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Decide on the Spot

Which way to go with a giant gastric ulcer?

January 12, 2017 | Bjorn Rembacken

A large gastric ulcer was discovered in 65-year-old man who had no significant comorbidities. Two set of biopsy samples (16 samples in total) revealed only some ‘probably reactive atypia.’ The images show the endoscopic appearance of the lesion. A CT has confirmed the presence of a large gastric ulcer with a couple of small nodes nearby that were reported as ‘likely to be reactive.’

Case Question 1

What would you do next?

a)     Reassure the patient and organise a follow up in 3 months to confirm healing

b)     Organise for another set of biopsy samples to be taken in the next week or so

c)     Organise an endoscopic ultrasound (EUS)

d)     Organise a laparoscopy and wedge biopsy

e)     Organise a distal gastrectomy

  • Case question 1 answer and discussion
Case question 1 answer and discussion

Correct answer: d.

Discussion

This situation is a frequent conundrum in clinical practise. Of course, such cases should be discussed in your local cancer meeting. Poor healing appears to be more frequent in the elderly, those who have significant comorbidities and with certain drug treatments, such as NSAIDs, potassium chloride, bisphosphonates, doxycycline or nicorandil. Chronic gastric ulceration has also been reported secondary to nearby infiltrating adenocarcinoma, lymphoma or stromal tumours, cytomegalovirus (CMV) infection and lymphoma.

A paper from the H2-receptor era reported on the outcomes of 129 ‘giant gastric ulcers’ (defined in this study as ulcers large enough to occupy at least one wall of the stomach).1 Compared with patients who had smaller gastric ulcers (presumably occupying less than a gastric wall), patients who had giant gastric ulcers were significantly older (p< 0.05), had more aggressive disease with a higher risk of bleeding, and presented more frequently with anorexia and weight loss. In this study, the most common location for a giant gastric ulcer was the gastric body.

The healing rate at 12 weeks was 88% for patients on cimetidine. Patients not offered maintenance therapy with cimetidine had a 50% risk of ulcer recurrence. Only two of the giant gastric ulcers identified finally proved to be malignant. Interestingly, a second review reported a similar ‘refractory gastric ulcer’ rate of 17% (that is, ulcers not healed after 8 weeks of treatment) even though ulcers were treated with full-dose lansoprazole.2 There was no difference in the healing rate between patients randomly allocated to receive 30 mg or 60 mg of lansoprazole.

As giant refractory gastric ulcers are far more likely to be benign than malignant, performing a gastrectomy would be premature in this case. Nevertheless, the report of atypia and the presence of a couple of small nodes nearby should not be ignored in a patient who would be a candidate for gastrectomy if cancer is ultimately confirmed. EUS with fine-needle aspiration (FNA) of the nodes would be reasonable but would of course only be of use in the unlikely event that the histology confirmed cancer.

The main choice now lies between taking another set of biopsy samples, perhaps using ‘jumbo biopsy forceps,’ or organising a laparoscopy with a gastric wedge biopsy. As I have seen several endoscopy-and-biopsy-negative cancers correctly identified by laparoscopy with a gastric wedge biopsy, I believe that this would be the best way forward for this patient. Even if a wedge biopsy conclusively rules cancer out, there is a risk of ulcer complications such as bleeding (12–44%) and perforation (1–2%).3 For this reason, a proportion of benign giant ulcers may ultimately be managed with a partial gastrectomy; however, perioperative mortality may be high with emergency surgery in an elderly patient.4,5,6 

References

  1. Raju GS, et al. Giant gastric ulcer: its natural history and outcome in the H2RA era. Am J Gastro 1999; 94: 3478–3486. http://www.nature.com/ajg/journal/v94/n12/abstract/ajg1999813a.html
  2. van Rensburg CJ, et al. A trial of lansoprazole in refractory gastric ulcer. Aliment Pharmacol Ther 1996; 10: 381–386. http://onlinelibrary.wiley.com/doi/10.1111/j.0953-0673.1996.00381.x/abstract
  3. Chua C-L, Jeyaraj P-R and Low C-H. Relative risks of complications in giant and nongiant gastric ulcers. Am J Surg 1992; 164: 94–97. http://www.americanjournalofsurgery.com/article/S0002-9610(05)80361-7/pdf
  4. Tsugawa K, et al. The therapeutic strategies in performing emergency surgery for gastroduodenal ulcer perforation in 130 patients over 70 years of age. Hepato-Gastroenterology 2001; 48: 156–162. https://www.ncbi.nlm.nih.gov/pubmed/?term=11268955
  5. Hemmer PHJ, et al. Results of surgery for perforated gastroduodenal ulcers in a Dutch population. Dig Surg 2012; 28: 360–366. https://www.karger.com/Article/Abstract/331320
  6. Buck DL, Vester-Andersen M and Møller MH. Surgical delay is a critical determinant of survival in perforated peptic ulcer. Br J Surg 2013; 100: 1045–1049. http://onlinelibrary.wiley.com/doi/10.1002/bjs.9271/abstract
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  • About the Author
About the Author

Bjorn Rembacken is at Leeds Teaching Hospitals NHS Trust, Leeds, UK. He was born in Sweden and qualified from Leicester University in 1987. He undertook his postgraduate education in Leicester and in Leeds. His MD was dedicated to inflammatory bowel disease. Dr Rembacken was appointed Consultant Gastroenterologist, Honorary Lecturer at Leeds University and Endoscopy Training Lead in 2005. Follow Bjorn on Twitter @Bjorn_Rembacken

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