Journal of Pediatric Surgery
Volume 43, Issue 3 , Pages 466-472, March 2008

Partial splenectomy for children with congenital hemolytic anemia and massive splenomegaly

  • Diana L. Diesen

      Affiliations

    • Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA
  • ,
  • Sherri A. Zimmerman

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA
  • ,
  • Courtney D. Thornburg

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA
  • ,
  • Russell E. Ware

      Affiliations

    • Department of Hematology, St Jude Children's Research Hospital, Memphis, TN 38105, USA
  • ,
  • Michael Skinner

      Affiliations

    • Department of Surgery, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
  • ,
  • Keith T. Oldham

      Affiliations

    • Department of Surgery, Children's Hospital of Wisconsin, Milwaukee, WI 53201, USA
  • ,
  • Henry E. Rice

      Affiliations

    • Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA
    • Corresponding Author InformationCorresponding author. Division of Pediatric Surgery, Box 3815, Duke University Medical Center, Durham, NC 27710, USA. Tel.: +1 919 681 5077; fax +1 919 681 8353.

Abstract 

Partial splenectomy is an alternative to total splenectomy for the treatment of congenital hemolytic anemias (CHAs) in children, although the feasibility of this technique in the setting of massive splenomegaly is unknown. This study was designed to evaluate the safety and efficacy of partial splenectomy in children with CHAs and massive splenomegaly. This retrospective study examined 29 children with CHAs who underwent partial splenectomy. Children were divided into 2 groups based on splenic size: 8 children had splenic volumes greater than 500 mL, whereas 21 children had splenic volumes less than 500 mL. Outcome variables included perioperative complications, transfusion requirements, hematocrits, reticulocyte counts, bilirubin levels, splenic sequestration, and splenic regrowth. All 29 children underwent successful partial splenectomy with 0.02 to 10 years of follow-up. After partial splenectomy, children overall had decreased transfusion requirements, increased hematocrits, decreased bilirubin levels, decreased reticulocyte counts, and elimination of splenic sequestration. Children with massive splenomegaly had similar outcomes compared with children without massive splenomegaly. Long-term complications included 3 mild infections, 4 cases of gallstones requiring cholecystectomy, and 1 child who required completion splenectomy. Partial splenectomy is a safe, effective, and technically feasible option for children with various CHAs, even in the setting of massive splenomegaly.

Key words:: Congenital hemolytic anemia, Spherocytosis, Partial splenectomy, Splenomegaly

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0022-3468(07)00823-8

doi:10.1016/j.jpedsurg.2007.10.025

Journal of Pediatric Surgery
Volume 43, Issue 3 , Pages 466-472, March 2008