Bacillary angiomatosis of acquired immunodeficiency syndrome: Case report and literature review

1990 ◽  
Vol 22 (3) ◽  
pp. 525-529 ◽  
Author(s):  
F. Jimenez-Acosta ◽  
Rube J. Pardo ◽  
Robert J. Cohen ◽  
Edwin W. Gould ◽  
Neal S. Penneys
2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110477
Author(s):  
Shuangxia Dong ◽  
Zhou Lin ◽  
Shenghao Wu ◽  
Leyi Cai

Non-tuberculous mycobacterial spondylitis is a rare spinal infection, especially among patients without acquired immunodeficiency syndrome or other immune impairments. Because of its rarity and non-specific clinical manifestations, diagnosis is often delayed or missed. Here, we present a case of Mycobacterium chelonae spondylitis in an immunocompetent patient and review the relevant literature.


Author(s):  
Paulo Mendes Peçanha ◽  
Isabela Cruz Bahiense ◽  
Wdson Luis Lima Kruschewsky ◽  
Cláudia Biasutti ◽  
Carlos Urbano Gonçalves Ferreira Júnior ◽  
...  

1995 ◽  
Vol 104 (8) ◽  
pp. 668-672 ◽  
Author(s):  
John G. Batsakis ◽  
Jae Y. Ro ◽  
Elizabeth E. Frauenhoffer

The acquired immunodeficiency syndrome and other causes of immunosuppression have ushered in a variety of opportunistic infections. One of these is bacillary angiomatosis, a vasoproliferative lesion whose principal causative agent is Rochalimaea henselae. Bacillary angiomatosis, while preponderantly a cutaneous affliction, can be systemic, including involvement of the head and neck mucous membranes. Molecular technology and epidemiologic studies used to identify the bacterial agent of bacillary angiomatosis have also uncovered R henselae as the organism responsible for most cases of cat-scratch disease. Why the same organism promotes two different histopathologic lesions, as seen in bacillary angiomatosis and cat-scratch disease, is unknown.


2011 ◽  
Vol 15 (02) ◽  
pp. 245-248
Author(s):  
Flavia Silveira ◽  
Gabriel Bijos Faidiga ◽  
Tassiana do Lago ◽  
Camila Carrara Yassuda ◽  
Eduardo Tanaka Massuda ◽  
...  

Summary Introduction: Fungal mastoidits by Aspergillus fumigates predominantly occurs in immunosuppressed patients. Diagnosis is usually hard and disease is potentially fatal. Treatment is comprised of antifungal therapy, surgical debridement and immunosuppression correction. Case Report: This article reports a case of fungal mastoiditis in a patient with acquired immunodeficiency syndrome (AIDS). The treatment performed was that of surgery associated with antifungal therapy. The patient's facial nerve was not affected, what does not exclude potentially fatal complications of mastoiditis.


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