WBR0750: Difference between revisions
Jump to navigation
Jump to search
Rim Halaby (talk | contribs) Created page with "{{WBRQuestion |QuestionAuthor={{Rim}} |ExamType=USMLE Step 1 |MainCategory=Pathology |SubCategory=Musculoskeletal/Rheumatology |MainCategory=Pathology |SubCategory=Musculoskel..." |
Rim Halaby (talk | contribs) No edit summary |
||
| Line 20: | Line 20: | ||
|MainCategory=Pathology | |MainCategory=Pathology | ||
|SubCategory=Musculoskeletal/Rheumatology | |SubCategory=Musculoskeletal/Rheumatology | ||
|Prompt=A 62 year old woman presents to the physician's office complaining of muscle weakness. She notes that she has recently been unable to comb her hair but is able to button a shirt. She also explains that she has been unable to stand from a seated position. Review of systems shows she also complains of arthralgia involving the hand joints, wrists, and knees. Physical examination is remarkable for symmetric proximal muscle weakness. Inspection of her face shows periorbital violaceous erythema with edematous eyelids. Further inspection of her dorsal interphalangeal and metacarophalangeal joints of her hands also show violaceous flat-topped papules and plaques. Her lab work-up shows elevated levels of creatine kinase. EMG is performed; it shows patterns consistent with muscular impairment. | |Prompt=A 62 year old woman presents to the physician's office complaining of muscle weakness. She notes that she has recently been unable to comb her hair but is able to button a shirt. She also explains that she has been unable to stand from a seated position. Review of systems shows she also complains of arthralgia involving the hand joints, wrists, and knees. Physical examination is remarkable for symmetric proximal muscle weakness. Inspection of her face shows periorbital violaceous erythema with edematous eyelids. Further inspection of her dorsal interphalangeal and metacarophalangeal joints of her hands also show violaceous flat-topped papules and plaques. Her lab work-up shows elevated levels of creatine kinase. EMG is performed; it shows patterns consistent with muscular impairment. What is the most likely pathological feature of the patient's condition? | ||
What is the most likely pathological feature of the patient's condition? | |||
|Explanation=The patient is presenting with symptoms and signs consistent with dermatomyositis. Dermatomyositis is an inflammatory myopathy chaacterized by symmetric proximal weakness with truncal weakness. Pain may or may not be present in dermatomyositis. Physical exmimnation typically shows Gottron papules, defined as violaceous flat-topped papules and plaques in the dorsal aspect of the hand, and heliotrope rash, defined as periorbital violaceous erythema with periorbital edema. The latter is specific for dermatomyositis. Work-up shows elevation of muscle biomarkers, such as creatine kinase. Pathologically, dermatomyositis is considered a perimysial inflammation with lymphocytic infiltration generally confined to the septa. | |Explanation=The patient is presenting with symptoms and signs consistent with dermatomyositis. Dermatomyositis is an inflammatory myopathy chaacterized by symmetric proximal weakness with truncal weakness. Pain may or may not be present in dermatomyositis. Physical exmimnation typically shows Gottron papules, defined as violaceous flat-topped papules and plaques in the dorsal aspect of the hand, and heliotrope rash, defined as periorbital violaceous erythema with periorbital edema. The latter is specific for dermatomyositis. Work-up shows elevation of muscle biomarkers, such as creatine kinase. Pathologically, dermatomyositis is considered a perimysial inflammation with lymphocytic infiltration generally confined to the septa. | ||
| Line 33: | Line 32: | ||
Dalakas M. Polymyositis, dermatomyositis, and inclusion-body myositis. N Engl J Med. 1991; 325:1487-1498. | Dalakas M. Polymyositis, dermatomyositis, and inclusion-body myositis. N Engl J Med. 1991; 325:1487-1498. | ||
