scholarly journals Dysphagia Lusoria

2020 ◽  
Vol 120 (12) ◽  
pp. 941
Author(s):  
Karl Andersen ◽  
Ryan Hoff ◽  
Dean Silas
Keyword(s):  
Dysphagia Lusoria

Dysphagia lusoria: utility of high‐resolution impedance manometry to identify true disease

2021 ◽  
Author(s):  
Jennifer Wellington ◽  
Joseph Kim ◽  
Donald O. Castell ◽  
Guofeng Xie
Keyword(s):  
High Resolution ◽  
Dysphagia Lusoria

scholarly journals Case report: a step-wise management of concurrent presentation of congenital single lung and aberrant right subclavian artery in an infant girl

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Keon Young Park ◽  
Kevin C. Janek ◽  
Joshua L. Hermsen ◽  
Petros V. Anagnostopoulos ◽  
Hau D. Le
Keyword(s):  
Subclavian Artery ◽  
Tissue Expander ◽  
Rare Condition ◽  
Aberrant Right Subclavian Artery ◽  
Cross Sectional ◽  
Unique Challenge ◽  
Surgical Interventions ◽  
Tracheal Compression ◽  
Dysphagia Lusoria ◽  
Infant Girl

Abstract Introduction Congenital single lung (CSL) is a rare condition, and symptomatic patients often present with respiratory distress or recurrent respiratory infection due to mediastinal shift causing vascular or airway compression. Aberrant right subclavian artery (ARSA) is another rare congenital anomality that can lead to tracheal or esophageal compressions. There is only one other case of concurrent presentation of CSL and ARSA reported, which presented unique challenge in surgical management of our patient. Here we present a step-wise, multidisciplinary approach to manage symptomatic CSL and ARSA. Case presentation An infant girl with a prenatal diagnosis of CSL developed worsening stridor and several episodes of respiratory illnesses at 11 months old. Cross-sectional imaging and bronchoscopic evaluation showed moderate to severe distal tracheomalacia with anterior and posterior tracheal compression resulting from severe mediastinal rotation secondary to right-sided CSL. It was determined that her tracheal compression was mainly caused by her aortic arch wrapping around the trachea, with possible additional posterior compression of the esophagus by the ARSA. She first underwent intrathoracic tissue expander placement, which resulted in immediate improvement of tracheal compression. Two days later, she developed symptoms of dysphagia lusoria due to increased posterior compression of her esophagus by the ARSA. She underwent transposition of ARSA to the right common carotid with immediate resolution of dysphagia lusoria. As the patient grew, additional saline was added to the tissue expander due to recurrence in compressive symptoms. Conclusions Concurrent presentation of CSL and ARSA is extremely rare. Asymptomatic CSL and ARSA do not require surgical interventions. However, if symptomatic, it is crucial to involve a multidisciplinary team for surgical planning and to take a step-wise approach as we were able to recognize and address both tracheomalacia and dysphagia lusoria in our patient promptly.

Right supra- Clavicular approach for simultaneous treatment of dysphagia lusoria and cervical rib with scalene node biopsy: A case report

2008 ◽  
Vol 24 (1) ◽  
pp. 32-34
Author(s):  
Uday Eknathrao Jadhav ◽  
Raghavendra Chikkatur ◽  
Nageshwar Rao ◽  
Manish Puranik ◽  
Jyoti Magar ◽  
...  
Keyword(s):  
Case Report ◽  
Simultaneous Treatment ◽  
Cervical Rib ◽  
Dysphagia Lusoria ◽  
Node Biopsy

A common symptom in two uncommon coexistent conditions: Glomus jugulare tumor and dysphagia lusoria

2012 ◽  
Vol 114 (8) ◽  
pp. 1193-1196
Author(s):  
Shivam Om Mittal ◽  
Bahman Jabbari ◽  
Duarte G. Machado
Keyword(s):  
Common Symptom ◽  
Glomus Jugulare Tumor ◽  
Glomus Jugulare ◽  
Dysphagia Lusoria

Dysphagia lusoria

1944 ◽  
Vol 154 (3-4) ◽  
pp. 313-320 ◽  
Author(s):  
W. Schneider
Keyword(s):  
Dysphagia Lusoria

Dysphagia lusoria: Report of a series of six cases

2014 ◽  
Vol 38 (3) ◽  
pp. e45-e49 ◽  
Author(s):  
Houda Jalal ◽  
Redouane El Idrissi ◽  
Amine Azghari ◽  
Laaziza Ouazzani ◽  
Nadia Benzzoubeir ◽  
...  
Keyword(s):  
Dysphagia Lusoria

scholarly journals Dysphagia lusoria: A late onset presentation

2013 ◽  
Vol 19 (15) ◽  
pp. 2433 ◽  
Author(s):  
Alice Louise Bennett
Keyword(s):  
Late Onset ◽  
Dysphagia Lusoria

Hybrid-Therapie eines Dysphagia-lusoria-Rezidives mittels thorakalem Stentgraft und Transposition der A. subclavia

2020 ◽  
Vol 25 (8) ◽  
pp. 664-666
Author(s):  
B. Geier ◽  
H. Freis ◽  
A. Brach ◽  
M. Michels ◽  
J. O. Düsterwald ◽  
...  
Keyword(s):  
Dysphagia Lusoria

scholarly journals Co-Occurrence of Rarest Type of Dysphagia Lusoria (Type N-1) and Eosinophilic Esophagitis in a Cognitively Disabled Individual

2019 ◽  
Vol 2019 ◽  
pp. 1-6
Author(s):  
Kishore Kumar ◽  
Jasbir Makker ◽  
Hassan Tariq ◽  
Ariyo Ihimoyan ◽  
Chime Chukwunonso ◽  
...  
Keyword(s):  
Subclavian Artery ◽  
Eosinophilic Esophagitis ◽  
Previous History ◽  
Food Allergies ◽  
Aberrant Right Subclavian Artery ◽  
Food Impaction ◽  
Diagnostic Challenge ◽  
Dysphagia Lusoria ◽  
Extrinsic Compression ◽  
History Of

Dysphagia is an expressive symptom, described by an individual as “difficulty in swallowing.” Dysphagia due to esophageal compression from an aberrant right subclavian artery is rare, and it is termed as “dysphagia lusoria.” We present a rare case of co-occurrence of dysphagia lusoria with esophageal eosinophilia in a patient with cognitive disability which portends a case with diagnostic challenge and treatment dilemma. A 31-year-old man with intellectual disability, cerebral palsy, previous history of feeding difficulty, and esophageal food impaction presented with esophageal foreign body impaction. He has no known history of atopy and food allergies. There was no laboratory evidence of peripheral eosinophilia. The IgE-mediated allergic test was unremarkable. His prior presentation revealed a diagnosis of eosinophilic esophagitis. The imaging studies showed proximal esophageal dilatation with extrinsic compression at the level of the upper esophagus. The foreign bodies were removed successfully through the help of upper endoscopy. Subsequent evaluation revealed a rare type of dysphagia lusoria (type N-1) due to an aberrant left subclavian artery arising from the right-sided aortic arch. The patient’s family refused further management of artery lusoria. Prolonged stasis of secretions and food in the esophagus can also lead to increased esophageal eosinophils. In our case, it remains undetermined whether increased number of esophageal eosinophils resulted from primary eosinophilic esophagitis or due to prolonged food stasis from esophageal compression caused by an aberrant subclavian artery. However, food impaction right above the compression site makes dysphagia lusoria the likely etiology.

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