IP Archives of Cytology and Histopathology Research

Print ISSN: 2581-5725

Online ISSN: 2456-9267

CODEN : IACHCL

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Get Permission Grandhi, Durga, Lakshmi, Madhuri, and Theja: Collagenising gastritis


Introduction

Collagenous gastritis is a rare and poorly understood condition characterized by the presence of a thickened subepithelial collagen layer in the gastric mucosa. This disorder shows a bimodal age distribution, affecting both pediatric patients and adults, but with different patterns of involvement. In children, the collagen deposition typically affects the gastric body or fundus, while in adults, it predominantly involves the antrum. Although the exact etiology remains unknown, patients often present with non-specific gastrointestinal symptoms. Here, we report a case of collagenous gastritis in a 50-year-old male who presented with recurrent vomiting, highlighting the challenges in diagnosis and management of this uncommon disease.

Case Report

A 50 year old male patient came to medical gastroenterology department with complaints of vomiting. There is significant history of alcohol intaske.Endoscopy was done and multiple spots were identified in the stomach. Multiple biopsies were taken and send to our department for histopathologicalexamination.We received multiple grey white mucosal bits which were processed routinely and examined.

On microscopy mucosa was seen lined by columnar epithelium. Lamina propria showed extensive areas of collagenisation with fibrosis with entrapment of mucosal glands. Inflammatory cells predominantly lymphocytes, eosinophils were seen. Vangieson demonstrated collagen bands confirming the diagnosis of collagenising gastritis.

Figure 1

Scanner view; 10Xx100 showing collagen bands

https://s3-us-west-2.amazonaws.com/typeset-prod-media-server/a16e18d1-f0fb-4dd1-98e5-9bbce4a5318dimage1.png
Figure 2

40X100 showing glands within collagen Van Gieson stain positive for collagen

https://s3-us-west-2.amazonaws.com/typeset-prod-media-server/a16e18d1-f0fb-4dd1-98e5-9bbce4a5318dimage2.png

Discussion

Collagen gastritis is a very rare clinicopathological entity.1

Etiology of the disease was proposed to be due to primary vascular abnormality causing increased vascular permeability and collagen deposition.2

It covers under the broad category of collagenous gastroenteritis which includes collagenous gastritis and collagenous colitis. These are charecterised by mucosal subepithelial collagen deposition along with mucosal inflammatory infiltrate.3, 4, 5, 6 Paediatric patients presenting with upper GI symptoms with abdominal pain and anaemia where adults present with autoimmune proctitis and caeliac disease.7, 8 Upper endoscopy is recommended diagnostic modality.

More cases are needed to be documented to establish a standard therapeutic strategy.

Conclusion

This is an uncommon entity with autoimmune etiology requiring further documentation.

Source of Funding

None.

Conflict of Interest

None.

References

1 

T Rustagi M Rai JV Scholes Collagenous gastroduodenitisJ Clin Gastroenterol20114597949

2 

NM Hijaz SS Septer J Degaetano TM Attard Clinical outcome of pediatric collagenous gastritis: case series and review of literatureWorld J Gastroenterol2013199147884

3 

OH Nielson LB Riis S Danese RD Bojesen C Soendergaard Proximal collagenous gastroenteritides: clinical management. A systematic reviewAnn Med20144653117

4 

P Gopal BJ McKenna The collagenous gastroenteritides: similarities and differencesArch Pahol Lab Med20101341014859

5 

O Brain C Rajaguru B Warren J Booth S Travis Collagenous gastritis: reports and systematic reviewEur J Gastroenterol Hepatol20092112141924

6 

HJ Freeman Complications of collagenous colitisWorld J Gastroenterol2008141116435

7 

C Lagorce-Pages B Fabini R Bouvier JY Scoazec L Durand JF Flejou Collagenous gastritis: a report of six casesAm J Surg Pathol200125911749

8 

H Zhou G Rossi Collagenous Gastritis: An Entity Distinct from Collagenous ColitisJ Clin Pathol201164870511



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Article type

Case Report


Article page

167-168


Authors Details

Bhavana Grandhi*, K Durga, P Maanasa Lakshmi, R Madhuri, P Divya Theja


Article History

Received : 05-06-2024

Accepted : 13-07-2024


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