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12月19日 Myxomatous &.Cerebral Infarctions
A 25-year-old woman with a history of depression, mitral-valve prolapse, and migraine presented with a 3-day history of fever, arthralgia, and a severe generalized headache that was not characteristic of her previous migraines. On examination, the patient was afebrile, with a pulse rate of 120 beats per minute and a blood pressure of 98/41 mm Hg. She was somnolent but easily arousable, with normal mentation, and the neurologic examination was normal. Laboratory studies showed a normocytic anemia and severe thrombocytopenia. A peripheral-blood smear revealed few platelets and some schistocytes. Thrombotic thrombocytopenic purpura(血栓性血小板减少性紫癜)was suspected, plasma exchange and corticosteroid therapy were initiated with improvement of her symptoms and hematologic abnormalities. However, five days after discharge, the patient returned because of a recurrent headache and emesis, and falling platelet count to 23,000 per cubic millimeter. Blood cultures now showed β-hemolytic group C streptococcus. A trans-esophageal echocardiogram revealed ruptured chordae tendineae of the mitral valve leaflet(二尖瓣腱索断裂), possible leaflet perforation, and severe regurgitation. This suggested infective endocarditis, not thrombotic thrombocytopenic purpura, as the unifying diagnosis. This case discussed “How a clinical presentation prompted an incorrect diagnosis”, and asks clinicians to re-sweep the case and the correct diagnosis of Myxoma" should’ve been made earlier. 12月5日 lymphoma with myocardial infiltration
A 20-year-old man presented to the emergency department after a syncopal episode. During the previous 2 weeks, he had had persistent low-grade fever, anorexia, rhinorrhea, and headache. On the morning of admission, he felt weak and then collapsed while walking into a room; he had no other antece’dent symptoms. Once he regained consciousness, he reported having dyspnea. In the emergency department, the patient remained hypotensive and dyspneic. Electrocardiography (ECG) showed a right bundle-branch block with right-axis deviation, a finding that had not been present 8 months earlier. Two years earlier, the patient had received the diagnosis of stage IV pre–T-cell lymphoblastic lymphoma at the age of 18 years. Despite a complete remission after induction and consolidation chemotherapy, he had had a recurrence within the year. After the patient’s initial presentation with hypotension, syncope, and ECG evidence of right heart strain, the treating physicians pursued the diagnosis of pulmonary embolism. The patient’s long-term use of corticosteroids also prompted consideration of sepsis and adrenal insufficiency. In the process of the evaluation, he was found to have cardiomyopathy. A comparison with previous imaging revealed that there had been rapid progression of ventricular-wall thickening; this was immediately recognized to be pathologic and to point to an infiltrative process. |
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