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Methods of Examination
In the following section, the main methods used for the investigation
and diagnosis of disorders of the stomach and duodenum are
explained. In addition, x-ray and ultrasound examinations
can be carried out.
Endoscopy
Illumination and inspection of body cavities and hollow organs
the aid of an endoscope. At the same time, a tissue sample
(biopsy) can be taken for further examination, possibly in
combination with an ultrasound examination (endosonography),
and minor surgical procedures can be carried out (e.g. electro
or laser coagulation, endoscopic implantation of stents to
expand the digestive tract).
Gastroduodenoscopy
Endoscopic examination of the stomach and duodenum using a
special flexible endoscope (gastroscope) with the facility
to carry out a biopsy (removal of a tissue sample) and minor
surgical procedures (above all the cauterisation (haemostasis)
of bleeding from any ulcers in the stomach or duodenum, removal
of small tumours (polyps), laser therapy, etc.).
When should a gastroscopy be carried out?
- in the case of persistent discomfort of unclear origin in
the upper abdomen
- in the case of any repeated discharge of blood or anaemia
of unclear origin
- in the case of suspicion of gastric or duodenal ulcers
- in the case of gastric polyps or malignant tumours (gastric
carcinoma)
How is a Gastroscopy or Oesophagogastroduodenoscopy
carried out?
Following anaesthetisation of the mucous membrane of the throat,
a flexible endoscope is passed via the mouth, throat and oesophagus
into the stomach and duodenum. If patients wish, they can
be given a strong sedative in order that they remain largely
unaware of the procedure. The advantage of this form of examination
is that changes which indicate disease can immediately be
seen and biopsied in order to conduct a fine-tissue analysis
of the mucous membrane. Minor surgical procedures, such as
cauterisation (haemostasis) can also be carried out via the
endoscope.
2. Major Disorders
of the Stomach and Duodenum
- Gastritis
- Ulcers (gastric and duodenal
ulcers)
- Gastric and duodenal haemorrhages
- Benign and malignant tumours
- Celiac disease (non-tropical
sprue)
- Lactose intolerance
Disorder
1 Gastritis
1. Definition
Gastritis is a chronic inflammation of the mucous membrane
of the stomach. In most cases, gastritis causes no symptoms
and is simply a chance find in the course of a gastroscopy.
Many people have gastritis without being aware of it. The
commonest cause is an infection with the helicobacter pylori
bacterium. In addition, drugs such as those used to treat
rheumatism, alcohol and other chemicals can cause gastritis.
Other physical disorders (e.g. autoimmune gastritis) can cause
a chronic inflammation of the mucous membrane of the stomach.
2. Symptoms / Signs
Normally, there are no symptoms or signs.
3. Complications and Risks
Gastritis is significant because it lays the ground for subsequent
diseases such as gastric ulcers and (very occasionally) gastric
tumours.
4. Diagnosis / Preliminary Investigations
Usually, a special diagnosis is not required. In most cases
the diagnosis is made by chance during a gastroscopy.
5. Therapy / Treatment
In the case of simple gastritis, no treatment is required.
6. After-care
No after-care or follow-up examinations are required.
Disorder 2 Gastric
and Duodenal Ulcers
1. Definition and Cause
Gastric and duodenal ulcers are highly localised deep lesions
in the mucous membrane, which reach deep into the wall of
the stomach or duodenum. In most cases, ulcers are caused
by infection through the helicobacter pylori bacterium. In
addition, anti-rheumatic drugs are often the cause of gastric
ulcers and also, but to a lesser extent, duodenal ulcers.
2. Symptoms / Signs
The pain caused by ulcers consists of a dull burning sensation
which is difficult to localise, but which lies somewhere in
the middle of the upper abdomen. Sometimes the pain radiates
into the back or towards the navel. A feeling of general malaise,
nausea and vomiting can also occur as a result of ulcers.
A gastric ulcer often causes discomfort after meals, while
a duodenal ulcer is more prone to cause discomfort when the
stomach is empty.
