presentation1.pptx, radiological imaging of bronchiectasis

Radiological imaging of bronchiectasis.

Dr/ ABD ALLAH NAZEER. MD.

Clinical Findings:Classical clinical triad: chronic cough, excess sputum production and repeated infection Hemoptysis.Shortness of breath.Wheezing.Fever is rare even with infection.

Morphological-types-of-bronchiectasis.

Imaging FindingsLocation

Proximal, frequently upper lobe, bronchiectasis is characteristic of allergic bronchopulmonary aspergillosis (ABPA)Bronchiectasis from viral or pyogenic infections is usually at the basesTuberculous bronchiectasis is usually at the apicesDiffuse bronchiectasis

Impaired mucus clearing e.g. cystic fibrosis and KartagenerChronic diffuse airways disease (chronic bronchitis, asthma, bronchiolitis obliteransImmune deficiency states

CT is the study of choice with a sensitivity of up to 97% and a specificity up to 99%Signet ring appearance on CT : normally, the vessel is larger than the corresponding bronchus

In bronchiectasis, the bronchus is larger than the corresponding vessel“Tramlines” or “honeycombing” represents dilated, thickened bronchial wallsVolume loss due to destruction of lung tissueMultiple small nodular densities from plugged alveoliLack of normal, bronchial taperingNon uniform bronchial dilationCystic lesions, often with air-fluid levels, and frequently in a clusterBronchial wall thickening.

MRI has potential in the imaging of bronchiectasis, particularly in conditions such as CF, in which young patients may require serial imaging for disease monitoring and assessment of response to treatment. Compared to HRCT, the ability of MR to provide functional imaging and lack of radiation could compensate for its limited spatial resolution. With improvement in MRI techniques, recent studies have shown good reproducibility and good correlation with PFT results.Further work is required to improve spatial resolution, develop robust validated scoring systems and evaluate correlations with clinical outcomes.Currently cost, limited availability and limited spatial resolution limit the use of MRI in bronchiectasis largely to the research arena. Although hyperpolarized noble gas imaging has great potential in terms of provision of functional data, technical issues and set-up and ongoing costs suggest its role will be limited to research for the foreseeable future.

ScintigraphyPrior to the advent of HRCT, ventilation (with or without perfusion) scintigraphy was used to aid disease evaluation in bronchiectasis. DOLLERY and HUGH-JONES studied the physiological implications of bronchiectasis and found reduced blood flow and impaired ventilation in bronchiectatic areas. V/Q scintigraphy typically demonstrates matched ventilation and perfusion defects, reflecting abnormal ventilation secondary to bronchiectasis and associated small airways obstruction V/Q scintigraphy and lung function are additive tools to aid diagnosis and guide therapeutic management. The ongoing issue of radiation dose and absence of useful anatomical information, however, limit the value of V/Q scintigraphy in routine practice.

Chest radiographyChest radiography (CXR) is usually the initial study performed in both suspected bronchiectasis and the evaluation of nonspecific respiratory symptoms, such as dyspnea and hemoptysis, when bronchiectasis may be identified incidentally. Signs on CXR include the identification of parallel linear densities, tram-track opacities, or ring shadows reflecting thickened and abnormally dilated bronchial walls. These bronchial abnormalities form a spectrum from subtle or barely perceptible 5-mm ring shadows to obvious cysts. Tubular branching opacities conforming to the expected bronchial branching pattern may result from fluid or mucous filling of bronchi. Peribronchial fibrosis results in a loss of definition of vessel walls. Signs of complications/exacerbations, such as patchy densities due to mucoid impaction and consolidation, volume loss secondary to bronchial mucoid obstruction or chronic cicatrisation, are also seen. In the more diffuse forms of bronchiectasis, such as cystic fibrosis (CF), generalized hyperinflation and oligaemia are often present, consistent with severe small airways obstruction.

Chest radiography showing a) cystic bronchiectasis with multiple cystic airspaces and b) cylindrical bronchiectasis and tram track opacities in a cystic fibrosis patient.

