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Encyclopedia of Health and Medicine

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multiple myeloma 157<br />

therapy may also be appropriate for people who<br />

cannot take methylene blue.<br />

Recovery is generally complete when the cause<br />

is toxic exposure. Genetic disorders <strong>of</strong> the hemoglobin<br />

or the enzyme mechanisms that regulate<br />

the balance between methemoglobin <strong>and</strong> hemoglobin<br />

may result in chronic methemoglobinemia<br />

<strong>and</strong> consequently the need for ongoing treatment<br />

(such as oral methylene blue) to prevent toxic<br />

accumulations.<br />

Risk Factors <strong>and</strong> Preventive Measures<br />

The most common cause <strong>of</strong> methemoglobinemia<br />

is toxic exposure to substances that cause oxidation,<br />

which overwhelms the body’s normal mechanisms<br />

for managing cell metabolism. Avoiding<br />

chemicals, including drugs, that may cause methemoglobinemia<br />

is not simple, as they number in<br />

the dozens <strong>and</strong> include such commonly used<br />

medications as nitrates (cardiovascular) <strong>and</strong> topical<br />

anesthetics. People who have genetic disorders<br />

that interfere with hemoglobin production <strong>and</strong><br />

function have increased risk for methemoglobinemia<br />

<strong>and</strong> should make every effort to avoid known<br />

causative agents.<br />

See also ENVIRONMENTAL HAZARD EXPOSURE; G6PD<br />

DEFICIENCY; OCCUPATIONAL HEALTH AND SAFETY; OXY-<br />

GEN–CARBON DIOXIDE EXCHANGE; SICKLE CELL DISEASE.<br />

monocyte A LEUKOCYTE (white BLOOD cell), also<br />

called an agranulocyte, that has a single-lobed<br />

nucleus <strong>and</strong> contains no granules in its cytoplasm.<br />

The BONE MARROW <strong>and</strong> the LYMPH nodes produce<br />

monocytes, which have a two-phase existence in<br />

the body. During the first phase, the monocyte circulates<br />

in the blood <strong>and</strong> the lymph, functioning as<br />

a PHAGOCYTE that consumes pathogenic particles in<br />

the circulation. After about 24 hours the monocyte<br />

migrates into the tissue to enter its second<br />

phase <strong>of</strong> life. Once in the tissue the monocyte<br />

matures, becoming a fixed phagocytic cell called a<br />

macrophage that may acquire a specific name,<br />

depending on its location. About half <strong>of</strong> the body’s<br />

macrophages migrate to the lymphatic structures.<br />

Most <strong>of</strong> the remainder reside in the LIVER,<br />

where they are called Kupffer cells. Macrophages<br />

that settle in the layers <strong>of</strong> the SKIN are Langerhans<br />

cells, <strong>and</strong> those that inhabit the BONE are osteoclasts.<br />

Two to 8 percent <strong>of</strong> the body’s leukocytes are<br />

monocytes; a normal monocyte count is 200 to<br />

1100 monocytes per microliter <strong>of</strong> whole blood.<br />

The number <strong>of</strong> monocytes in circulation may<br />

increase with INFECTION, LEUKEMIA, LYMPHOMA, many<br />

other types <strong>of</strong> cancer, <strong>and</strong> AUTOIMMUNE DISORDERS<br />

in which there is active INFLAMMATION <strong>and</strong> autoimmune<br />

activity. The number <strong>of</strong> monocytes in circulation<br />

may decrease in aplastic ANEMIA <strong>and</strong> with<br />

steroid medications.<br />

For further discussion <strong>of</strong> monocytes within the<br />

context <strong>of</strong> blood <strong>and</strong> lymph structure <strong>and</strong> function<br />

please see the overview section “The Blood<br />

<strong>and</strong> Lymph.”<br />

See also CELL STRUCTURE AND FUNCTION; ERYTHRO-<br />

CYTE; GRANULOCYTE; HEMATOPOIESIS; SKIN-ASSOCIATED<br />

LYMPHOID TISSUE (SALT).<br />

multiple myeloma A CANCER <strong>of</strong> the BONE MARROW<br />

in which PLASMA cells, also called myeloma cells or<br />

myelocytes, proliferate, accumulating as lesions<br />

(growths) to develop within the BONE marrow cavities<br />

<strong>of</strong> the bones. The lesions prevent normal<br />

functioning <strong>of</strong> the bone marrow. They also damage<br />

bone tissue <strong>and</strong> weaken the bone structure.<br />

Plasma cells derive from lymphocytes that migrate<br />

to the bone marrow. Their function is to produce<br />

immune antibodies, or immunoglobulins, that are<br />

essential for the body’s IMMUNE RESPONSE. They<br />

generally make up less than 5 percent <strong>of</strong> the cells<br />

in the bone marrow. In multiple myeloma plasma<br />

cells make up 10 percent or more <strong>of</strong> the bone<br />

marrow’s cells. The cancerous plasma cells <strong>of</strong> multiple<br />

myeloma overproduce certain immune antibodies<br />

called monoclonal proteins or M-proteins.<br />

M-proteins alter the ways in which immunoglobulins<br />

bind with B-cell lymphocytes in the blood,<br />

reducing their ability to fight INFECTION.<br />

The M-proteins also activate specialized phagocytic<br />

cells in the bone, called osteoclasts, accelerating<br />

the deconstruction phase <strong>of</strong> bone remodeling<br />

(the process through which bone tissue continuously<br />

replenishes). Osteoclastic activity releases<br />

excessive calcium into the bloodstream, affecting<br />

numerous body systems, including cardiovascular<br />

function <strong>and</strong> renal (kidney) function. The KIDNEYS<br />

produce ERYTHROPOIETIN (EPO), the HORMONE that<br />

stimulates the bone marrow to produce erythrocytes<br />

(red blood cells). Damage to the kidneys

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