CLINICAL CASE: THE SYNDROME OF KASABACH-MERRITT (SCM)
https://doi.org/10.24412/2790-1289-2021-1123126
Abstract
Relevance. Kazabach-Merritt syndrome is extremely rare in children's practice. Clinical manifestations are diverse, which complicates the timely diagnosis and treatment of this di sease.
Purpose: to attract the attention of pediatricians, neonatologists and pediatricians to the timely diagnosis of rare hematological syndromes.
Materials and methods. An extended examination of the child and a thorough differential diagnosis with other vascular anomalies were carried out.
Results. Based on the assessment of anamnesis, clinical laboratory and instrumental examination methods, the diagnosis of SCM was established.
Conclusions. The diagnosis of SCM requires an extended examination of the child and careful differentiation with other vascular anomalies.
About the Authors
G. N. Balmagambetova
«Center of Perinatology and Pediatric Cardiac Surgery»
Kazakhstan
Kazakhstan
S. A. Lisogor
«Center of Perinatology and Pediatric Cardiac Surgery»
Kazakhstan
Kazakhstan
V. M. Shmonin
NEI «Kazakh-Russian Medical University»
Kazakhstan
Kazakhstan
References
1. Современная педиатрия 7(95) / 2018, Случай синдрома Казабаха-Мерритта у ребенка, Н.И. Макеева, Ю.В. Одинец, И.Н. Поддубная, С.147.
Review
For citations:
Balmagambetova G.N., Lisogor S.A., Shmonin V.M. CLINICAL CASE: THE SYNDROME OF KASABACH-MERRITT (SCM). Actual Problems of Theoretical and Clinical Medicine. 2021;(1):123-126. (In Russ.) https://doi.org/10.24412/2790-1289-2021-1123126
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