par Guillaume, Marie-Paule 
;Driessens, Natacha ;Libert, Maryse ;De Bels, David ;Corazza, Francis ;Karmali, Rafik
Référence European journal of internal medicine, 17, 7, page (503-504)
Publication Publié, 2006-11
;Driessens, Natacha ;Libert, Maryse ;De Bels, David ;Corazza, Francis ;Karmali, Rafik Référence European journal of internal medicine, 17, 7, page (503-504)
Publication Publié, 2006-11
Article révisé par les pairs
| Résumé : | Hemophagocytic syndrome (HPS) is a clinical entity that combines non-specific clinical and biological features. The diagnosis is usually confirmed by a bone marrow examination. HPS may be primary or secondary to a malignancy or to an infectious or autoimmune disease. Since it was first described, various agents have been implicated, including viruses, bacteria, and parasites. In HIV patients, many cases occur with lymphoma or with a variety of opportunistic infections due to CMV, HHV8, Pneumocystis carinii, Mycobacterium tuberculosis, MAC, toxoplasmosis, and even pneumococcus. We report here a case of an AIDS patient presenting a HPS secondary to an extracerebral form of systemic toxoplasmosis that was only revealed by specific PCR in tissue other than the CNS. |
