In the reticular pattern
there are too many lines, either as a result of thickening of the interlobular
septa or as a result of fibrosis as in honeycombing.
·
Septal thickening
Thickening of the lung interstitium by fluid, fibrous tissue, or infiltration by cells results in a pattern of reticular opacities due to thickening of the interlobular septa.
Although thickening of the interlobular septa is relatively common in patients with interstitial lung disease, it is uncommon as a predominant finding and has a limited differential diagnosis (Table).
Thickening of the lung interstitium by fluid, fibrous tissue, or infiltration by cells results in a pattern of reticular opacities due to thickening of the interlobular septa.
Although thickening of the interlobular septa is relatively common in patients with interstitial lung disease, it is uncommon as a predominant finding and has a limited differential diagnosis (Table).
Smooth septal thickening is usually seen in interstitial pulmonary
edema (Kerley B lines on chest film); lymphangitic spread of carcinoma or
lymphoma and alveolar proteinosis.
Nodular or irregular
septal thickening occurs
in lymphangitic spread of carcinoma or lymphoma; sarcoidosis and silicosis.
c carcinomatosis
On the left we see focal
irregular septal thickening in the right upper lobe in a patient with a known
malignancy.
This finding is typical for lymphangitic carcinomatosis.
There are also additional findings, that support this diagnosis like mediastinal lymph nodes and a nodular lesion in the left lung, that probably represents a metastasis.
This finding is typical for lymphangitic carcinomatosis.
There are also additional findings, that support this diagnosis like mediastinal lymph nodes and a nodular lesion in the left lung, that probably represents a metastasis.
Pulmonary lymphangitic
carcinomatosis (PLC)
In 50% of patients the septal thickening is
focal or unilateral.
This finding is helpful in distinguishing PLC from
other causes of interlobular septal thickening like Sarcoidosis or cardiogenic
pulmonary edema.
Hilar lymphadenopathy is visible in 50% and
usually there is a history of (adeno)carcinoma.
Identical findings can be seen in patients with
Lymphoma and in children with HIV infection, who develop Lymphocytic
interstitial pneumonitis (LIP), a rare benign infiltrative lymphocytic disease.
On the left a patient
who had a CT to rule out pulmonary embolism.
There is a combination of smooth septal thickening and ground-glass opacity with a gravitational distribution.
The diagnosis based on this CT was cardiogenic pulmonary edema.
There is a combination of smooth septal thickening and ground-glass opacity with a gravitational distribution.
The diagnosis based on this CT was cardiogenic pulmonary edema.
Cardiogenic pulmonary
edema generally results
in a combination of septal thickening and ground-glass opacity.
There is a tendency for hydrostatic edema to
show a perihilar and gravitational distribution.
Thickening of the peribronchovascular
interstitium, which is called peribronchial cuffing, and fissural thickening
are also common.
Common additional findings are an enlarged heart
and pleural fluid.
Usually these patient are not imaged with HRCT
as the diagnosis is readily made based on clinical and radiographic findings,
but sometimes unsuspected hydrostatic pulmonary edema is found.
On the left a patient
with both septal thickening and ground glass opacity in a patchy distribution.
Some lobules are affected and others are not.
This combination of findings is called 'crazy paving'.
Crazy paving was thought to be specific for alveolar proteinosis, but is also seen in many other diseases such as pneumocystis carinii pneumonia, bronchoalveolar carcinoma, sarcoidosis, nonspecific interstitial pneumonia (NSIP), organizing pneumonia (COP), adult respiratory distress syndrome and pulmonary hemorrhage.
Some lobules are affected and others are not.
This combination of findings is called 'crazy paving'.
Crazy paving was thought to be specific for alveolar proteinosis, but is also seen in many other diseases such as pneumocystis carinii pneumonia, bronchoalveolar carcinoma, sarcoidosis, nonspecific interstitial pneumonia (NSIP), organizing pneumonia (COP), adult respiratory distress syndrome and pulmonary hemorrhage.
Alveolar proteinosis
is a rare diffuse lung disease of unknown
etiology characterized by alveolar and interstitial accumulation of a periodic
acid-Schiff (PAS) stain-positive phospholipoprotein derived from surfactant.
is a rare diffuse lung disease of unknown etiology characterized by alveolar and interstitial accumulation of a periodic acid-Schiff (PAS) stain-positive phospholipoprotein derived from surfactant
Honeycombing
represents the second reticular pattern
recognizable on HRCT.
Because of the cystic appearance, honeycombing is also discussed in the chapter discussing the low attenuation pattern.
Pathologically, honeycombing is defined by the presence of small cystic spaces lined by bronchiolar epithelium with thickened walls composed of dense fibrous tissue.
Honeycombing is the typical feature of usual interstitial pneumonia (UIP).
Because of the cystic appearance, honeycombing is also discussed in the chapter discussing the low attenuation pattern.
Pathologically, honeycombing is defined by the presence of small cystic spaces lined by bronchiolar epithelium with thickened walls composed of dense fibrous tissue.
Honeycombing is the typical feature of usual interstitial pneumonia (UIP).
See my article
on HRCT
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