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1.
Vestn Otorinolaringol ; 88(3): 73-77, 2023.
Article in Russian | MEDLINE | ID: mdl-37450395

ABSTRACT

Choristoma is one of the varieties of congenital developmental anomalies, where one or another normal tissue of the body is located in an atypical place for itself. The short literary review of choristoma of middle ear is presented in article. A rare clinical cases of salivary gland choristoma of the middle ear (5-year-old girl with left-sided conductive hearing loss of III degree) and glial choristoma of the mastoid (19-year-old man with signs of chronic suppurative otitis media of the right ear) are described.


Subject(s)
Choristoma , Otitis Media, Suppurative , Male , Female , Humans , Child, Preschool , Young Adult , Adult , Choristoma/diagnosis , Ear, Middle , Hearing Loss, Conductive/diagnosis , Hearing Loss, Conductive/etiology , Salivary Glands , Otitis Media, Suppurative/complications , Otitis Media, Suppurative/diagnosis
2.
Vestn Otorinolaringol ; 87(4): 84-88, 2022.
Article in Russian | MEDLINE | ID: mdl-36107186

ABSTRACT

The describes a clinical observation of a combination of jugulotympanic paraganglioma of the left temporal bone with multifocal congenital hemangioma. The interest of the case is that such a combination of pathologies is extremely rare. A comprehensive study and surgical treatment of a patient with this clinical diagnosis was carried out. In the diagnosis, objective otorhinolaryngological studies, otomicroscopy and MSCT of the temporal bones and MRI of the middle ear with contrast were used. Surgical intervention was performed under multicomponent anesthesia with tracheal intubation, transmastoid access. The postoperative management of the patient after surgical treatment is described.


Subject(s)
Glomus Jugulare Tumor , Hemangioma , Paraganglioma , Ear, Middle , Hemangioma/complications , Hemangioma/diagnosis , Hemangioma/surgery , Humans , Paraganglioma/diagnosis , Paraganglioma/diagnostic imaging , Temporal Bone/pathology
3.
Vestn Otorinolaringol ; 86(1): 11-14, 2021.
Article in Russian | MEDLINE | ID: mdl-33720644

ABSTRACT

The lesion of middle ear as a variant of clinical manifestation of secondary tuberculosis, according to international scientific literature, is a rare condition. However, in terms of real clinical practice, the proportion of this pathology should not be underestimated due to the wide spread of tuberculosis infection among the population of developing countries, including the Russian Federation. One of the risk factors for the systemic spread of mycobacterial flora is a concomitant HIV infection, which often acts as an opportunistic pathological agent for tuberculosis. The treatment of such a state is always challenging because of the high aggressiveness of bacteria and the low immunological resistance of the patient. This article presents a clinical case of bilateral tuberculosis otitis media, which was a manifestation of tuberculosis infection that developed on the background of HIV infection.


Subject(s)
HIV Infections , Otitis Media , Tuberculosis , Ear, Middle , HIV Infections/complications , HIV Infections/diagnosis , Humans , Otitis Media/complications , Otitis Media/diagnosis , Russia , Tuberculosis/complications , Tuberculosis/diagnosis
4.
Vestn Otorinolaringol ; 85(4): 6-10, 2020.
Article in Russian | MEDLINE | ID: mdl-32885629

ABSTRACT

A retrospective analysis of the results of surgical treatment of 436 patients (332 adults and 104 children under the age of 15 years) with acquired middle ear cholesteatoma was performed to identify possible predictors of relapse of the process and a prospective assessment of the results of surgical treatment. It was revealed that the leading factors in the development of residual pathology were: the presence of cholesteatoma in the area of destruction of the bone wall of the canal of the facial nerve, cholesteatoma of the hypothympanum, cholesteatoma in the place of destruction of the bone wall of the posterior cranial fossa. The key reasons for the formation of recurrent pathology were: children under 15 years of age, closed surgery, pathological changes in the tympanic orifice of the auditory tube and the presence of cholesteatoma in its lumen. Performing a closed operation in adults with pathology of the tympanic orifice of the auditory tube increases the risk of recurrent cholesteatoma by 18.6%, and in children by 20%. The choice of a closed method of surgical intervention for the epitympanic type of the disease can increase the risk of residual pathology by 17.2% in adults and 27.8% in children.


Subject(s)
Cholesteatoma, Middle Ear , Adult , Child , Ear, Middle , Humans , Prognosis , Prospective Studies , Retrospective Studies
5.
Vestn Otorinolaringol ; 85(3): 23-27, 2020.
Article in Russian | MEDLINE | ID: mdl-32628378

ABSTRACT

OBJECTIVE: To conduct a retro- and prospective analysis of the clinical characteristics and results of surgical treatment of patients with congenital temporal bone cholesteatoma. PATIENTS AND METHODS: On the basis of the SPb Scientific Research Institute of ENT of the Ministry of Health of Russia 23 patients were diagnosed with congenital temporal bone cholesteatoma for the period from 2011 to 2018. There were 11 men (47.8%), 12 women (52.2%), the age of patients - from 2 to 44 years. The M.J. Levenson criteria were used to verify congenital middle ear cholesteatoma. (1986). According to intrasurgery findings, we identified congenital cholesteatoma of the middle ear stages according to the ChOLE classification. Other types of congenital temporal bone cholesteatoma included the patients with congenital atresia of the external auditory opening, combined with congenital temporal bone cholesteatoma; we found a patient with exostoses obstructing the external auditory canal combined with congenital cholesteatoma of the middle ear; and a patient with congenital cholesteatoma of the temporal bone pyramid. RESULTS: An increase in the incidence of congenital temporal bone cholesteatoma was noted, which is probably due to increased awareness of specialists and the wider use of imaging research methods. A relationship was revealed between the stage of congenital cholesteatoma according to the ChOLE classification and the necessary volume of surgical intervention. Of the total number of cases of congenital temporal bone cholesteatoma, 26.1% were the patients with anomalies in the development of the outer and middle ear. CONCLUSIONS: All patients with suspected congenital temporal bone cholesteatoma require a temporal bone MSCT and middle ear MRI in DWI mode.


Subject(s)
Cholesteatoma, Middle Ear , Cholesteatoma , Ear Canal , Female , Humans , Male , Prospective Studies , Russia , Temporal Bone
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