Natural history of asplenism in APECED - Patient report

Citation
J. Starzyk et al., Natural history of asplenism in APECED - Patient report, J PED END M, 14(4), 2001, pp. 443-449
Citations number
40
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
ISSN journal
0334018X → ACNP
Volume
14
Issue
4
Year of publication
2001
Pages
443 - 449
Database
ISI
SICI code
0334-018X(200104)14:4<443:NHOAIA>2.0.ZU;2-J
Abstract
Only a few reports on patients with hypo/asplenism associated with APECED h ave been published, yet hyposplenism has been found in approximately half o f the studied patients. The 7-year follow-up in our only patient with APECE D revealed a decrease of spleen size from normal to half-size by ultrasound and CT examinations. Scintigraphy of the liver and spleen demonstrated a p rogressively diminishing splenic uptake of the tracer from low to complete absence, Peripheral blood smears revealed permanent thrombocytosis with the presence of Howell-Jolly bodies when functional asplenism was reached. The cause of autoimmunization and hyposplenism in APECED is unknown, We hypoth esize that hyposplenism depends primarily on local AIRE gene dysfunction in the spleen, and secondarily on an AIRE gene-mediated autoagressive process . In our opinion, hypo/asplenism in APECED disease might not be noticed in patients with APECED if not directly examined. Thus we emphasize the necess ity of searching for hyposplenism in ail patients with APECED, and recommen d scintigraphy.