Laparoscopic splenectomy (LS) is an alternative to open surgery, However, t
here is a theoretic risk of splenosis and abdominal cavity dissemination of
splenic cells if the splenic capsule is broken, as seen by experimental ev
idence of tumoral cell mobilization by the pneumoperitoneum, We evaluated t
he features of splenosis after splenectomy operated via an open approach or
under laparoscopic control in an experimental model in the rat, A total of
65 Sprague-Dawley rats were distributed in seven groups that included the
open approach, CO2 pneumoperitoneum LS, or wall lift LS with or without a s
plenic graft, Splenic function was evaluated 90 day later through (1) scint
igraphy with Tc-labeled heat-damaged erythrocytes; (2) determination of cir
culating "pitted" cells; and (3) analysis of the distribution of splenic pu
lp in the peritoneal cavity, Scintigraphy did not show viable residual tiss
ue in any group after splenectomy; splenic activity in the splenic fossa wa
s observed in 40% of the animals with grafts. Splenectomy increased the "pi
t" cell count, but it was reduced to normal values with a splenic graft. Ne
cropsy showed normal splenic tissue in the splenic fossa in 100% of animals
with a graft. Abdominal implants were observed significantly more frequent
ly after CO2 LS than after the open surgery or a wall lift LS (80% vs. 20%
vs, 30%; p < 0.05), In addition, trocar site implants were observed with CO
2 LS (n = 3) or wall lift LS (n = 2), whereas there were no implants in the
wound in the open group. We conclude that in an experimental rat model the
pneumoperitoneum may facilitate abdominal splenosis after LS if the spleni
c capsule is ruptured or if splenic tissue spills compared with surgery wit
hout gas (open or laparoscopic).