BackgroundColorectal cancer takes the second place in the highly developed countries morbidity increases, for females it takes place after breast cancer, for males after lung cancer colorectal cancer occupies about 3-5% from the cancer of digestive tract. In the western Europe, united states of America it occuries 12.6% on males and 14% on females, for Pathological structure it occurs mostly in the proximal part and adenocarcinoma is diagnosed 95%. Colorectal carcinoma occurs more at the age of 20-40 but people aged 40-50 are mostly affected and males are affected more. Lately it has tendency of increasing amond the population 40-120 case on 100000 in a year approximately 5-10 people are affected newly. For our country by health statistical information colon cancer was 94 from it 49 occur on females, cancer of rectal and anus canal was 237, from it 99 occur on females, 37 case of colorectal cancer are registered newly in a year approximately, 19 occurs on females cancer of rectal and anus canal was 45 from them 16 are registered newly on females the number of patients with colorectal cancer has tendency of increasing. Among Mongolian population morbidity of colorectal cancer is increasing nowadays but any research has not been done to reveal pathology early and to diagnose. This became base of our research work.GoalAim of our study is to define peculiarity of colorectal cancer and its early pathology and to study some factor of aetiology connectea with cancer forming.Objectives:1. To define peculiarity of pathology of colorectal cancer.2. To diagnose early pathology of colorectal cancer by pathological method.3. To diagnose colorectal carcinoma by international histological classification and determine cell secretion degree.4. To define some genetic peculiarity of factors which affects to colorectal carcinoma.Novelty of research workNovelty of research work is to study colorectal carcinoma and its early pathology in combination with the method of endoscopy and molecular biology.Materials and MethodsIn the research 315 biopsy material of 142 patients with colorectal carcinoma of 2004-2008, 56 biopsy material of colorectal endoscopy of 2007-2008 are involved.1. Histological basic painting method.2. Method of molecular biology. We revealed affect of human papilloma virus infection in 39 surgical and endoscopyic material by using general GP5, GP6, MY11 primer in PSR.ResultsIn our study totally 198 people were involved from them (average age 45.8+ - 0.4), 46.0%(n=91)-male, 54% (n=107) female. If we see people involved in the study by age classification, 8 (5.9%) at the age of 20-29, 21 (10.3%) at the age of 30-39, 39 (19.3%) at the age of 40-49,45 (22.4%) at the age of 50-59, 56 (27.7%) at the age of 60-69, over 70-79 (14.3%). If we see colorectal carcinoma by anatomical location most location was in 45 (22.7%) in sigma, 52 (26.2%) in rectus. Seeing from endoscopic biopsy analyse pathology which involved whole colorectus occupied 10 (35.6%). By international histological classification of cancer which was adopted from WHO. In our study polyp occupies 21 (10.6%), adenoma 24(12.1%), adenocarcinoma 137 (69.2%), metastatic carcinoma 6 (3%), chronic inflammation or with change dysplasia 10 (5.1%). If we see endoscopic biopsy analyse it is 56 (28.3%) of people involved in the research. Hyper plastic polyp 21 (36.1%), adenoma 6 (25%), adenomatous polyp 8 (33.3%) occupces, Tubular adenoma polyp 7 (29.2%), villous adenoma 3 (12.5%) from carcinoma adenomatous carcinoma occupces 98 (71.5%), mucous carcinoma 7 (5.1%), carcinoma with flat cell 8 (5.8%), carcinoma with ring cell 5 (5.1%), carcinoma witout secretion 13 (9.5%), carcinoma with metastases 6 (4.3%), one of factors of etiology which affects to colorectal carcinoma is human papilloma virus. In the biopsy material of surgery and endoscope involved in the research it reveals negative in sensitive primer which reveals all the type of papilloma virus.Conclusions:1. Colorectal carcinoma occurs 19.3% at the age of 40-49, 22.4% at the age of 50-59, 27.7% at the age of 60-69, it has tendency of increasing rohen age becomes older. It occurs 14% over 70.2. By location of anatomy colorectal carcinoma it occupies 50-60% in sigma and rectus.3. Noncarcinomous polyp of colorectal carcinoma is situated in many parts of intestine carcinoma with many polyp occupies 35.6%of total carcinoma.4. By histological classification mostly carcinomous and noncarcinomous carcinoma of epithel and adenomous cell originated occupy.5. Papilloma virus hasn’t been releaved in the sample endoscopic sample.

