Differentials

Common

Acute bronchitis

History

acute onset cough, wheeze and/or dyspnea, rhinorrhea, sore throat

Exam

may be normal, cough with variable degrees of hemoptysis, normal to mildly elevated temperature, rhonchi, expiratory wheezing

1st investigation
  • CXR:

    normal or faint diffuse infiltrates

  • sputum culture:

    bacteria most often recovered: Haemophilus influenzae, Streptococcus pneumoniae, Moraxella catarrhalis, less commonly Bordetella pertussis; viral agents: respiratory syncytial virus, rhinovirus, echovirus, parainfluenza, herpesvirus, coxsackievirus, influenza, coronavirus, adenovirus

    More
Other investigations
  • bronchoscopy:

    nondiagnostic, or small amount of blood in airways, signs of inflammation

    More

Chronic bronchitis

History

frequent cough with excessive mucus production; chest pressure or pain; triggers include tobacco smoke, cannabis, air pollutants, and various infectious agents

Exam

may be normal, cough with variable degrees of hemoptysis, rhonchi, expiratory wheezing, barrel chest, hyper-resonance on percussion, poor air movement on auscultation

1st investigation
  • CXR:

    Increased anteroposterior ratio, flattened diaphragm, increased intercostal spaces, and hyperlucent lungs may be seen

    More
  • spirometry:

    FEV1/FVC ratio <0.70

Other investigations
  • bronchoscopy:

    nondiagnostic, or small amount of blood in airways, signs of chronic inflammation

Pulmonary tuberculosis

History

history of travel to endemic areas, exposure to people with tuberculosis (TB), risk factors for HIV, history of incarceration or homelessness; cough, dyspnea, weight loss, fever, joint aches, night sweats

Exam

cachexia, fever, lymphadenopathy, rales, consolidation, decreased breath sounds if pleural effusion is present

1st investigation
  • CXR:

    may demonstrate atelectasis from airway compression, pleural effusion, consolidation, pulmonary infiltrates, mediastinal or hilar lymphadenopathy, upper zone fibrosis

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  • sputum acid-fast bacilli smear and culture:

    presence of acid-fast bacilli (Ziehl-Neelsen stain) in specimen.

    More
  • nucleic acid amplification (NAAT):

    positive for M tuberculosis

    More
Other investigations
  • bronchoscopy and bronchoalveolar lavage:

    positive for acid-fast bacilli

    More
  • contrast-enhanced chest computed tomography scan:

    primary TB: mediastinal tuberculous lymphadenitis with central node attenuation and peripheral enhancement, delineated cavities; postprimary TB: centrilobular nodules and tree-in-bud pattern

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  • lateral flow urine lipoarabinomannan (LF-LAM) assay:

    positive

    More

Lung abscess

History

high fever (>101°F [>38.5°C]), productive cough, purulent sputum, weight loss, malaise, fever, night sweats, alcoholism, risk factors for aspiration; massive hemoptysis may occur with chronic abscesses

Exam

fever, cardiac murmur, signs of gingival disease, cachexia, halitosis, amphoric or cavernous breath sounds, inspiratory crackles and/or bronchial breathing, decreased breath sounds; nail clubbing may occur with chronic abscesses

1st investigation
  • CBC:

    leukocytosis, anemia

  • CXR:

    consolidation with central cavitation and air-fluid level, cavity wall thick and irregular

  • sputum Gram stain:

    one predominant gram-positive or -negative organism and neutrophils in aerobic infections; mixed flora with many neutrophils in anaerobic infections

  • sputum culture:

    often only see growth of normal respiratory flora in polymicrobial anaerobic infections; growth of infecting organism in aerobic infections

  • blood culture:

    positive for infecting organism in aerobic infections, bacteremia, and septic embolism; seldom positive in anaerobic infections

Other investigations
  • contrast-enhanced chest CT scan:

    thick-walled, usually round cavity with irregular margins forming an acute angle with chest wall, no signs of compression of surrounding lung

    More

Pneumonia

History

fever, cough, dyspnea, chest pain, malaise

Exam

dullness to percussion, fever, unilateral rales, hypoxemia

1st investigation
  • CXR:

    lobar or segmental infiltrates

    More
  • sputum Gram stain:

    visualization of suspected infecting organisms such as gram-negative rods, gram-positive cocci

  • sputum culture:

    growth of infecting organism

  • blood culture:

    may be positive for infecting organism

Other investigations

    Primary lung cancer

    History

    new cough, dyspnea (worse at night or in recumbent position), chest pain, weight loss, occurrence of paraneoplastic syndrome

