Medical Image of the Month: Idiopathic Right Lower Lobe Pulmonary Vein Thrombus

Figure 1. CT angiogram chest sagittal view: showing low density filling defect consistent with pulmonary vein thrombus (yellow arrow).

Figure 2. A: CT angiogram chest axial view showing right lower lobe pulmonary vein thrombus. B: the vein (red arrow) is well differentiated by his lower contrast than the adjacent artery (blue arrows).

A 62-year-old man with a medical history notable only for a seasonal allergy, presented to the emergency department with complaints of shortness of breath with productive cough for 2 months which were worsening for the last 2 weeks. CTA chest revealed low density filling defect in the RLL vein consistent with RLL vein thrombus (Figures 1 and 2). After a comprehensive work up to rule out malignancy and hypercoagulable disorders, a diagnosis of idiopathic pulmonary vein thrombosis was made. The patient received heparin and was discharged with rivaroxaban.

Pulmonary vein thrombosis is a rare disease but can be fatal, usually patient presents with non-specific symptoms such as cough and shortness of breath (1). The etiology in most of cases is hypercoagulable disorders, malignancies, atrial fibrillation, post lung operations such as lobectomy and lung transplantation, or could be idiopathic as in our patient.

Timothy Jon Rolle MD¹ and Mohammad Abdelaziz Mahmoud MD, DO^2
1Department of Radiology and the ²Internal Medicine Residency

Midwestern University Arizona College of Osteopathic Medicine

Canyon Vista Medical Center
Tucson, AZ USA

Reference

1. Chaaya G, Vishnubhotla P. Pulmonary vein thrombosis: a recent systematic review. Cureus. 2017 Jan 23;9(1):e993. [CrossRef] [PubMed]

Cite as: Rolle TJ, Mahmoud MA. Medical image of the month: idiopathic right lower lobe pulmonary vein thrombus. Southwest J Pulm Crit Care. 2020;20(1):7-8. doi: https://doi.org/10.13175/swjpcc048-19 PDF

Medical Image of the Month: Pneumoperitoneum with Rigler’s Sign

Figure 1. CT of the abdomen with contrast showing a large quantity of free air within the peritoneal cavity. The etiology of her free intraperitoneal air was not evident on this imaging study.

Figure 2. An upright chest radiograph performed six months later again demonstrates a large amount of free air under the hemidiaphragms, outlining both the spleen and the superior surface of the liver. Rigler’s sign (air on both the peritoneal and luminal side of bowel wall (arrows) - which clearly delineates the bowel wall) is in noted and supports the diagnosis of free intraperitoneal air.

Clinical Presentation: A 70-year-old Asian-American woman presented to the hospital with a distended and tympanic abdomen. She was otherwise asymptomatic. Her past medical history was significant only for an uncomplicated colonoscopy the previous summer. A CT scan showed free air within the peritoneal cavity (Figure 1). She was managed conservatively without a surgical intervention. After six months without a chest x-ray continued to show free air (Figure 2). She underwent an elective exploratory laparotomy without identification of a cause for her free intraperitoneal air. Her pneumoperitoneum completely resolved on follow up imaging.

Discussion: Pneumoperitoneum is a condition which commonly presents as an acute abdomen (1). Causes are numerous and include penetrating and blunt abdominal trauma, perforation of viscus, diaphragmatic rupture, fistula formation – among other etiologies. Work-up of pneumoperitoneum varies depending on the suspected etiology. In the presence of hemodynamic instability or peritoneal signs, the patient should proceed to an exploratory laparotomy immediately following airway maintenance and resuscitation. In the setting of a perforation or sepsis, broad-spectrum intravenous antibiotics are indicated. Stable patients are managed expectantly with NPO status, intravenous fluids resuscitation, serial vitals/abdominal imaging/labs, and nasogastric tube decompression if indicated for obstructive etiologies.

