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PP 6.17<br />

Community-acquired septicemic pneumonia caused by a multiresistant<br />

Staphylococcus aureus strain, resulting in multiple organ involvement exacerbated<br />

by extensive immune activation<br />

Roberto Manfredi, Sergio Sabbatani<br />

Infectious Diseases, University of Bologna, Italy<br />

Introduction<br />

Antibiotic-resistant gram-positive cocci are of increasing concern, and immune activation<br />

promped by microbial products (bacterial superantigens) may play a major role in the<br />

pathogenesis of disseminated, life-threatening Staphylococcus aureus infection.<br />

Patient and Methods<br />

An exceptional case report of community-acquired, severe infection caused by a<br />

methicillin-resistant S. aureus strain,responsible for pneumonia, septic shock, and<br />

scattered septic embolism, and accompanied by diffuse polyvisceritis and thrombophlebitis<br />

as signs of an extensive immune system activation, was seen in a otherwise healthy<br />

40-year-old man.<br />

Results<br />

The striking features of S. aureus polyvisceral disease (pneumonia, septicemia, and<br />

pulmonary and hepato-splenic septic embolism), were associated with multiple<br />

immune-mediated focal manifestations (massive pleuric-pericardial effusion, mycocarditis,<br />

and multiple lower limb thrombophlebitis). In vitro resistance to all beta-lactams,<br />

fluoroquinolones, macrolides, and aminoglycosides, apparently did not justify the<br />

clinical-microbiological failure of a glycopeptide-based combination therapy. Only the<br />

administration of combined linezolid-rifampicin-tetracycline together with intensive care<br />

support, achieved a slowly progressive ameliorement, while the polyvisceritis (associated<br />

by an immune-activation syndrome documented by increased CD4+, CD34+, and CD4-<br />

CD8- T-lymphocyte subsets), caused dysreactive disease at multiple body sites, and<br />

required a prolonged high-dose steroid therapy. A complete clinical, laboratory, and<br />

instrumental recovery was reached only three months after admission.<br />

Conclusions<br />

This report raises multiple questions about the epidemiology, pathogenesis, clinical<br />

presentation and manifestations, and management of complicated S. aureus infection,<br />

with special focus on the immune system activation possibly triggered by microbial<br />

antigens, and the therapeutic role of steroids and novel antibiotics targeted against<br />

resistant gram-positive cocci.<br />

“ Focusing FIRST on PEOPLE “ 234 w w w . i s h e i d . c o m

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