2017
DOI: 10.5847/wjem.j.1920-8642.2017.01.012
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Toxoplasma encephalitis and AIDS in a patient with seizure and altered mental status: A case report

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Cited by 5 publications
(7 citation statements)
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“…Toxoplasmosis can cause severe clinical symptoms and even death in infants, pregnant women and immunocompromised individuals [ 2 , 3 ]. This parasite can infect all host tissues, but the central nervous system and muscles are the predilection sites [ 4 ]. Tachyzoites of T. gondii can invade almost all nucleated cells but have a particular affinity for nerve cells, resulting in T. gondii encephalitis [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…Toxoplasmosis can cause severe clinical symptoms and even death in infants, pregnant women and immunocompromised individuals [ 2 , 3 ]. This parasite can infect all host tissues, but the central nervous system and muscles are the predilection sites [ 4 ]. Tachyzoites of T. gondii can invade almost all nucleated cells but have a particular affinity for nerve cells, resulting in T. gondii encephalitis [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…In antiviral therapy, non-nucleoside reverse transcriptase inhibitors nevirapine and efavirenz can cause severe skin eruption. [10,11] Anti-tuberculosis drugs are the second most common cause of drug-induced erythroderma in our study. It is suggested that AIDS patients should be tested for tuberculosis infection early, and skin changes should be closely observed during the course of anti-tuberculosis treatment.…”
Section: Discussionmentioning
confidence: 73%
“…It has been reported that the drug eruption rate in HIV-positive patients is 100 times that of HIVnegative patients. [10][11][12] However, AIDS patients with drug-induced erythroderma is rare, and the mechanism is still unclear. [13] Common agents that cause druginduced erythroderma in HIV-negative persons include carbamazepine antiepileptic drugs, sulfa antibiotics, penicillins, and cephalosporins.…”
Section: Discussionmentioning
confidence: 99%
“…If seropositive without evidence of active toxoplasma encephalitis and a CD4 of <100µL, it is recommended to initiate prophylactic TMP-SMX. Prophylaxis/secondary prophylaxis may be discontinued with response to ART by an increase in CD4 + counts to >200 cells/µL for >3 months [9]. Of note ruling out G6PD deficiency should be done prior to initiation of treatment given association with severe hemolytic anemia.…”
Section: Discussionmentioning
confidence: 99%