Long-term outcome after DNA-based prophylactic neck surgery in children at risk of hereditary medullary thyroid cancer

2019 ◽  
Vol 33 (4) ◽  
pp. 101274 ◽  
Author(s):  
Andreas Machens ◽  
Henning Dralle
Surgery ◽  
2009 ◽  
Vol 146 (5) ◽  
pp. 906-912 ◽  
Author(s):  
Elisabeth Schellhaas ◽  
Charlotte König ◽  
Karin Frank-Raue ◽  
Heinz-J. Buhr ◽  
Hubert G. Hotz

2008 ◽  
Vol 32 (5) ◽  
pp. 754-765 ◽  
Author(s):  
Elizabeth Fialkowski ◽  
Mary DeBenedetti ◽  
Jeffrey Moley

1994 ◽  
Vol 18 (4) ◽  
pp. 583-587 ◽  
Author(s):  
Friedrich L�ngle ◽  
Thomas Soliman ◽  
Nikolaus Neuhold ◽  
Gerold Widhalm ◽  
Bruno Niederle ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Nicholas S. Mastronikolis ◽  
Sofia P. Spiliopoulou ◽  
Vassiliki Zolota ◽  
Theodoros A. Papadas

Horner’s syndrome is characterized by a combination of ipsilateral miosis, blepharoptosis, enophthalmos, facial anhidrosis, and iris heterochromia in existence of congenital lesions. The syndrome results from a disruption of the ipsilateral sympathetic innervation of the eye and ocular adnexa at different levels. Though rare, thyroid and neck surgery could be considered as possible causes of this clinical entity. We present a case of Horner’s syndrome in a patient after total thyroidectomy and neck dissection for medullary thyroid cancer with neck nodal disease and attempt a brief review of the relevant literature.


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