An Episode of Moshkovitz Syndrome in an 11-year-old Child: a Clinical Observation
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Creator Asya Bekovna Revazova, Tatiana Temirbolatovna Boraeva, Ulyana Viktorovna Matveeva, Lyudmila Voldemarovna Pavlovskaya, Alina Yurievna Maslova,, Hadji-Murat Huseyevich Erkenov, Ratmir Amirovich Magomedov
Title An Episode of Moshkovitz Syndrome in an 11-year-old Child: a Clinical Observation
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Publisher TuEngr Group
Publication Year 2565
Journal Title International Transaction Journal of Engineering, Management, & Applied Sciences & Technologies
Journal Vol. 13
Journal No. 8
Page no. 13A8F: 1-9
Keyword Thrombotic Thrombocytopenic purpura, Moshkovitz syndrome, Microangiopathic hemolytic anemia, Thrombocytopenia.
URL Website http://TuEngr.com/V13-8.html
Website title ITJEMAST V13(8) 2022 @ TuEngr.com
ISSN 2228-9860
Abstract Moshkovitz syndrome, which is also called thrombotic thrombocytopenic purpura (TTP), is an extremely severe multimorbid pathology. TTP is characterized by a very aggressive course, requiring immediate initiation of treatment in the first hours of occurrence, because, without fast and properly selected therapy, the mortality rate approaches 100% regardless of age. The foundation of Moshkovitz syndrome is a sharp increase in platelet aggregation with the formation of thrombi consisting of platelets and von Willebrand factor in small vessels of organs. The target organs that are affected in the first place are the brain, lungs, and kidneys. There is a sharp development of thrombocytopenia, microangiopathic hemolytic anemia, and ischemia in the most important organs. It is difficult to diagnose the disease due to the absence of specific symptoms. The disease often develops suddenly against the background of full health and in most cases resembles ARVI. In children, TTP is very rare, and therefore it is difficult for clinicians to verify the disease and determine a therapy strategy. The article presents an analysis of a clinical case of an 11-year-old girl with Moshkovitz syndrome.
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