Sections View Full Chapter Figures Tables Videos Annotate Full Chapter Figures Tables Videos Supplementary Content +++ BASOPHILS ++ The basophil is the least common granulocyte. Normal basophil count is 0.015 to 0.08 × 109/L. The causes of basopenia (decreased numbers) and basophilia (increased numbers) are listed in Table 33–1. ++Table Graphic Jump LocationTABLE 33–1CONDITIONS ASSOCIATED WITH ALTERATIONS IN NUMBERS OF BASOPHILSView Table||Download (.pdf) TABLE 33–1 CONDITIONS ASSOCIATED WITH ALTERATIONS IN NUMBERS OF BASOPHILS Decreased Numbers (Basopenia) Hereditary absence of basophils (very rare) Elevated levels of glucocorticoids Hyperthyroidism or treatment with thyroid hormones Ovulation Hypersensitivity reactions Urticaria Anaphylaxis Drug-induced reactions Leukocytosis (in association with diverse disorders) Increased Numbers (Basophilia) Allergy or inflammation Ulcerative colitis Drug, food, inhalant hypersensitivity Erythroderma, urticaria Juvenile rheumatoid arthritis Endocrinopathy Diabetes mellitus Estrogen administration Hypothyroidism (myxedema) Infection Chickenpox Influenza Smallpox Tuberculosis Iron deficiency Exposure to ionizing radiation Neoplasia “Basophilic leukemias” (see text) Myeloproliferative neoplasms (especially chronic myelogenous leukemia; also polycythemia vera, primary myelofibrosis, essential thrombocythemia) Carcinoma +++ BASOPENIA ++ Hereditary absence of basophils is very rare. Other causes include high doses of glucocorticoids, hyperthyroidism or therapy with thyroid hormones, ovulation, hypersensitivity reactions, or leukocytosis in association with diverse disorders. +++ BASOPHILIA ++ Causes include allergy or inflammation, endocrinopathies (diabetes mellitus, hypothyroidism), infections, iron deficiency, exposure to ionizing radiation, and neoplasias. Basophilia occurs in virtually all patients with chronic myelogenous leukemia (CML). De novo acute basophilic leukemia is very rare, but marrow basophilia may be associated uncommonly with other subtypes of acute myelogenous or acute promyelocytic leukemia. Basophils in acute or chronic clonal myeloid diseases are derived from the malignant clone and occasionally may cause symptoms of histamine release (flushing, pruritus, hypotension) or severe peptic ulcer disease reflecting hypersecretion of gastric acid and pepsin. +++ MAST CELLS AND SECONDARY CHANGES IN NUMBERS ++ Mast cells are produced in the marrow and then transit the blood to the tissues where they reside. They cannot be identified in transit in the blood of healthy individuals by standard techniques. Mast cells contain mediators that may be preformed in granules (eg, histamine, heparin, and chemotactic factors) or newly formed (eg, arachidonic acid metabolites, such as prostaglandin D2 and leukotrienes). An increased number of mast cells may be seen in tissues of immunoglobulin E–associated disorders and connective tissue disorders, at infection sites, and in the lymph nodes and marrow in a variety of benign and malignant tumors (Table 33–2). ++Table Graphic Jump LocationTABLE 33–2CONDITIONS ASSOCIATED WITH SECONDARY CHANGES IN MAST CELL NUMBERSView Table||Download (.pdf) TABLE 33–2 CONDITIONS ASSOCIATED WITH SECONDARY CHANGES IN MAST CELL NUMBERS Decreased Numbers Long-term treatment with glucocorticoids Primary or acquired immunodeficiency disorders (certain mast cell populations) Increased Numbers IgE-associated disorders Allergic rhinitis Asthma Urticaria Connective tissue disorders Rheumatoid arthritis Psoriatic arthritis Scleroderma Systemic lupus erythematosus Infectious diseases Tuberculosis Syphilis Parasitic diseases Neoplastic disorders Lymphoproliferative diseasesa (lymphoplasmacytic lymphoma/Waldenström ... Your Access profile is currently affiliated with [InstitutionA] and is in the process of switching affiliations to [InstitutionB]. Please select how you would like to proceed. Keep the current affiliation with [InstitutionA] and continue with the Access profile sign in process Switch affiliation to [InstitutionB] and continue with the Access profile sign in process Get Free Access Through Your Institution Learn how to see if your library subscribes to McGraw Hill Medical products. Subscribe: Institutional or Individual Sign In Error: Incorrect UserName or Password Username Error: Please enter User Name Password Error: Please enter Password Sign in Forgot Password? Forgot Username? Download the Access App: iOS | Android Sign in via OpenAthens Sign in via Shibboleth You already have access! Please proceed to your institution's subscription. Create a free profile for additional features.