Количество страниц: 4 с.
Клинический случай мультисистемного воспалительного синдрома / М. С. Саввина, В. М. Аргунова, Т. Е. Бурцева [и др.] ; Якутский научный центр комплексных медицинских проблем, Республиканская больница N 1 -Национальный центр медицины, Санкт-Петербургский государственный педиатрический медицинский университет, Северо-Восточный федеральный университет им. М. К. Аммосова // Якутский медицинский журнал. - 2023. - N 2 (82). - C.135-138. - DOI: 10.25789/YMJ.2023.82.33
DOI: 10.25789/YMJ.2023.82.33
Количество страниц: 3 с.
This article presents a clinical case of chronic myeloproliferative disease (CPMD) in 57-years-old male, which first manifested with acute Q-positive myocardial infarction. The patient successfully underwent recanalization, transluminal balloon angioplasty with stenting of the anterior descending coronary artery. Based on thrombocytosis and bone marrow examination the patient was diagnosed with essential thrombocythemia. This case demonstrates the possible insidious onset of the disease. The absence of typical presentation further complicates the diagnosis of CMPD.
Клинический случай острого инфаркта миокарда в дебюте хронического миелопролиферативного заболевания / Х. А. Куртанов, Т. Н. Александрова, Н. И. Павлова, И. И. Мулина, И. Е. Соловьева, М. А. Варламова, Л. М. Неустроева, А. Т. Дьяконова // Якутский медицинский журнал. — 2018. — N 2 (62). — С. 120-122
DOI: 10.25789/YMJ.2018.62.39
Количество страниц: 4 с.
The article presents the clinical case of management of a child with a genetic metabolic disease until setting a correct diagnosis propionic acidemia. The full – term child aged 11 days had developed metabolic crisis, which was taken as an expression of neonatal pathology, such as neonatal jaundice, perinatal CNS lesion. On a background of detoxification the patient had the clinical positive dynamics, but a bright period lasted only two weeks. Due to a main disease the child had secondary immunodeficiency, which resulted in recurrent pneumonias. The patient was examined in three ways: changes of peripheral blood – leukopenia, thrombocytopenia, anemia; neurological symptoms – soporous condition, lethargy, refusal of meals, oppression of all reflexes, muscular hypotension; in view of anamnesis, impossibility of a comparison all the clinical symptoms to one diagnosis tap genetic research. The lack of the methodology of tandem mass spectrometry extended the time of correct diagnosis and timely treatment.
Клинический случай пропионовой ацидемии / С. Н. Алексеева, А. Л. Сухомясова, Г. И. Софронова, З. П. Андросова, С. А. Кондратьева, Е. Е. Гуринова, П. В. Павлова // Якутский медицинский журнал. — 2018. — N 3 (63). — С. 99-102 – DO: 10.25789/YMJ.2018.63.32 .
DOI: 10.25789/YMJ.2018.63.32
Количество страниц: 4 с.
Клинический случай синдрома Вискотта-Олдрича / О. Н. Иванова, Т. Е. Бурцева, Н. Н. Протопопова, С. А. Кондратьева, Д. М. Фурман, М. П. Слободчикова // Якутский медицинский журнал. — 2020. — N 2 (70). — С. 104-106. – DOI: 10.25789/YMJ.2020.70.31.
DOI: 10.25789/YMJ.2020.70.31
Количество страниц: 4 с.
Spontaneous pneumothorax most commonly occurs among able-bodied male population at the age of 20-40; thus revealing not only medical but also social significance of the problem. We have described the case of spontaneous pneumothorax of a 17-year old male adolescent, admitted to the department of pulmonology of the Pediatric center, Republic Hospital ө1 – National Center of Medicine. The significance of the case results from clinical manifestation of the spontaneous pneumothorax associated with a severe and acute attack of the bronchial asthma
Клинический случай спонтанного пневмоторакса у юноши 17 лет на фоне бронхиальной астмы / О. Н. Иванова, Т. Е. Бурцева, М. П. Черкашин [и другие] // Якутский медицинский журнал. — 2020. — N 1 (69). — С. 124-126. – DOI: 10.25789/YMJ.2020.69.32.
