What are the dangers of leukopenia?

Written by Tang Zhuo
Endocrinology
Updated on September 27, 2024
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Leukopenia is a relatively common hematological disease that can occur at any age. It is characterized by a persistent peripheral blood white blood cell count below 4×10^9/L. The onset of the disease is mostly slow, with mild symptoms. Common symptoms include fatigue, palpitations, dizziness, and pharyngitis, making individuals more susceptible to pharyngitis or mucosal ulceration. Other symptoms include reduced appetite, limb soreness, insomnia, and frequent dreaming. Individuals with leukopenia are also more prone to viral and bacterial infections. Some infections can lead to severe symptoms such as high fever, chills, and body aches. However, if there is a significant decrease in the total number of white blood cells, with the absolute neutrophil count dropping below 0.5×10^9/L, this condition is referred to as neutropenia. In such cases, symptoms may include chills, high fever, sore throat, headache, joint pain, and in severe cases, it can even lead to death.

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Written by Zhang Jun Jun
Endocrinology
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Leukopenia and thrombocytopenia are what diseases

Diseases caused by decreased white blood cells and platelets are often related to our hematological system, since both white blood cells and platelets are produced by our hematopoietic factors. When there is a decrease in both white blood cells and platelets, we generally consider that there might be an issue with our hematopoietic system. The most common conditions could be diseases related to the hematological system, such as leukemia, or aplastic anemia. These conditions can cause a decrease in the mentioned indices. Another disease is cirrhosis, especially in patients in the compensatory stage, which can lead to hyperfunctioning of the spleen. The spleen is also an immune organ, as well as a part of our hematopoietic system, so when the spleen is hyperactive, it can also result in decreased white blood cells and platelets.

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Written by Zhao Xin Lan
Endocrinology
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Treatment methods for leukopenia

First, it is necessary to identify the cause of leukopenia. Common causes include viral infections and poor bone marrow hematopoiesis, and some medications can also cause this condition. Therefore, symptomatic treatment mainly involves the use of medications that increase white blood cells. For mild leukopenia, oral medications commonly used include Li Xuesheng, squalene, and Vitamin B4 to promote the proliferation of white blood cells. In more severe cases, granulocyte colony-stimulating factors may be used. Of course, the main method of treatment still depends on the different causes of each patient. Once leukopenia occurs, it is necessary to go to the hospital for an examination to clearly determine the cause of the decrease in white blood cells, so that targeted treatment can be provided. (Please use medications under the guidance of a professional physician and do not self-medicate.)

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Written by Zhang Jun Jun
Endocrinology
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Is leukopenia very harmful?

Leukopenia primarily depends on the extent of the decrease in white blood cells, which can be classified into mild, moderate, and severe levels. Mild leukopenia generally means less than 4.0 X 10⁹/L, and if granulocytes are decreased, it typically means an absolute value of granulocytes less than 2.0 X 10⁹/L. A lack of granulocytes indicates a more severe condition, usually less than 0.5 X 10⁹/L. For patients with mild leukopenia, special preventive measures are generally not necessary. However, for moderate and severe leukopenia, the greatest risk is an increased chance of infection, as white blood cells are a marker of our ability to defend against external threats. With fewer of these defensive guards, the probability of resisting infections and the chance of acquiring infections significantly increase. Therefore, for patients with moderate leukopenia, their rate of infection increases, and it is important to take precautions, reduce visits to public places, maintain hygiene, and eliminate chronic infectious foci. For patients with severe leukopenia, aseptic isolation measures should be adopted. For patients who have infections, it is crucial to find sensitive antibiotics, preferably broad-spectrum antibiotics. If there is a concurrent fungal or viral infection, antifungal or antiviral medications should also be used, as the decrease in white blood cells can destroy a person's immune capacity, lowering immunity and increasing the chance of infections and the invasion of pathogenic bacteria, which in severe cases could even lead to sepsis or septic shock.

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Written by Liu Lei
Endocrinology
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What causes leukopenia?

Leukopenia mainly has the following three causes: 1) Drugs; 2) Infections; 3) Diseases that cause disturbances in white blood cell production. Drugs primarily include antibiotics such as sulfonamide antibiotics and penicillin; anti-tuberculosis drugs like rifampicin and isoniazid; anti-thyroid drugs such as methimazole and propylthiouracil; antipyretic analgesics like aminopyrine, indomethacin, and ibuprofen; and antihistamines such as diphenhydramine. Additionally, most chemotherapy drugs can cause a decrease in white blood cells. Viral infections can lead to a decrease in white blood cells or severe bacterial infections, such as sepsis and septicemia, along with some chronic infections. Diseases that cause disturbances in the production of white blood cells mainly refer to certain hematological diseases, such as aplastic anemia or malignant tumors that invade the bone marrow and affect hematopoiesis. Furthermore, there are some less common causes of leukopenia, such as familial inheritance and granulocyte distribution disorders.

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Written by Zhang Jun Jun
Endocrinology
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What are the symptoms of leukopenia?

The most common cause of leukopenia is viral infections, along with some severe bacterial infections. Common symptoms of viral and bacterial infections include dizziness, headache, nausea, vomiting, chills, fever, cough, expectoration, abdominal pain, diarrhea, urgent urination, and frequent urination. Generally, further examinations can be conducted through blood draws and routine tests of blood, urine, and stool cultures. If there is an accompanying hematological disease, such as thrombocytopenia, symptoms can include general weakness, body aches, and bone pain; further bone marrow examinations should be conducted.