    Exam

    clubbing, focal wheezing, diminished breath sounds in pleural effusion or central obstruction

    1st investigation
    • CXR:

      may be normal or show segmental atelectasis, lobar collapse, obstructive pneumonitis, pleural effusion

      More
    • chest CT scan:

      from solitary lung nodule to endobronchial obstruction with atelectatic lobe or lung, mediastinal/hilar lymphadenopathy, and/or pleural effusion

    • bronchoscopy:

      vascular lesions: may obstruct airways distal to tumor, subtle granular appearance, or erythematous mucosa; polypoid or papillary infiltrative with superficial erosions

      More
    Other investigations
    • PET-fluorodeoxyglucose scan:

      positive uptake of 18-fluorodeoxyglucose (FDG) in metabolically active nodules

      More

    Lung metastasis

    History

    symptoms related to the primary neoplastic site, pain, weight loss, malaise, cough, dyspnea

    Exam

    clubbing, focal wheezing

    1st investigation
    • chest CT scan:

      one or multiple nodules of variable sizes, from diffuse micronodular shadows (miliary) to well-defined masses, often irregular, often in the periphery of the lower lung zones, sometimes with cavitation; may see lymphadenopathy

      More
    Other investigations
    • PET-fluorodeoxyglucose scan:

      increased uptake in pulmonary nodules and at primary site

      More
    • bronchoscopy with biopsy:

      positive for malignant cells

      More
    • sputum cytology:

      positive for malignant cells

      More

    Anticoagulants, thrombolytic agents

    History

    exposure to anticoagulants, antiplatelet therapy, thrombolytic agents

    Exam

    ecchymosis, petechiae, may be normal

    1st investigation
    • INR:

      may be prolonged

      More
    • PTT:

      may be prolonged

      More
    Other investigations
    • bronchoscopy:

      bleeding

      More

    Toxic inhalation

    History

    exposure to smoke inhalation, solvents, trimellitic anhydride

    Exam

    may be normal, cough with variable degrees of hemoptysis

    1st investigation
    • CXR:

      atelectasis; airspace opacity

    • ABG with carboxyhemoglobin (CO-Hg) level:

      severe metabolic acidosis; CO-Hg level >15%

    • pulse oximetry:

      hypoxemia

    • ECG:

      arrhythmias, ischemia

    Other investigations
    • bronchoscopy:

      bleeding

      More

    Bronchiectasis

    History

    frequent cough with excessive mucus production and little seasonal variation, dyspnea, pleurisy, fatigue, weight loss; history of cystic fibrosis, alpha-1 antitrypsin deficiency, underlying immunodeficiency

    Exam

    cough almost always present, with variable degrees of hemoptysis, crackles, wheezing, clubbing

    1st investigation
    • CXR:

      may be normal or show obscured hemidiaphragm, thin-walled ring shadows with or without fluid levels, tram lines, tubular or ovoid opacities

    • chest CT scan:

      dilated bronchi with thickened walls extending to the lung periphery; bronchial diameter larger than accompanying pulmonary artery, creating "signet ring" appearance, endobronchial mucus impaction

      More
    • sputum culture:

      pathogens most often recovered: Pseudomonas, Haemophilus influenzae, Streptococcus pneumoniae, Moraxella catarrhalis, Mycobacterium avium, Aspergillus, viral pathogens

    Other investigations
    • bronchoscopy:

      small amount of blood in airways, signs of chronic inflammation

      More
    • spirometry:

      obstructive physiology with decrease in FEV1/FVC ratio below normal limit

    Pulmonary thromboembolism

    History

    dyspnea, pleuritic chest pain, syncope

    Exam

    tachycardia, unilateral lower extremity edema, split S2 with loud P2, diaphoresis, tachypnea

    1st investigation
    • CT pulmonary angiogram (CTPA):

      low-attenuation filling defects within a well-opacified pulmonary artery, clot, vessel cutoff, rim sign

      More
    • Echocardiography:

      abnormal RV ejection pattern (“60-60 sign”); reduced contractility of the RV free wall compared with the RV apex “McConnell sign”); RV dilatation and hypokinesis; RV diameter/LV diameter >0.9; interventricular septal flattening and paradoxical leftward septal motion; tricuspid regurgitation; pulmonary hypertension

      More
    • D-dimer:

      positive

      More
    Other investigations
    • ventilation-perfusion (V/Q) radionuclide scan:

