A gastric stump cancer with unusual appearance

Ferdane Sapmaz1*, Sebahat Başyiğit1, Metin Uzman1, Gülçin Güler Şimşek2, Tolga Akkan1, Yaşar Nazlıgül1,

1Department of Gastroenterology, Keçiören Education and Training Hospital, Ankara, Turkey, 2Department of Pathology, Keçiören Education and Training Hospital, Ankara, Turkey

*Corresponding Author: Ferdane Sapmaz, MD Keçiören Education and Training Hospital, Phone: +90 505 357 61 84, E-mail: ferda-sapmaz@hotmail.com

Submitted: 22 November 2015 / Accepted: 12 December 2015

DOI: http://dx.doi.org/10.17532/jhsci.2015.289


ABSTRACT

A 60 year old man was referred to our hospital with the chief complaints of abdominal pain and vomiting. He underwent a distal gastrectomy with a Billroth II gastrojejunostomy for a peptic ulcer 13 years ago. Esophagogastroduodenoscopy (EGD) did not reveal any gross lesion in the stomach but depigmented areas were seen in the anastomosis line. The histopathology of the anastomotic area revealed poorly differentiated adenocarcinoma. Gastric stump cancers can be polypoid, fungating, ulcerated and diffusely infiltrating tumors respectively. In our case, the appearance of adenocarcinoma was quite different from that described in the classification system.

Keywords: gastric stump; cancer; appearance.


INTRODUCTION

Globally, gastric cancer is the fourth most common cancer in men, the fifth most common cancer in women, and the second leading cause of death due to cancer (1). It is often diagnosed in an advanced stage. Survival from gastric cancer remains low in the Western world, with reported 5-year survival rates of 10–30% (2), in contrast to survival rates in Asia of 69% (3). The prognosis for gastric cancer depends on its stage; so, detection in the early stage of disease is important, when complete and curative removal is possible.

Gastric stump carcinoma (GSC) is defined as a carcinoma occurring in the gastric remnant at least 5 years after surgery for benign peptic ulcer disease (4). The incidence of GSC has not yet declined because of the long time interval until the development of GSC in the operated stomach; the incidence may increase in the following years as surgery was commonly performed until the early 1980’s. Increased frequency of GSC after partial gastrectomy was reported in several studies (5). Fifteen to twenty years after distal gastrectomy, the risk of GSC steeply rises. Average latency period until manifestation of carcinoma in the gastric stump is 20-27 years (6).

Endoscopy is regarded as the most sensitive and specific diagnostic method in patients suspected of harboring gastric cancer. Endoscopy allows direct visualization of tumor location, the extent of mucosal involvement, and biopsy (or cytologic brushings) for tissue diagnosis (7).

Various macroscopic classification systems have been developed for gastric adenocarcinoma. One of the more common is the Borrmann system, with classifications of type’s I-IV for polypoid, fungating, ulcerated, and diffusely infiltrating tumors, respectively (8).

But occasionally some gastric cancers may not fit into any of the existing macroscopic classification.

Here we report the case of a 60-year-old man with an unusual macroscopic appearance of adenocarcinoma in the resected stomach, who was admitted because of abdominal pain, nausea, and vomiting.

CASE REPORT

A 60 year old man was admitted to our hospital with the chief complaints of repeated abdominal pain, nausea and vomiting. He underwent a distal gastrectomy with a Billroth II gastrojejunostomy for a peptic ulcer 13 years previously. The histopathology of the surgical specimen revealed an active peptic ulcer and there was no evidence of malignancy, no pathological lymph nodes, and Helicobacter pylori stain was negative. A physical examination on admission, there is epigastric tenderness without rebound or guarding and with hyperactive bowel sound. Rectal examination was normal, and his stool was negative for occult blood. Other systems were unremarkable. All routine laboratory tests were normal. Further investigation revealed elevated carcinoembryonic antigen (CEA) >500 ng/mL. Esophagogastroduodenoscopy (EGD) did not reveal any gross lesion in the stomach but depigmented areas were seen in the anastomosis line (Figure 1). Endoscopic biopsies were obtained from existing depigmented areas. The histopathology of the anastomotic area revealed poorly differentiated adenocarcinoma (Figure 2). The patient was referred to surgery clinic for the availability of operation.

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FIGURE 1 Endoscopic unusual appearance remnant gastric adenocarcinoma

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FIGURE 2 (A) Glands that show prominent cytological atypia within inflammatory exudate and the histopathological examination findings observed with regenerative epithelial change (Hematoxylin-eosin staining; x 40). (B) The immunohistochemical examination with pancytokeratin

DISCUSSION

Gastric stump cancer (GSC), first described by Balfour in 1922 (9), is defined as a carcinoma occurring in the gastric remnant after partial gastric resection for peptic ulcer disease.