Rigler’s sign is well-demonstrated in the abdominal radiograph (figure 2). Rigler’s sign is the presence of air on both the luminal and peritoneal side of the bowel wall – which clearly delineates the bowel wall (1). This sign is highly suggestive of free intraperitoneal air. Rigler’s sign can be seen on a supine abdominal radiograph and can be helpful in the identification of free intraperitoneal air in a patient who may be too ill for upright radiographs or CT imaging.

Mohammad A. Mahmoud MD DO, Jonathon P. Mahn DO, and Alexander E. Brahmsteadt, MSIV.

Midwestern University | Arizona College of Osteopathic Medicine

Canyon Vista Medical Center

Sierra Vista, AZ USA

Reference

1. Levine MS, Scheiner JD, Rubesin SE, Laufer I, Herlinger H. Diagnosis of pneumoperitoneum on supine abdominal radiographs. AJR Am J Roentgenol. 1991 Apr;156(4):731-5.

Cite as: Mahmoud MA, Mahn JP, Brahmsteadt AE. Medical image of the month: pneumoperitoneum with Rigler's sign. Southwest J Pulm Crit Care. 2019;19(6):156-7. doi: https://doi.org/10.13175/swjpcc047-19 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 

Medical Image of the Week: Plastic Bronchitis

Figure 1. Cast removed from the right main stem.

Figure 2. Casts removed from right lower lobe.

Plastic Bronchitis is a rare syndrome characterized with expectoration of bronchial casts.  Conditions associated with plastic bronchitis in adults include asthma, allergic bronchopulmonary aspergillosis, cystic fibrosis, bronchiectasis, tuberculosis, amyloidosis, sickle cell anemia and rheumatoid arthritis. In children, is its associated with congenital heart diseases (1).

Typical casts are large and branched. These can be expectorated or removed endoscopically as in our case of a 52-year old man with respiratory failure (Figures 1 and 2). The exact etiology of his plastic bronchitis remains obscure. These casts were removed using a bronchoscope with a cryotherapy probe. 

Lauren Estep MD and Bhupinder Natt MD FACP

Division of Pulmonary, Allergy, Critical Care and Sleep

Banner-University Medical Center, Tucson, AZ USA

Reference

1. Itkin MG, McCormack FX, Dori Y. Diagnosis and treatment of lymphatic plastic bronchitis in adults using advanced lymphatic imaging and percutaneous embolization. Ann Am Thorac Soc. 2016 Oct;13(10):1689-96. [CrossRef] [PubMed]

Cite as: Estep L, Natt B. Medical image of the week: plastic bronchitis. Southwest J Pulm Crit Care. 2018;16(1):28. doi: https://doi.org/10.13175/swjpcc005-18 PDF 

Medical Image of the Week: Vascular Occlusion

Figure 1. Left arm angiogram showing complete occlusion of ulnar artery (red arrow).

Figure 2. Angiogram showing left radial artery complete occlusion (red arrow).

Figure 3. Left hand with necrotic fingers.

The patient is a 39 year-old woman with no significant past medical history presenting with progressive left hand pain for five days. The patient denied a history of Raynaud’s phenomenon or clotting disorders. She had no radial pulse on presentation and angiogram showed severe complete occlusion of the radial and ulnar arteries (Figures 1 and 2). She had an initial partial response with intra-arterial verapamil and nitroglycerin but her hand ischemia did not improve on heparin or with intra-arterial tissue plasminogen activator. Autoimmune and coagulation work-ups were negative. Her left hand finger necrosis at time of discharge is shown (Figure 3).  Further evaluation is ongoing for coagulation disorders.

Allison Shapiro MD, Carmen Luraschi-Monjagatta MD, Matthew Schreiber MD.

Department of Internal Medicine, Pulmonary and Critical Care, University of Nevada School of Medicine, Las Vegas, NV

Reference as: Shapiro A, Luraschi-Mongagatta C, Schreiber M. Medical image of the week: vascular occlusion. Southwest J Pulm Crit Care. 2014;9(1):36-7. doi: http://dx.doi.org/10.13175/swjpcc093-14 PDF