The majority of white blood cells are either neutrophils (band cells and polymorphonuclear granulocytes, 35-70%) or lymphocytes (20-45%). Leucocytopenia is almost always caused by a reduced number of neutrophils.
Lymphocytopenia is only seldom associated with a specific disease. It may be seen in acute or chronic infections caused by a variety of microbes as well as both in congenital and acquired immune deficiency states.
Reference values
Leucocytopenia: white blood cells < 3.4 × 109 /l
Lymphocytopenia: blood lymphocytes < 1.2 × 109 /l
Neutropenia: blood neutrophils < 1.5-2.0 × 109 /l
Degree of neutropenia:
mild: neutrophils 1.0-1.5 × 109 /l
moderate: neutrophils 0.5-1.0 × 109 /l
severe: neutrophils < 0.5 × 109 /l
Agranulocytosis: a syndrome characterised by an unexpected, drug-induced severe neutropenia and associated infection. The term is not usually used as a synonym for severe neutropenia.
A decreased number of B-lymphocytes predisposes the patient to bacterial infections whereas a decreased number of T-lymphocytes predisposes the patient to infections caused by viruses, certain bacteria, (mycobacteria, salmonella, listeria), fungi (candida, aspergillus) and parasites (toxoplasma). In HIV infection, the helper T cells count (CD4) is monitored and used as an indicator of the patient's susceptibility to infections.
Neutropenia predisposes the patient to bacterial infections. The susceptibility to infections is dependent on, for example,
the degree of neutropenia
neutrophils 1.0-1.5 × 109 /l: slightly increased risk of infection
neutrophils < 0.5 × 109 /l: significant risk of infection
whether the patient has co-existing conditions that increase the risk of infection:
immunosuppressive illness and/or medication
poorly functioning bone marrow
skin and/or mucous membrane ulcers.
The bacterial infections in a neutropenic patient may vary from mild oral (ulceration) and upper respiratory tract infections to life-threatening septic infections.
No purulent discharge will form in the absence of neutrophils. The diagnosis and localisation of an infection may therefore prove difficult in a neutropenic patient. In neutropenia, an infection will spread quickly throughout the body.
Lymphocytopenia is often encountered in acute infections. It is not associated with any specific disease.
It may also be present in autoimmune diseases, allergies, chronic infections (tuberculosis, histoplasmosis, brucellosis), in association with malignancies as well as in congenital immune deficiency states.
Lymphocytopenia may also be associated with some medications, e.g.
Cancer drugs and some immunosuppressive drugs will consistently cause neutropenia in all users.
Some drugs will cause neutropenia only occasionally in a small proportion of users (idiosyncratic neutropenia).
Agranulocytosis is a life-threatening drug-induced complication, and its relative risk is high during the use of clozapine Clozapine Therapy, antithyroid drugs, metamizole and sulfasalazine (may also be associated with other drugs).
A drug that is suspected to be causing neutropenia must be discontinued immediately. A patient must never be administered a drug that has caused him/her agranulocytosis or severe idiosyncratic neutropenia in the past.
Many viruses are able to attenuate the production of neutrophils. In some cases, neutropenia continues for several weeks after the patient has recovered from the viral infection itself.
Bacterial infections usually cause neutrophilia rather than depress the cell production in the bone marrow (mycobacterial infections form an exception as the infection may involve the bone marrow itself). In severe infections, the neutrophil consumption by the tissues is usually not sufficient to cause neutropenia because a healthy bone marrow is able to increase its neutrophil production manifold. If the bone marrow functioning is impaired (e.g. blood disease, after cytotoxic treatment, alcoholism), neutropenia will occur much more readily during infections.
Some chronic infections (tuberculosis, typhoid fever, brucellosis, malaria) cause splenomegaly, and consequent hypersplenism may cause neutropenia.
Immunologic neutropenia
Alloimmune neonatal neutropenia
In autoimmune neutropenia, neutrophils are destroyed because the body inappropriately develops antibodies to its own neutrophils and also possibly to their precursor cells. Even at its worst, the neutropenia will only be moderate, and the susceptibility to infections is relatively low in relation to the degree of neutropenia.
In certain autoimmune diseases, e.g. in systemic lupus erythematosus, neutropenia is fairly common.
Neutropenia as a feature in haematological diseases
A haematological disease should be suspected if the blood picture shows, in addition to neutropenia, abnormalities in the other cell lines or in the differential white cell count. Neutropenia on its own is an abnormal finding suggestive of a malignant disease. If malignant blood disease is suspected, a bone marrow sample must be collected.
Abnormal distribution of neutrophils in the circulatory system
Half of the neutrophils in the blood are loosely bound to the blood vessel walls (margination), and they are quickly released to the circulating neutrophil pool during stressful situations. In some healthy individuals, the proportion of the marginated neutrophil pool is significantly higher than normal, leading to nominal neutropenia, i.e. pseudoneutropenia, where the risk of infection is not increased.
Splenomegaly of any aetiology may cause hypersplenism and associated anaemia, thrombocytopenia and/or neutropenia. In systemic lupus erythematosus, even a normal sized spleen may be overactive.
Chronic idiopathic neutropenia
Acquired, significant neutropenia without any obvious cause is sometimes encountered in healthy individuals (exclusion diagnosis). The condition is not associated with an increased risk of infection and does not signify the onset of any other disease process.
Congenital and hereditary neutropenia
Cyclic neutropenia. Symptomatic neutropenia (i.e. infections) occurs at regular intervals, usually about every three weeks, lasting a few days at a time. Diagnosis is usually made within the first 12 months of life; later in milder cases.
Severe congenital neutropenia is rare (e.g. Kostmann syndrome). Neutropenia may be associated with hereditary functional disorders of B- and T-lymphocytes as well as with some congenital developmental and metabolic diseases.
Investigations in neutropenia
The urgency of the investigations is mainly dependent on the degree of neutropenia, the patient's symptoms and whether there are grounds to suspect a malignant blood disease.
If the patient presents with severe neutropenia with an acute onset, investigations should start immediately. The aetiology may include drug-induced agranulocytosis or a blood disease. Acute leukaemia may be suggested by blast cells seen in the differential white blood cell count; the total white cell count may be low, normal or high.
It is usually safe to monitor only, if the neutropenia is mild or moderate, the differential white blood cell count is normal and the patient has no anaemia and/or thrombocytopenia. In most of such cases, the neutropenia is caused by a medicine taken by the patient or a viral infection. Neutropenia may also be associated with an underlying disease, e.g. systemic lupus erythematosus, or splenomegaly.
It is important to establish whether neutropenia is a new, acquired finding or whether it has been present for a long time. It is important to check old laboratory reports and take a careful history. A true, clinically significant neutropenia will cause recurrent infections and, in some patients, ulceration in the buccal mucosa. In some ethnic populations and individual families, the neutrophil counts of healthy individuals may be lower than normal reference values. Pseudoneutropenia may be demonstrated with a prednisolone test (40 mg orally; a neutrophil count is taken before and 4-5 hours after the medicine), which will show an abnormally strong increase in the neutrophil count.