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pubmed-article:8965482pubmed:abstractTextThis article reviews Pneumocystis carinii and presents four cases in the miniature dachshund. The cases presented with hyperpnoea, tachypnoea and exercise intolerance. There were also clinical signs suggestive of immune incompetence in all the dogs. P carinii pneumonia was diagnosed in all four cases on transtracheal aspirate cytology. Immunological studies showed low globulin levels on serum electrophoresis, decreased lymphoblast transformation response (in the two cases that were tested) and a deficiency of immunoglobulins A, G and M. Light and electron microscopy as well as anti-canine immunoglobulin G immunoperoxidase staining studies were performed on one case which had died because of the disease. From these four cases, it appears that P carinii pneumonia in the miniature dachshund may be the result of an immunodeficiency. It does not, however, appear to be a classic primary severe combined immunodeficiency syndrome as the dogs appeared to respond to treatment, did not show growth failure and did not manifest overwhelming commensurate bacterial infections.lld:pubmed
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pubmed-article:8965482pubmed:issn0022-4510lld:pubmed
pubmed-article:8965482pubmed:authorpubmed-author:SpencerJ AJAlld:pubmed
pubmed-article:8965482pubmed:authorpubmed-author:LobettiR GRGlld:pubmed
pubmed-article:8965482pubmed:authorpubmed-author:LeisewitzA...lld:pubmed
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pubmed-article:8965482pubmed:volume37lld:pubmed
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pubmed-article:8965482pubmed:pagination280-5lld:pubmed
pubmed-article:8965482pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:8965482pubmed:year1996lld:pubmed
pubmed-article:8965482pubmed:articleTitlePneumocystis carinii in the miniature dachshund: case report and literature review.lld:pubmed
pubmed-article:8965482pubmed:affiliationDepartment of Medicine, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, South Africa.lld:pubmed
pubmed-article:8965482pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8965482pubmed:publicationTypeReviewlld:pubmed
pubmed-article:8965482pubmed:publicationTypeCase Reportslld:pubmed