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3.2. CLIMA ESCOLAR

3.2.2. CLIMA SOCIAL ESCOLAR: CONCEPTO E IMPORTANCIA

About 75.0% of early gastric carcinomas were well differentiated while the remaining 25.0% were moderately differentiated. Also about 37.2% of advanced tumours were well differentiated while 30.2% and 32.6% respectively were moderately and poorly differentiated. These findings seem to suggest a possible association between the histologic grade and depth of invasion of the tumour with most early carcinomas and a significantly smaller number of advanced carcinomas being well differentiated.

Moreover, there were no poorly differentiated early gastric carcinomas in the series.

6.7 PATTERNS OF METASTASIS

In all, a total of 37 cases were assessed. Of these, table 8 shows that 22 cases (59.5%) had lymph node metastasis while 3 cases (8.1%) had omental metastasis. There was 1 case each (2.7%) with metastasis to the liver and umbilicus. Metastasis was absent in 27.0% of cases. Neither the specific group nor the total number of lymph nodes involved in each case could be assessed. No lymph nodes were included in the tissues sent in cases which showed omental and hepatic metastases. The only case

with umbilical metastasis was a biopsy specimen Table 10 shows that a total of 21(63.6%) out of the 33 cases of advanced gastric carcinoma showed evidence of metastatic spread as opposed to 3 (75.0%) of the 4 cases of superficial carcinomas.

Eighteen cases (54.5%) of advanced carcinomas had evidence of metastasis to the peri-gastric lymph nodes while 2 cases (6.0%) and 1 case (3.0%) each showed metastasis to the omentum and liver respectively. All cases of metastasis from superficial carcinomas were to peri-gastric lymph nodes.

6.8 ASSOCIATED INCIDENTAL FINDINGS 6.8.1 Helicobacter pylori

A total of 79 (81.4%) out of the 97 cases reviewed for the study showed evidence of chronic gastritis in the surrounding, apparently non neoplastic gastric tissue. Table 9 shows that out of these 79 cases, forty-three (54.4%) had histological evidence of helicobacter pylori infection. No H. pylori was found in the absence of chronic gastritis. The association between chronic gastritis and the presence of H. pylori was found to be statistically significant with a p-value of 0.000.

6.8.1.1 H. pylori, Patients’ Age and Sex

H. pylori was detected in all age groups. Table 9 shows that H. pylori was found in 6(33.3%) of patients younger than 40 years and 37(46.8%) of those 40 years and older. It was present in 33.3% of patients in the 20-29 year age group and 30.0% of those in the 30-39 year age group. H. pylori was also found in 60.0%, 41.4% and

45.8% of patients in the 40-49, 50-59 and 60-69 year age groups respectively while it was detected only in 40.0% of those in the 70-79 year age group. It was present in the only case above 80 years old. There was, however, no significant relationship between the presence of H. pylori and the patients’ age (p=0.298).

H. pylori was found in 39.6% of males and 50.0% of females. There was also no significant relationship between the patient’s sex and the presence of H. pylori (p=0.306)

6.8.1.2 H. pylori and Histological Type of Gastric Carcinoma

Table 9 also shows that H. pylori was found in 60% of patients with diffuse carcinoma and in 41.9% of patients with the intestinal type carcinoma. However, no significant association was found between H. pylori and the Lauren’s histological type of the carcinoma (p= 0.292).

6.8.1.3 H. pylori, Gross Growth Pattern and Topography of Gastric Carcinoma According to table 9, H. pylori was found in 46.7% of excavated tumours, 39.7% of fungating types, 66.7% of ulcerative tumours and 66.7% of diffusely infiltrating tumours. However, there was no significant association between the gross growth pattern of the tumours and the presence of H. pylori (p=0.494).

It was also found in 45.7% of antro-pyloric tumours, 25.0% of cardia tumours, 42.9% of corporal tumours and 40.0% of fundal tumours. There was no significant

association between the topographical location of the tumours and the presence of H. pylori (p=0.871).

