Hyper-reactive malarial splenomegaly in a European patient after residencein Africa.

Citation
H. Granier et al., Hyper-reactive malarial splenomegaly in a European patient after residencein Africa., REV MED IN, 20(5), 1999, pp. 431-433
Citations number
10
Categorie Soggetti
General & Internal Medicine
Journal title
REVUE DE MEDECINE INTERNE
ISSN journal
02488663 → ACNP
Volume
20
Issue
5
Year of publication
1999
Pages
431 - 433
Database
ISI
SICI code
0248-8663(199905)20:5<431:HMSIAE>2.0.ZU;2-T
Abstract
Introduction. - Hyper-reactive malarial splenomegaly (HMS) syndrome related to abnormal immunologic response to repeated malarial infections is unusua l in European expatriates. Exegesis. - We report the case of a 72-year-old white male patient who had been residing in the Congo and developed a typical clinical features of hyp eractive malarial syndrome characterized by massive splenomegaly wit hypers plenism, high titers of malarial IgM antibodies, IgM macroglonulinemia, liv er and medullary lymphocytic proliferation, and a clinical and immunologica l response to long-trm chloroquine therapy. Conclusion. - Criteria for the diagnosis of hyper-reactive malarial splenom egaly are useful. However, making a distinction from malignant lymphoprolif erative disorders is difficult, as a sustained response to chloroquine is r equired. Therefore, chloroquine appears to have a regulatory effect on the immune system. (C) 1999 Elsevier, Paris.