Количество страниц: 3 с.
The article describes a case of effective application of the valvular bronchoblocation method in an acute progressive form of tuberculosis - caseous pneumonia, in a patient with multidrug-resistant tuberculosis pathogen (MDR MBT).
Клинический случай эффективного применения клапанной бронхоблокации в комплексном лечении больного с казеозной пневмонией с множественной лекарственной устойчивостью возбудителя туберкулеза / Н. А. Гуляева, В. Д. Адамова, А. С. Делахов, А. Е. Варламов ; Медицинский институт Северо-Восточного федерального университета им. М. К. Аммосова, ГБУ РС(Я) Научно-практический центр "Фтизиатрия" им. Е. Н. Андреева // Якутский медицинский журнал. - 2024. - N 2 (86). - С. 105-107. - DOI: 10.25789/YMJ.2024.86.25
DOI: 10.25789/YMJ.2024.86.25
Количество страниц: 5 с.
The purpose of the report was to present our own observation of clinical cases with Ullrich congenital muscular dystrophy in two unrelated Yakut families. The cause of the disease in the first family was two mutations in a compound heterozygous state: c.1561C>T and c.2329T>C in the COL6A2 gene; in the second family, the c.2329T>C mutation in the COL6A2 gene in a homozygous state. Despite the rarity of the disease, neurologists and geneticists, when identifying symptoms of myopathy, delayed motor development, and the presence of hypermobility in the distal joints, contrasting with retractions of the proximal and axial joints, must be alert to Ullrich CMD. Next-generation sequencing techniques make it easier to diagnose the disease.
Врожденная миодистрофия Ульриха: описание клинических случаев / П. И. Голикова, Г. Д. Москвитин, А. Л. Сухомясова [и др.] ; Медицинский институт Северо-Восточного федерального университета им. М. К. Аммосова, Медико-генетический центр Республиканской больницы 1-Национального центра медицины // Якутский медицинский журнал. - 2024. - N 2 (86).- С. 98-102. - DOI: 10.25789/YMJ.2024.86.23
DOI: 10.25789/YMJ.2024.86.23
Количество страниц: 4 с.
The article demonstrates a clinical case of Sweet's syndrome associated with hypomethylating agents in patient with myelodysplastic syndrome. The recurrent course of Sweet's syndrome and the ineffectiveness of maintenance doses of prednisolone required a revision of the treatment tactics for myelodysplastic syndrome with the abolition of hypomethylating agents. Therapeutic tactics for patients with a rare disease, Sweet's syndrome, should be selected individually, taking into account the form of the disease and concomitant pathology.
Клинический случай развития синдрома свита у пациентки с миелодиспластическим синдромом / У. В. Семенова, А. И. Борисов, Т. Н. Александрова [и др.] ; Медицинский институт Северо-Восточного федерального университета им. М. К. Аммосова, Республиканская больница 1-Национальный центр медицины // Якутский медицинский журнал. - 2024.- N 2 (86). - С. 94-97. - DOI: 10.25789/YMJ.2024.86.22
DOI: 10.25789/YMJ.2024.86.22
Количество страниц: 4 с.
The additional retention elements were determined taking into account the individual anatomical-topographical variability of the pliability zones location, exit places of neurovascular bundles and places with dense mucous membrane on the upper jaw, which create negative pressure zones medial to the borders of the prosthetic bed to improve the retention of complete removable laminar dentures on the upper jaw. The developed method considerably reduces the probability of vascular compression with microcirculation disturbance and traumatization of soft tissues to which the prosthetic construction adjoins and excludes fracture of the base of the complete removable laminar dentures. In case of depressurization of external valve zones, this method at the expense of additional internal valve zones located in places where there is sufficient pliability and there are no neurovascular bundles and exostoses provides an increase in the degree of retention and stabilization of complete removable prosthetic constructions on the upper jaw during their operation.
Способ улучшения фиксации полных съёмных протезов на беззубой верхней челюсти при помощи последовательно-замкнутых клапанных зон / И. Д. Ушницкий, Н. И. Борисов, И. С. Пинелис, А. В. Юркевич ; Медицинский институт Северо-Восточного федерального университета им. М. К. Аммосова, Клиника ООО "Гармония", Читинская государственная медицинская академия, "Дальневосточный государственный медицинский университет" Министерства здравоохранения Российской Федерации // Якутский медицинский журнал. - 2024. - N 2 (86). - С. 35-38. - DOI: 10.25789/YMJ.2024.86.09
DOI: 10.25789/YMJ.2024.86.09
Количество страниц: 5 с.
Stereotypies, along with tics, are the most common hyperkineses, especially among children, but there is limited research on this movement disorder in adults. The aim of the study is to assess the prevalence and nature of stereotypies among adults without neurological and intellectual disorders and to determine its relationship with tics and associated psychiatric symptoms. The method of online survey and face-to-face examination revealed a high prevalence of stereotypies and tics in adults and their high association with anxiety and obsessive-compulsive symptoms.