      PE likely when an area of ventilation is not perfused

      More
    • CXR:

      nonspecific parenchymal infiltrates, atelectasis, hemidiaphragm elevation, pleural effusion

      More

    Mitral valve stenosis

    History

    chronic dyspnea, dyspnea on exertion, orthopnea, paroxysmal nocturnal dyspnea, palpitations; may become clinically apparent with pregnancy-induced hemodynamic changes; history of recurrent respiratory infections (group A hemolytic streptococci) during childhood, rheumatic fever, rheumatic heart disease, living in endemic areas for mitral stenosis, atherosclerotic heart disease, and/or mitral annular calcification

    Exam

    reduced pulse pressure, elevated jugular venous distension, plethoric cheeks, right ventricular lift, atrial fibrillation, diastolic rumble, opening snap, loud S1, loud P2, hoarseness (recurrent laryngeal nerve impingement by the left atrium)

    1st investigation
    • CXR:

      dilated left atrium, variable cardiomegaly, calcified mitral valve, increased interstitial markings with Kerley-B lines

    • ECG:

      atrial fibrillation with right ventricular hypertrophy, left atrial enlargement with long P wave (>120 milliseconds), broad notched P waves in lead II

    • transthoracic echocardiogram:

      leaflet thickening, commissural fusion, chordal shortening, chordal fusion

    Other investigations

      Left ventricular failure

      History

      history of hypertension, diabetes mellitus, dyslipidemia, or tobacco use; coronary, valvular, or peripheral vascular disease; dyspnea, palpitations, chest discomfort, orthopnea, paroxysmal nocturnal dyspnea, fatigue

      Exam

      neck vein distension, hepatojugular reflux, rales, S3 gallop, cardiomegaly, tachycardia

      1st investigation
      • transthoracic echocardiogram:

        systolic heart failure: depressed and dilated left and/or right ventricle with low ejection fraction; diastolic heart failure: left ventricular ejection fraction normal but left ventricular hypertrophy and abnormal diastolic filling patterns

      • ECG:

        evidence of previous infarct, left ventricular hypertrophy, or atrial enlargement; may be conduction abnormalities and abnormal QRS duration

      • CXR:

        cardiomegaly, pulmonary vascular congestion, Kerley B lines, pleural effusions

      • BUN and creatinine:

        normal to elevated

      • blood glucose:

        elevated in diabetes

      • thyroid function tests:

        hypothyroidism: elevated thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), decreased free thyroxine (FT4); hyperthyroidism: decreased TSH, elevated FT4

      • blood lipids:

        elevated in dyslipidemia

      • B-type natriuretic peptide (BNP)/N-terminal pro BNP levels:

        elevated

      Other investigations

        Coagulopathy

        History

        association with advanced liver and kidney disease, hematologic malignancy, recent cytotoxic chemotherapy, specific disorders of coagulation cascade (factor deficiency); menorrhagia

        Exam

        petechiae, small capillary hemorrhages, ecchymoses, hematomas, hemarthrosis

        1st investigation
        • INR and PTT:

          elevated

        • BUN and creatinine:

          may be elevated

        Other investigations
        • specific coagulation factor deficiency:

          decreased or absent

        • thrombin time:

          elevated

        Thrombocytopenia

        History

        may present with purpura, or be associated with gestation, HIV, liver disease, myelodysplastic syndrome; may be drug-induced

        Exam

        purpura, mucosal bleeding, epistaxis, signs of liver disease

        1st investigation
        • peripheral blood smear:

          thrombotic microangiopathy (schistocytes)

        • CBC with differential:

          low platelet count

          More
        Other investigations
        • LFTs:

          may be normal; elevated in HELLP syndrome

        • lactate dehydrogenase:

          elevated in hemolysis

        • haptoglobin:

          low level with hemolysis

        • INR/PTT:

          elevated in disseminated intravascular coagulation

        • fibrinogen:

          low in disseminated intravascular coagulation

        • D-dimer:

          elevated in disseminated intravascular coagulation

        Disseminated intravascular coagulation

        History

        fever, cough, dyspnea, confusion, epistaxis, bleeding gums; possible history of sepsis, obstetric complications such as placental abruption, snake bite, malignancy (e.g., acute promyelocytic leukemia), or tissue trauma (e.g., surgery)

        Exam

        petechiae, gastrointestinal or genitourinary tract bleeding, hypotension, tachycardia, pleural friction rub

        1st investigation
        • CBC with differential:

          pancytopenia

        • peripheral blood smear:

          thrombotic microangiopathy (schistocytes)

