Pathological differences between forceps biopsy specimens and endoscopic resection specimens in early gastric cancer patients

Article information

Kosin Med J. 2014;29(2):117-124
Publication date (electronic) : 2014 December 18
doi : https://doi.org/10.7180/kmj.2014.29.2.117
1Department of Internal Medicine, Eulji University Hospital, Daejon, Korea
Corresponding Author : Sae Hee Kim, Department of Internal Medicine, Eulji University Hospital, 1306, Dunsan-dong, Seo-gu, Daejeon, 302-799, Korea TEL: +82-42-611-3065 FAX: +82-42-611-3947 E-mail: cozy129@eulji.ac.kr
Received 2013 August 20; 2013 November 21; Accepted 2013 December 16.

Abstract

Abstract

Objective:

Endoscopic resection(ER) is effective therapy on EGC and which is treated according to the histological diagnosis of forcep biopsy. But sometimes the histological diagnosis of forcep biopsy and post-ER does not match with each other and it might lead to wrong treatment. The aim of this study is to find the frequency of histologic differences between forcep biopsy and post-ER, and to confirm the characteristics of lesions which make errors.

Methods:

We selected the confirmed cancer cases of 141 patients of 1359 gastric tumor lesions which were treated under the ER in Eulji university hospital from May 2005 to March 2013. They were sorted by the age and sex of patient, location of lesion, present of ulcer and depression to identify the discordance between forcep biopsy and ER. The discordant group was compared with non-cancer-diagnosed controlled group, retrospectively.

Results:

70 cases(5.5%) of 1283 cases of “cancer negative” in forceps biopsy were fo䴸nd to be diagnosed cancer on final diagnosis of cancer by post-ER result. In this discordant group showed characteristics of bigger size that are with more frequently in tumor size D15mm(17.9% vs. 31.4%, p=0.03), have depressed lesion(ᄀ 4.3% vs. 41.4%, p<0.01) and have 䴸lceration(2.4% vs.18.6%, p<0.01) than that of 84 control gro䴸p not diagnosed cancer.

Conclusions:

In cases of tumor with size D15mm, presented with depressed lesion and ulceration, we should consider combined cancer, even the result of forcep biopsy was negative. Therefore, more careful and accurate resection should be taken with characters listed above.

Clinicopatholgical characteristics of the study subjects

Pathological differences between forceps biopsy specimens and endoscopic resection specimens

Analysis of the Predictable Factors of Pathological Differences between Non-cancer and Cancer after Endoscopic Resection

Analysis of the Predictable Factors of Pathological Differences between Non- Poorlv Differentiated and Poorly Differentiated after Endoscopic Resection

References

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Article information Continued

Table 1.

Clinicopatholgical characteristics of the study subjects

Clinicopatholgical characteristics of 137 patients (141 lesions)
Age, years, median (range) 67 (41-89)
Sex, Male/Fcmale (%) 100/37 (73.0/27.0)
Lociition, n (%)  
  Upper (cardia, fundus, upper body) 12(8.5)
  Mid (mid body, lower body, angle) 51 (36.2)
  Lower (antrum, pylorus) 78 (55.3)
Lesion diameter, mm, median (range) 10(1-50)
Gross lypc, n (%)  
  Protruded 11 (7.8)
  Flat elevated 20(14.2)
  Flat 32 (22.7)
  Flat depressed 30 (21.3)
  Depressed or Ulcerative 4 (2.8)
  Combined 44 (31.2)
Biopsy pathology, group classification, n (%)  
  Non-adenomatous neoplasm 5 (3.5)
  Adeoma & CIS 65 (46.1)
  Adenocarcinoma & other cancers 71 (50.4)
Histological type of cancer, forceps biopsy, n (%)  
  WD 42 (59.2)
  MD 23 (32.4)
  PD 4(5.6)
  Other cancers (carcinoid tumor, mucinous carcinoma) 2(2.8)
Endoscopic resection method, n (%)  
  Endoscopic mucosal resection 27(19.1)
  Endoscopic submucosal dissection 114 (80,9)

CIS, carcinoma in situ: WD, well differentiated; MD, moderate differentiated; PD. poorly differentiated;

EMR, endoscopic mucosal resection; ESD, endoscopic submucosal dissection.

Table 2.

Pathological differences between forceps biopsy specimens and endoscopic resection specimens

Forceps biopsy specimens Endoscopic resection specimens
  Non- adenomatous neoplasm Adenoma&CIS Adenocarcinoma Other cancers
WD MD PD
Non-adenomatous neoplasm (n=5) - - 1 1 1 2
Adenoma & CIS(n=65) - - 46 14 4 i
Adenocarcinoma (n 二 69) WD (n=42) 0 6 24 10 2 0
MD (n-23) 0 1 6 14 2 0
PD (n=4) 0 0 0 0 4 0
Other cancers (n=2) 0 0 0 0 0 2

CIS, carcinoma in situ; WD, well differentiated; MD, moderate differentiated; PD, poorly differentiated.

Table 3.

Analysis of the Predictable Factors of Pathological Differences between Non-cancer and Cancer after Endoscopic Resection

  Endoscopic resection specimens P-value
Non-cancer (n=84) Cancer (n=70)
Age      
  <65 50 (59.5%) 36 (51.4%) 0.16
  ≧ 65 34 (40.5%) 34 (48.6%)  
Sex      
  Male 60(71.4%) 49 (70.0%) 0.42
  Female 24 (28.6%) 21 (30.0%)  
Location      
  Upper 5 (6.0%) 7(10.0%) 0.18
  Mid 27(32.1%) 29 (41.4%) 0,12
  Lower 52(61.9%) 34 (48.6%) 0.05
Tumor size      
  <15 69(82.1%) 48 (68.6%) 0.03
  ≧ 15 15 (17.9%) 22 (31.4%)  
Depression      
  Present 12(14.3%) 29 (41.4%) <0,01
  Absent 72 (S5.7%) 41 (58.6%)  
Ulceration      
  Present 2 (2.4%) 13 (18.6%) <0.01
  Absent 82 (87.6%) 57(81.4%)  

Table 4.

Analysis of the Predictable Factors of Pathological Differences between Non- Poorlv Differentiated and Poorly Differentiated after Endoscopic Resection

  Endoscopic resection specimens P-value
Non-PD (n= 23) PD (n=9)
Age      
  <65 52 (42.3%) 2 (22.2%) 0.08
  ≧ 65 71 (57.7%) 7 (77.8%)  
Sex      
  Male 91 (74.0%) 6 (66.7%) 0.33
  Female 32 (26.0%) 3 (33.3%)  
Location      
  Upper 10(8,1%) 0 (0%)  
  Mid 43 (35.0%) 6 (66.7%) 0.03
  Lower 70 (56.9%) 3 (33.3%) 0,07
Tumor size      
  <15 81 (65.9%) 6 (66.7%) 0.48
  ≧15 42 (34.1%) 3 (33.3%)  
Depression      
  Present 62 (50.4%) 6 (66.6%) 0.16
  Absent 6i (49.6%) 3 (33.3%)  
Ulceration      
  Present 32 (26.0%) 2 (22.2%) 0.40
  Absent 91 (74.0%) 7 (77.8%)  

PD, poorly differentiated