Abstract
A patient with profound panhypogammaglobulinaemia due to common variable immunodeficiency developed two discrete intra-cranial space-occupying lesions, 10 years apart, requiring craniotomy. Histological examination revealed the intra-cranial masses to be granulomata of unknown aetiology on both occasions.
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- Delaney P. Neurologic manifestations in sarcoidosis: review of the literature, with a report of 23 cases. Ann Intern Med. 1977 Sep;87(3):336–345. doi: 10.7326/0003-4819-87-3-336. [DOI] [PubMed] [Google Scholar]
- Eibl M. M., Mannhalter J. W., Zlabinger G., Mayr W. R., Tilz G. P., Ahmad R., Zielinski C. C. Defective macrophage function in a patient with common variable immunodeficiency. N Engl J Med. 1982 Sep 23;307(13):803–806. doi: 10.1056/NEJM198209233071307. [DOI] [PubMed] [Google Scholar]
- Guerra I. C., Fawcett W. A., 4th, Redmon A. H., Lawrence E. C., Rosenblatt H. M., Shearer W. T. Permanent intrinsic B cell immunodeficiency caused by phenytoin hypersensitivity. J Allergy Clin Immunol. 1986 Apr;77(4):603–607. doi: 10.1016/0091-6749(86)90353-2. [DOI] [PubMed] [Google Scholar]
- Leen C. L., Bath J. C., Brettle R. P., Yap P. L. Sarcoidosis and primary hypogammaglobulinaemia: a report of two cases and a review of the literature. Sarcoidosis. 1985 Sep;2(2):91–95. [PubMed] [Google Scholar]