        • serum INR and activated PTT:

          elevated

        • serum fibrinogen:

          low

        • D-dimer:

          elevated

        Other investigations

          Uncommon

          Aspergilloma

          History

          mostly asymptomatic, commonly secondary to underlying chronic lung disease; weight loss, chronic cough, malaise

          Exam

          cough, variable hemoptysis

          1st investigation
          • CXR:

            upper lobe mobile intracavitary mass with an air crescent in the periphery

          • high-resolution chest CT scan:

            upper lobe cavitary mass with intracavitary contents and adjacent pleural thickening

            More
          Other investigations

            Endobronchial and pulmonary mucormycosis

            History

            underlying diabetes mellitus, immunosuppressed state, hematologic disorder or transplant, chronic renal failure, chronic steroid use; fever, cough, dyspnea, hemoptysis

            Exam

            sinusitis if upper airway is involved, wheezing if lower airway is involved, normal exam if only lung parenchyma is involved

            1st investigation
            • CXR:

              pulmonary infiltrates

            • high-resolution chest CT scan:

              unilateral or bilateral infiltrates, cavity, endobronchial mass may mimic tumor

            • CT guided needle biopsy:

              non-septate or minimally septate broad, ribbon-like hyphae

              More
            Other investigations
            • bronchoscopy and bronchoalveolar lavage:

              non-septate or minimally septate broad, ribbon-like hyphae

              More

            Endobronchial neuroendocrine tumor (carcinoid)

            History

            asymptomatic; may cause cough, dyspnea, wheezing if nodule is endobronchial

            Exam

            often normal exam, unilateral wheezing may be present

            1st investigation
            • CXR:

              may be normal or show solitary nodule, segmental atelectasis, lobar collapse, obstructive pneumonitis

            • chest CT scan:

              solitary lung nodule, endobronchial nodule, parenchymal nodule

              More
            • bronchoscopy with biopsy:

              raised, pinkish, vascular, lobulated lesions; biopsy positive for malignant cells

              More
            Other investigations

              Aspiration of foreign body

              History

              may be asymptomatic, cough paroxysms, localized wheezing, choking crisis; most common in children <15 years of age; associated with alcohol misuse, sedative use, poor dentition, neurologic disease, loss of consciousness, seizure in older adults

              Exam

              focal wheezing, choking crisis, focal decrease in breath sounds

              1st investigation
              • CXR:

                atelectasis, pulmonary infiltrates

                More
              • bronchoscopy:

                chronic foreign body usually covered with mucus and granulation tissue

                More
              Other investigations
              • chest CT scan:

                associated air trapping, atelectasis

                More

              Aspiration of gastric contents

              History

              history of GERD, age >70 years, general anesthesia, cerebrovascular disease; fever, intractable cough, dyspnea, alcohol misuse

              Exam

              fever, crackles, wheezing, dyspnea

              1st investigation
              • CXR:

                patchy airspace consolidations

              Other investigations
              • chest CT scan:

                opacities in dependent segments

                More

              Broncholithiasis

              History

              chronic cough, occasional chest pain, may be asymptomatic; history of recurrent pneumonias in same location

              Exam

              rarely wheezing due to airway obstruction

              1st investigation
              • chest CT scan:

                calcified mediastinal adenopathy or bronchial obstruction

              Other investigations
              • bronchoscopy:

                splayed or irregular carinas

                More

              Tracheoesophageal fistula

              History

              feeding difficulties, recurrent aspiration pneumonia, cough

              Exam

              labored breathing, coughing, choking, and cyanosis are nonspecific findings

              1st investigation
              • CXR:

                mediastinal air, gas-filled gastrointestinal tract, dependent infiltrates; insertion of a nasogastric tube may show coiling in the upper pouch

              • upper gastrointestinal series:

                spilling of contrast into the trachea

                More
              Other investigations
              • bronchoscopy:

                presence of a fistula

              Bronchial telangiectasia

              History

              sometimes associated with hereditary hemorrhagic telangiectasia, recurrent epistaxis

              Exam

              mucocutaneous telangiectasia, pulmonary bruit, stigmata of right-to-left shunting such as cyanosis and clubbing

              1st investigation
              • CT angiography:

                presence of arteriovenous malformations

              Other investigations
              • bronchoscopy:

                nonspecific network of submucosal dilated vessels

              Airway trauma

              History

              recent history of high-velocity accident, blunt trauma to neck or chest, or exposure to explosive blast; iatrogenic hemoptysis may occur with traumatic intubation, bronchoscopy, and endobronchial therapeutic maneuvers