3. Complications and Risks
Around 10% of ulcers lead to complications. The most common
complication is a haemorrhage or a perforation into the abdominal
cavity or into neighbouring organs.
4. Diagnosis
A gastroduodenoscopy is the best method of investigation as,
in addition to enabling a diagnosis to be made, certain treatments
can be carried out, such as cauterisation (haemostasis). Tissue
samples can also be taken, to assist in distinguishing between
benign and (rare) malignant ulcers. At the same time, confirmation
can be obtained as to whether a helicobacter pylori infection
is present.
5. Therapy / Treatment
Nowadays, excellent treatment is available for ulcers using
drugs which inhibit the production of gastric acid. Normally,
ulcers become pain-free within a few days and heal within
4-6 weeks. If there is a helicobacter pylori infection, a
course of antibiotics must also be taken. If the ulcers have
been caused by medication (e.g. anti-rheumatic drugs), the
patient should stop taking these, or only take them along
with medication which reduces the production of gastric acid.
6. After-care
A follow-up examination is only required in the case of a
gastric ulcer after 6 to 8 weeks, so that it is certain that
the ulcer has healed and is not malignant. However, in the
event of certain complications, occasional check-ups must
be carried out.
Disorder 3 Gastric
and Duodenal Haemorrhages
1. Definition
Haemorrhages from the oesophagus (cf.), the stomach and the
duodenum are classified as upper gastro-intestinal bleeding,
as in many cases there is also vomiting of blood.
The most common causes are:
- Gastric and duodenal ulcers
- Superficial mucositis (erosions)
- Varicose veins in the oesophagus or in the stomach (mainly
in conjunction with disorders of the liver - cf.)
- Rupture of the mucous membrane of the stomach (Mallory-Weiss
Syndrome) in the case of serious vomiting
- Tumours
- Vascular defects
- Other rarer causes
2. Symptoms / Signs
The most common symptom is the vomiting of blood, the passing
of black stools or blood in the stools. In addition, due to
anaemia, general physical weakness is experienced. Occasionally,
the only symptoms of a minor haemorrhage are anaemia and iron
deficiency.
3. Complications and Risks
Serious haemorrhages can be life-threatening, causing shock
and circulatory collapse, and leading to death.
4. Diagnosis / Preliminary Investigations
A gastroscopy is the main method of investigation, as an immediate
diagnosis can be made.
5. Therapy / Treatment
Many haemorrhages stop of their own accord. Most haemorrhages
which are still ongoing can be treated during a gastroscopy.
Very occasionally, surgical haemostasis is required. The specific
therapy to be carried out is determined by the cause of the
haemorrhage.
6. After-care
After-care is only required in serious cases. However, where
the cause is related to the helicobacter plyori bacterium,
tests must be carried out to confirm that the bacterium has
been successfully eradicated.
Disorder 4 Benign
and Malignant Tumours
1. Tumours
We distinguish between benign and malignant tumours. Examples
of benign tumours are:
- Non-adenomatous polyps
- Adenomatous polyps
Examples of malignant tumours:
- gastric carcinomas
- primary gastric lymphomas (MALT-lymphoma)
- Carcinoid tumours (Duodenum) and other rare types of tumours
such as the Gastrointestinal Stromal Tumor (GIST)
1. Gastric Polyps
Definition
A polyp is a protrusion of the tissue into the gastric cavity.
They can occur with a stem, be spherical, or be broad-based
and can vary considerably in their size. According to examination
under a microscope, they can be classified in various categories
which are significant in the treatment and prognosis.
Frequency
The proportion of benign gastric polyps in relation to all
new growths in the stomach is around 15%-20%. As one gets
older, this percentage increases. Multiple Polyps in the stomach
occur in - Polyposis-Syndrome.
- Gardner's Syndrome
- Peutz-Jeghers Syndrome
- Cronkhite-Canada Syndrome
- Juvenile polyposis
- Hereditary adenomatous polyposis
Up to 50% of patients with hereditary adenomatous polyposis
have gastric and duodenal adenomas. These have a very high
tendency to become malignant. In the other syndromes, the
development of malignancy is not so frequent.
