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Br J Dermatol ; 135(6): 982-7, 1996 Dec.
Article in English | MEDLINE | ID: mdl-8977724

ABSTRACT

Bacillary angiomatosis is an unusual systemic vascular proliferation seen predominantly in patients with the acquired immunodeficiency syndrome. These vascular lesions are due to infection with a Bartonella species, most commonly B. henselae, but sometimes B. quintana. It is treatable and often curable, but without therapy may be life-threatening. Clinically, the disorder often resembles several different vascular disorders, particularly pyogenic granuloma and Kaposi's sarcoma. We now report a clinically typical patient with bacillary angiomatosis who was HIV seronegative, but who had idiopathic thrombocytopenic purpura, was status-post splenectomy and to whom long-term systemic prednisone had been administered.


Subject(s)
Angiomatosis, Bacillary/diagnosis , Glucocorticoids/adverse effects , HIV Seronegativity , Prednisolone/adverse effects , Purpura, Thrombocytopenic, Idiopathic/complications , Adult , Angiomatosis, Bacillary/drug therapy , Angiomatosis, Bacillary/pathology , Anti-Bacterial Agents/therapeutic use , Azithromycin/therapeutic use , Glucocorticoids/therapeutic use , Humans , Male , Prednisolone/therapeutic use , Purpura, Thrombocytopenic, Idiopathic/drug therapy , Purpura, Thrombocytopenic, Idiopathic/pathology , Skin/pathology
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