              Exam

              tachypnea, wheezing, chest or neck pain; external signs may or may not indicate magnitude of trauma

              1st investigation
              • CXR:

                presence of widened mediastinum

                More
              • chest CT scan:

                fractures, hematomas, patchy or diffuse infiltrates in the lung parenchyma that do not conform to segmental or lobar anatomy

              Other investigations
              • bronchoscopy:

                distal hemorrhage, pulmonary contusion, aspirated material

                More

              Dieulafoy disease

              History

              congenital origin; history of comorbidities: cardiovascular disease, hypertension, chronic renal failure, diabetes, or alcohol misuse

              Exam

              Dieulafoy disease is a vascular anomaly characterized by the presence of a tortuous dysplastic artery in the submucosa; cases involving a subepithelial bronchial artery have caused hemoptysis; most cases involve the gastrointestinal tract

              1st investigation
              • bronchoscopy:

                arterial bleeding in area of ulcer or nodule; raised nipple or visible vessel without an ulcer, in absence of bleeding

              • endoscopy:

                arterial bleeding in area of ulcer or nodule; raised nipple or visible vessel without an ulcer, in absence of bleeding

              Other investigations

                Thoracic endometriosis

                History

                catamenial symptoms (within 24-48 hours of onset of menstruation); may have dysmenorrhea, dyspareunia; chest pain, shortness of breath

                Exam

                no physical findings; pelvic tenderness, cul-de-sac nodularity may be present

                1st investigation
                • no test required:

                  diagnosis is clinical

                Other investigations
                • chest CT scan:

                  may be negative; pulmonary or pleural nodules seen during menses

                Pulmonary artery aneurysm

                History

                congenital or related to pulmonary artery catheter complication

                Exam

                nonspecific; chest pain may be present

                1st investigation
                • CT angiography:

                  presence of pulmonary artery aneurysm

                Other investigations

                  Fat embolism

                  History

                  dyspnea, fever, changes in mental status; usually 24-72 hours after long-bone fracture or liposuction

                  Exam

                  hypoxemia, tachypnea, changes in mental status; petechiae in the head, neck, anterior chest, and axillae

                  1st investigation
                  • no test required:

                    diagnosis is clinical

                  Other investigations

                    Tumor thromboembolism

                    History

                    history of mucin-secreting adenocarcinomas (breast, lung, stomach, colon), hepatoma, prostate cancer, choriocarcinoma, or renal cell carcinoma

                    Exam

                    tachypnea, hypoxemia, tachycardia

                    1st investigation
                    • CT angiography:

                      diagnosis is made in conjunction with high clinical suspicion; isolated vascular filling defect may be difficult to distinguish from blood clot

                    Other investigations
                    • ECG:

                      right-heart strain

                    • surgery:

                      histopathologic demonstration of tumor cells in the pulmonary vasculature

                    Arteriovenous malformation

                    History

                    dyspnea; history of stroke, brain abscess, cirrhosis (hepatopulmonary syndrome); personal or family history of hereditary hemorrhagic telangiectasia

                    Exam

                    pulmonary bruit; arteriovenous communications or telangiectasia in skin, mucous membranes, and other organs; cyanosis, clubbing; neurologic signs from cerebral aneurysms, cerebral emboli, or metastatic abscess; stigmata of advanced liver disease (jaundice, small liver, ascites, skin spider angiomata)

                    1st investigation
                    • chest CT with contrast:

                      round or oval nodule(s) with feeding artery and draining vein; pulmonary arteriole enlargement in dependent portions of the lungs

                      More
                    Other investigations
                    • pulmonary angiography:

                      confirms presence and location of malformations, identifies feeding arterial and venous structures

                      More
                    • transthoracic contrast echocardiography:

                      delayed shunting suggests transpulmonary shunting

                    • radionuclide perfusion scanning:

                      does not typically define a pulmonary arteriovenous malformation anatomically, but can confirm or identify the presence of a right-to-left shunt

                      More
                    • ABG analysis:

                      decreased partial pressure of oxygen, decreased oxygen saturation when arteriovenous flow is severe

                      More

                    Pulmonary hemorrhagic syndromes

                    History

                    cough, fever, dyspnea; history of bone marrow transplant; history of connective tissue disease or vasculitis

                    Exam

                    usually negative; presence of leukocytoclastic vasculitis, arthritis, or synovitis, indicative of connective tissue disease

                    1st investigation
                    • CXR:

                      alveolar infiltrates, usually patchy or diffuse

                    • CBC:

                      decreased hemoglobin level

                    • bronchoscopy with bronchoalveolar lavage and/or lung biopsies:

                      sequential lavage yields progressively more hemorrhagic fluid; cytology shows hemosiderin-laden macrophages; lung biopsies may show capillaritis, vasculitis or immune complex deposition.

