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Biomedical Journal of Scientific & Technical Research

May, 2022, Volume 44, 2, pp 35288-35289

Case Report

Case Report

Glandulocystic Gastric Polyposis

Mohamed Hajri, Sahir Omrani, Wael Ferjaoui*, Rami Guizani and Rached Bayar

Author Affiliations

Department of General surgery, Mongi Slim University Hospital, Faculty of medicine of Tunis, Tunisia

Received: May 22, 2022 | Published: May 30, 2022

Corresponding author: Wael Ferjaoui, Department of General surgery, Mongi Slim University Hospital, Faculty of medicine of Tunis, Tunisia

DOI: 10.26717/BJSTR.2022.44.007015

Abstract

Keywords: Polyposis Adenomatous Familial; Gastric Glandulocystic Polyposis; Total Gastrectomy

Case Report

It is about a 43-year-old patient with no past medical history who consulted for dyspeptic disorders and vomiting. The clinical examination was without abnormalities. Esophagogastroduodenoscopy revealed innumerable sessile polyps in the cardia, fundus, and body of the stomach. The gastric antrum was free of polyps. Biopsies from the gastric body and antrum were negative for H. pylori infection. A colonoscopy was performed showing the appearance of diffuse recto-colonic polyposis. The diagnosis of Polyposis Adenomatous Familial (PAF) was retained and a genetic investigation was initiated within the family. The patient was operated on and a total prophylactic Colo proctectomy was performed. The postoperative follow-up was simple. The anatomopathological study showed an appearance of recto colic PAF without signs of degeneration. Periodic monitoring of gastric lesions was planned. But the vomiting became uncontrollable and the laboratory tests showed electrolyte disturbances which were difficult to balance (compensate). Surgery was decided and a total gastrectomy was performed (Figure 1). Pathological examination of the operative specimen was in favor of gastric glandulocystic polyposis without signs of dysplasia or degeneration. PAFassociated fundic gland polyps are reported to occur in 20% to 84% of patients. Histopathologically, they are characterized by cystically dilated and irregularly budded fundic glands in a background of otherwise normal gastric mucosa. There is a clear role for surveillance of FGPs in patients with an inherited polyposis syndrome due to the increased risk of dysplasia and cancer. In our case, surgery was necessary vu the impact of vomiting on the patient’s quality of life and on the electrolyte balance [1,2].

Figure 1: Operative specimen showing gastric polyposis.

References

    1. Brown HR, Hardisty JF (1990) Oral cavity, esophagus and stomach. In: Pathology of the Fischer Rat. In: Boorman GA, Montgomery CA, MacKenzie WF (Eds.)., Academic Press, San Diego, USA, p. 9-30.
    2. Frantz JD, Betton GR, Cartwright ME, Crissman JW, Macklin AW, et al. (1991) Proliferative lesions of the non-glandular and glandular stomach in rats GI-3. In Guides for Toxicologic Pathology. STP/ARP/AFIP, Washington, DC, p. 1-20.
Case Report

Glandulocystic Gastric Polyposis

Mohamed Hajri, Sahir Omrani, Wael Ferjaoui*, Rami Guizani and Rached Bayar

Author Affiliations

Department of General surgery, Mongi Slim University Hospital, Faculty of medicine of Tunis, Tunisia

Received: May 22, 2022 | Published: May 30, 2022

Corresponding author: Wael Ferjaoui, Department of General surgery, Mongi Slim University Hospital, Faculty of medicine of Tunis, Tunisia

DOI: 10.26717/BJSTR.2022.44.007015

Abstract

Keywords: Polyposis Adenomatous Familial; Gastric Glandulocystic Polyposis; Total Gastrectomy