Complications of Anomalous Origin of the Right Subclavian Artery: Case Report and Review of the Literature

1991 ◽  
Vol 5 (4) ◽  
pp. 385-388 ◽  
Author(s):  
Donald L. Akers ◽  
Richard J. Fowl ◽  
James Plettner ◽  
Richard F. Kempczinski
Keyword(s):  
Case Report ◽  
Subclavian Artery ◽  
Anomalous Origin ◽  
Review Of The Literature ◽  
The Right

Republished: Multiple anomalies in the origin and course of vertebral arteries and aberrant right subclavian artery in a child with moyamoya syndrome

2018 ◽  
Vol 10 (6) ◽  
pp. e14-e14
Author(s):  
Pınar Beyaz ◽  
Nadia Khan ◽  
Gerasimos Baltsavias
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Subclavian Artery ◽  
Anomalous Origin ◽  
Aberrant Right Subclavian Artery ◽  
Moyamoya Syndrome ◽  
Vertebral Arteries ◽  
The Common ◽  
The Right ◽  
First Time

Here we report, for the first time, a combination of five-vessel aortic arch, anomalous origin of the right vertebral artery (VA) from the common carotid artery (CCA), an aberrant right subclavian artery (SCA), and bilateral symmetrical segmental agenesis of VAs.In this case report, we present a patient with moyamoya syndrome (MMS) and Down syndrome (DS) who has bilateral symmetrical segmental agenesis of VAs, left VA originating from aortic arch and anomalous origin of right VA arising from CCA in combination with an aberrant right SCA. Therefore, five vessels are originating from aortic arch. Here, we report, for the first time, a combination of five-vessel aortic arch with an aberrant right SCA and symmetrical segmental agenesis of both VAs. The possible embryological mechanisms of the anomalies as well as an relation with MMS and DS are discussed.

scholarly journals Clear cell sarcoma of the right lumbar region: A case report and review of the literature

2014 ◽  
Vol 8 (4) ◽  
pp. 1625-1627
Author(s):  
XUE-LI YANG ◽  
SAN-JUN LU ◽  
JIE XUE ◽  
YAN-FEN WU ◽  
JUN-LING SHI
Keyword(s):  
Case Report ◽  
Clear Cell ◽  
Clear Cell Sarcoma ◽  
Lumbar Region ◽  
Review Of The Literature ◽  
Cell Sarcoma ◽  
The Right

scholarly journals Angiosarcoma of the Heart: Case Report

2020 ◽  
Vol 3 (11) ◽  
pp. 01-07
Author(s):  
Marc Vanderheyden ◽  
Sofie Dhaeyer ◽  
Chirik Wah Lau ◽  
Vanessa Meert ◽  
Jan Leeman ◽  
...  
Keyword(s):  
Case Report ◽  
Malignant Tumors ◽  
Local Relapse ◽  
Review Of The Literature ◽  
Poor Survival ◽  
Right Heart ◽  
Course Of Disease ◽  
Metastatic Recurrence ◽  
Primary Angiosarcoma ◽  
The Right

Cardiac angiosarcomas are rare malignant tumors, predominantly affecting the right heart with poor survival outcomes. The current mainstay of treatment consists of surgery with or without chemotherapy, but often yields limited results with local relapse or metastatic recurrence. This case report describes 2 patients with primary angiosarcoma located in the right atrium. One patient received neo-adjuvant and adjuvant chemotherapy; both were scheduled for surgical resection. The course of disease is described followed by a comprehensive review of the literature.

Intracardiac varices of the right atrium: a case report and review of the literature

1995 ◽  
Vol 48 (2) ◽  
pp. 177-181 ◽  
Author(s):  
Phillip J. Harrity ◽  
Henry D. Tazelaar ◽  
William D. Edwards ◽  
Thomas A. Orszulak ◽  
William K. Freeman
Keyword(s):  
Case Report ◽  
Right Atrium ◽  
Review Of The Literature ◽  
The Right

scholarly journals Recurrent Pindborg Tumor of the Maxilla: A Case Report and Review of the Literature

2013 ◽  
Vol 92 (2) ◽  
pp. 84-87 ◽  
Author(s):  
Gangadhara Somayaji ◽  
Aroor Rajeshwary ◽  
Sullia Ramesh ◽  
Sullia Dinesh
Keyword(s):  
Case Report ◽  
Nasal Cavity ◽  
Nasal Obstruction ◽  
Radical Surgery ◽  
Odontogenic Tumor ◽  
Review Of The Literature ◽  
Calcifying Epithelial Odontogenic Tumor ◽  
Pindborg Tumor ◽  
The Right ◽  
Epithelial Odontogenic Tumor

We report a case of recurrent Pindborg tumor (calcifying epithelial odontogenic tumor) of the maxilla. The patient was a 34-year-old woman who had been previously diagnosed with Pindborg tumor and treated with curettage. She was subsequently referred to us for evaluation of nasal obstruction. Examination revealed the presence of a mass lesion in the right nasal cavity and right maxilla, which was identified as a recurrence of her earlier Pindborg tumor. The patient was treated with maxillectomy with orbital preservation. Pindborg tumor is a rare odontogenic tumor; when it does occur, it is more often seen in the mandible than in the maxilla. While this tumor is often treated with curettage alone, the aggressive nature of the recurrence in our patient necessitated radical surgery. We report this case to highlight the need to be suitably aggressive in treating these types of tumors in order to avoid recurrence.

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