                    Other investigations
                    • erythrocyte sedimentation rate:

                      usually elevated

                    • urinary sediment:

                      may be present

                      More
                    • ANA, C-ANCA, anti-GBM, and anti-DNA antibodies:

                      may be positive

                      More
                    • pulmonary function test with diffusing capacity of the lung for carbon monoxide:

                      usually restrictive pattern with elevated diffusing capacity of the lung for carbon monoxide

                    Granulomatosis with polyangiitis (formerly Wegener granulomatosis)

                    History

                    cough, chest pain, dyspnea, rhinorrhea, epistaxis, ear/sinus pain, hoarseness, fever, fatigue, anorexia, weight loss

                    Exam

                    palpable purpura, painful ulcers, uveitis, wheezing, sinus tenderness

                    1st investigation
                    • chest CT scan:

                      solitary or multiple lung nodules; airways are frequently affected

                    • antineutrophil cytoplasmic antibody:

                      usually positive

                      More
                    Other investigations
                    • bronchoscopy:

                      presence of necrotizing granulomatous inflammation and pauci-immune vasculitis in small and medium blood vessels on biopsy

                      More
                    • CT-guided transthoracic needle aspiration:

                      presence of necrotizing granulomatous inflammation

                      More

                    Systemic vasculitis

                    History

                    complaints of arthralgias, myalgias, malaise, fatigue for several months before more specific signs or symptoms develop

                    Exam

                    specific organ involvement, which may demonstrate a pattern of disease (e.g., eosinophilic granulomatosis with polyangitis is associated with poorly controlled asthma)

                    1st investigation
                    • erythrocyte sedimentation rate:

                      >100 mm/hour

                    • C-reactive protein:

                      elevated

                    • antineutrophil cytoplasmic antibody:

                      positive

                    • BUN and creatinine:

                      normal or elevated

                      More
                    • urinalysis:

                      may show hematuria, proteinuria, red blood cell casts

                      More
                    Other investigations
                    • biopsy of affected tissue:

                      vessel wall necrosis, fibrinoid necrosis, karyorrhexis (destructive fragmentation of the nucleus of a dying cell), red blood cell extravasation

                      More

                    Congenital heart disease

                    History

                    from asymptomatic to disabling symptoms: progressive heart disease, dyspnea, fatigue, orthopnea, paroxysmal nocturnal dyspnea

                    Exam

                    frothy pink sputum, stigmata of right-to-left shunting (cyanosis, clubbing), heart murmur

                    1st investigation
                    • echocardiogram:

                      reflects the congenital cardiac defect

                      More
                    Other investigations

                      Tricuspid endocarditis

                      History

                      history of intravenous drug use, mitral valve prolapse, or congenital heart disease; fever, malaise, fatigue, chest pains, weakness, night sweats, palpitations

                      Exam

                      fever, Janeway lesions, Osler nodes, splinter hemorrhages, cardiac murmur

                      1st investigation
                      • CBC:

                        elevated white blood cells

                      • blood cultures:

                        bacteremia, fungemia

                      • ECG:

                        prolonged PR interval; nonspecific ST/T wave abnormalities; atrioventricular block

                      • echocardiogram:

                        mobile valvular vegetations

                      Other investigations
                      • urinalysis:

                        red blood cell casts, white blood cell casts, proteinuria, pyuria

                      Bronchogenic cyst

                      History

                      usually asymptomatic unless infected or results in airway obstruction; incidental finding

                      Exam

                      asymptomatic; cough, dyspnea

                      1st investigation
                      • CXR:

                        sharply circumscribed, round or oval opacity in medial third of lower lobe

                        More
                      • chest CT scan:

                        nonenhancing homogeneous attenuation near water density; a smooth, thin wall; typically presents as a cystic mediastinal mass

                        More
                      Other investigations

                        Factitious hemoptysis

                        History

                        frequently young patients, healthcare workers; evidence of self-inflicted wounds or interventions capable of causing hemoptysis supports the diagnosis

                        Exam

                        absence of an alternative etiology on workup

                        1st investigation
                        • clinical history and exam:

                          diagnosis is clinical with a high index of suspicion; tests may not be indicated

                        Other investigations

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