BACKGROUND OF STUDY: Adenocarcinoma cancer is the most common cancer in the world and the gastric happens rare however gastric neuroendocrine carcinoma is one of the leading causes of cancer death in the world and its pathogenesis and pathology diagnosis haven’t been not studied well. Our study is based on it. AIMS: 1.To determine by age and sex the 70 adenocarcinoma cases which diagnosed by endoscope at the National Cancer Center of Mongolia in 2013-2016 and to diagnose histology method of WHO. 2. To study the gastric cancer in pathology department by immunohistochemistry. MATERIAL AND METHODOLOGY: We worked on 70 patients with gastric cancer in 4th department at the National Cancer Center of Mongolia from 2013 until 2016. RESULT OF STUDY: We determined 70 patients with gastric cancer and of the 70 patients which diagnosed by pathology and immunohistochemistry 35 cases were 50.0% (Adenocarcinoma), 15 cases were 21.4% (gastric neuroendocrinecarcinoma), 2 cases were 2.9% (GIST-gastrointestinalstromal tumor), and 18 cases 25.7% (dysplasia). By sex of the 70 patients 39 cases 56% were males, 31 cases 44% were females and by age 17 cases 24.29% were 51-60 years old, 24 cases 34.29% were 61-70 years old. This results is shown the early 40 years old people has the great risk of this cancer. CONCLUSION: In our study 35 CD56 specific tissues were diagnosed by Ki67 markers and of them 15 cases were gastric neuroendocrine carcinoma and 18 cases were dysplasia determined.

: Background: According to the statistics, Gastrointestinal disorders (GIDs) are the second of the leading five diseases among Mongolians, with an estimated 20% of GIDs by pathological diagnosis in 2022. Additionally, esophageal adenocarcinoma is ranked in the 4^th of the 10 most common cancer. Esophageal adenocarcinoma and its predispositions, and pathological changes are mostly located lower part of esophagus. Barret’s esophagus (BE) is consequences of goblet cell replaces the stratified squamous epithelium due to chronic gastroesophageal reflux disease. If BE transfers to the dysplasia, its probability of carcinogenesis is 30-125 times higher, and 0.8% of dysplastic patients with BE diagnosed with esophageal adenocarcinoma. Pathologists play a critical role in confirming the diagnosis of BE and BE-associated dysplasia. Goblet cells are almost always identifiable on routine hematoxylin and eosin-stained sections with Alcian blue (at pH 2.5). Purpose: To diagnose the esophageal biopsies via pathological immunohistochemical assay. Methods and materials: We investigated 130 biopsies in 2017-2019 years from NFCH, and 254 biopsies in SSCH. Result A total of 384 biopsies were collected from both national central hospitals and hematoxylin and eosin-stained results were Barret’s esophagus (50 biopsy or 13%), followed by dysplasia (66 or 17%), GERD (55 or 14%), squamous cell carcinoma (49 or 13%), chronic erosive lesions (41 or 11%), chronic esophagitis (40 or 10%), polyp (19 or 5%), adenocarcinoma (15 or 4%), acute esophageal erosion (5 or 1%), hyperplastic polyp (36 or 9%), and were others (8 or 2%), respectively.
As a result of immunohistochemical re staining of 50 biopsies with BE, Alcian blue were 87,8% and PAS were 97,4%.

Background: Gastroesophageal reflux disease (GERD) composes up to 28% of the esophageal disorders, and diagnosis of GERD is associated with a 10-15% of risk of Barrett’s esophagus, change of normal squamous epithelium of the distal esophagus to a columnar-lined intestinal metaplasia. It is reported that gastrointestinal (GI) disorders are the second out of five leading diseases in ambulatory diagnosed diseases and in 2022, esophageal adenocarcinoma is ranked in the fourth of the 10 most prevalent cancers among Mongolian population. When the Barrett’s esophagus changes shift to dysplasia, risk of esophageal adenocarcinoma development rises 30-125 folds and every year, 0.8% of population with dysplastic changes suffer from esophageal carcinoma. Although specific staining methods for histochemical analysis has been introduced into pathological laboratories detecting protein, fat, nucleic acid and enzymes that contained in cells, there isn’t study has been conducted to investigate the diagnostic specificity of Alcian blue and PAS staining method among population with Barrett’s esophagus. Aim: We aimed to make a differential diagnosis with basic and histochemical staining method in esophageal biopsies from Second Central Hospital of Mongolia (SCHM) and Mongolia-Japan hospital of MNUMS. Results: A total of 589 biopsies were collected from the SCHM and Mongolia-Japan Hospital of MNUMS and hematoxylin and eosin-stained results were Barret’s esophagus (43 biopsies or 7.3%), followed by Squamous cell carcinoma (46 or 7.8%), GERD (60 or 10.2%), hyperplastic polyp (92 or 15.6%), chronic erosive lesions (242 or 41%), polyp (94 or 15.9%), adenocarcinoma (12 or 2%), respectively. We have re-examined 43 cases with Barrett’s esophagus staining with Alcian blue and PAS and as a result, acidic mucin will be blue, neutral mucin will be purple, mixed mucin will be blue-purple and nucleus will be stained blue, respectively. Immunohistochemical re-staining of 43 biopsies with BE, Alcian blue were 87.8% and PAS were 97.4%. Conclusion Barrett›s esophagus, esophageal papilloma and hyperplastic polyps are comprising most of the esophageal precancerous disorders, and 9.8% of esophageal carcinoma was diagnosed. Histochemical re-staining of esophageal intestinal metaplastic changes is significantly beneficial to confirmation of the diagnosis.