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HOW READ CHEST XR -11




     ANAS SAHLE ,MD
Brief review
POSITION
                             PA                                                   AP


                                                       QUALITY
                ROTATION                               PENETRATION                      INSPIRATION




                                                        LESION
OPACIT
 OPACITY
                           Homo
                       Heterogenous     Wellill defined           Zone
                                                                            Centralperipher
                                                                                               Silhouet sign
                                                                                   al
   Y                       Necrotic
  PATCHY

                                             HILUMMEDIASTINAL
  NODULE                                 Central deviasionwided

   MASS
                                            COSTO-PHRENIC ANGEL
                                                  Freeoblitern
  CAVITARY



                                                         OTHER
INFILTIRATION
                                        Bone soft tissuediaphragm
Consolidation

Infection
 causes                    Non-infection causes



                        Broncho-
                                         WEGNER              Cardiac
Pneumonia   Lymphoma    alveolar   COP             Sarcoid
                                         disease             failure
                       carcinoma
Solitary Pulmonary Nodule(SPN)
                         Appearance
 Margin                  Calcification                cavitation

             Comparison with a
                      Size
             previous x-ray to >8mm
          <8mm
             Assess growth over
             time. Location
   Upperhillar zone                     Lowerbasesup-pleural


                 Associated abnormalities
Lymph node enlargement                   Rib destruction/erosion
Cavitary lesion
 Air +
               Air-fluid level                          Air only
tissue
                                                   Wall thickness

              Straight     Wavy               Thick                        Thin
         1.   Fungal ball.
         2.   Rupture hydatid cyct                                           site
         3.   Necrotic tumor
                           ruptured
         4.   Blood glot Hydatid
              Abscess                  Irregular    Regular
                                                                Peripheral          Central
                                      inner wall   inner wall
                            cyst


                                                                Emphesemato
                                      Cavitating   Chronic          us          pneumatoc
                                      neoplasm     abscess                         ele
                                                                   bulla
LINEAR PATTERN
                LINEAR PATTERN
LEFT VENTRICULAR FAILURE Perihilar and peripheral basal septal lines,
                         changes acutely and resolves with diuretics



Normal ageing             Coarsening of lung markings in lower zones, no
                          change on review of recent films



Lymphangitis              Coarse nodular and linear thickening of
                          markings, known malignancy, often associated
                          with pleural effusion, rapid clinical
                          deterioration of patient
LINEAR PATTERN
               LINEAR PATTERN
Atelectasis       Short thin lines, often basal, new on review of
                  previous films



Subsegmental      Longer thicker bands, often perihilar or basal,
collapse          suggest recent infection or infarction



Scarring          Any length, persist over time unchanged

Fibrosis          Volume loss is key, persists over time
Causes of fibrosis
  Mid zone lung              Lower zone lung Upper zone lung
tuberculosis                 Drug indused fibrosis        sarcoidosis
                             (most common)

Chronic extrinsic allergic   UIP
alveolitis

Radio-therapy                Asbestose-related fibrosis


Ankylosing spondylitis


Progressive massive
fibrosis

histoplasmosis
CASE-1
•   A 50-year-old male smoker is evaluated for chronic shortness of breath.
•   On physical examination his vital signs are:
     – pulse 110 bpm;
     – Temperature normal;
     – respirations 30/min with use of accessory muscles and pursed-lip breathing;
     – blood pressure 110/78 mm Hg.
•   Other pertinent findings are:
     – heart exam: apex beat (impulse) is medial to the mid-clavicular line
     – generalized decreased breath sounds on lung exam;
•   ABGs (FiO2 0.21):
     – pH 7.38; PCO2 47 mm Hg; PO2 67 mm Hg.
•   PFTs/spirometry:
     – FVC 2.80 L (67% of predicted);
     – FEV1 1.56 (50% of predicted);
     – FEV1/FVC% 56%;
     – TLC 134% of predicted;
     – RV 170% of predicted;
     – DLCO 43% of predicted.
     – There is no reversibility with bronchodilators.
CASE-1
POSITION            •PA CXR

QUALITY             •Good Technical Quality

                     •Bilateral linar (vascular)infitration .
                     •Laminar opacity from right hilum.
LESION               •Hyper-lucency area at lower right zone.




