Early gastric post-transplantation lymphoproliferative disorder and H pylori detection after kidney transplantation: A case report and review of the literature
Cl. Nash et al., Early gastric post-transplantation lymphoproliferative disorder and H pylori detection after kidney transplantation: A case report and review of the literature, CAN J GASTR, 14(8), 2000, pp. 721-724
The incidence of post-transplantation lymphoproliferative disorder (PTLD) i
n the adult renal transplant population ranges from 0.7% to 4% The majority
of cases involve a single site and arise, on average, seven months after t
ransplantation. Histopathology usually reveals B-cell proliferative disease
and has been standardized into its own classification. Treatment modalitie
s consist: of decreased immunosuppression, eradication of Epstein-Barr viru
s, surgical resection, systemic chemotherapy and monoclonal antibody therap
y; however, mortality remains high, typically with a short survival time. I
n patients who have undergone renal transplantation, approximately 10% of t
hose with PTLDs present with gastrointestinal symptomatology and disease. R
eported sites include the stomach, and small and large bowel. Very few case
s of Helicobacter pylori or mucosal-associated lymphoid tissue have been de
scribed in association with PTLD. In the era of cyclosporine immunosuppress
ion, the incidence of PTLD affecting the gastrointestinal tract may be incr
easing in comparison with the incidence seen with the use of older immunosu
ppression regimens. A case of antral PTLD and H pylori infection occurring
three months after renal transplantation is presented, and the natural hist
ory and management of gastric PTLD are reviewed.