Granulomatous disease in selective IgA deficiency
Identifieur interne : 001B48 ( Main/Exploration ); précédent : 001B47; suivant : 001B49Granulomatous disease in selective IgA deficiency
Auteurs : Vidya Limaye ; Tim Lu ; Eugene Ang ; Amirtharajan Krishnan ; Pravin Hissaria [Australie] ; David Gillis [Australie]Source :
- APLAR Journal of Rheumatology [ 0219-0494 ] ; 2007-09.
English descriptors
- Teeft :
- Adelaide, Aplar, Aplar journal, Case report, Core biopsy, Cvid, Facial nerve palsy, Further example, Granuloma, Granulomatous, Granulomatous disease, Haemophilus type, Heerfordt, Heerfordt syndrome, Immune, Immune function, Microbial antigens, Ndings, Neurosarcoidosis, Normal range, Prednisolone, Previous report, Protective immunity, Rheumatology, Rheumatology department, Royal adelaide hospital, Salivary, Salivary glands, Sarcoidosis, Selective immunoglobulin, Serum angiotensin, Streptococcus pneumoniae, Submandibular, Syndrome, Taci, Taci gene, Uoroscein angiogram.
Abstract
Although common variable immunodeficiency (CVID) is sometimes associated with sarcoidosis/granulomatous disease, there have only been isolated reports of selective immunoglobulin A (IgA) deficiency and granulomatous disease. We present a patient with IgA deficiency who developed Heerfordt syndrome, a variant of neurosarcoidosis. This specific entity has not been previously reported to occur in IgA deficiency. Our case expands the reported associations of IgA deficiency and provides another example to the paucity of reported cases of sarcoidosis occurring in patients with IgA deficiency. As CVID and IgA deficiency have common underlying genetic factors, such an association is biologically plausible.
Url:
DOI: 10.1111/j.1479-8077.2007.00298.x
Affiliations:
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antigens</term><term>Ndings</term><term>Neurosarcoidosis</term><term>Normal range</term><term>Prednisolone</term><term>Previous report</term><term>Protective immunity</term><term>Rheumatology</term><term>Rheumatology department</term><term>Royal adelaide hospital</term><term>Salivary</term><term>Salivary glands</term><term>Sarcoidosis</term><term>Selective immunoglobulin</term><term>Serum angiotensin</term><term>Streptococcus pneumoniae</term><term>Submandibular</term><term>Syndrome</term><term>Taci</term><term>Taci gene</term><term>Uoroscein angiogram</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Although common variable immunodeficiency (CVID) is sometimes associated with sarcoidosis/granulomatous disease, there have only been isolated reports of selective immunoglobulin A (IgA) deficiency and granulomatous disease. We present a patient with IgA deficiency who developed Heerfordt syndrome, a variant of neurosarcoidosis. This specific entity has not been previously reported to occur in IgA deficiency. Our case expands the reported associations of IgA deficiency and provides another example to the paucity of reported cases of sarcoidosis occurring in patients with IgA deficiency. 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