6.8.2 Gastric Glandular Atrophy

Table 10 shows the pattern of gastric glandular atrophy in patients with gastric carcinoma. Seventeen (21.5%) patients had gastric atrophy in the presence of chronic gastritis. On the other hand there were no cases of gastric atrophy in the absence of chronic gastritis.

6.8.2.1 Age of Patients and Occurrence of Gastric Atrophy

Gastric atrophy was found only in patients 40 years and older, occurring in 17(21.5%) of such cases (p=0.03). Gastric atrophy was found in 2(11.8%) cases in the 40-49 year age-group and 4(23.5%) cases in the 50-59 year age-group. The highest number of cases was found in the 60-69 year age-group with 6(35.3%) cases while there were 5(29.4%) cases in the 70-79 year age-group. There was only one case (5.9%) of mild atrophy. Moderate and severe atrophy each accounted for 11(64.7%) and 5(29.4%) cases respectively (figure 4).

6.8.2.2 Gastric Atrophy, Chronic Gastritis, Histological Type and Topography of Gastric Carcinoma

Table 10 shows that glandular atrophy was found in 24.6% of intestinal-type tumours and none of the diffuse type tumours (p=0.268). Glandular atrophy was also found in 19.8% of antro-pyloric tumours, 25.0% of fundal tumours and none of

cardia or corporal tumours. Glandular atrophy was found in 17 patients (21.5%) with gastritis but not in the absence of gastritis. The association between gastric glandular atrophy and chronic gastritis was also found to be statistically significant with a p-value of 0.03.

6.8.3 Intestinal Metaplasia

Table 11 shows the pattern of intestinal metaplasia in patients with gastric carcinoma. Thirty-seven patients (46.8%) with evidence of chronic gastritis had intestinal metaplasia while only one patient (5.6%) had intestinal metaplasia in the absence of any histological evidence of chronic gastritis (p=0.001).

6.8.3.1 Age and Occurrence of Intestinal Metaplasia

Table 11 shows that intestinal metaplasia was present only in 2 patients (11.1%) younger than 40 years but in 36 patients (45.6%) older than 40 years with a p value of 0.007. Figure 5 also shows the age distribution of intestinal metaplasia with 2 cases in the 30-39 year age-group and 6 cases in the 40-49 year age-group. Intestinal metaplasia was not found in patients younger than 30 years of age. The 50-59 year age-group had the highest frequency with 12 cases while there were 8 and 9 cases respectively in the 60-69 and 70-79 year age-groups respectively. It was present in the only case in the 80-100 year age-group. Both cases in the 30-39 year age-group were complete intestinal metaplasia. However, with advancing age the frequency of incomplete metaplasia increases accounting for more than 50% of the cases in each age-group.

6.8.3.2 Intestinal Metaplasia, Chronic Gastritis, Histological Type and Topography of Gastric Carcinoma.

According to table 11 intestinal metaplasia was found in only 30% of diffuse carcinomas and 40.7% of intestinal-type tumours (p=0.582). Intestinal metaplasia was also found in 40.7% of antropyloric tumours, 42.9% of corporal tumours, 66.7%

of fundal tumours and none of cardia tumours (p=0.440). Thirty-seven patients (46.8%) with associated gastritis and only 1 patient (5.6%) without chronic gastritis had evidence of intestinal metaplasia (p=0.001).

Although each of these associated incidental findings do not individually show any significant association with Lauren’s histological type of gastric carcinoma, logistic regression analysis, however, shows a significant relationship between gastric carcinoma of Lauren’s type and the presence of H. pylori, chronic gastritis, gastric atrophy and intestinal metaplasia, with a value of 0.000 (p<0.0001).

