrospective Studies
;
Rheumatology
;
Rituximab
;
Sinusitis
9.HRCT and MRI image of bilateral large vestibular aqueduct syndrome.
Youyou GUO ; Yongmei LI ; Chun ZENG ; Jingjie WANG ; Yi LIU ; Ping YIN ; Dan LIAO
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2016;30(5):361-365
OBJECTIVE:
To explore. HRCT and MRI three-dimensional fast imaging employing steady state ac-quisition(3D-FIESTA) imaging features and clinical characteristics of bilateral large vestibular aqueduct syndrome(LVAS).
METHOD:
The imaging and clinical features of 14 cases of bilateral LVAS identified over a 5-year periodwere retrospectively analyzed. All patients underwent HRCT and MRI 3D-FIESTA scanning of head and neck;MRI three dimensional reconstructions of internal acoustical meatus were also completed at the same time.
RESULT:
Audiogram showed mild to moderate hearing loss and was progressive. The cut-off values for the coronal midpointand operculum planes on the HRCT scan to diagnose an EVA were 1. 5 mm and 4. 3 mm respectively; the averagevalue was 2. 4 mm. VA expansion degree were not linked to the degree of hearing loss. MRI showed VA andlymph sac abnormalities. Concomitant image finding was cochlear hypoplasia.
CONCLUSION
HRCT and MRI 3D-FI-ESTA are important examinations for accurate diagnosis of LVAS. HRCT can acquire the specific size of reamedVA. MRI and 3D reconstructions of internal acoustical meatus can noninasive show more intuitive display ofLVAS and other inner ear malformations than HRCT.
Ear, Inner
;
Head
;
Hearing Loss
;
Hearing Tests
;
Humans
;
Imaging, Three-Dimensional
;
Magnetic Resonance Imaging
;
Retrospective Studies
;
Temporal Bone
;
Tomography, X-Ray Computed
;
Vestibular Aqueduct
;
pathology
;
Vestibular Diseases
;
diagnosis
10.A Case of Relapsing Polychondritis Presenting with Diffuse Tracheobronchial Involvement.
Kyung Mo YOO ; Jiwon HWANG ; Joong Kyong AHN
Journal of Rheumatic Diseases 2015;22(6):374-377
Relapsing polychondritis is a rare autoimmune disease involving the cartilaginous structures of the whole body. Its diagnosis can be difficult when the typical clinical features such as auricular chondritis are absent. Here, we report on a case of a 51-year-old female who presented with cough, dyspnea, and polyarthritis. Chest computed tomography showed the diffuse involvement of tracheobronchial cartilage. According to Damiani's criteria, she was diagnosed as relapsing polychondritis even though there was no unique involvement of auricular cartilage, and high dose steroid and immunosuppressive therapy were then started. This case indicated that patients who have tracheobronchial cartilage involvement without definite auricular chondritis should be considered for relapsing polychondritis as a differential diagnosis.
Arthritis
;
Autoimmune Diseases
;
Cartilage
;
Cough
;
Diagnosis
;
Diagnosis, Differential
;
Dyspnea
;
Ear Cartilage
;
Female
;
Humans
;
Middle Aged
;
Polychondritis, Relapsing*
;
Thorax

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