This is the last post in the series of basics of HRCT. links to the previous posts are given at the end of this post.
DIFFERENTIAL DIAGNOSIS OF INTERSTITIAL LUNG DISEASE
DIFFERENTIAL DIAGNOSIS OF INTERSTITIAL LUNG DISEASE
Reticular pattern
1.
Lymphangitic
carcinomatosis: irregular septal thickening, usually focal or unilateral 50%
adenopathy', known carcinoma.
2.
Cardiogenic pulmonary
edema: incidental finding in HRCT, smooth septal thickening with basal
predominance (Kerley B lines), ground-glass opacity with a gravitational and
perihilar distribution, thickening of the peribronchovascular interstitium
(peribronchial cuffing)
3.
Lymphangitic
carcinomatosis.
4.
Lymphangitic
carcinomatosis with hilar adenopathy.
5.
Alveolar proteinosis:
ground glass attenuation with septal thickening (crazy paving).
6.
Cardiogenic pulmonary
edema.
Nodular pattern
1.
Hypersensitivity
pneumonitis: ill defined centrilobular nodules.
2.
Miliary TB: random
nodules
3.
Sarcoidosis: nodules
with perilymphatic distribution, along fissures, adenopathy.
4.
Hypersensitivity
pneumonitis: centrilobular nodules, notice sparing of the area next to pleura
and fissure.
1.
Sarcoidosis: nodules
with perilymphatic distribution, along fissures, adenopathy.
2.
TB: Tree-in-bud
appearance in a patient with active TB.
3.
Langerhans cell
histiocytosis: early nodular stage before the typical cysts appear.
4.
Respiratory
bronchiolitis in infection.
1.
Chronic eosinophilic
pneumonia with peripheral areas of ground glass opacity.
2.
Sarcoid end-stage with
massive fibrosis in upper lobes presenting as areas of consolidation. Notice
lymphadenopathy.
3.
Chronic eosinophilic
pneumonia with peripheral areas of consolidation.
4.
Broncho-alveolar cell
carcinoma with both areas of ground glass opacity and consolidation
1.
Non specific
interstitial pneumonitis (NSIP): ground glass with traction bronchiectasis, no
honeycombing.
2.
Cryptogenic organizing
pneumonia (COP).
3.
Sarcoidosis end-stage:
consolidation as a result of massive fibrosis perihilar and in upper lobes.
4.
COP.
1.
Lymphangiomyomatosis
(LAM): uniform cysts in woman of child-bearing age; no history of smoking;
adenopathy and pleural effusion; sometimes pneumothorax.
2.
LCH: multiple round
and bizarre shaped cysts; smoking history.
3.
Honeycombing
4.
Centrilobular emphysema:
low attenuation areas without walls.
1.
Centrilobular
emphysema: low attenuation areas without walls. Notice the centrilobular artery
in the center.
2.
Langerhans cell
histiocytosis (LCH): multiple thick walled cysts; smoking history.
3.
Honeycombing.
4.
Lymphangiomyomatosis
(LAM): regular cysts in woman of child-bearing age.
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