|AnswerA=Endomysial inflammation | |AnswerA=Endomysial inflammation | ||
|AnswerAExp=Endomysial inflammation is characteristic of polymyositis | |AnswerAExp=Endomysial inflammation is characteristic of polymyositis | ||
Revision as of 22:41, 28 October 2013
| Author | [[PageAuthor::Rim Halaby, M.D. [1]]] |
|---|---|
| Exam Type | ExamType::USMLE Step 1 |
| Main Category | MainCategory::Pathology |
| Sub Category | SubCategory::Musculoskeletal/Rheumatology |
| Prompt | [[Prompt::A 62 year old woman presents to the physician's office complaining of muscle weakness. She notes that she has recently been unable to comb her hair but is able to button a shirt. She also explains that she has been unable to stand from a seated position. Review of systems shows she also complains of arthralgia involving the hand joints, wrists, and knees. Physical examination is remarkable for symmetric proximal muscle weakness. Inspection of her face shows periorbital violaceous erythema with edematous eyelids. Further inspection of her dorsal interphalangeal and metacarophalangeal joints of her hands also show violaceous flat-topped papules and plaques. Her lab work-up shows elevated levels of creatine kinase. EMG is performed; it shows patterns consistent with muscular impairment. What is the most likely pathological feature of the patient's condition?]] |
| Answer A | AnswerA::Endomysial inflammation |
| Answer A Explanation | AnswerAExp::Endomysial inflammation is characteristic of polymyositis |
| Answer B | AnswerB::Perimysial inflammation |
| Answer B Explanation | AnswerBExp::Perimysial inflammation is characteristic of dermatomyositis. |
| Answer C | AnswerC::Non-caseating granulomas |
| Answer C Explanation | AnswerCExp::Non-caseating granulomas are commonly seen in sarcoidosis. |
| Answer D | AnswerD::Precipitation of monosodium urate crystals |
| Answer D Explanation | AnswerDExp::Precipitation of monosodium urate crystals is characteristic of gout. |
| Answer E | AnswerE::Autoimmune inflammatory destruction of synovial joints |
| Answer E Explanation | AnswerEExp::Rheumatoid arthritis (RA) is characterized by the autoimmune inflammatory destruction of synovial joints. |
| Right Answer | RightAnswer::B |
| Explanation | [[Explanation::The patient is presenting with symptoms and signs consistent with dermatomyositis. Dermatomyositis is an inflammatory myopathy chaacterized by symmetric proximal weakness with truncal weakness. Pain may or may not be present in dermatomyositis. Physical exmimnation typically shows Gottron papules, defined as violaceous flat-topped papules and plaques in the dorsal aspect of the hand, and heliotrope rash, defined as periorbital violaceous erythema with periorbital edema. The latter is specific for dermatomyositis. Work-up shows elevation of muscle biomarkers, such as creatine kinase. Pathologically, dermatomyositis is considered a perimysial inflammation with lymphocytic infiltration generally confined to the septa.
Dermatomyositis has a bimodal peak incidence. In adult patients > 50 years of age, the diagnosis of dermatomyositis prompts the investigation of a malignancy due to frequent association. This is not true, however, for those diagnosed at young age. Educational Objective: Dermatomyositis is characterized by perimysial inflammation. References: Khan S, Christopher-Stine L. Polymyositis, dermatomyositis, and autoimmune necrotizing myopathy: clinical features. Rheum Dis Clin N Am. 2011; 37:143-158. Dalakas M. Polymyositis, dermatomyositis, and inclusion-body myositis. N Engl J Med. 1991; 325:1487-1498. |
| Approved | Approved::No |
| Keyword | WBRKeyword::polymyositis, WBRKeyword::dermatomyositis, WBRKeyword::myopathy, WBRKeyword::inflammatory, WBRKeyword::proximal, WBRKeyword::muscle, WBRKeyword::weakness, WBRKeyword::perimysial, WBRKeyword::inflammation, WBRKeyword::endomysial, WBRKeyword::myopathies, WBRKeyword::gottron, WBRKeyword::papules, WBRKeyword::gottron's, WBRKeyword::heliotrope, WBRKeyword::rash |
| Linked Question | Linked:: |
| Order in Linked Questions | LinkedOrder:: |