MEDIASTINALHilum   •Central trachea and mediasteinal.
                    •Dangle heart.

ANGELS              •Hazy left angleirregular
                    diaphragm(flat)
                    •No
OTHER
CASE-1
• 1. What is the most likely diagnosis?
• a. Bronchial asthma with status asthmaticus
• b. Emphysema
• c. Chronic bronchitis
• d. Tuberous sclerosis
• 2. Associated with the above condition is
• a. Obstructive sleep apnea
• b. Increased IgE levels
• c. Respiratory failure with increased A-aDO2
  gradient
• d. Clubbing
CASE-2
• A 38-year-old man is admitted with progressive shortness of breath
• and cough.
• He denies any fever, chills, or purulent sputum production.
• He wants to be evaluated to determine the reasons for his symptoms.
• On exam, he is afebrile and has decreased breath sounds with hyper-
  resonant upper lung field more obvious on the right.
• ABGs on RA: pH 7.35; PCO2 38mm Hg; PO2 78 mm Hg.
• Spirometry:
   – (FVC) 1.72 (70% of predicted);
   – (FEV1)1.34 L (60% of predicted);
   – FEV1/FVC% 76%;
   – TLC 4.1 L (100% of predicted);
   – TLC by helium dilution method 3.4 (71%);
   – DLCO 70% of predicted.
   – There is no bronchodilator response.
CASE-2
POSITION            •PA CXR

QUALITY             •Poor Technical Quality

                     •Large bulla extend at right upper and
                     middle zone.
LESION               •Vascular marking crowded at lower
                     zone.
                     •Hyperlucensy area at left upper zone.



MEDIASTINALHilum   •Central trachea and mediasteinal.


ANGELS              •Free

                    •No
OTHER
CASE-2
•   1. What is the most likely diagnosis?
•   a. Severe emphysema
•   b. Bulla
•   c. Pneumothorax
•   d. Bronchiectasis
•   2. What is the next management option?
•   a. Place a chest tube urgently
•   b. Increase bronchodilator dosage and frequency
•   c. Start chest physical therapy
•   d. Perform CT scan of chest
CASE-3
• A 39-year-old man, a smoker since age 16, is seen
  in the clinic with complaints of fever, cough, and
  production of yellowish sputum.
• He has been chronically short of breath, but
  these symptoms have increased over the last
  week after he developed a flulike illness.
• On exam, he is febrile and looks ill.
• Lung exam reveals diffuse wheezing with
  egophony and whispering pectoriloquy on the
  right side.
• ABGs show PO2 of 55 mm Hg on room air,
• sputum is negative for TB.
CASE-3
POSITION            •PA CXR

QUALITY             •Poor Technical Quality

                     •Multiple air-fluid level at right middle
                     zone.
LESION               •Area of hyperlucensy at right and left
                     upper zone.




MEDIASTINALHilum   •Central trachea and mediasteinal.


ANGELS              •Free

                    •No
OTHER
CASE-3
• 1. The next step in the management of this patient
  would be
• a. Arrange with intervention radiology to do a needle
  aspiration
• b. Consult thoracic surgery for lung reduction surgery
• c. Start antibiotic and O2 therapy
• d. Admit patient in an isolation room
• 2. Appropriate measures at the first follow-up
  should include
•   a. Pneumococcal and influenza vaccine
•   b. Allergy testing
•   c. Detailed occupational history
•   d. Genetic counseling
CASE-4
• A 31-year-old African American man is admitted
  with increasing cough, fever, and sputum
  production.
• He gives a history of repeated infections and
  “pneumonias” since childhood.
• Lung exam reveals:
   – diffuse rhonchi
   – bilateral crackles, more so in the left lung field.
• Routine labs are normal except for a poly-
  morphonuclear leuko-cytosis.
CASE-4
POSITION            •PA CXR

QUALITY             •Poor Technical Quality

                     •Bilateral nodulo-reticular pattern
                     crowded at lower,middle zone and cyct-
LESION               like apperance.




