Anterior Mediastinal Mass in a Patient With Graves’ Disease

2006 ◽  
Vol 81 (5) ◽  
pp. 1904-1906 ◽  
Author(s):  
Kazuki Yamanaka ◽  
Haruhiko Nakayama ◽  
Katsuya Watanabe ◽  
Yoichi Kameda
2010 ◽  
Vol 76 (1) ◽  
pp. 113-115
Author(s):  
Robert D. Rice ◽  
David M. Parker ◽  
Dominic M. Gallo ◽  
Cletus A. Arciero

2019 ◽  
Vol 08 (01) ◽  
pp. e24-e26 ◽  
Author(s):  
Christopher James Kennedy ◽  
David James William Paton

Background Thymic hyperplasia is a recognized complication of Graves' disease that can present radiologically as an anterior mediastinal mass. Case Description We present a unique case of massive thymic hyperplasia occurring in a 24-year-old female without a known history of thyroid or other systemic disease in whom Graves' disease first manifested intraoperatively during thymectomy for presumed neoplasia. Conclusion We suggest that the work-up of all anterior mediastinal masses should include a comprehensive search for medical causes of reversible thymic enlargement.


2019 ◽  
Vol 25 ◽  
pp. 294
Author(s):  
Losty Torres Potter ◽  
Gustavo Meyreles-Chaljub ◽  
Natalia Weare-Regales ◽  
Pedro Troya ◽  
Madeline Candelario-Cosme

Thorax ◽  
1985 ◽  
Vol 40 (6) ◽  
pp. 469-470 ◽  
Author(s):  
H C Ford ◽  
T Savage ◽  
J W Delahunt

2002 ◽  
Vol 77 (5) ◽  
pp. 495-499 ◽  
Author(s):  
ADRIANE I. BUDAVARI ◽  
MICHAEL D. WHITAKER ◽  
RICHARD A. HELMERS

1982 ◽  
Vol 55 (3) ◽  
pp. 587-588 ◽  
Author(s):  
THOMAS A. BERGMAN ◽  
CARY N. MARIASH ◽  
JACK H. OPPENHEIMER

2002 ◽  
Vol 77 (5) ◽  
pp. 495-499 ◽  
Author(s):  
Adriane I. Budavari ◽  
Michael D. Whitaker ◽  
Richard A. Helmers

2012 ◽  
Vol 15 (3) ◽  
pp. 170
Author(s):  
Hee Moon Lee ◽  
Dong Seop Jeong ◽  
Pyo Won Park ◽  
Wook Sung Kim ◽  
Kiick Sung ◽  
...  

A 54-year-old man was referred to our institution with hemoptysis and hoarseness of 1 year's duration. A computed tomography (CT) scan showed an anterior mediastinal mass (2.5 cm x 1.0 cm), which was diagnosed as thymoma. The tumor was resected under a sternotomy. The tumor had invaded the anterior wall of the ascending aorta. With the patient under cardiopulmonary bypass, the aortic wall invaded by the mass was resected, and arterial reconstruction was performed with patch material. The tumor was revealed to be a tumor of neuronal origin. The patient's postoperative course was uneventful. The patient was discharged on postoperative day 9. One year after the operation, a follow-up chest CT evaluation showed no specific complications or recurrence.


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