July 2018 Imaging Case of the Month

Michael B. Gotway, MD

Department of Radiology

Mayo Clinic Arizona

Scottsdale, AZ USA

Imaging Case of the Month CME Information  

Completion of an evaluation form is required to receive credit and a link is provided on the last panel of the activity.

0.25 AMA PRA Category 1 Credit(s)™

Estimated time to complete this activity: 0.75 hours

Lead Author(s): Michael B. Gotway, MD. All Faculty, CME Planning Committee Members, and the CME Office Reviewers have disclosed that they do not have any relevant financial relationships with commercial interests that would constitute a conflict of interest concerning this CME activity. 

Learning Objectives: As a result of completing this activity, participants will be better able to:

1. Interpret and identify clinical practices supported by the highest quality available evidence.
2. Establish the optimal evaluation leading to a correct diagnosis for patients with pulmonary, critical care and sleep disorders.
3. Translate the most current clinical information into the delivery of high quality care for patients.
4. Integrate new treatment options for patients with pulmonary, critical care and sleep related disorders.

Learning Format: Case-based, interactive online course, including mandatory assessment questions (number of questions varies by case). Please also read the Technical Requirements.

CME Sponsor: University of Arizona College of Medicine at the Arizona Health Sciences Center.

Current Approval Period: January 1, 2017-December 31, 2018

Clinical History: An 81–year old non-smoking woman presented with complaints of shortness of breath for one month, more so when laying down. The patient had a history of Sjögren syndrome established 13 years earlier. She notes a history of dryness of the eyes and upper airways. Her medications included 5 mg prednisone daily as well as various vitamins and supplements. While she complained of several medication “allergies,” none were serious and most appeared to represent side effects or untoward reactions to medications as opposed to true allergic reactions. Her past medical history included arthritis, possible obstructive sleep apnea, kidney stones, and orthostatic hypotension, the latter thought to be related to her Sjögren syndrome. Her surgical history included a sternotomy for thymoma resection years earlier.

Her physical examination was unremarkable except for diminished breath sounds at the left base; her vital signs were within normal limits.

Frontal and lateral chest radiography (Figure 1) was performed.

Figure 1. Frontal (A) & lateral (B) chest radiography.

Which of the following represents the most accurate assessment of the chest radiographic findings? (click on the correct answer to be directed to the second of eleven pages)

1. Chest radiography shows an elevated left hemidiaphragm
2. Chest radiography shows bibasilar fibrotic-appearing opacities
3. Chest radiography shows cavitary pulmonary lesions
4. Chest radiography shows multifocal bronchiectasis
5. Chest radiography shows small pulmonary nodules

Cite as: Gotway MB. July 2018 imaging case of the month. Southwest J Pulm Crit Care. 2018;17(1):15-27. doi: https://doi.org/10.13175/swjpcc086-18 PDF 

Medical Image of the Week: Pulmonary Artery Dilation

Figure 1.  Axial section of the thoracic CT scan showing the massively dilated pulmonary trunk and artery.

The upper limit of the normal diameter of the main pulmonary artery on CT scan is 29 mm and of the right interlobar artery is 17 mm (1). A dilated pulmonary artery can arise from a variety of disease states. Most commonly from one of the many causes of pulmonary hypertension including idiopathic, previously termed primary, pulmonary artery hypertension (PAH). Other less common causes of pulmonary arterial dilation include pulmonary valvular stenosis, atrial septal defect, and idiopathic dilatation of the pulmonary artery.

Our patient is 66-year-old man with exertional dyspnea who was found to have a dilated pulmonary artery on thoracic CT scan during his work up (Figure 1).  His case is suspected to be idiopathic dilatation (1). This is a rare disease with estimates around 0.6% of patients with known congenital heart disease. The estimates in the general population are unknown. There have been a few different diagnostic criteria proposed, but most contain the following:

1. Dilation of the pulmonary trunk 
2. Absence of abnormal intracardiac or extracardiac shunts
3. Absence of chronic heart or lung disease
4. Absence of arterial diseases such as syphilis, arteriosclerosis or arteritis
5. Normal pressures in the right ventricle and pulmonary artery

Patients are usually asymptomatic or with minimal symptoms of dyspnea such as our patient. Rarely, it can present dramatically from compression of nearby structures. This includes constriction of the trachea or major branches or sudden cardiac death from compression of the left main coronary artery.

Tiffany Ynosencio MD and Swathy Puthalapattu MD

Division of Pulmonary, Allergy, Critical Care and Sleep

Banner-University Medical Center and Southern Arizona VA Health Care System

Tucson, AZ USA

Reference

1. Malviya A, Jha PK, Kalita JP, Saikia MK, Mishra A. Idiopathic dilatation of pulmonary artery: A review. Indian Heart J. 2017 Jan-Feb;69(1):119-24. [CrossRef] [PubMed]

Cite as: Ynosencio T, Puthalapattu S. Medical image of the week: pulmonary artery dilation. Southwest J Pulm Crit Care. 2018;16(1):46-7. doi: https://doi.org/10.13175/swjpcc012-18 PDF