MEDIASTINALHilum   •Central trachea and mediasteinal.


ANGELS              •Free

                    •No
OTHER
CASE-4
• 1. What is the most likely diagnosis?
•   a. Bronchiectasis
•   b. Cystic fibrosis
•   c. Sarcoidosis
•   d. Allergic bronchopulmonary aspergillosis
• 2. What is the next management option?
•   a. Bronchoscopy
•   b. Steroid Rx
•   c. Antibiotics and postural drainage
•   d. Surgical consult
DISCUSSION
• The history is suggestive of bronchiectasis,
  and the bilateral cystic-appearing lesions on
  the CXR are consistent with that diagnosis.
• Cystic fibrosis is generally predominant in the
  upper zone.
• Sarcoidosis rarely presents with this history,
  and the fibrotic changes in sarcoidosis are
  usually in the upper lobes.
• Allergic bronchopulmonary aspergillosis is
  seen with an underlying asthmatic condition.
CASE-5
• A 24-year-old male law student presents with
  a 3-wk history of increasing dyspnea.
• He has a history of chronic sputum production
  of about 100 cc of purulent material each day
  for many years.
• In the past, he was hospitalized for a left
  pneumothorax.
• He is on inhaled bronchodilator as an
  outpatient.
CASE-5
POSITION            •PA CXR

QUALITY             •Good Technical Quality

                     •Bilateral cyct-like opacity apperance.
                     •At middle zone near hilum and extend
LESION               to left upper zone (fibrosis).




MEDIASTINALHilum   •Central trachea and mediasteinal.


ANGELS              •Freeflated diaphragm.

                    •No
OTHER
CASE-5
• 1. Physical exam will most likely show
•   a. Clubbing
•   b. Koilonychia
•   c. Oncholysis
•   d. Pectus excavatum
• 2. Spirometry will most likely show
•   a. FVC 60%; FEV1 40%; ratio 66%
•   b. FVC 60%; FEV1 62%; ratio 90%
•   c. Normal
•   d. Normal except mild decrease in FEF25–75
• 3. The most helpful treatment option would be
•   a. Increase bronchodilator therapy
•   b. Start broad-spectrum antibiotic therapy
•   c. Initiate anti-pseudomonas antibiotic regimen
•   d. Start oral steroids
DISCUSSION
• The history and chest x-ray are consistent with
  cystic fibrosis with bilateral cystic upper zone
  predominance.
• Physical exam would reveal clubbing;
  spirometry would show a mixed obstructive
  with restrictive picture.
• The best option would be to initiate anti-
  pseudomonas antibiotics.
How  read  chest xr  11

