scholarly journals Barium sulphate aspiration pneumonia in a cat with megaesophagus and dextroposition of the aortic arch: case report

2018 ◽  
Vol 70 (5) ◽  
pp. 1453-1458
Author(s):  
J.A. Barrera-Zarate ◽  
B.A. Paiva ◽  
D.P. Ferreira ◽  
F.S. Alves ◽  
J.P.H. Sato ◽  
...  

ABSTRACT A six-month-old female cat suffered aspiration of an abundant amount of barium sulfate during a radiographic procedure for the diagnosis of megaesophagus. Latero-lateral contrast radiography revealed severe dilation of the thoracic esophagus cranial to the base of the heart. Persistence of the right aortic arch was suspected and later confirmed during corrective surgery. Accumulation of barium sulfate, used as a contrast agent, was clearly observed in the lumen of the bronchi, bronchioles, and alveoli in the radiographic image. Days after the surgery, the animal developed severe respiratory distress, which resulted in death. Cytology results and histology analysis using polarized light demonstrated that the lumen of bronchi, bronchioles, and alveoli exhibited evident histiocytic infiltration with cytoplasm filled by abundant amorphous refractive granular material consistent with barium sulfate. In this report, we describe the anatomical, cytological, histopathological (using polarized light), and x-ray findings of a case of barium sulfate aspiration pneumonia in a cat resulting from the use of this contrast medium for the diagnosis of megaesophagus secondary to persistent right aortic arch.

2020 ◽  
Vol 30 (6) ◽  
pp. 892-893
Author(s):  
Toyohide Endo ◽  
Daigo Ochiai ◽  
Mamoru Tanaka

AbstractThe right aortic arch is a congenital vascular anomaly, which may form a vascular ring. However, prenatal identification of the branching pattern of brachiocephalic vessels is often limited. In this paper, we clearly demonstrated the branching pattern of brachiocephalic vessels in a case of right aortic arch with an aberrant left subclavian artery using HDlive Flow imaging.


Surgery Today ◽  
1998 ◽  
Vol 28 (1) ◽  
pp. 76-78 ◽  
Author(s):  
Masahiko Yano ◽  
Hitoshi Shiozaki ◽  
Atsuo Murata ◽  
Masatoshi Inoue ◽  
Shigeyuki Tamura ◽  
...  

1991 ◽  
Vol 43 (5) ◽  
pp. 305-307 ◽  
Author(s):  
D. Glew ◽  
G.G. Hartnell

2000 ◽  
Vol 64 (9) ◽  
pp. 727-728 ◽  
Author(s):  
Ichiya Yamazaki ◽  
Kiyotaka Imoto ◽  
Yukio Ichikawa ◽  
Jiro Kondo ◽  
Yoshinori Takanashi

1999 ◽  
Vol 67 (4) ◽  
pp. 1194-1202 ◽  
Author(s):  
Doff B McElhinney ◽  
Wayne Tworetzky ◽  
Frank L Hanley ◽  
Abraham M Rudolph

2021 ◽  
Vol 11 (17) ◽  
pp. 8171
Author(s):  
Kohei Tokuyama ◽  
Hiro Kiyosue ◽  
Hiroshi Baba ◽  
Yoshiki Asayama

An anomalous origin of the right vertebral artery (VA) is a rare anomaly that is much rarer than that of the left VA. It can be divided into a few patterns, including aortic origin, right carotid or brachiocephalic arterial origin, and duplicated origin. In embryological development, the VA is made up of a longitudinal anastomosis between cervical segments. The mechanism of the anomalous origin of the right VA can be explained by the persistence of the cervical segmental artery and the regression point of the 4th right aortic arch. Although the anomaly is usually found incidentally on imaging modalities, it can be a potential cause of complication during surgical and interventional procedures. However, there are a lot of reports about the radiomics of the anomaly. Therefore, we discuss the potential relationship between the anomalous origin of the right VA and radiomics. As the take-home message, understanding several patterns of anomalous origin of the right VA with their embryology and imaging findings is important for surgical and endovascular interventions to avoid intraprocedural complications.


2014 ◽  
Vol 28 (2) ◽  
pp. 235-240
Author(s):  
Nobumasa Takahashi ◽  
Atsushi Morio ◽  
Naoya Katsuragi ◽  
Kazuki Nakahara ◽  
Kenji Suzuki

1998 ◽  
Vol 11 (1) ◽  
pp. 177
Author(s):  
Byung Pil Cho ◽  
Ho Suck Kang ◽  
Young Chul Yang ◽  
Tae Sun Hwang ◽  
Ji Won Kim

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