Therapy
A distinction is made on examination under the microscope
between adenomatous and non-adenomatous polyps. Adenomas must
be completely removed due to the risk of their becoming malignant.
This is normally carried out in the course of a gastroscopy.
Larger tumours normally require the surgical partial excision
of the stomach. The removal of non-adematous polyps is optional,
as these are not expected to become malignant.
Malignant Tumours
1. Gastric Adenocarcinoma
Causes: Gastric carcinomas can be caused by a multitude of
factors. Genetic (hereditary) factors appear to play a minor
role. There is a clearer connection, however, with infections
with the helicobacter pylori bacterium, which has been discovered
to increase the risk up to sixfold. Helicobacter infections
cause microscopic injuries to the mucous membrane, and, in
the course of the repeated healing process, defective regeneration
can occur leading to the formation of a carcinoma.
Frequency
40 in every 100 000 population develop gastric carcinomas
every year. The disease is more common among men then women.
Symptoms
Gastric carcinoma is often asymptomatic for a long time, or
develops only with uncharacteristic symptoms. The most common
symptoms are: - Weight loss - Pain in the upper abdomen -
Frequent vomiting - Intolerance of food (normally meat)
Therapy and Prognosis
The preferred treatment is radical surgical removal. In the
course of the operation, the whole stomach is removed (or
in certain cases only part of the stomach) and replaced by
part of the small intestine. If it is not possible to remove
the carcinoma in full, due to a serious spread of the tumour
or metastasis, supplementary medication similar to a form
of chemotherapy is used. Where there is little spread of the
tumour, the chances of survival for 5 years or more are reckoned
to be 80%.
2. Primary Gastric Lymphoma of MALT-type
Definition Malignant lymphomas are cancer-like tumours growing
from the lymphatic tissue which is to be found in the bone
marrow, the lymph glands and almost every organ of the body
or which migrates to the relevant tissue in the course of
an inflammation or infection. The cells of this tissue, lymphocytes,
are primarily responsible for the immune defences in the body
and play a significant role in the event of inflammation or
infection. White blood cells also originate from the lymphatic
tissue. The primary gastric lymphoma of the MALT type (mucosa-associated-lymphoid-tissue)
is the most common malignant gastric lymphoma. The tumour
growth is restricted to the stomach for a considerable period
before spreading in its late stages to the lymph nodes and
other organs. The causes have yet to be clarified, but in
most cases an infection with the helicobacter pylori bacterium
(see above) is present, and it is therefore assumed that this
is a significant factor in the development of gastric lymphomas.
Symptoms and Signs
The most common symptoms are indigestion, pain in the upper
abdomen, general malaise and vomiting. Later, patients can
experience weight loss. There are no specific symptoms which
permit a clear diagnosis.
Diagnosis / Preliminary Investigations
In order to make a diagnosis, a gastroscopy and biopsy must
be carried out. The histological examination can then give
a definitive diagnosis. Where it is suspected, clarification
will also be sought as to whether a helicobacter pylori infection
is present.
Therapy / Treatment
In the early stages it is often sufficient to eradicate the
helicobacter pylori infection. After this has been done, the
lymphoma regresses. In more advanced stages, an operation,
x-ray therapy or chemotherapy will be considered.
After-care
The chances of a cure in the case of this malignant tumour
are relatively good. After successful treatment, regular follow-up
examinations by the family physician or a specialist are required.
3. Carcinoid Tumours
The carcinoid tumour is a common hormone-producing tumour
of the gastro-intestinal tract. It affects intestinal cells
which mainly produce a hormonal substance known as serotonin.
The majority of these tumours are found in the duodenum (30%),
the appendix (45%), or in the rectum (10%).
The main symptoms for patients are a sudden and recurring
feeling of heat and reddening of the face, often combined
with serious diarrhoea and tachycardia.