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How read chest xr 11

  • 1. HOW READ CHEST XR -11 ANAS SAHLE ,MD
  • 3. POSITION PA AP QUALITY ROTATION PENETRATION INSPIRATION LESION OPACIT OPACITY Homo Heterogenous Wellill defined Zone Centralperipher Silhouet sign al Y Necrotic PATCHY HILUMMEDIASTINAL NODULE Central deviasionwided MASS COSTO-PHRENIC ANGEL Freeoblitern CAVITARY OTHER INFILTIRATION Bone soft tissuediaphragm
  • 4. Consolidation Infection causes Non-infection causes Broncho- WEGNER Cardiac Pneumonia Lymphoma alveolar COP Sarcoid disease failure carcinoma
  • 5. Solitary Pulmonary Nodule(SPN) Appearance Margin Calcification cavitation Comparison with a Size previous x-ray to >8mm <8mm Assess growth over time. Location Upperhillar zone Lowerbasesup-pleural Associated abnormalities Lymph node enlargement Rib destruction/erosion
  • 6. Cavitary lesion Air + Air-fluid level Air only tissue Wall thickness Straight Wavy Thick Thin 1. Fungal ball. 2. Rupture hydatid cyct site 3. Necrotic tumor ruptured 4. Blood glot Hydatid Abscess Irregular Regular Peripheral Central inner wall inner wall cyst Emphesemato Cavitating Chronic us pneumatoc neoplasm abscess ele bulla
  • 7. LINEAR PATTERN LINEAR PATTERN LEFT VENTRICULAR FAILURE Perihilar and peripheral basal septal lines, changes acutely and resolves with diuretics Normal ageing Coarsening of lung markings in lower zones, no change on review of recent films Lymphangitis Coarse nodular and linear thickening of markings, known malignancy, often associated with pleural effusion, rapid clinical deterioration of patient
  • 8. LINEAR PATTERN LINEAR PATTERN Atelectasis Short thin lines, often basal, new on review of previous films Subsegmental Longer thicker bands, often perihilar or basal, collapse suggest recent infection or infarction Scarring Any length, persist over time unchanged Fibrosis Volume loss is key, persists over time
  • 9. Causes of fibrosis Mid zone lung Lower zone lung Upper zone lung tuberculosis Drug indused fibrosis sarcoidosis (most common) Chronic extrinsic allergic UIP alveolitis Radio-therapy Asbestose-related fibrosis Ankylosing spondylitis Progressive massive fibrosis histoplasmosis
  • 10. CASE-1 • A 50-year-old male smoker is evaluated for chronic shortness of breath. • On physical examination his vital signs are: – pulse 110 bpm; – Temperature normal; – respirations 30/min with use of accessory muscles and pursed-lip breathing; – blood pressure 110/78 mm Hg. • Other pertinent findings are: – heart exam: apex beat (impulse) is medial to the mid-clavicular line – generalized decreased breath sounds on lung exam; • ABGs (FiO2 0.21): – pH 7.38; PCO2 47 mm Hg; PO2 67 mm Hg. • PFTs/spirometry: – FVC 2.80 L (67% of predicted); – FEV1 1.56 (50% of predicted); – FEV1/FVC% 56%; – TLC 134% of predicted; – RV 170% of predicted; – DLCO 43% of predicted. – There is no reversibility with bronchodilators.
  • 12. POSITION •PA CXR QUALITY •Good Technical Quality •Bilateral linar (vascular)infitration . •Laminar opacity from right hilum. LESION •Hyper-lucency area at lower right zone. MEDIASTINALHilum •Central trachea and mediasteinal. •Dangle heart. ANGELS •Hazy left angleirregular diaphragm(flat) •No OTHER
  • 13. CASE-1 • 1. What is the most likely diagnosis? • a. Bronchial asthma with status asthmaticus • b. Emphysema • c. Chronic bronchitis • d. Tuberous sclerosis • 2. Associated with the above condition is • a. Obstructive sleep apnea • b. Increased IgE levels • c. Respiratory failure with increased A-aDO2 gradient • d. Clubbing
  • 14. CASE-2 • A 38-year-old man is admitted with progressive shortness of breath • and cough. • He denies any fever, chills, or purulent sputum production. • He wants to be evaluated to determine the reasons for his symptoms. • On exam, he is afebrile and has decreased breath sounds with hyper- resonant upper lung field more obvious on the right. • ABGs on RA: pH 7.35; PCO2 38mm Hg; PO2 78 mm Hg. • Spirometry: – (FVC) 1.72 (70% of predicted); – (FEV1)1.34 L (60% of predicted); – FEV1/FVC% 76%; – TLC 4.1 L (100% of predicted); – TLC by helium dilution method 3.4 (71%); – DLCO 70% of predicted. – There is no bronchodilator response.
