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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor={{Rim}}, {{AJL}} {{Alison}}
|QuestionAuthor= {{YD}} (Reviewed by  {{YD}} and  {{AJL}})
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Microbiology
|MainCategory=Microbiology
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|MainCategory=Microbiology
|MainCategory=Microbiology
|SubCategory=Neurology
|SubCategory=Neurology
|MainCategory=Microbiology
|MainCategory=Microbiology
|MainCategory=Microbiology
|MainCategory=Microbiology
|MainCategory=Microbiology
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|MainCategory=Microbiology
|MainCategory=Microbiology
|SubCategory=Neurology
|SubCategory=Neurology
|Prompt=A 28-year-old HIV-positive female presents to the emergency room with a high grade fever, headache, weakness, and tonic-clonic seizures. The patient has a recent history of anorexia. Laboratory work-up reveals CD4 count = 80 cells/µL per year. Head computer tomography (CT) scan demostrates multiple ring enhancing lesions in the frontal lobes. The patient requires treatment with a medication that uses which of the following mechanisms of action?
|Prompt=A 28-year-old HIV-positive woman is brought to the emergency department (ED) with an episode of tonic-clonic seizure. The patient's family reports that the patient has recently lost weight and has been having complaints of high-grade fever and headaches for the past few days. The patient has been non-compliant with her anti-retroviral therapy for the past few weeks. Laboratory work-up in the ED is remarkable for CD4 count=80 cells/µL. Head computed tomography (CT) scan demonstrates multiple ring-enhancing lesions in the frontal lobes. The patient is administered empiric pharmacotherapy and is admitted to the hospital. What is the mechanism of action of the drug administered to this patient to treat her condition?
|Explanation=[[Cerebral toxoplasmosis]], caused by ''[[Toxoplasma gondii]]'', is an opportunistic parasitic infection that frequently infects HIV-positive patients with CD4 counts < 100 cells/µL per year. [[Toxoplasmosis]] manifest with fever, headache, and new-onset seizures.  Multiple [[ring-enhancing lesions]] upon cranial CT scan are characteristic. Treatment of [[cerebral toxoplasmosis]] includes [[pyrimethamine]], a [[dihydrofolate reductase inhibitor]], and [[sulfadiazine]], a [[sulfa drug]] that is a [[dihydropteroate synthetase]] inhibitor.
|Explanation=''Toxoplasma gondii'' is an obligatory intracellular opportunistic parasite that commonly infected patients with advanced HIV disease. It is transmitted as cysts in meat or in cat feces. ''Toxoplasma gondii'' infection is typically latent, whereby patients remain asymptomatic until the parasite reactivates at low CD4 levels < 100 cells/µL. Infection with ''Toxoplasma gondii'' typically manifests with [[cerebral toxoplasmosis]], which is characterized by a subacute-onset of high-grade fever and headache that eventually progress to involve focal neurological deficits, seizures, confusion, and death.  Multiple [[ring-enhancing lesions]] on head CT scan or brain MRI are characteristic and are an indication for initiation of empiric therapy for coverage of cerebral toxoplasmosis among HIV-positive patients. The diagnosis of cerebral toxoplasmosis is usually confirmed with elevated anti-toxoplasma IgG concentrations. First-line therapy for cerebral toxoplasmosis includes combination of pyrimethamine (dihydrofolate reductase inhibitor) and sulfadiazine (dihydropteroate synthetase inhibitor). Leucovorin is also added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis. Patients usually report improvement in symptoms within 2 days of administration of pharmacotherapy, and complete resolution follows within 2 weeks of pharmacotherapy. Less commonly, patients present with extracerebral toxoplasmosis, such as chorioretinitis or pneumonitis.
 