(a) (b)

Chest radiographs: Demonstrate thin-walled, cystic structures in right lower lobe (white arrow), some with air-fluid levels (yellow arrows).

Cystic bronchiectasis with air-fluid levels.

CT signs of bronchiectasisSignet ring appearance on CT: normally, the vessel is larger than the corresponding bronchus in bronchiectasis, the bronchus is larger than the corresponding vessel.Bronchial dilation, the cardinal sign of bronchiectasis, is characterised on HRCT by a bronchoarterial ratio (BAR) of .1, lack of bronchial tapering, and visibility of airways within 1 cm of the pleural surface or abutting the mediastinal pleural surface. “Tramlines” or “honeycombing” represents dilated, thickened bronchial walls.Volume loss due to destruction of lung tissue.Multiple small nodular densities from plugged alveoli.Lack of normal, bronchial taperingNon uniform bronchial dilationCystic lesions, often with air-fluid levels, and frequently in a clusterBronchial wall thickening.

SIGNET RING SIGN. Chest CT shows small bronchiectasis.

SIGNET RING SIGN. Chest CT shows small bronchiectasis.

Bronchiectasis. Signet-ring sign.

Axial CT scan. Lower lobe bronchiectasis. Signet-ring sign.

Axial CT scan. Lower lobe bronchiectasis. Signet-ring sign.

High-resolution computed tomography image showing non tapering bronchi, in keeping with bronchiectasis.

Lack of bronchial tapering.

Young adult with cystic fibrosis. Coronal CT scan. Widespread bronchiectasis. Lack of bronchial tapering

Varicose bronchiectasis.

Varicose bronchiectasis with cystic bronchiectasis.

Varicose bronchiectasis.

Cylindrical bronchiectasis.

Cylindrical bronchiectasis.

Cylindrical bronchiectasis.

Categories of bronchiectasis. Normal bronchus (arrow) (A), cylindrical bronchiectasis with lack of bronchial tapering (arrow) (B), varicose bronchiectasis with string-of-pearls appearance (arrow) (C), and cystic bronchiectasis (arrow) (D).

BA CD

Abnormal bronchial contour.

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High-resolution computed tomography image demonstrating bronchiectasis with bronchial wall thickening (asterisk) and mucous plugging (arrow) in the right lower lobe.

Bronchial wall thickening

Inspiratory high-resolution computed tomography image showing bronchiectasisand widespread areas of low attenuation, representing air-trapping.

Air-trapping Sign.

High-resolution computed tomography showing a) proximal bronchiectasis affecting segmental airways and b) high attenuation mucous plugs in patients with allergic bronchopulmonary aspergillosis. No intravenous contrast medium was used in (b).

a)b)

Mucous plugs Impaction.

Cystic Bronchiectasis. CT: Markedly dilated bronchi are seen, some with air-fluid levels (yellow arrows), mostly in the right lung.

Cystic changes with air-fluid levels.

High-resolution computed tomographyimage showing cystic bronchiectasis.

Cystic Bronchiectasis. CT: Markedly dilated bronchi are seen, some with air-fluid levels.

Cystic Bronchiectasis. CT: Markedly dilated bronchi are seen, some with air-fluid levels.

Cystic Bronchiectasis. X-Ray and CT: Dilated bronchi are seen, some with air-fluid levels.

Cystic Bronchiectasis.

Endoluminal Obstruction by Tumor Most carcinoid tumors are primarily endobronchial lesions, occurring in the central, main, or segmental bronchi. Some small tumors are located entirely within the lumen. However, some display a dominant extraluminal component with only a small part of the tumor lying within the airway (iceberg lesion). A variety of other benign and malignant neoplasms can also result in obstruction leading to focal bronchiectasis.

Carcinoid. This predominantly endobronchial tumor, arising before bifurcation of left upper and lower lobe bronchi, causes distal bronchiectasis. Transverse images of tumor (arrow, A) and distal bronchiectasis (arrows, B).

