Panhemocytopenia

Panhemocytopenia is a rare blood disorder characterized by a decrease in the number of all types of blood cells and a decrease in the amount of hemoglobin in the blood. The occurrence of this disease is associated with a disruption in the formation of blood cells, including red blood cells, white blood cells and platelets. Panhemocytopenia is caused by genetic abnormalities of the immune complex of the blood system.

Clinical manifestations of the pathology include weakness, fatigue, dizziness, loss of appetite, diarrhea, constipation, frequent colds and other diseases. Less commonly, patients experience nausea, vomiting and abdominal pain. As the disease progresses, chest pain and headaches occur, and leg pain may occur. At the stage of the expanded picture, a serious condition is observed: high fever, joint pain, significant weight loss. Some patients additionally experience episodes of arterial hypertension and hyperthermia.

In general, the risk of panhemocytopenia increases with age. Most often it develops in people over 65 years of age, especially after repeated operations. That is why during a routine examination you need to pay attention to a general blood test. Regular consultations and examinations will help to identify the problem in a timely manner. In most cases, the disease is not fatal. With the complete exclusion of physical activity, the patient only needs vitamin support. Every effort is made to

Panhemocytopenia (panhæmocytopënia), anisocytosis, monocytosis - the presence in the blood of a large number of mature mononuclear and several dozen subnuclear granulocytes of the monocytic series. These changes are most often manifestations of some infectious or tumor disease and are usually regarded as laboratory signs detected during a general clinical analysis