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High-resolution computed tomography

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High-resolution computed tomography (HRCT) is a type of computed tomography (CT) with specific techniques to enhance image resolution. It is used in the diagnosis of various health problems, though most commonly for lung disease, by assessing the lung parenchyma.

High-resolution computed tomography
Pulmon fibrosis.PNG
HRCT of lung showing extensive fibrosis possibly from usual interstitial pneumonitis. There is also a large emphysematous bulla.
ICD-9-CM 87.41

Contents

TechniqueEdit

 
High-resolution computed tomographs of a normal thorax, taken in the axial, coronal and sagittal planes, respectively. Click here to scroll through the image stacks.

HRCT is performed using a conventional CT scanner. However, imaging parameters are chosen so as to maximize spatial resolution:[1]

  • A narrow slice width is used (usually 1–2 mm)
  • A high spatial resolution image reconstruction algorithm is used
  • Field of view is minimized, so as to minimize the size of each pixel
  • Other scan factors (e.g. focal spot) may be optimized for resolution at the expense of scan speed

Depending on the suspected diagnosis, the scan may be performed in both inspiration and expiration. The patient may also lie prone (face down) rather than the more usual supine (face up).

As HRCT's aim is to assess a generalized lung disease, the test is conventionally performed by taking thin sections 10–40 mm apart. The result is a few images that should be representative of the lungs in general, but that cover only approximately one tenth of the lungs.[2]

Because HRCT does not image the whole lungs (by using widely spaced thin sections), it is unsuitable for the assessment of lung cancer or other localised lung diseases. Similarly, HRCT images have very high levels of noise (due to thin sections and high-resolution algorithm), which may make them non-diagnostic for the soft-tissues of the mediastinum.

Intravenous contrast agents are not used for HRCT[3] as the lung inherently has very high contrast (soft tissue against air), and the technique itself is unsuitable for assessment of the soft tissues and blood vessels, which are the major targets of contrast agents.

Impact of modern CT technologyEdit

The technique of HRCT was developed with relatively slow CT scanners, which did not make use of multi-detector (MDCT) technology. The parameters of scan duration, z-axis resolution and coverage were interdependent. To cover the chest in a reasonable time period with a conventional chest CT scan required thick sections (e.g., 10mm thick) to ensure contiguous coverage. As performing contiguous thin sections required unacceptably prolonged scan time, HRCT examination was performed with widely spaced sections. Because of the different scan parameters for conventional and HRCT examinations, if a patient required both, they had to be performed sequentially.

Modern MDCT scanners are able to overcome this interdependence, and are capable of imaging at full resolution yet retain very fast coverage - images can then be reconstructed retrospectively from the volumetric raw data. Because of this, it may be possible to reconstruct inspiratory HRCT-like images from the data taken from a 'normal' chest CT scan.[4]

Alternatively, the scanner could be configured to perform contiguous 1mm sections for a HRCT examination - this provides greater diagnostic information as it examines the entire lung, and permits the use of multi-planar reconstruction techniques. However, it brings the expense of irradiating the entire chest (instead of approximately 10%) when performed using widely spaced sections.[5]

Lung diseaseEdit

HRCT is used for diagnosis and assessment of interstitial lung disease, such as pulmonary fibrosis, and other generalized lung diseases such as emphysema and bronchiectasis.

NodularityEdit

The presence of nodules on high resolution CT is a keystone in understanding the appropriate differential. Typically, the distribution of nodules is divided into perilymphatic, centrilobular and random categories. Furthermore, nodules can be ill-defined, implying they are in the alveoli, or well defined, suggesting an interstitial position. Distribution and appearance allow understanding of the disease process relative to the secondary lobule of the lung, the smallest anatomic unit with surrounding connective tissue, usually 1–2 cm across.[6]

Perilymphatic nodularity deposits at the periphery of the secondary lobule and tends to respect pleural surfaces and fissures. Sarcoidosis, lymphangitic spread of carcinoma, silicosis, coal worker's pneumoconiosis, and more rare diagnoses such as lymphoid interstitial pneumonitis and amyloidosis are included in the differential. Centrilobular nodularity deposits at the center of the secondary lobule, but spares pleural surfaces. Differential includes endobronchial tuberculosis, bronchopneumonia, endobronchial spread of tumor, and again silicosis or coal workers’ pneumoconiosis. For randomly distributed nodules, the differential includes miliary tuberculosis, fungal pneumonia, hematogenous metastasis and diffuse sarcoidosis.[6]

Prone versus supine positionEdit

Because the bases of the lungs lie posteriorly in the chest, a mild degree of collapse under the lungs' own weight can occur when the patient lies on their back. As the very base of the lungs may be the first region affected in several lung diseases, most notably asbestosis or usual interstitial pneumonia (UIP), the patient may be asked to lie prone to improve sensitivity to early changes of these conditions.

