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In hematology, plasma cell dyscrasias (also termed plasma cell disorders and plasma cell proliferative diseases) are a spectrum of progressively more severe monoclonal gammopathies in which a clone or multiple clones of pre-malignant or malignant plasma cells (sometimes in association with lymphoplasmacytoid cells or B lymphocytes) over-produce and secrete into the blood stream a myeloma ...
Factor X deficiency (X as Roman numeral ten) is a bleeding disorder characterized by a lack in the production of factor X (FX), an enzyme protein that causes blood to clot in the coagulation cascade. Produced in the liver FX when activated cleaves prothrombin to generate thrombin in the intrinsic pathway of coagulation.
Inborn deficiency of factor X is very rare (1:1,000,000), and may present with epistaxis (nosebleeds), hemarthrosis (bleeding into joints) and gastrointestinal blood loss. . Apart from congenital deficiency, low factor X levels may occur occasionally in a number of disease stat
Transfusion transmitted infection, from blood transfusions that are given as treatment. Hemophilia [7] Adverse reactions to clotting factor treatment. Hemophilia [7] Anemia: Von Willebrand disease [8] Exsanguination (bleeding to death) Von Willebrand disease [8] Acute leukemia [5] Vitamin K deficiency [6] Cerebral hemorrhage: Wiskott–Aldrich ...
Coagulopathy (also called a bleeding disorder) is a condition in which the blood's ability to coagulate (form clots) is impaired. [1] This condition can cause a tendency toward prolonged or excessive bleeding (bleeding diathesis), which may occur spontaneously or following an injury or medical and dental procedures.
Treatment is guided by the severity and specific cause of the disease. Treatment focuses on eliminating the underlying problem, whether that means discontinuing drugs suspected to cause it or treating underlying sepsis. Diagnosis and treatment of serious thrombocytopenia is usually directed by a hematologist.
Health authorities around the world are still grappling with lessons learned at the start of the Covid-19 pandemic and trying to determine the best way to prevent a new one.. Many researchers have ...
Among patients with Evans syndrome, the prevailing causes of death were bleeding, infections, and hematological cancer. [ 4 ] It has been observed that there is a risk of developing other autoimmune problems and hypogammaglobulinemia , [ 30 ] in one cohort 58% of children with Evans syndrome had CD4-/CD8- T cells which is a strong predictor for ...