TABLE 1: AGE AND SEX DISTRIBUTION OF PATIENTS WITH GASTRIC CARCINOMA

AGE GROUP SEX TOTAL (%)

MALE FEMALE

20-29 2 (66.7) 1 (33.3) 3 (3.1)

30-39 4 (40.0) 6 (60.0) 10 (10.3)

40-49 9 (60.0) 6 (40.0) 15 (15.5)

50-59 17 (58.6) 12 (41.4) 29 (29.9)

60-69 13 (54.2) 11 (45.8) 24 (24.7)

70-79 8 (53.3) 7 (46.7) 15 (15.5)

80-100 0 (0.0) 1 (100.0) 1 (1.0)

TOTAL 53 (54.6) 44 (45.4) 97 (100.0)

P=0.855

TABLE 2: TOPOGRAPHICAL DISTRIBUTION OF GASTRIC CARCINOMAS WITHIN THE STOMACH.

GROSS TOPOGRAPHY TOTAL

(%) ANTRUM

(%)

CARDIA (%)

CORPUS (%)

FUNDUS (%)

TYPE I 53(65.4) 1(25.0) 2(28.6) 2(40.0) 58(59.8)

TYPE II 21(25.9) 2(50.0) 5(71.4) 2(40.0) 30(30.9)

TYPE III 5(6.2) 0(0.0) 0(0.0) 1(20.0) 6(6.2)

TYPE IV 2(2.5) 1(25.0) 0(0.0) 0(0.0) 3(3.1)

TOTAL 81(83.5) 4(4.1) 7(7.2) 5(5.2) 97(100.0)

P=0.056

TABLE 3: GROSS MACROSCOPIC GROWTH PATTERNS OF GASTRIC CARCINOMA (BORRMAN’S CLASSIFICATION)

AGE-GROUP

GROSS GROWTH PATTERN

TOTAL (%) FUNGATING

(TYPE I) (%) EXCAVATED (TYPE II) (%) ULCERATIVE (TYPEIII) (%)

DIFFUSELY INFILTRATG (TYPEIV) (%)

20-29

1(50.0) 1(50.0) 0(0.0) 0(0.0) 2(5.4) 30-39

3(75.0) 0(0.0) 0(0.0) 1(25.0) 4(10.8) 40-49

2(33.3) 3(50.0) 1(16.7) 0(0.0) 6(16.2)

50-59

5(45.5) 6(54.5) 0(0.0) 0(0.0) 11(29.7) 60-69

4(50.0) 3(37.5) 0(0.0) 1(12.5) 8(21.6) 70-79

4(66.7) 2(33.3) 0(0.0) 0(0.0) 6(16.2)

TOTAL 19(51.4) 15(40.5) 1(2.7) 2(5.4) 37(100.0)

P=0.928

TABLE 4: HISTOLOGICAL TYPES OF GASTRIC CARCINOMA (WHO)

AGE-GROUP

WHO

TOTAL

MUCINOUS (%)

(%) PAPILLARY(%) SIGNET RING (%) TUBULAR(%) 20-29

0(0.0) 0(0.0) 1(33.3) 2(66.7) 3(3.1) 30-39

0(0.0) 2(20.0) 0(0.0) 8(80.0) 10(10.3) 40-49

0(0.0) 2(13.3) 0(0.0) 13(86.7) 15(15.50

50-59

5(17.2) 3(10.3) 4(13.8) 17(58.7) 29(29.9) 60-69

2(8.3) 0(0.0) 5(20.8) 17(70.8) 24(24.7) 70-79

4(26.7) 2(13.3) 0(0.0) 9(60.0) 15(15.5) 80-100

0(0.0) 0(0.0) 0(0.0) 1(100.0) 1(1.0)

TOTAL 11(11.3) 9(9.3) 10(10.3) 67(69.1) 97(100.0)

P=0.223

TABLE 5: HISTOLOGICAL TYPES OF GASTRIC CARCINOMA (LAUREN)

AGE GROUP

LAUREN

TOTAL (%)

DIFFUSE(%) INTESTINAL (%) MIXED(%)

