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Case Report Submitted by: Ashley Roberts, MS4 Faculty reviewer: Sandra Oldham, M.D Date accepted: 25 August 2010 Radiological Category: Principal Modality : Thoracic Chest CT

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Page 1: Slide 1 - Welcome to the Texas Medical Center

Case Report

Submitted by: Ashley Roberts, MS4

Faculty reviewer: Sandra Oldham, M.D

Date accepted: 25 August 2010

Radiological Category: Principal Modality : Thoracic Chest CT

Page 2: Slide 1 - Welcome to the Texas Medical Center

Case History

HPI: 74yo white female presented to an OSH with sudden onset bradycardia, dizziness, chest pain and SOB after a several week history of dry cough.

She was transferred to MHH at the request of the family after developing altered mental status.

Denies sick contacts or a previous history of respiratory difficulties.

PMH: HTN, HLD, multiple TIAs, Afib for 1.5yrs, lung contusion many years ago.

Home meds: Plavix, Coumadin, Amiodarone, Nifedipine, Nexium, Gabapentin, Toprol

PSH: tonsillectomy, glaucoma

Allergies: PCN, Demerol

FH: Positive for CVAs and CAD.

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Case History

SH: Denies T/A/D. Previously held jobs include work in a rug factory and as a hospital aid. She has lived near both coal refineries and sugar factories, as well as in Pasadena. Currently works at Wal-Mart.

ROS: negative except for HPI.

Relevant PE:

BP: 121/56, P 62-66, RR 20-33, SpO2: 94-98% on 4-5L NC

Gen: Well-nourished, NAD

CV: S1,S2, RRR. No murmur

Pulm: Bilateral diffuse dry crackles, particularly in the lower lobes. Mild expiratory wheezing.

Abd: WNL

Extr: No clubbing/cyanosis, edema.

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Radiological Presentations

PA Chest X-rays show blunting of the left costophrenic angle. Lateral Shows clear evidence of effusion with possible bilateral involvement.

No previous studies were available for comparison

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Radiological Presentations

CT Chest without contrast, lung window, coronal and axial sections

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Radiological Presentations

CT Chest without contrast, mediastinal window, axial sections

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Radiological Presentations

CT Chest without contrast, axial sections

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Radiological Presentations

CT Chest without contrast, coronal sections

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• Amyloidosis

• Pneumoconiosis

• Amiodarone toxicity

• Calcified Pulmonary Metastases

• Hemachromatosis

Which one of the following is your choice for the appropriate diagnosis? After your selection, go to next page.

Test Your Diagnosis

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2 view Chest X-ray shows bilateral effusions.

Unenhanced CT scan shows scattered areas of ground glass opacitiies, and focal areas of dense lung consolidations containing air bronchograms in the basilar segments of the bilateral lower lobes. Adjacent to these consolidations are moderate bilateral pleural effusions. High attenuation is also noted in the liver parenchyma.

• Amyloidosis

• Pneumoconiosis

• Amiodarone toxicity

• Calcified Pulmonary Metastases

• Hemachromatosis

Findings:

Differentials:

Findings and Differentials

Each of these diagnoses present patterns of high attenuation on CT

Page 11: Slide 1 - Welcome to the Texas Medical Center

2 view Chest X-ray shows bilateral effusions.

Unenhanced CT scan shows focal areas of dense lung consolidations containing air bronchograms in the basilar segments of the bilateral lower lobes. Adjacent to these consolidations are moderate bilateral pleural effusions. High attenuation is also noted in the liver parenchyma.

• Amyloidosis

• Pneumoconiosis

• Calcified Pulmonary Metastases

• Hemochromatosis

• Amiodarone toxicity

Findings:

Differentials:

Findings and Differentials

- Rarely occurs in the lungs, and liver findings will be hypodense

- (coal) CT appearance is of multiple hyperdense nodules- No liver involvement

-Liver will be hyperattenuated, but no lung involvement

- Bingo!

- Have an appearance of focal calcification within a pulmonary nodule rather than a generally hyperattenuated appearance

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Given the unique radiological presentation, and the patient’s history of atrial fibrillation, her images are consistent with Amiodarone-induced pulmonary toxicity (AIPT).

Amiodarone is one of the most widely prescribed anti-arrhythmic in the US due to it’s multiple clinical applications and it’s cardiovascular efficacy.

Indications include both ventricular and supraventricular arrhythmias. It does not exacerbate CHF, nor is it pro-arrhythmic.

The patients that benefit the most from the use of amiodarone are those with: Afib, LV dysfunction, acute sustained arrhythmias, and those with ICDs and symptomatic shocks.

