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Results for “CAT-SCRATCH DISEASE”

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PubMed1991

Bacillary angiomatosis.

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Acquired Immunodeficiency Syndrome↗
PubMed1991

Bacillary angiomatosis.

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Acquired Immunodeficiency Syndrome↗
PubMed1991

Household pets and human infections.

Because many Americans keep a wide variety of household pets, they are exposed to the many pet-associated diseases that are transmitted in various ways, including through bites, scratches, saliva, excreta, and respiration. This article briefly describes a number of the illnesses that may be acquired from household pets.

Animals↗
PubMedDate not supplied

[Causative agent of benign lymphoreticulosis].

A causative agent ("D" strain) was isolated from the contents of an affected lymph node of a patient with beningn lymphoreticulosis. According to the biological and antigenic properties this agent is identified with Chlamydia but is a distinct species. The chlamydial etiology of benign lymphoreticulosis is determined also by the complement-fixation test with sera from convalescents.

Animals↗
PubMed1978

Cat scratch disease with involvement of intra-parotid lymph nodes. Case report.

A case of cat scratch disease, presenting as a parotid tumor, is described. In its oculo-glandular form, this disease may be associated with swelling of the intraparotid lymph nodes, and the possibility should be considered in the differential diagnosis of parotid tumors in children. A careful history, and skin testing with cat scratch antigen, may aid in the diagnosis of this condition.

Cat-Scratch Disease↗
PubMed1992

Macrophages (histiocytes) in various reactive and inflammatory conditions express different antigenic phenotypes.

The purpose of this study was to determine whether human tissue macrophages (M phi s) in various inflammatory/reactive conditions express different immunophenotypes. Using a large panel of monoclonal antibodies to monocyte/M phi-related antigens and a frozen-section immunoperoxidase technique, the following conditions were studied: granulomatous inflammation of unknown etiology, sarcoidosis, cat-scratch fever, toxoplasmosis, Gaucher's disease, and juvenile xanthogranulomas. The results show that there is immunophenotypic variation of the M phi s among the various inflammatory/reactive conditions. For example, the M phi s in cat-scratch fever are nearly unique in the expression of the "early inflammation" antigen identified by antibody 27E10, and the M phi s in juvenile xanthogranulomas, unlike those in most of the other conditions, lacked the antigen detected by antibody 25F9. The M phi s in Gaucher's disease differed from those in the other disorders by the combined absence of CD11b, CD14, G16/1, CD1a, CD25, and CD30. The inflammatory/reactive M phi s also exhibited differences from those in "normal" tissues, namely, a tendency toward acquisition of the antigens identified by antibodies Mac 387 and G16/1 and the more uniform expression of the "activation" antigens CD25, CD30, and CD71. The antigenic variations described here probably reflect differences in antigenic stimuli and M phi function. In addition to the possible biologic implications, this M phi immunophenotypic diversity may have practical diagnostic applications.

Antigens↗