A fatal case of common variable hypogammaglobulinemia (CVH) is described. The patient presented with fulminant haemolytic anaemia. Post mortem examination revealed evidence of chronic hypogammaglobulinemia.
FudenbergHH, GoodRA, GoodmanHC. Primary immunodeficiencies. Report of a World Health Organisation Committee. Pediatrics1971; 47; 927–946.
2.
AshersonGL, WebsterADB. Diagnosis and treatment of immunodeficiency disease. Oxford, Blackwell Scientific Publications; 1980, pp 37–60.
3.
NelAE. Primary acquired hypogammaglobulinaemia complicated by antibody mediated haemolysis and pernicious anaemia. A case report. S Afr Med J1983; 64: 326–328.
4.
GehaRS, SchnecbergerE, MederE, RosenPS. Heterogeneity of ‘acquired’ or common variable hypogammaglobulinemia. N Engl J Med1974; 291: 1–6.
5.
LanningM, KouvalainenK, SimilaS, RaunioV.Agammaglobulinemia with arthritis and coeliac disease developing after infectious mononucleosis. Scand J Infect, Dis1977; 9: 144–148.
6.
AndimanWA, EastmanR, MartinK.Opportunistic lymphoproliferations associated with Epstein-Barr viral DNA in infants and children with AIDS. Lancet1988; ii: 1390–1393.
7.
LungML, LamWK, SoSY. Evidence that respiratory tract is major reservoir for Epstein-Barr virus. Lancet1985; i: 889–892.
8.
LeenCLS, YapPL, WilliamsPE. Tolerance of Scottish National Blood Transfusion Service intravenous immunoglobulin in patients with primary hypogammaglobuninaemia; report of 1235 infections. Scot Med J1988; 33: 303–306.
9.
ThompsonRA, Rees-JonesA.The antibody deficiency syndrome, a report on current management. J Infect1979; 1: 49–60.