However, amiodarone use must be closely monitored.…

Discussion

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Pharmacokinetics:

•Amiodarone is highly lipid-soluble and contains an iodinated component. –It is the iodinated component that is responsible for the high attenuation appearance on CT

•It tends to accumulate in adipose tissue and highly perfused organs such as the liver, lungs, and spleen.

•It is metabolized in the liver via the cytochrome p450 system and has a half-life of approximately 6 months.

•Of note, neither amiodarone nor it’s metabolite are able to be removed by dialysis.

Discussion

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Amiodarone is well-known to have adverse effects involving multiple organs. Among them are:

Corneal deposits

Thyroid dysfunction (both hyper- and hypo-)

Bone marrow suppression

Abnormal liver function tests

Coagulopathies

Drug-drug interactions

The most serious and clinically limiting side effect, however, is AIPT.

Discussion

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Pulmonary toxicity occurs both by direct cytotoxic effects through the generation of free radicals, and by a cell-mediated immune reaction. High concentrations of the drug accumulate within macrophages and type II pneumocytes.

Lung biopsy of patients with AIPT show diffuse interstitial pneumonitis, hyperplasia of type II pneumocytes, thickening of alveolar septae with inflammatory infiltrate, and varying degrees of fibrosis.

Discussion

Image borrowed from the Veterans AffairsNational Department of Electron Microscopy

Microstructural exam shows characteristic lamellated myelin bodies, and foamy macrophages. These findings are present even in the absence of toxicity.

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Clinical presentation

-Incidence of AIPT varies from 2-15% depending on the prescribed dose.

-The most common presentation is one of a subacute pneumonia after months to years of amiodarone use:

-Non-productive cough, progressive shortness of breath, fever, and malaise -+/- pleuritic chest pain

-PFTs will demonstrate a restrictive pattern

-In severe cases it can also present as a rapidly progressive pneumonitis with development of ARDS

-Particularly in patients receiving contrast for pulmonary angiography and -Patients undergoing cardiac or pulmonary surgery

Discussion

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Risk factors for the development of AIPT:

-Dose-dependent effect, particularly with respect to the total cumulative dose-Patients most at risk are those receiving >/= 400mg daily for >2 months OR those receiving 200mg daily for >2 years-That said, AIPT can occur at any time during treatment

Other risk factors include:-Male sex-Age-Pre-existing lung disease-Potentially race (higher incidence in a Japanese population in one study)-Exposure to supplemental oxygen

Discussion

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Radiographic presentation:

CXR: will reveal patchy or diffuse infiltrates, often bilaterally, and sometimes with a ground glass appearance.

HRCT:

Lung: -Ground glass opactities; in early disease, these may be peripheral-Infiltrates: interstitial, alveolar, or both. Usually bilateral-Areas of high attenuation due to amiodarone accumulation-Peripheral lung nodules or masses-Dense bibasilar reticular opacities, which suggest fibrosis-Pleural thickening and effusions

Abdomen:-High attenuation in the liver and spleen

Discussion

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Diagnosis and Treatment:

-AIPT should be suspected in any patient on amiodarone therapy with new onset or worsening pulmonary symptoms or changes on CXR

-CXR, and PFTs should be obtained at baseline, and a CXR should be obtained yearly so that toxicity can be closely monitored.

-Have a low threshold for getting new CXR and PFTs if clinically indicated.

-If diagnosis is confirmed, discontinue the drug and begin systemic steroids-The long half-life of amiodarone may mean that things will get worse before they get better. -Steroids should be given for 6 months to a year.

-Cases of relapse have been documented with early steroid withdrawal, particularly in patients with a large amount of adipose tissue.

Discussion

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Amiodarone-induced lung toxicity

Diagnosis

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Marchiori E, et al. Diffuse High-Attenuation Pulmonary Abnormalities: A Pattern-Oriented Diagnostic Approach on High resolution CT. American Journal of Roentgenology 2005; 184: 273-282

Wolkove N, Baltzan M. Amiodarone Pulmonary Toxicity. Canadian Respiratory Journal 2009; 16(2): 43-48

Georgiades CS, et al. Amyloidosis: Review and CT Manifestations. Radiographics, March 2004; 24(2): 405-416

Merck Manual’s Online Medical Library: Coal Worker’s Pneumoconiosis. http://www.merck.com/mmhe/sec04/ch049/ch049f.html

Beo SB, et al. Atypical Pulmonary Metastases: Spectrum of Radiographic Findings. Radiographics, March 2001; 21:403-417

Vassallo P, Trohman G. Prescribing Amiodarone: An Evidence-Based Review of Clinical Indications. JAMA 2007; 298(11): 1312-1322

References