20-29

1(33.3) 2(66.7) 0(0.0) 3(3.1)

30-39

0(0.0) 10(100.0) 0(0.0) 10(10.3) 40-49

0(0.0) 15(100.0) 0(0.0) 15(15.5)

50-59

4(13.8) 24(82.8) 1(3.4) 29(29.9) 60-69

5(20.8) 19(79.2) 0(0.0) 24(24.7) 70-79

0(0.0) 15(100.0) 0(0.0) 15(15.5) 80-100

0(0.0) 1(100.0) 0(0.0) 1(1.0)

TOTAL 10(10.3) 86(88.7) 1(1.0) 97(100.0)

P=0.434

FIGURE 1: SEX DISTRIBUTION OF GASTRIC CARCINOMA ACCORDING TO LAUREN’S SCHEME

mixed intestinal

diffuse

Lauren

50

40

30

20

10

0

frequency

female male

Sex

P=0.512

FIGURE 2: GROWTH PATTERNS OF GASTRIC CARCINOMA OF LAUREN’S TYPE

mixed intestinal

diffuse

Lauren

50

40

30

20

10

0

frequency

ulcerative schirrous fungating excavated Gross

P=0.709

FIGURE 3: LOCATION OF GASTRIC CARCINOMA OF LAUREN’S TYPE

mixed intestinal

diffuse

Lauren

80

60

40

20

0

frequency

fundus corpus cardia antrum Location

P=0.964

TABLE 6: HISTOLOGICAL DIFFERENTIATION OF GASTRIC CARCINOMA

AGE-GROUP

DIFFERENTIATION

TOTAL (%)

WELL(%) MODERATE (%) POOR(%)

20-29

1(33.3) 1(33.3) 1(33.3) 3(3.1) 30-39

4(40.0) 3(30.0) 3(30.0) 10(10.3) 40-49

8(53.3) 1(6.7) 6(40.0) 15(15.5) 50-59

10(34.5) 10(34.5) 9(31.0) 29(29.9) 60-69

11(45.8) 7(29.2) 6(25.0) 24(24.7) 70-79

5(33.3) 8(53.3) 2(13.3) 15(15.5) 80-100

1(100.0) 0(0.0) 0(0.0) 1(1.0)

TOTAL 40(40.3) 30(30.9) 27(27.8) 97(100.0)

P=0.592

TABLE 7: DEPTH OF INVASION OF THE STOMACH WALL BY GASTRIC CARCINOMA

GROSS

DEPTH

TOTAL (%) SUPERFICIAL

(%)

ADVANCED (%)

TYPE I

1(3.7) 26(96.3) 27(57.5)

TYPE II

2(12.5) 14(87.5) 16(34.0)

TYPE III

1(100.0) 0(0.0) 1(2.1)

TYPE IV

0(0.0) 3(100.0) 3(6.4)

TOTAL 4(8.5) 43(91.5) 47(100.0)

P=0.007

TABLE 8: PATTERN OF METASTASIS ACCORDING TO DEPTH OF TUMOUR INVASION

METASTATIC SITE

DEPTH

TOTAL (%)

SUPERFICIAL

(%) ADVANCED (%)

ABSENT

1(25.0) 12(36.4) 13(35.1) LIVER

0(0.0) 1(3.0) 1(2.7)

LYMPH

NODE 3(75.0) 18(54.5) 21(56.8)

OMENTUM

0(0.0) 2(6.0) 2(5.4)

TOTAL

4(10.8) 33(89.2) 37(100.0)

P=0.860

TABLE 9: PATTERN OF HELICOBACTER-LIKE ORGANISMS (HLO) ACCORDING TO SOME VARIABLES

HLO

Present Absent Total X2 P value

AGE

< 40 years

>40years 6(33.3)

37(46.8) 12(66.7)

42(53.2) 18

79 1.083 0.298

SEX

Male

Female 21(39.6)

