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Created page with "{{WBRQuestion |QuestionAuthor=William J Gibson |ExamType=USMLE Step 1 |MainCategory=Microbiology, Pathology |SubCategory=Neurology, Infectious Disease |MainCategory=Microbiolo..." |
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|MainCategory=Microbiology, Pathology | |MainCategory=Microbiology, Pathology | ||
|SubCategory=Neurology, Infectious Disease | |SubCategory=Neurology, Infectious Disease | ||
|MainCategory=Microbiology, Pathology | |||
|MainCategory=Microbiology, Pathology | |MainCategory=Microbiology, Pathology | ||
|MainCategory=Microbiology, Pathology | |MainCategory=Microbiology, Pathology | ||
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|SubCategory=Neurology, Infectious Disease | |SubCategory=Neurology, Infectious Disease | ||
|Prompt=A 56 year old woman is brought to the emergency room by her husband. He reports that one week ago she appeared to be increasingly forgetful. At first forgetting things like the car keys, then forgetting appointments. Now she has forgotten the names of her children and her home address. Physical exam is remarkable for an abnormal gait and widespread neurologic deficits particularly in executive function. Brain biopsy would most likely show which of the following? | |Prompt=A 56 year old woman is brought to the emergency room by her husband. He reports that one week ago she appeared to be increasingly forgetful. At first forgetting things like the car keys, then forgetting appointments. Now she has forgotten the names of her children and her home address. Physical exam is remarkable for an abnormal gait and widespread neurologic deficits particularly in executive function. Brain biopsy would most likely show which of the following? | ||
|Explanation=The patient in this vignette is suffering from Creutzfeldt-Jakob disease, an infectious disease caused by the abnormal aggregation of prions. Prions are an abnormally folded protein composed of beta pleated sheets which act as a scaffold to induce the conversion of other proteins into an abnormally folded prion state as well. | |Explanation=The patient in this vignette is suffering from Creutzfeldt-Jakob disease, an infectious disease caused by the abnormal aggregation of prions. Prions are an abnormally folded protein composed of beta pleated sheets which act as a scaffold to induce the conversion of other proteins into an abnormally folded prion state as well. Creutzfeldt-Jakob disease is characterized by the rapid onset of dementia in otherwise well people. It is universally fatal and there is no treatment. | ||
|AnswerA=Lymphocytic infiltrate | |AnswerA=Lymphocytic infiltrate | ||
|AnswerAExp= | |AnswerAExp=This corresponds to encephalitis, which may show more systemic symptoms such as fever and focal neurologic deficits. | ||
|AnswerB=Alpha Synuclein deposits | |AnswerB=Alpha Synuclein deposits | ||
|AnswerBExp= | |AnswerBExp=This corresponds to Lewy Body dementia which would not have the acute onset seen in this patient. | ||
|AnswerC=Beta pleated sheets | |AnswerC=Beta pleated sheets | ||
|AnswerCExp= | |AnswerCExp=See explanation | ||
|AnswerD=Abnormally phosphorylated tau protein | |AnswerD=Abnormally phosphorylated tau protein | ||
|AnswerDExp= | |AnswerDExp=This corresponds to Neurofibrillary tangles, pathologic changes associated with Alzheimer’s disease. Alzheimer’s disease does not have the acute onset seen in this patient. | ||
|AnswerE=Beta-amyloid deposits | |AnswerE=Beta-amyloid deposits | ||
|AnswerEExp= | |AnswerEExp=This corresponds to the composition of senile plaques, pathologic changes seen in Alzheimers disease. Alzheimer’s disease does not have the acute onset seen in this patient. | ||
|EducationalObjectives=Creutzfeldt-Jakob disease is characterized by rapidly progressive dementia, and is caused by prions which are proteins folded as beta pleated sheets. | |||
|References=First Aid 2014 page 483 | |||
|RightAnswer=C | |RightAnswer=C | ||
|WBRKeyword=Neurology, Pathology, Neuropathology, Prion, Creutzfeldt-Jakob disease, Dementia, Mental status change, | |||
|Approved=Yes | |Approved=Yes | ||
}} | }} |
Revision as of 02:02, 11 September 2014
Author | PageAuthor::William J Gibson |
---|---|
Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Microbiology, MainCategory::Pathology |
Sub Category | SubCategory::Neurology, SubCategory::Infectious Disease |
Prompt | [[Prompt::A 56 year old woman is brought to the emergency room by her husband. He reports that one week ago she appeared to be increasingly forgetful. At first forgetting things like the car keys, then forgetting appointments. Now she has forgotten the names of her children and her home address. Physical exam is remarkable for an abnormal gait and widespread neurologic deficits particularly in executive function. Brain biopsy would most likely show which of the following?]] |
Answer A | AnswerA::Lymphocytic infiltrate |
Answer A Explanation | AnswerAExp::This corresponds to encephalitis, which may show more systemic symptoms such as fever and focal neurologic deficits. |
Answer B | AnswerB::Alpha Synuclein deposits |
Answer B Explanation | AnswerBExp::This corresponds to Lewy Body dementia which would not have the acute onset seen in this patient. |
Answer C | AnswerC::Beta pleated sheets |
Answer C Explanation | AnswerCExp::See explanation |
Answer D | AnswerD::Abnormally phosphorylated tau protein |
Answer D Explanation | AnswerDExp::This corresponds to Neurofibrillary tangles, pathologic changes associated with Alzheimer’s disease. Alzheimer’s disease does not have the acute onset seen in this patient. |
Answer E | AnswerE::Beta-amyloid deposits |
Answer E Explanation | AnswerEExp::This corresponds to the composition of senile plaques, pathologic changes seen in Alzheimers disease. Alzheimer’s disease does not have the acute onset seen in this patient. |
Right Answer | RightAnswer::C |
Explanation | [[Explanation::The patient in this vignette is suffering from Creutzfeldt-Jakob disease, an infectious disease caused by the abnormal aggregation of prions. Prions are an abnormally folded protein composed of beta pleated sheets which act as a scaffold to induce the conversion of other proteins into an abnormally folded prion state as well. Creutzfeldt-Jakob disease is characterized by the rapid onset of dementia in otherwise well people. It is universally fatal and there is no treatment. Educational Objective: Creutzfeldt-Jakob disease is characterized by rapidly progressive dementia, and is caused by prions which are proteins folded as beta pleated sheets. |
Approved | Approved::Yes |
Keyword | WBRKeyword::Neurology, WBRKeyword::Pathology, WBRKeyword::Neuropathology, WBRKeyword::Prion, WBRKeyword::Creutzfeldt-Jakob disease, WBRKeyword::Dementia, WBRKeyword::Mental status change |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |