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Stomach Cancer
Stomach Cancer
SURGICAL ANATOMY
SURGICAL ANATOMY
INTRODUCTION
The stomach functions as:
Posterior vagus gives criminal nerves of Grassi, which supply lower oesophagus and fundus of stomach, which, if not cut properly during
vagotomy, may lead to recurrent ulcer.
Vagus also gives splanchnic branches (hepatic and coeliac branches), ends as nerve of Latarjet which supplies the antrum and maintains the antral
pump.
Parietal branches help in HCl secretion, which is an important concept in vagotomy that is done as a treatment in duodenal ulcer.
Truncal vagotomy with posterior gastrojejunostomy is done for chronic duodenal ulcer with pyloric stenosis.
Highly selective vagotomy (HSV) is done in case of uncomplicated chronic duodenal ulcer which is not responding to available medical line of
treatment.
In HSV, nerve of Latarjet is retained so as to retain antral pump and no drainage is required. Here only the fibres entering the stomach are ligated
close to the lesser curve to reduce the acid secretion.
In selective vagotomy splanchnic branches are retained but it is presently not done.
LYMPHATICS
The stomach is divided into four lymphatic territories as follows:
First, divide the stomach into right two-third and left one-third by a line along its long axis. Now divide the right two-third into upper two-third (area 1) and lower one-third (area
4), and left one-third into upper one-third (area 3) and lower two-third (area 2).
Area 1 is the largest area along the lesser curvature. The lymph from this area is drained into left gastric lymph nodes along the left gastric artery. These lymph nodes also drain
the abdominal part of the esophagus.
Area 2 includes the pyloric antrum and pyloric canal along the greater curvature of the stomach. (The carcinoma of the stomach most frequently occurs in this area.) The lymph
from this area is drained into right gastroepiploic lymph nodes along the right gastroepiploic artery and pyloric nodes, which lie in the angle between the first and second parts
of the duodenum.
Area 3 (also called pancreaticosplenic area) drains into pancreaticosplenic (pancreaticolienal) nodes along the splenic artery.
Area 4 includes the pyloric antrum and pyloric canal along the lesser curvature of the stomach. The lymph from this area is drained into right gastric nodes along the right
gastric artery and hepatic nodes along the hepatic artery.
The efferents from all these lymph node groups pass to the coeliac nodes.
Efferents from coeliac nodes enter the cysterna chyli through intestinal lymph trunk.
Gastric carcinoma: It commonly occurs in the region of pyloric antrum along the greater curvature of the stomach. The gastric cancer spreads by
lymph vessels to the left supraclavicular lymph nodes. The enlarged and palpable left supraclavicular node (Virchow’s node) may be the first sign of
gastric cancer (Troisier’s sign). The cancer cells reach the left supraclavicular lymph node through the thoracic duct.
HISTOLOGY
The gastric epithelial cells are mucus producing and are turned over rapidly. In the pyloric part of the stomach, and also
the duodenum, mucus-secreting glands are found.Most of the specialised cells of the stomach (parietal and chief cells) are
found in the gastric crypts. The stom- ach also has numerous endocrine cells.
PARIETAL CELLS
These are in the body (acid-secreting portion) of the stomach and line the gastric crypts, being more abundant distally.
They are responsible for the production of hydrogen ions to form hydrochloric acid. The hydrogen ions are actively
secreted by the proton pump, a hydrogen–potassium-ATPase (Sachs), which exchanges intraluminal potassium for
hydrogen ions. The potassium ions enter the lumen of the crypts passively, but the hydrogen ions are pumped against an
immense con- centration gradient (1 000 000:1).
CHIEF CELLS
These lie principally proximally in the gastric crypts and produce pepsinogen. Two forms of pepsinogen are described:
pepsinogen I and pepsinogen II. Both are produced by the chief cell, but pepsinogen I is produced only in the stomach. The
ratio between pepsinogens I and II in the serum decreases with gastric atrophy. Pepsinogen is activated in the stomach to
produce the digestive protease, pepsin.