|EducationalObjectives=
Cerebral toxoplasmosis, frequently occurring in HIV-positive individuals  with CD4 count < 100 cells/µL per year, often manifests with a fever, headache, and new-onset seizures.
Treatment of [[cerebral toxoplasmosis]] includes [[pyrimethamine]], a [[dihydrofolate reductase inhibitor]], and [[sulfadiazine]], a [[sulfa drug]] that is a [[dihydropteroate synthetase]] inhibitor.
|References= First Aid 2014 page 151
 
|AnswerA=Inhibition of heme polymerase activity
|AnswerA=Inhibition of heme polymerase activity
|AnswerAExp=[[Chloroquine]], an antimalarial drug, is a plasmodium heme polymerase inhibitor.
|AnswerAExp=[[Chloroquine]] is an antimalarial drug that acts by inhibition of plasmodium heme polymerase.
|AnswerB=Inhibition of dihydrofolate reductase activity
|AnswerB=Inhibition of dihydrofolate reductase activity
|AnswerBExp=[[Pyrimethamine]], a drug frequently used to treat [[toxoplasmosis]], is a dihydrofolate reductase inhibitor.
|AnswerBExp=[[Pyrimethamine]] is a dihydrofolate reductase inhibitor indicated for the treatment of [[cerebral toxoplasmosis]] when combined with sulfadiazine. Leucovorin is often added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis.
|AnswerC=Free radical toxicity of organism’s DNA
|AnswerC=Free radical toxicity of organism’s DNA
|AnswerCExp=[[Metronidazole]], an [[antibiotic]] and antiprotozoal, forms free radical metabolites that are toxic to bacterial DNA.
|AnswerCExp=[[Metronidazole]] is an antimicrobial agent that forms free radical metabolites, which are toxic to bacterial DNA.
|AnswerD=Blockade of peptide bond formation at 50S ribosomal subunit
|AnswerD=Blockade of peptide bond formation at the 50S ribosomal subunit
|AnswerDExp=Several [[antibiotics]], including [[chloramphenicol]], [[macrolides]], [[clindamycin]], [[streptogramins]], and [[linezolid]], block peptide bond formation at the 50S ribosomal subunit.
|AnswerDExp=Several [[antibiotics]], including [[chloramphenicol]], [[macrolides]], [[clindamycin]], [[streptogramins]], and [[linezolid]], block peptide bond formation at the 50S ribosomal subunit.
|AnswerE=Inhibition of DNA polymerase activity
|AnswerE=Inhibition of DNA polymerase activity
|AnswerEExp=Antiviral medications, such as [[acyclovir]], [[ganciclovir]], [[foscarnet]], and [[cidofovir]] are DNA polymerase inhibitors.
|AnswerEExp=Antiviral medications, such as [[acyclovir]], [[ganciclovir]], [[foscarnet]], and [[cidofovir]], are DNA polymerase inhibitors.
|EducationalObjectives=Infection with ''Toxoplasma gondii'' typically manifests with [[cerebral toxoplasmosis]], which is characterized by a subacute-onset of high-grade fever, headache that eventually progress to involve focal neurological deficits, seizures, confusion, and death. It is commong among HIV-positive patients with low CD4 levels < 100 cells/µL. Leucovorin is also added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis.
|References=Jayawardena S, Singh S, Burzyantseva O, et al. Cerebral toxoplasmosis in adult patients with HIV infection. Clin Med J Resid Hosp Physician. 2008;44(7):17-24.<br>
First Aid 2014 page 151
|RightAnswer=B
|RightAnswer=B
|WBRKeyword=Toxoplasma gondii, toxomplasmosis, HIV, seizure, ring enhancing lesion, pyrimethamine, dihydrofolate reductase inhibitor
|WBRKeyword=Toxoplasma gondii, Fever, Cerebral toxoplasmosis, Leucovorin, Sulfadiazine, Mechanism of action, Toxomplasmosis, HIV, Seizure, Ring enhancing lesion, Pyrimethamine, Dihydrofolate reductase inhibitor
|Approved=Yes
|Approved=Yes
}}
}}