The clinical medical examination normally reveals nothing.
However, typical indicators are found in the laboratory analysis
of blood and urine. In order to locate the tumour, conventional
imaging procedures are used, namely abdominal x-rays, ultrasound,
CAT or MRI, at the same time locating or excluding secondary
tumours (metastases), most particularly in the liver.
In order to treat the disease, the tumour and the section
of the intestine affected must in the first place be surgically
removed. If it is not possible to do this completely because
of the spread of the tumour or metastasis, a supplementary
form of chemotherapy will be used.
Disorder 5 Celiac Disease
(Non-Tropical Sprue)
1. Definition
A disorder of the small intestine which involves atrophy of
the villi (villous flattening), digestion problems and diarrhoea
and which is caused by intolerance of gluten (gliadin), a
constituent part of certain forms of grain. Hereditary factors
are of significance in this disorder.
2. Symptoms / Signs
Most patients suffer from diarrhoea and in time experience
evident weight loss. Other symptoms include general weakness,
abdominal discomfort, signs of malnutrition, and, most particularly,
signs of vitamin deficiency.
3. Complications and Risks
The vitamin deficiency can lead to an increased tendency to
haemorrhage, which can lead to serious haemorrhages. Due to
protein deficiency, oedemas can occur in the legs. The abdomen
can become increasingly bloated. In childhood, the disorder
can also affect growth. Skin diseases can also occur. If the
disorder is left untreated for a lengthy period, malignancies
can also occur in the lymph cells (lymphoma).
4. Diagnosis / Preliminary Investigations
The most important form of examination is a duodenoscopy in
order to make a biopsy. A diagnosis can normally be made on
examining the tissue sample under the microscope. The diagnosis
can be confirmed by testing the blood for antibodies to constituent
elements of grain (gliadin or endomysium antibodies). On initial
diagnosis, an ultrasound examination of the abdomen should
be carried out to exclude a lymphoma.
5. Therapy / Treatment
Patients must avoid eating cereals (wheat, rye, oats, barley)
for the rest of their lives. They also require detailed advice
on their diet. Treatment with drugs is only required in the
event of complications.
6. After-care
Where there are no longer any symptoms, the family physician
can carry out regular follow-up examinations at fairly lengthy
intervals. If symptoms recur, the family physician or a gastro-intestinal
specialist should be contacted as soon as possible. Patients
are also recommended to join their regional/national support
group for the disease, such as the Swiss Support Group for
Celiac Disease, which regularly provide information on the
latest findings and offer advice on how to deal with the condition.
Disorder
6 Lactose Intolerance
1. Definition
Patients with lactose intolerance experience difficulties
in the digestion of lactose in the small intestine. The congenital
deficiency of lactase, an enzyme which breaks down lactose,
is known as primary lactose intolerance. Secondary lactose
intolerance occurs when another disorder of the small intestine
causes a reduction in the level of lactose. This can happen,
for example, if celiac disease goes untreated.
2. Symptoms / Signs
The most common symptoms are diarrhoea, distension, abdominal
cramps, and flatulence, most particularly after the consumption
of milk and dairy products.
3. Complications and Dangers
Symptoms of malnutrition, general malaise, weight loss
4. Diagnosis / Preliminary Investigations
If the disease is suspected, a so-called lactose tolerance
test can be carried out. The patient is given a precisely
measured amount of lactose to drink. Thereafter, the traces
of lactose in the blood are regularly measured at short intervals.
If there is no increase in these traces, this indicates that
the disease is present.
5. Therapy / Treatment
In the case of the primary form, the patient must follow a
milk and dairy product-free diet. Yoghurt and sometimes certain
varieties of cheese can however be eaten without difficulty.
In the case of the secondary form, treatment of the underlying
illness is also of fundamental importance.
6. After-care
After-care is not necessary if the symptoms do not recur.
In the case of the secondary form, following treatment of
the underlying disease, a further lactose tolerance test is
advisable.
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