Carcinoid. This predominantly endobronchial tumor, arising before bifurcation of left upper and lower lobe bronchi, causes distal bronchiectasis. Coronal oblique image (C) and volume-rendering reformation (D) in similar orientation as A and B show central carcinoid tumor (arrows) and distal bronchiectasis (arrowheads, C).

Broncholithiasis Calcified or ossified material within the bronchial lumen can cause focal bronchiectasis. By far the most common cause of broncholithiasis is erosion by and extrusion of a calcified adjacent lymph node, usually associated with a long-standing focus of necrotizing granulomatous lymphadenitis, especially after tuberculosis. Nevertheless, the frequency of broncholithiasis complicating granulomatous infection is quite low. The most common sites are the proximal right middle lobe bronchus and the origin of the anterior segmental bronchus of the upper lobes because of airway anatomy and lymph node distribution.

Broncholithiasis. Calcified left upper lobe endobronchial broncholithiasis (arrow) from previous tuberculosis exposure is seen on transverse image (A), minimum-intensity-projection reformation in coronal oblique plane (B), and volume-rendering reformation (C) in similar orientation. In C, arrow points to distal bronchiectasis.

Congenital stenosis of left mainstem bronchus. Transverse images show stenosis (arrow, A), distal bronchiectasis, and mucoid impaction (arrows, B).

Airway stenosis causing focal bronchiectasis can result from a broad spectrum of entities including infection, intubation stricture, healing of a tracheostomy stoma, tracheobronchopathia osteochondroplastica, amyloidosis, relapsing polychondritis, sarcoidosis, and fibrosing mediastinitis.

Focal bronchiectasis (idiopathic) in left lower lobe (arrow).

Bronchial Atresia The most common cause of congenital focal bronchiectasis is bronchial atresia, characterized by obliteration of a bronchus with distal bronchiectasis, mucoid impaction, and air trapping that is most commonly seen in the left upper lobe. In this rare lesion, the bronchial tree peripheral to the point of obliteration is patent and the lung parenchyma is overinflated because of collateral air drift.

Bronchial atresia. Transverse image of focal bronchiectasis (arrow) distal to bronchial atresia associated with hyperlucency and hyperexpansion of left lung.

Post-radiation fibrosis. Right para-mediastinal fibrotic changes, which developed after treatment of lung cancer, are associated with traction bronchiectasis (arrows).

Young adult with cystic fibrosis. Chronic right upper lobe collapse (arrow)

Young adult female with cystic fibrosis. Long standing middle and lingular collapse (arrows) Background severe bronchiectasis.

Cystic Fibrosis The most common cause of congenital upper-lung-predominant bronchiectasis is cystic fibrosis, commonly associated with enlarged lung volumes and interstitial alterations. An autosomal recessive genetic disorder causing ineffective clearance of secretions, cystic fibrosis presents with recurrent pneumonias, sinusitis, pancreatic insufficiency, and infertility. Milder forms of cystic fibrosis, however, can remain unrecognized until adulthood.

Cystic fibrosis. Transverse (A) and coronal (B) images show upper lobe predominance of cystic bronchiectasis (arrows) and volume loss, enlarged lung volumes, and diffuse heterogeneous attenuation.

Young adult with cystic fibrosis. Arrow: Cylindrical (tubular) bronchiectasis.

Elderly male with idiopathic pulmonary fibrosis. Arrow: varicose bronchiectasis.

Sarcoidosis. Transverse images show fibrosis and traction bronchiectasis (arrows, B) that predominantly involve upper lobes.

Sarcoidosis Parenchymal involvement by sarcoidosis can lead to upper and mid lung fibrosis and traction bronchiectasis, typically associated with multiple nodules in a perilymphatic distribution. Mediastinal and bilateral symmetric lymphadenopathy is common, although it can regress as the interstitial disease worsens

Kartagener's syndrome. Transverse CT image confirms dextrocardia (asterisk is in left ventricle) and bronchiectasis (arrows) that predominantly affects midportion of lungs.

