Bma Illustrated Medical Dictionary

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abdominal wall. The mesentery con-
tains the blood vessels, nerves, and
lymphatic vessels for the intestines.
mesotheliomaA cancerous tumour of
the pleura. Exposure to asbestos dust is
a risk factor (see asbestos-related dis-
eases). Symptoms, which do not always
occur, include cough, chest pain, and
breathing difficulty, especially if a pleu-
ral effusiondevelops. Diagnosis is made
with a chestX-ray followed by pleural
biopsyor examination of a fluid sample
from any effusion. If the tumour is
small, surgery is often successful. There
is no effective treatment for large
tumours, although radiotherapy may
alleviate symptoms.
mesotheliumA type of epitheliumcov-
ering the peritoneum, the pleura, and
the pericardium.
mesteroloneAn androgen hormone
(male sex hormone) used as replace-
ment therapy in hypogonadismbecause
testosterone cannot be given orally.
Side effects can include prostate prob-
lems, headache, and depression.
mestranolAn oestrogen drugused in
some oral contraceptives.
metabolic disordersA group of dis-
orders in which some aspect of body
chemistry is disturbed. Some metabolic
disorders result from an inherited mal-
function or deficiency of an enzyme(see
metabolism, inborn errors of). Others
result from under- or overproduction of
a hormone that controls metabolic acti-
vity, such as occurs in diabetes mellitus
and hypothyroidism.

metabolismA collective term for all the
chemical processes that take place in
the body. It is divided into catabolism
(breaking down of complex substances
into simpler ones) and anabolism
(building up of complex substances
from simpler ones). Usually, catabolism
releases energy, while anabolism uses it.
The energy needed to keep the body
functioning at rest is called the basal
metabolic rate (BMR). It is measured in
joules (or kilocalories) per square metre
of body surface per hour. The BMR
increases in response to factors such as
stress, fear, exertion, and illness, and is
controlled principally by various hor-
mones, such as thyroxine, adrenaline
(epinephrine), and insulin. (See also
metabolism, inborn errors of;metabolic
disorders.)
metabolism, inborn errors ofInher-
ited defects of body chemistry. Inborn
errors of metabolism are caused by
single genedefects, which lead to ab-
normal functioning of an enzyme.
Some of these gene defects are harm-
less, but others are severe enough to
result in death or physical or mental
handicap. Examples include Tay–Sachs
disease, phenylketonuria, Hurler’s syn-
drome, and Lesch–Nyhan syndrome.
Collectively, inborn errors of meta-
bolism affect around 1 child in 5,000.
Symptoms are usually present at or
soon after birth. They may include
unexplained illness or failure to thrive,
developmental delay, floppiness, per-
sistent vomiting, or seizures.
Routine tests are performed on new-
born babies for some genetic disorders,
such as phenylketonuria.
Treatment is not needed for some
inborn errors of metabolism. For others,
avoidance of a specific environmental
factor may be sufficient. In some cases,
the missing enzyme or the protein that
it produces can be manufactured using
genetic engineering techniques, or a
vitamin supplement can help compen-
sate for the defective enzyme. If the
enzyme is made in blood cells, a bone
marrow transplantmay provide a cure.
People with a child or a close relative
who is affected may benefit from genetic
counsellingbefore planning a pregnancy.

MESOTHELIOMA METABOLISM, INBORN ERRORS OF

M


MESENTERY

Stomach

Large
intestine

Mesentery

Small
intestine
(pulled
aside to
reveal
mesentery)
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