Affiliation:
1. Department of Paediatrics University Medical Center Ulm (UUMC) Ulm Germany
2. Department of Paediatric Surgery UUMC Ulm Germany
3. Department of Paediatrics Helios Clinic Berlin‐Buch Germany
4. Department of Paediatric Surgery Helios Clinic Berlin‐Buch Germany
Abstract
AbstractIntroductionSubtotal or total splenectomy are recommended in severe and should be considered in intermediate forms of hereditary spherocytosis (HS). Data on laparoscopic subtotal splenectomy (LSTS) in HS patients are sparse.MethodsThirty three patients with HS (median age 10.7 years (yrs), range 1.8–15.5) underwent LSTS. Baseline and follow‐up investigation included haematological parameters, microscopic analysis of pitted erythrocytes (pitE), and B‐cell subpopulations assessed by flow cytometry. Results were compared to those of non‐splenectomised HS patients, HS patients after total splenectomy (TS), and healthy individuals.ResultsAfter LSTS, haemoglobin levels were normalised in all patients. During median long‐term follow‐up of 3.9 yrs (range 1.1–14.9), only four patients presented mild anaemia. Despite re‐growing of the remnant spleen none of the patients required a second surgical intervention. As compared to TS, PitE in LSTS patients were significantly lower and indicated normal to only moderately decreased spleen function. Relative but not absolute IgM memory B‐cell counts were reduced in both LSTS and TS patients.ConclusionsLSTS is effective for the treatment of patients with HS. A small remnant spleen is sufficient to provide adequate phagocytic function and to induce a pool of IgM memory B‐cells.
Subject
Hematology,General Medicine
Cited by
2 articles.
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