  • 16. POSITION •PA CXR QUALITY •Poor Technical Quality •Large bulla extend at right upper and middle zone. LESION •Vascular marking crowded at lower zone. •Hyperlucensy area at left upper zone. MEDIASTINALHilum •Central trachea and mediasteinal. ANGELS •Free •No OTHER
  • 17. CASE-2 • 1. What is the most likely diagnosis? • a. Severe emphysema • b. Bulla • c. Pneumothorax • d. Bronchiectasis • 2. What is the next management option? • a. Place a chest tube urgently • b. Increase bronchodilator dosage and frequency • c. Start chest physical therapy • d. Perform CT scan of chest
  • 18. CASE-3 • A 39-year-old man, a smoker since age 16, is seen in the clinic with complaints of fever, cough, and production of yellowish sputum. • He has been chronically short of breath, but these symptoms have increased over the last week after he developed a flulike illness. • On exam, he is febrile and looks ill. • Lung exam reveals diffuse wheezing with egophony and whispering pectoriloquy on the right side. • ABGs show PO2 of 55 mm Hg on room air, • sputum is negative for TB.
  • 20. POSITION •PA CXR QUALITY •Poor Technical Quality •Multiple air-fluid level at right middle zone. LESION •Area of hyperlucensy at right and left upper zone. MEDIASTINALHilum •Central trachea and mediasteinal. ANGELS •Free •No OTHER
  • 21. CASE-3 • 1. The next step in the management of this patient would be • a. Arrange with intervention radiology to do a needle aspiration • b. Consult thoracic surgery for lung reduction surgery • c. Start antibiotic and O2 therapy • d. Admit patient in an isolation room • 2. Appropriate measures at the first follow-up should include • a. Pneumococcal and influenza vaccine • b. Allergy testing • c. Detailed occupational history • d. Genetic counseling
  • 22. CASE-4 • A 31-year-old African American man is admitted with increasing cough, fever, and sputum production. • He gives a history of repeated infections and “pneumonias” since childhood. • Lung exam reveals: – diffuse rhonchi – bilateral crackles, more so in the left lung field. • Routine labs are normal except for a poly- morphonuclear leuko-cytosis.
  • 24. POSITION •PA CXR QUALITY •Poor Technical Quality •Bilateral nodulo-reticular pattern crowded at lower,middle zone and cyct- LESION like apperance. MEDIASTINALHilum •Central trachea and mediasteinal. ANGELS •Free •No OTHER
  • 25. CASE-4 • 1. What is the most likely diagnosis? • a. Bronchiectasis • b. Cystic fibrosis • c. Sarcoidosis • d. Allergic bronchopulmonary aspergillosis • 2. What is the next management option? • a. Bronchoscopy • b. Steroid Rx • c. Antibiotics and postural drainage • d. Surgical consult
  • 26. DISCUSSION • The history is suggestive of bronchiectasis, and the bilateral cystic-appearing lesions on the CXR are consistent with that diagnosis. • Cystic fibrosis is generally predominant in the upper zone. • Sarcoidosis rarely presents with this history, and the fibrotic changes in sarcoidosis are usually in the upper lobes. • Allergic bronchopulmonary aspergillosis is seen with an underlying asthmatic condition.
  • 27. CASE-5 • A 24-year-old male law student presents with a 3-wk history of increasing dyspnea. • He has a history of chronic sputum production of about 100 cc of purulent material each day for many years. • In the past, he was hospitalized for a left pneumothorax. • He is on inhaled bronchodilator as an outpatient.
  • 29. POSITION •PA CXR QUALITY •Good Technical Quality •Bilateral cyct-like opacity apperance. •At middle zone near hilum and extend LESION to left upper zone (fibrosis). MEDIASTINALHilum •Central trachea and mediasteinal. ANGELS •Freeflated diaphragm. •No OTHER
  • 30. CASE-5 • 1. Physical exam will most likely show • a. Clubbing • b. Koilonychia • c. Oncholysis • d. Pectus excavatum • 2. Spirometry will most likely show • a. FVC 60%; FEV1 40%; ratio 66% • b. FVC 60%; FEV1 62%; ratio 90% • c. Normal • d. Normal except mild decrease in FEF25–75 • 3. The most helpful treatment option would be • a. Increase bronchodilator therapy • b. Start broad-spectrum antibiotic therapy • c. Initiate anti-pseudomonas antibiotic regimen • d. Start oral steroids
  • 31. DISCUSSION • The history and chest x-ray are consistent with cystic fibrosis with bilateral cystic upper zone predominance. • Physical exam would reveal clubbing; spirometry would show a mixed obstructive with restrictive picture. • The best option would be to initiate anti- pseudomonas antibiotics.