The lung bases are often inconsistent in appearance in patients due to the potential for atelectasis causing positional ground glass or consolidative opacities. When the patient is positioned prone, or on their belly, the lung bases can expand further and help distinguish atelectasis from early fibrosis. In patients with normal chest radiographs, prone scans have been found useful in 17% of cases, particularly in excluding posterior lung abnormalities. In patients with abnormal findings on chest radiographs, prone scans are only useful in 4% of cases. The scans may be more useful in patients with basilar predominant disease processes, such as asbestosis and idiopathic pulmonary fibrosis.[6]

Airways diseases, such as emphysema or bronchiolitis obliterans, cause air trapping on expiration, even though they may cause only minor changes to lung structure in their early stages. To enhance sensitivity for these conditions, the scan may be performed in both inspiration and expiration.

HRCT may be diagnostic for conditions such as emphysema or bronchiectasis. While HRCT may be able to identify pulmonary fibrosis, it may not always be able to further categorize the fibrosis to a specific pathological type (e.g., non-specific intersitial pneumonitis or desquamative interstitial pneumonitis). The major exception is UIP, which has very characteristic features, and may be confidently diagnosed on HRCT alone.[7]

Where HRCT is unable to reach a definitive diagnosis, it helps locate an abnormality, and so helps planning a biopsy, which may provide the final diagnosis.

Other miscellaneous conditions where HRCT is useful include:

Organ transplant patients, particularly lung, or heart-lung transplant recipients, are at relatively high risk of developing pulmonary complications of the long-term drug and immunosuppressive treatment. The major pulmonary complication is bronchiolitis obliterans, which may be a sign of lung graft rejection.

HRCT has better sensitivity for bronchiolitis obliterans than conventional radiography.[8][9] Some transplant centers may arrange annual HRCT to screen for this.

See alsoEdit

ReferencesEdit

  1. ^ "ACR–STR Practice Parameter for the Performance of High-Resolution Computed Tomography (HRCT) of the Lungs in Adults" (PDF). American College of Radiology. 2015. Retrieved 27 June 2017. 
  2. ^ Worthy, S. (11 March 1995). "High resolution computed tomography of the lungs". BMJ. 310 (6980): 616–616. doi:10.1136/bmj.310.6980.616. PMC 2549004 . 
  3. ^ Peros-Golubicic, Tatjana; Sharma, Om P. (2007). Clinical Atlas of Interstitial Lung Disease. Springer. p. 19. ISBN 9781846283260. 
  4. ^ Schoepf, U. Joseph (2005). Multidetector-Row CT of the Thorax. Springer. p. 84. ISBN 9783540300069. 
  5. ^ Schwarz, Marvin I.; King, Talmadge E. (2011). Interstitial Lung Disease. Shelton, CT: PMPH. p. 106. ISBN 9781607950240. 
  6. ^ a b c Naidich, W. Richard Webb, Nestor L. Müller, David P. (2014). High-resolution CT of the lung (5th ed.). ISBN 978-1451176018. 
  7. ^ Gotway, M. B; Freemer, M. M; King, T. E (1 June 2007). "Challenges in pulmonary fibrosis · 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias". Thorax. 62 (6): 546–553. doi:10.1136/thx.2004.040022. PMC 2117220 . 
  8. ^ Chan, A; Allen, R (March 2004). "Bronchiolitis obliterans: an update". Current Opinion in Pulmonary Medicine. 10 (2): 133–41. PMID 15021183. 
  9. ^ "Imaging in Bronchiolitis Obliterans Organizing Pneumonia: Overview, Radiography, Computed Tomography". Medscape. WebMD. 6 January 2017. Retrieved 29 June 2017. 

External linksEdit