Latest revision as of 00:32, 28 October 2020

 
Author [[PageAuthor::Yazan Daaboul, M.D. (Reviewed by Yazan Daaboul, M.D. and Alison Leibowitz [1])]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Microbiology
Sub Category SubCategory::Neurology
Prompt [[Prompt::A 28-year-old HIV-positive woman is brought to the emergency department (ED) with an episode of tonic-clonic seizure. The patient's family reports that the patient has recently lost weight and has been having complaints of high-grade fever and headaches for the past few days. The patient has been non-compliant with her anti-retroviral therapy for the past few weeks. Laboratory work-up in the ED is remarkable for CD4 count=80 cells/µL. Head computed tomography (CT) scan demonstrates multiple ring-enhancing lesions in the frontal lobes. The patient is administered empiric pharmacotherapy and is admitted to the hospital. What is the mechanism of action of the drug administered to this patient to treat her condition?]]
Answer A AnswerA::Inhibition of heme polymerase activity
Answer A Explanation [[AnswerAExp::Chloroquine is an antimalarial drug that acts by inhibition of plasmodium heme polymerase.]]
Answer B AnswerB::Inhibition of dihydrofolate reductase activity
Answer B Explanation [[AnswerBExp::Pyrimethamine is a dihydrofolate reductase inhibitor indicated for the treatment of cerebral toxoplasmosis when combined with sulfadiazine. Leucovorin is often added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis.]]
Answer C AnswerC::Free radical toxicity of organism’s DNA
Answer C Explanation [[AnswerCExp::Metronidazole is an antimicrobial agent that forms free radical metabolites, which are toxic to bacterial DNA.]]
Answer D AnswerD::Blockade of peptide bond formation at the 50S ribosomal subunit
Answer D Explanation [[AnswerDExp::Several antibiotics, including chloramphenicol, macrolides, clindamycin, streptogramins, and linezolid, block peptide bond formation at the 50S ribosomal subunit.]]
Answer E AnswerE::Inhibition of DNA polymerase activity
Answer E Explanation [[AnswerEExp::Antiviral medications, such as acyclovir, ganciclovir, foscarnet, and cidofovir, are DNA polymerase inhibitors.]]
Right Answer RightAnswer::B
Explanation [[Explanation::Toxoplasma gondii is an obligatory intracellular opportunistic parasite that commonly infected patients with advanced HIV disease. It is transmitted as cysts in meat or in cat feces. Toxoplasma gondii infection is typically latent, whereby patients remain asymptomatic until the parasite reactivates at low CD4 levels < 100 cells/µL. Infection with Toxoplasma gondii typically manifests with cerebral toxoplasmosis, which is characterized by a subacute-onset of high-grade fever and headache that eventually progress to involve focal neurological deficits, seizures, confusion, and death. Multiple ring-enhancing lesions on head CT scan or brain MRI are characteristic and are an indication for initiation of empiric therapy for coverage of cerebral toxoplasmosis among HIV-positive patients. The diagnosis of cerebral toxoplasmosis is usually confirmed with elevated anti-toxoplasma IgG concentrations. First-line therapy for cerebral toxoplasmosis includes combination of pyrimethamine (dihydrofolate reductase inhibitor) and sulfadiazine (dihydropteroate synthetase inhibitor). Leucovorin is also added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis. Patients usually report improvement in symptoms within 2 days of administration of pharmacotherapy, and complete resolution follows within 2 weeks of pharmacotherapy. Less commonly, patients present with extracerebral toxoplasmosis, such as chorioretinitis or pneumonitis.

Educational Objective: Infection with Toxoplasma gondii typically manifests with cerebral toxoplasmosis, which is characterized by a subacute-onset of high-grade fever, headache that eventually progress to involve focal neurological deficits, seizures, confusion, and death. It is commong among HIV-positive patients with low CD4 levels < 100 cells/µL. Leucovorin is also added to the combination to reduce the risk of hematologic adverse events associated with pyrimethamine-induced inhibition of folic acid synthesis.
References: Jayawardena S, Singh S, Burzyantseva O, et al. Cerebral toxoplasmosis in adult patients with HIV infection. Clin Med J Resid Hosp Physician. 2008;44(7):17-24.
First Aid 2014 page 151]]

Approved Approved::Yes
Keyword WBRKeyword::Toxoplasma gondii, WBRKeyword::Fever, WBRKeyword::Cerebral toxoplasmosis, WBRKeyword::Leucovorin, WBRKeyword::Sulfadiazine, WBRKeyword::Mechanism of action, WBRKeyword::Toxomplasmosis, WBRKeyword::HIV, WBRKeyword::Seizure, WBRKeyword::Ring enhancing lesion, WBRKeyword::Pyrimethamine, WBRKeyword::Dihydrofolate reductase inhibitor
Linked Question Linked::
Order in Linked Questions LinkedOrder::