ENDOCRINE CELLS
The stomach has numerous endocrine cells, which are critical to its function. In the gastric antrum, the mucosa contains G
cells, which produce gastrin. Throughout the body of the stomach, enterochromaffin-like (ECL) cells are abundant and
produce histamine, a key factor in driving gastric acid secre- tion. In addition, there are large numbers of
somatostatinproducing D cells throughout the stomach, and somatostatin has a negative regulatory role. The peptides and
neuropep- tides produced in the stomach are discussed later.
AETIOLOGY
1.ENVIRONMENTAL/OCCUPATIONAL/DIET/HABITS
*Smoking/alcohol/obesity
*Low vegetable diet,diet with low vit A and C
*Consuming red meat ,smoked salmon fish,cabbage, diet rich in nitrosamines, lead
*Viral infections like EBV virus
*occupational-Rubber/coal wrkers
2.PRECANCEROUS LESION
*H.pylori infection,chronic gastritis
*Pernicious anemia
*Intestinal metaplasia
*Adenomatous polyps
*Bening gastric ulcer
*Previous gastric surgeries
3.GENETIC AND FAMILIAL
*Mutation in E –CADHERIN and APC gene
*Inactivation of tumor suppressor gene p53
*Loss of heterozygosity in BCL2 gene
*HNPCC carriers
*Li Fraumen syndrome
*Blood group A
*Monozygotic twins carry more risk than dizygotic twins
*When both parents have gastric cancer,the sibbiling are at a risk of diffuse proximal
gastric ulcer
*Mutation of H –ras oncogene and over expression of c- cerb B2 gene
PATHOLOGY
Intestinal metaplasia
Dysplasia
ATROPHIC GASTRITIS
Cancer stomach
PATHWAYS OF SPREAD
PROGNOSTIC FACTORS
CLINICAL FEATURES:
Most Patients present with advanced stage because they are no early specific signs and symptoms.
Symptoms:
Recent onset of loss appetite and weight
early satiety fatigue
Dyspepsia
Epigastric discomfort
upper abdominal pain (non radiating)
haematemesis, Melaena
SPECIFIC SYMPTOMS DEPEND ON SITE OF TUMOUR
Krukenberg tumors
Irish node ( enlarged axillary node )
Cutaneous secondaries
INVESTIGATIONS
FLEXIBLE ENDOSCOPY
CONTRAST RADIOLOGY
ULTRASONOGRAPHY(ENDOSCOPIC USG)
CT & MRI
PET – CT
LAPAROSCOPY
TO CONFIRM THE DIAGNOSIS
Flexible upper GI Endoscopy with directed
biopsy followed by histopathological
examination of the sample
Flexible Upper GI Endoscopy
EGD(esophago gastro duodenoscopy)
Visual examination of the upper intestinal tract using a lighted, flexible fiberoptic or
video endoscope
Gold standard
More sensitive than conventional radiology (95% accuracy)
Advantages
- outpatient procedure
- no radiation exposure
- targeted biopsy form the lesion can be taken at the same setting
- diagnosis can be made more accurately
INDICATIONS
Ulcers in the upper GI tract
Tumours of the stomach or oesophagus
Severe/persistent Dysphagia
Undiagnosed upper abdominal pain or indigestion
Intestinal bleeding
Esophagitis and heartburn – unresponsive to medical therapy
Gastritis
CONTRAINDICATIONS
Shock
Acute MI
Peritonitis
Acute perforation
Corrosive injuries of oesophagus
IF YOU SEE ULCER ASK YOURSELF BENIGN OR MALIGNANT
BENIGN MALIGNANT
Round to oval punched Irregular outline with
out lesion with straight necrotic or haemorrhagic
walls and flat smooth base base
Smooth margins with Irregular and raised margins
normal surrounding
mucosa Anywhere
Mostly on lesser curvature Any size
Majority <2cm Prominent and oedematous
Normal adjoining rugal rugal folds that usually do
folds that extend to the not extend to the margins
margins of the base
Contrast Radiology
Single contrast/ Double contrast
Barium meal
Advantages
- sensitivity comparable to endoscopy
- Non invasive procedure
FINDINGS IN CARCINOMA STOMACH