22(50.0) 32(60.4)

22(50.0) 53

44 1.049 0.306

GROSS

Type I Type II Type III Type IV

23(39.7) 14(46.7) 4(66.7) 2(66.7)

35(60.3) 16(53.3) 2(33.3) 1(33.3)

58 30 6 3

2.400 0.494

HISTOLOGY

Diffuse Intestinal Mixed

6(60.0) 36(41.9) 1(100.0)

4(40.0) 50(58.1) 0(0.00)

10 86 1

2.463 0.292

TOPOGRAPHY

Antrum Cardia Corpus Fundus

37(45.7) 1(25.0) 3(42.9) 2(40.0)

44(54.3) 3(75.0) 4(57.1) 3(60.0)

81 4 7 5

0.709 0.871

GASTRITIS

Present

Absent 43(54.4)

0(0.0) 36(45.6)

18(100.0) 79

18 17.599 0.000

TABLE 10: PATTERN OF GASTRIC GLANDULAR ATROPHY ACCORDING TO SOME VARIABLES

ATROPHY

Present Absent Total X2 P value

AGE

< 40 years

>40years 0(0.0)

17(21.5) 18(100.0)

62(78.5) 18

79 4.697 0.03

SEX

Male

Female 7(13.2)

10(22.7) 46(86.8)

34(77.3) 53

44 1.507 0.220

GROSS

Type I Type II Type III Type IV

10(17.2) 4(13.3) 3(50.0) 0(0.0)

48(828) 26(86.7) 3(50.0) 3(100.0)

58 30 6 3

5.383 0.146

HISTOLOGY

Diffuse Intestinal Mixed

0(0.0) 17(19.8) 0(0.0)

10(100.0) 69(80.2) 1(100.0)

10 86 1

2.636 0.268

TOPOGRAPHY

Antrum Cardia Corpus Fundus

16(19.8) 0(0.0) 0(0.0) 1(20.0)

65(80.2) 4(100.0) 7(100.0) 4(80.0)

81 4 7 5

2.637 0.451

GASTRITIS

Present

Absent 17(21.5)

0(0.0) 62(78.5)

18(100.0) 79

18 4.697 0.030

TABLE 11: PATTERN OF INTESTINAL METAPLASIA ACCORDING TO SOME VARIABLES

INTESTINAL METAPLASIA

Present Absent Total X2 P value

AGE

< 40 years

>40years 2(11.1)

36(45.6) 16(88.9)

43(54.4) 18

79 7.305 0.007

SEX

Male

Female 20(37.7)

18(40.9) 33(62.3)

26(59.1) 53

44 0.102 0.750

GROSS

Type I Type II Type III Type IV

25(43.1) 11(36.7) 2(33.3) 0(0.0)

33(56.9) 19(63.3) 4(66.7) 3(100.0)

58 30 6 3

2.473 0.480

HISTOLOGY

Diffuse Intestinal Mixed

3(30.0) 35(40.7) 0(0.0)

7(70.0) 51(59.3) 1(100.0)

10 86 1

1.081 0.582

TOPOGRAPHY

Antrum Cardia Corpus Fundus

33(40.7) 0(0.0) 3(42.9) 2(40.0)

48(59.3) 4(100.0) 4(57.1) 3(60.0)

81 4 7 5

2.701 0.440

GASTRITIS

Present

Absent 37(46.8)

1(5.6) 42(53.2)

17(94.4) 79

18 10.484 0.001

FIGURE 4: DISTRIBUTION OF GASTRIC GLANDULAR ATROPHY AMONG THE DIFFERENT AGE GROUPS

80-100 70-79

60-69 50-59

40-49 30-39

20-29

Agegroup

25

20

15

10

5

0

frequency

severe moderate mild absent Atrophy

P=0.876

FIGURE 5: PATTERN OF INTESTINAL METAPLASIA AMONG THE DIFFERENT AGE GROUPS.