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Two Women with Hemoptysis Ellen Barbouche, MD Primary Care Conference 8 June 2005 NO FINANCIAL DISCLOSURE
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Objectives Review differential diagnosis of hemoptysis Update role of imaging in evaluation of hemoptysis Explore specific diagnoses of presented cases –Clinical features –Diagnostics –Treatment and outcomes
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Patient #1, History 46 year old female with hypertension 25 pack/year history tobacco, 1 ppd Investment broker and horsewoman Productive cough for 5 days Blood streaked sputum for 24 hours No shortness of breath, rhinitis, or fever Slight pleuritic, anterior chest tightness
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Patient #1, Exam T 97.8, P 100, BP 124/92, pulse ox 97% Purulent right posterior nare No cervical, supraclavicular, or axillary nodes Bilateral rhonchi, clear after cough Heart: RRR, no S3, no murmur
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Patient #2, History 42 year old, previously healthy 25 pack/year history tobacco, 1ppd Machinist for 6 months and horsewoman One week cough, occasional bloody sputum Slight dyspnea No rhinitis, chest pain, or fevers Swollen, painful right ankle
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Patient #2, Exam T 97.0, P 88, RR 12, BP 128/78, pulse ox 98% Nares without mucus or lesion Lungs clear bilaterally Heart: RRR, no murmur, gallop, or rub No cervical, supraclavicular, or axillary nodes Hot, red, swollen left ankle
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Hemoptysis Distinguish from upper respiratory tract or GI Airways disease *MOST COMMON –Tertiary hospital study: bronchiectasis, bronchogenic carcinoma, bronchitis Hirshberg, B et al. Chest 1997;112:440. Pulmonary parenchymal disease Pulmonary vascular disease Other
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Evaluation of Hemoptysis History and physical Chest radiograph Lab guided by history Possible CT versus bronchoscopy –High resolution chest CT demonstrated more tumors than bronchoscopy, but not bronchitis McGuinness, G et al. Chest 1994;105:1155.
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Patient #1, Chest Radiograph
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Patient #1, Initial Course Treatment with azithromycin for community acquired, atypical pneumonia 2 week follow up –Decreased cough intensity and sputum production –Decreased, but persistent, dime-sized hemoptysis
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Patient #1, Chest Radiograph
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Patient #1, Chest CT
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Patient #1, Pulmonary Consult Bronchoscopy –Organizing pneumonitis with 49% eosinophilia –Cultures negative
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Acute Eosinophilic Pneumonia Idiopathic, possibly hypersensitivity reaction to inhaled antigen –1:10K US military in Iraq March 2003-2004 Schorr, AF et al. JAMA 2004;292:2997. –Resolution of AEP despite smoking Kitihara, Y et al. Int Med 2003;42:1016. Classic presentation: one week febrile illness with cough and dyspnea 2/3 patients progress to respiratory failure requiring mechanical ventilation Philit, F et al. Am J Resp Crit Care Med 2002;166:1235.
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Acute Eosinophilic Pneumonia Peripheral eosinophilia develops later in course, not at presentation CXR: subtle reticular opacities progressing to bilateral, diffuse mixed alveolar and reticular opacities CT: bilateral, patchy ground-glass or reticular opacities BAL > 25% eosinophilia
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AEP, Treatment Uniformly responsive to steroids Typically continue steroids 2-4 weeks after symptom and CXR abnormality resolution Allen, JN et al. AM J Resp Crit Care Med 1994;150:1423.
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Patient #1, Post Rx CT
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Patient #2, Chest Radiograph
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Patient #2, Laboratory WBC 18.9K, 15K neutrophils Hemoglobin 10.3, Platelets 275K Sedimentation rate 47, CRP 5 Creatinine 1.1 UA Protein 1+, WBC 6-10, RBC >50 C-ANCA >1:1280 ANA negative
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Wegener’s Granulomatosis, Respiratory Involvement Multisystem vasculitis “Classic” – respiratory tract and kidneys “Limited” – respiratory tract largely Symptoms –Rhinorrhea, often bloody, with oral or nasal ulcers –Cough, hemoptysis, and pleuritic pain –Fever, malaise, eye symptoms, arthritis, rash
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Wegener’s, Laboratory Findings Leukocytosis, normocytic anemia, elevated sedimentation rate C-ANCA –Positive >90% limited OR classic –Majority: autoantibodies to proteinase 3 –Minority: p-ANCA with myeloperoxidase antibodies UA –Limited Wegener’s normal UA –Renal involvement may elevate creatinine, and show proteinuria or active sediment
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Wegener’s Chest Radiography Nodules, possibly cavitary –Single or multiple –Approximately 50% cavitary Alveolar opacities –< 5% alveolar hemorrhage Pleural opacities Cordier, JF et al. Chest 990;97:906
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Wegener’s Diagnosis Histopathologic evidence of vasculitis and granuloma –Most likely from lung biopsy –Renal biopsy more likely to show focal segmental necrotizing glomerulonephritis Jennette, JC et al. Am J Kidney Dis 1994;24:130. Compatible clinical presentation
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Wegener’s Treatment Cyclophosphamide, with or without steroids Serious morbidity and mortality due to cyclophosphamide 60-80% recurrence WGETRG NEJM 2005;352:351.
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Patient #2, Course Difficult due to chest pain, likely related to Wegener’s Severe anemia due to renal insufficiency, pulmonary hemorrhage, and cyclophosphamide Very gradual improvement, though not yet able to work
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Hemoptysis, Conclusions Multiple possible sources of hemoptysis –Bronchiectasis, bronchoalveolar carcinoma, bronchitis most common from lower respiratory tract Most effective work up: history and physical plus chest radiography –Above guide lab, HRCT, and bronchoscopy
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Specific Diagnoses Acute Eosinophilic Pneumonia –Idiopathic –Frequently very severe –Excellent response to steroids Wegener’s Granulomatosis –Vasculitis affecting respiratory tract + kidneys –Usually c-ANCA + –Dangerous treatment with frequent recurrences
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