Таппахов, А. А. Распространенность стереотипий среди взрослых без неврологических расстройств и интеллектуального снижения / А. А. Таппахов, О. С. Нижегородова ; Северо-Восточный федеральный университет им. М. К. Аммосова, Медицинский институт // Якутский медицинский журнал. - 2024. - N 2 (86). - С. 13-17. - DOI: 10.25789/YMJ.2024.86.03
DOI: 10.25789/YMJ.2024.86.03
Количество страниц: 3 с.
The article presents а clinical case of a rare inflammatory myofibroblastic tumor of the abdominal cavity in a 6-year-old boy. The child had a high fever, laboratory tests revealed an increase in acute phase proteins, and according to instrumental studies - a large tumor of the abdominal cavity, without a clear organ affiliation. During laparoscopic revision, the possibility of total tumor removal was established; laparotomy was performed and the tumor was radically removed
Редкий случай воспалительной миофибробластической опухоли брюшной полости у ребенка / C. A. Николаева, В. Б. Егорова, C. A. Кондратьева, А. Ю. Тарасов, Е. П. Яковлев, Я. А. Мунхалова, С. А. Евсеева // Якутский медицинский журнал. - 2024. - N 1 (85). - С. 132-135. - DOI: 10.25789/ҮШ.2024.85.34
DOI: 10.25789/ҮШ.2024.85.34
Количество страниц: 3 с.
The article presents а clinical case of congenital autosomal recessive cataract, first identified in a 3-year-old Sakha child. Congenital cataract is a relatively rare pathology found in children, but it is often the cause of visual impairment and blindness. The restoration of a child's eyesight depends on the early detection and treatment of the disease Studies show that 30 to 50 % of congenital cataracts are caused by genetic mutations
Врожденная аутосомно-рецессивная катаракта у ребенка саха / M. C. Саввина, O. H. Иванова, В. Б. Егорова, Т. Е. Бурцева // Якутский медицинский журнал. - 2024. - N 1 (85). - С. 131-132. - DOI: 10.25789/ҮШ.2024.85.33
DOI: 10.25789/ҮШ.2024.85.33
Количество страниц: 4 с.
The article presents а clinical case of combination of Miller Fisher syndrome and unspecified peripheral T-cell lymphoma, which is an aggressive disease with an extremely poor prognosis. The pathogenetic treatment of the identified syndrome did not cause an improvement in the patient's condition and did not affect the expected unfavorable prognosis of the primary malignant disease, for which chemotherapy was not carried out due to the extremely serious condition of the patient. This case emphasizes the importance of an oncological search in patients with Miller Fisher syndrome and the mandatory determination of onconeural antibodies used in the diagnosis of paraneoplastic neurological syndrome, which occurs in malignant tumors of various histogenetic types
Сочетание синдрома Миллера Фишера и неспецифицированной периферической Т-клеточной лимфомы / А. Д. Макаров, Л. М. Атласова, А. В. Тобохов, А. А. Таппахов, С. С. Сосина, Д. Н. Семенов // Якутский медицинский журнал. - 2024. - N 1 (85). - С. 128-131. - DOI: 10.25789/ҮШ.2024.85.32
DOI: 10.25789/ҮШ.2024.85.32
Количество страниц: 4 с.
The article presents а case of the course of two severe autoimmune diseases (Crohn's disease and juvenile rheumatoid arthritis) in a Sakha teenager
Клинический случай сочетания болезни Крона иювенильного ревматоидного артрита у подростка саха / C. A. Евсеева, M. A. Шарина, Г. М. Мельчанова, О. Н. Иванова, Т. Е. Бурцева, И. С. Иванова ; Якутский научный центр комплексных медицинских проблем, Медицинский институт Северо-Восточного федерального университета им. М. К. Аммосова // Якутский медицинский журнал. - 2024. - N 1 (85).- С. 125-128. - DOI: 10.25789/ҮШ.2024.85.31
DOI: 10.25789/ҮШ.2024.85.31
Количество страниц: 4 с.
This paper presents the results of biocompatibility research of PN-90 polytetrafluoroethylene implanted in the subcutaneous fat space of laboratory animals (Wistar rats). The implantation of the polymer was carried out under general anesthesia in the subscapular region. Histological sections of tissues from the control area and adjacent to the implant were investigated. Around the implanted polytetrafluoroethylene there was an intensive growth of new vessels of various calibers combined with a severe fibroblasts proliferation. The polymeric material was also investigated by means of an IR spectrometer and a scanning electron before and after implantation According to the results of IR spectroscopy the chemical composition of the polymer remains unchanged. The surface of polytetrafluoroethylene after implantation was practically identical to the surface of the initial polymer Based on the data obtained, it can be concluded that polytetrafluoroethylene is biologically compatible and can be used in medicine as a base for implants
Исследование биологической совместимости политетрафторэтилена марки ПН-90 на экспериментальных животных / Д. Н. Сидорова, A. M. Спиридонов, И. П. Троев, Л. Г. Маринова, М. П. Кириллина, Г. А. Пальшин, Д. В. Сивцев, А. А. Дьяконов, Н. Н. Лазарева, А. А. Охлопкова // Якутский медицинский журнал. - 2024. - N 1 (85). - С. 109-112. - DOI: 10.25789/ҮШ.2024.85.27
DOI: 10.25789/ҮШ.2024.85.27