DOI: 10.25789/YMJ.2020.69.32
Количество страниц: 3 с.
The authors described the clinical observation of postoperative sternomediastinitis. The feasibility of a two-stage surgical treatment of this pathology was noted: the first stage is the removal of ligatures and necrectomy of the sternum, the second is the resection of the sternum with plastic replacement of the wound defect. At the integrity of the sternum, the authors propose to perform surgical intervention, including the preservation of bone tissue, sternal rheosteosynthesis.
Распространение носителей "индоевропейских" гаплотипов системы HLA по территории Евразии / И. П. Гурьев // Якутский медицинский журнал. — 2019. — N 3 (67). — С. 119-121. – DOI: 10.25789/YMJ.2019.67.33
DOI: 10.25789/YMJ.2019.67.33
Количество страниц: 4 с.
The article presents a clinical case of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome), which was diagnosed for the first time in a 27-year-old man with bronchial asthma, eosinophilia, and gastrointestinal tract involvement. A retrospective analysis of the disease demonstrates the difficulties in diagnosing this disease. In this clinical case, the diagnosis was made 1.5-2 years after the onset of the first manifestations of the disease, in the second period of the development of the disease, based on the symptoms of the disease that were identified in the patient: bronchial asthma, rhinosinusopathy, pulmonary infiltrates, hypereosinophilia, despite the absence of biological markers of vasculitis. This syndrome is infrequently in clinical practice; however, doctors of various specialties should be aware of identifying this syndrome in their patients
Асекритова, А. С. Клинический случай эозинофильного гранулематоза с полиангиитом: трудности диагностики и клиническая картина / А. С. Асекритова, Э. А. Емельянова, А. П. Далбараева // Якутский медицинский журнал. — 2020. — N 4 (72). — С. 122-125.
DOI: 10.25789/YMJ.2020.72.30
Количество страниц: 4 с.
The article presents a case of sex cord-stromal tumor of the fallopian tube in a 18-year-old female patient. Single cases of extra-ovarian localization of sex cord-stromal tumor have been described in the literature, however the primary lesion of fallopian tube still hasn`t been reported.
Клиническое наблюдение опухоли стромы полового тяжа маточной трубы / А. Е. Бирюков, Л. М. Михалева, К. Ю. Мидибер, В. В. Печникова // Якутский медицинский журнал. — 2019. — N 4 (68). — С. 119-121.
DOI: 10.25789/YMJ.2019.68.33
Количество страниц: 2 с.
The article is devoted to the description of the clinical course of Bruton's disease in a child. Bruton's disease is a genetic disease associated with impaired synthesis of serum immunoglobulins and B cells. The disease belongs to the primary immunodeficiency.
Иванова, О. Н. Клиническое описание болезни Брутона у ребенка в Республике Саха (Якутия) / О. Н. Иванова, Т. Е Бурцева, М. П. Слободчикова // Якутский медицинский журнал. — 2019. — N 4 (68). — С. 122-123.
DOI: 10.25789/YMJ.2019.68.34
Количество страниц: 4 с.
Cerebral amyloid angiopathy (CAA) is a disease of the small cerebral vessels and it mostly affects older people. CAA is characterized by progressive deposition of amyloid-beta in small arteries and arteries of medium caliber, as well as in the capillaries. Sporadic amyloid angiopathy is a cause of recurrent cerebral hemorrhage and cognitive impairment in the elderly. The latest scientific researches and a case report of a patient who suffered from cerebral amyloid angiopathy were used in order to prepare this article. The diagnosis and treatment of CAA are considered
Клиническое описание пациента с церебральной амилоидной ангиопатией / А. А. Таппахов, Т. Е. Попова, М. Н. Петрова [и другие] // Якутский медицинский журнал. — 2020. — N 1 (69). — С. 42-45
DOI: 10.25789/YMJ.2020.69.10