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Partial splenectomy in children undergoing liver transplantation or venous shunt for severe hypersplenism: A case control comparative study - 06/07/22

Doi : 10.1016/j.clinre.2022.101929 
Olivier Boillot a, b, c, , Sophie Chopinet c, Emilie Gregoire c, Laurent Milot d, Philippe Petit e, Barbara Rohmer f, Bertrand Roquelaure g, Anne Dariel h, Nicoleta Panait h, Jean Hardwigsen c, Jérôme Dumortier a, b
a Department of Digestive Diseases, Edouard Herriot Hospital, Hospices Civils de Lyon, France 
b University Claude Bernard Lyon 1, France 
c Aix-Marseille University, Assistance Publique des Hôpitaux de Marseille, Department of General Surgery and Liver Transplantation, la Timone Hospital, Marseille, France 
d Department of Radiology, Edouard Herriot Hospital, Hospices Civils de Lyon, France 
e Department of Pediatric Radiology, la Timone Hospital, Assistance Publique - Hôpitaux de Marseille, France 
f Department of Pediatry, Femme Mère Enfant Hospital, Hospices Civils de Lyon, France 
g Department of Pediatry, la Timone Hospital, Assistance Publique - Hôpitaux de Marseille, France 
h Department of Pediatric Surgery, la Timone Hospital, Assistance Publique - Hôpitaux de Marseille, France 

Address for correspondence and reprints: Hôpital Edouard Herriot, Pavillon D, 69437 Lyon Cedex 03, France.Hôpital Edouard HerriotPavillon D, 69437 Lyon Cedex 03France

Highlights

Hypersplenism is potentially life-threatening in children with portal hypertension and can persist after liver transplantation or portosystemic shunt.
Retrospective data from 16 children who underwent partial splenectomy and liver transplantation or portosystemic shunt were collected.
Partial splenectomy can be added to liver transplantation or portosystemic shunt and is effective and safe to treat severe hypersplenism.

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Abstract

Background and aim

Hypersplenism is a consequence of portal hypertension and splenomegaly secondary to cirrhosis or portal cavernoma in children. In order to avoid persistent hypersplenism and splenomegaly after liver transplantation (LT) or venous shunt (VS), partial splenectomy (PS) may represent a relevant therapeutic option. The aim of this retrospective study was to evaluate the results of PS performed in children presenting hypersplenism.

Methods

The following end-points were evaluated: (1) reversion of hypersplenism and its durability over time, (2) postoperative outcome, (3) courses of spleen size and volume and (4) comparison to a control group in which PS was not performed.

Results

Between 1996 and 2020, 16 children underwent PS associated with LT (8 cases) for cirrhosis or VS (8 cases) for portal cavernoma. From Day 0 to 1 month, mean platelet and white blood cell counts (WBC) dramatically improved from 48 ± 19 at day 0 to 176 ± 70 × 109/L (P < 0.0001) and from 2469 ± 853 to 7198 ± 3982/L (P = 0.001) respectively. PS allowed significant reduction of splenic length and volume from 176 ± 33 to 112 ± 24 cm (P < 0.0001) and from 1228 ± 464 to 450 ± 297 cm3 (P = 0.0003) respectively. After a mean follow-up of 92.6 ± 84.7 months (range: 4.1–210.7), 14 patients are alive with normal platelet and WBC counts and persistent spleen size reduction. Compared to control group, PS was associated with a significant platelet count rise from baseline to one year.

Conclusions

PS appears to be effective for treatment of hypersplenism and splenomegaly in combination with LT or VS without compromising outcome.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Hypersplenism, Splenomegaly, Partial splenectomy, Liver transplantation, Venous shunt, Outcome

Abbreviations : LT, VS, PS, WBC, SL, SV, CT, PHSLR, MRS, LLS, LD, LL, WL, SSSRS, GRWR, D, W, M, Y


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 This work did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.


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Vol 46 - N° 6

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