Immobile Cilia Syndrome This rare congenital cause of bronchiectasis, which primarily involves the middle lung, is characterized by ineffective clearing of secretions, causing bronchiectasis, recurrent pneumonias, sinusitis, and infertility. In 50% of cases, total situs inversus is present, a condition known as Kartagener's syndrome.

Mounier-Kuhn's syndrome. Enlarged mainstem bronchi (black arrows) and distal bronchiectasis (white arrows).

Mounier-Kuhn syndrome, also known as tracheobronchomegaly, is a rare congenital abnormality of the trachea and main bronchi characterized by cystic dilatation of the tracheobronchial tree and recurrent respiratory infections.

Mounier-Kuhn Syndrome. Two axial CT images of the thorax demonstrate marked dilatation of the trachea (T) and right (R) and left (L) main bronchi in this patient with Mounier-Kuhn syndrome. Notice the bronchiectasis (red arrows and red circle) in which the bronchi are larger than their accompanying blood vessel and there is tram=tracking of thickened bronchial walls seen in profile.

Elderly male with COPD and upper lobe bronchiectasis and scarring. New hemoptysis. Questionable soft tissue nodule within a left upper lobe bullous (arrow).

Axial CT scan on lung windows. Mycetoma within the left upper lobe bullous (arrow).

Coronal reformat demonstrating bilateral upper lobe bullae, scarring and bronchiectasis with a fungus ball on the left (arrow).

MPR in MIP demonstrates hypervascular area of bronchiectasis with multiple cysts containing air mucus at postero basal segment of left lower lobe.

MPR (oblique section) in MIP demonstrates area of bronchiectasis at posterior basal segment.

MPR (axial section) in MIP demonstrates areas of bronchiectasis at posterior basal segments at both sides.

CT show marked dilatation of the trachea, left and right bronchi with multiple diverticula (arrow heads), and bilateral cystic bronchiectasis.

HRCT features of NSIP include extensive ground-glass areas in the lung (black arrows) and traction bronchiectasis. This bronchiectasis frequently shows a parallel course through the lung, well depicted by sagittal reconstruction in D (black dotted arrows). There is no honeycombing in the lung. Cystic bronchiectasis is generally well documented by MPR images

Cystic bronchiectasis in middle lobe. Chest x ray and MDCT (axial, coronal and sagittal).

Bilateral cystic bronchiectasis.

Vascular abnormalities.Dilated bronchial arteries. These are best demonstrated post administration of intravenous contrast. These tortuous vessels extend along the central airways toward the hila. It is these vessels that are often responsible for hemoptysis, a symptom these patients may describe. Dilated main pulmonary artery. This usually indicates underlying pulmonary hypertension as a sequelae of chronic, severe lung disease. Other findingsLobar collapse.Mycetoma formation (Fungus ball) Aspergillus fumigatus is a fungus that may colonise dilated airways or bullae/cavities. It is an important cause of hemoptysis.

Contrast enhanced CT scan in a coronal reformat. Dilated bronchial arteries course through the mediastinum. (arrows).

Coronal reconstruction from high-resolution computed Tomography showing a bronchial collateral vessel.

a) Transverse magnetic resonance (T2-weighted half-Fourier acquisition single-shot turbo spin echo (HASTE)) image and b) corresponding computed tomography image in a 14-year-old female with cystic fibrosis. In both images, bronchial wall thickening, bronchiectasis, peripheral mucous plugging and dorsal consolidations are demonstrated, as shown by the arrows.

Bilateral upper lobes cystic bronchiectasis with air fluid level, MRI images.

MRI images with cystic bronchiectasis.

T1-weighted magnetic resonance imaging showing appearance a) before and b) after contrast medium in a 43-year-old cystic fibrosis patient. The post-contrast images demonstrate extensive bronchial wall enhancement and permit differentiation of a thickened wall from intrabronchial secretions, with intrabronchial fluid having an air–fluid level (arrow).

Diagnostic approach to bronchiectasis.

Thank You.