Cancer of the gastric stump is a well-known event after distal gastrectomy for benign peptic ulcer. Previous reports show gastric cancer in remnant stomach may be associated with the lower acidic environment in the gastric stump, duodenogastric reflux, Helicobacter pylori infection and Billroth II reconstruction (10).

In comparison to GSC after surgery for benign disease, carcinomas in the gastric stump occurring after surgery for malignant disease are thought to have a different mechanism of carcinogenesis. Matsui et al. divided their patients with GSC into three groups. The first group consisted of patients following surgery for benign disease, and the gastroduodenal reflux after Billroth-II reconstruction may lead to development of carcinoma. In the second group with a time interval of > 10 years and surgery after malignant disease, a genetic factor such as p53 may be related to metachronous multiple carcinogenesis. In the last group with a time interval of < 10 years, metachronous multiple carcinogenesis might be associated with diffuse intestinal metaplasia in the mucosa (11).

Gastric stump cancer usually occurs 20-30 years after gastrectomy and rarely < 10 years following the surgery. Early gastric stump cancer has a male preponderance, and the majority of lesions are found at the anastomotic site or at the lesser curvature of the stomach (12). The macroscopic appearance of gastric stump cancer and its classification system is the same as gastric cancers. Based on this situation, gastric stump cancers can be polypoid, fungating, ulcerated and diffusely infiltrating tumors respectively. Surveillance with endoscopy and multiple biopsies is the only way to diagnose tumors that are at an early stage and thus susceptible to surgical treatment with an excellent chance of overall good results and prognosis. In our case, the appearance of adenocarcinoma was quite different from that described in the classification system.

CONCLUSION

Gastric cancers, especially gastric stump cancers may have different appearances. Therefore a careful endoscopic examination and received biopsies are of paramount importance.

CONFLICT OF INTEREST

The authors declare that they have no competing interests.

REFERENCES

1. Fuchs CS, Mayer RJ, Gastric carcinomaN Engl J Med 1995; 333: 132-41. http://dx.doi.org/10.1056/NEJM199507063330107.

2. Karim-Kos HE, de Vries E, Soerjomataram I, Lemmens V, Siesling S, Coebergh JW, Recent trends of cancer in Europe:a combined approach of incidence, survival and mortality for 17 cancer sites since the 1990sEur J Cancer 2008; 44: 101345-89. http://dx.doi.org/10.1016/j.ejca.2007.12.015.

3. Nashimoto A, Akazawa K, Isobe Y, Miyashiro I, Katai H, Kodera Y, Gastric cancer treated in 2002 in Japan:2009 annual report of the JGCA nationwide registryGastric Cancer 2013; 16: 11-27. http://dx.doi.org/10.1007/s10120-012-0163-4.

4. Thorban S, Bottcher K, Etter M, Roder JD, Busch R, Siewert JR, Prognostic factors in gastric stump carcinomaAnn Surg 2000; 231: 2188-94. http://dx.doi.org/10.1097/00000658-200002000-00006.

5. Sasako M, Maruyama K, Kinoshita T, Okabayashi K, Surgical treatment of carcinoma of the gastric stumpThe British journal of surgery 1991; 78: 7822-4. http://dx.doi.org/10.1002/bjs.1800780718.

6. Ovaska JT, Havia TV, Kujari HP, Retrospective analysis of gastric stump carcinoma patients treated during 1946e1981Acta Chir Scand 1986; 152: 199-204.

7. Dicken BJ, Bigam DL, Cass C, Gastric adenocarcinoma:review and considerations for future directionsAnn. Surg 2005; 241: 127-39.

8. Japanese Gastric Cancer Association. Japanese Classification of Gastric Carcinoma 1998; 2nd English Edition. Gastric Cancer;

9. Balfour DC, Factors influencing the life expectancy of patients operated on for gastric ulcerAnnals of Surgery 1922; 76: 3405-8. http://dx.doi.org/10.1097/00000658-192209000-00014.

10. Fukuhara K, Osugi H, Takada N, Takemura M, Ohmoto Y, Kinoshita H, Quantitative determinations of duodenogastric reflux, prevalence of Helicobacter pylori infection, and concentrations of interleukin-8World J Surg 2003; 27: 5567-70. http://dx.doi.org/10.1007/s00268-003-6796-z.

11. Matsui N, Yao T, Akazawa K, Nawata H, Tsuneyoshi M, Different characteristics of carcinoma in the gastric remnant:histochemical and immunohistochemical studiesOncol Rep 2001; 8: 117-26. http://dx.doi.org/10.3892/or.8.1.17.

12. Laiyemo AO, Smoot DT, Metastatic gastric stump cancer occurring six years after a partial gastrectomy for gastric ulcerJ Natl Med Assoc 2008; 100: 6737-9.