Javascript must be enabled to continue!
Budd-Chiari syndrome at the young woman with thrombophilia and myeloproliferative disease
View through CrossRef
In the clinic of various diseases (especially hematological) Budd-Chiari syndrome occupies a signifi cant place. The occurrence of blood fl ow disorders in the portal vein system can be a manifestation and the only symptom that manifests itself in a number of diseases. Given the rapid development of portal hypertension, this syndrome requires rapid diagnosis and timely initiated therapeutic measures, as well as comprehensive research to identify the etiological cause of Budd-Chiari syndrome.Objectives: In this paper we demonstrated a clinical case of a young patient with Budd-Chiari syndrome, an unusual course and a combination of etiological factors.Materials and methods. Data from the medical history of the patient who was on treatment at the surgical department of the City Multi-profile Hospital № 2, Military-medical Academy St. Petersburg were used as materials.Result. The patient developed severe ascites 3 months after delivery, for which she was unsuccessfully examined by gynecologists to exclude ovarian tumors. Then, in the course of laboratory and instrumental studies, a final diagnosis was made of Budd-Chiari syndrom (thrombosis of the intrahepatic part of the inferior vena cava in the phase of partial recanalization against the background of chronic myeloproliferative disease and genetically determined thrombophilia.Conclusion: As this case shows, in the development of non-cirrhotic portal hypertension, it is necessary to exclude hepatic thrombosis, in the detection of which it is recommended to conduct a comprehensive examination to exclude all causes of this thrombosis (genetic analysis for thrombophylia, antiphospholipid syndrome, Jak-2 v617f for exclude polycythemia and myelofi brosis, examination for cancer pathology). Manifestation and the only symptom of thrombophilia and idiopathic myelofi brosis may be acute Budd-Chiari syndrome, which requires complex medical and surgical treatment, further observation and especially treatment of causal diseases.
LLC Global Media Technology
Title: Budd-Chiari syndrome at the young woman with thrombophilia and myeloproliferative disease
Description:
In the clinic of various diseases (especially hematological) Budd-Chiari syndrome occupies a signifi cant place.
The occurrence of blood fl ow disorders in the portal vein system can be a manifestation and the only symptom that manifests itself in a number of diseases.
Given the rapid development of portal hypertension, this syndrome requires rapid diagnosis and timely initiated therapeutic measures, as well as comprehensive research to identify the etiological cause of Budd-Chiari syndrome.
Objectives: In this paper we demonstrated a clinical case of a young patient with Budd-Chiari syndrome, an unusual course and a combination of etiological factors.
Materials and methods.
Data from the medical history of the patient who was on treatment at the surgical department of the City Multi-profile Hospital № 2, Military-medical Academy St.
Petersburg were used as materials.
Result.
The patient developed severe ascites 3 months after delivery, for which she was unsuccessfully examined by gynecologists to exclude ovarian tumors.
Then, in the course of laboratory and instrumental studies, a final diagnosis was made of Budd-Chiari syndrom (thrombosis of the intrahepatic part of the inferior vena cava in the phase of partial recanalization against the background of chronic myeloproliferative disease and genetically determined thrombophilia.
Conclusion: As this case shows, in the development of non-cirrhotic portal hypertension, it is necessary to exclude hepatic thrombosis, in the detection of which it is recommended to conduct a comprehensive examination to exclude all causes of this thrombosis (genetic analysis for thrombophylia, antiphospholipid syndrome, Jak-2 v617f for exclude polycythemia and myelofi brosis, examination for cancer pathology).
Manifestation and the only symptom of thrombophilia and idiopathic myelofi brosis may be acute Budd-Chiari syndrome, which requires complex medical and surgical treatment, further observation and especially treatment of causal diseases.
Related Results
Whole Exome Sequencing and Extended Thrombophilia Testing in Patients with Venous Thromboembolism
Whole Exome Sequencing and Extended Thrombophilia Testing in Patients with Venous Thromboembolism
Abstract
Introduction: Venous thromboembolism (VTE), defined as deep venous thrombosis (DVT) and pulmonary embolism (PE), is a cause of significant morbidity and mor...
Heritable and Acquired Thrombophilias in Clinical Practice
Heritable and Acquired Thrombophilias in Clinical Practice
Thrombosis is common in clinical practice. Venous thromboembolism in particular raises questions of a possible underlying hereditary or acquired thrombophilic state. Despite consid...
Heritable and Acquired Thrombophilias in Clinical Practice
Heritable and Acquired Thrombophilias in Clinical Practice
Thrombosis is common in clinical practice. Venous thromboembolism in particular raises questions of a possible underlying hereditary or acquired thrombophilic state. Despite consid...
The Association Study of Targeted DNA Methylation and Thrombophilia
The Association Study of Targeted DNA Methylation and Thrombophilia
Abstract
Objective
The aim of this study is to investigate the relationship of leukocytes DNA methylation in targeted sites and thrombophilia.
...
Chiari Malformasyonu Tarihçesi, Sınıflandırmaları
Chiari Malformasyonu Tarihçesi, Sınıflandırmaları
Chiari malformasyonları (CM), serebellumun beyin sapının ve kraniyo-servikal birleşkenin anatomik bozukluk anomalileriyle tanımlanan, serebellumun alt kısımları birlikte orta beyin...
Pediatrik Chiari Malformasyonları
Pediatrik Chiari Malformasyonları
Chiari malformasyonları, posterior fossa, arka beyin( serebellum, pons, medulla oblongata9 ve spinal kordun değişen derecelerde doğumsal anomalilerini tanımlayan bir hastalık grubu...
Chiari Malformasyonları Elektrofizyoloji
Chiari Malformasyonları Elektrofizyoloji
Chiari malformasyonu (CM), serebellar tonsillerin foramen magnum altına herniasyonu ile karakterize edilen bir nörolojik hastalıktır. Bu hastalık, beyin-omurilik sıvısının akışını ...
Membranous obstruction of the inferior vena cava (obliterative hepatocavopathy, Okuda)
Membranous obstruction of the inferior vena cava (obliterative hepatocavopathy, Okuda)
AbstractConfusion prevails throughout the world regarding the definition and classification of the Budd–Chiari syndrome. The original patients (Budd and Chiari) described had hepat...

