Sternotomy-sparing surgical dissection technique of a large thyroid substernal goiter with preservation of bilateral recurrent laryngeal nerves and parathyroid glands

ASVIDE ◽  
2021 ◽  
Vol 8 ◽  
pp. 006-006
Author(s):  
Allen Young ◽  
Harry Ching ◽  
Sabrina Ho ◽  
Robert Wang
1991 ◽  
Vol 100 (11) ◽  
pp. 944-950 ◽  
Author(s):  
Franca B. Sant'Ambrogio ◽  
Oommen P. Mathew ◽  
Hirokazu Tsubone ◽  
Giuseppe Sant'Ambrogio

Neurosurgery ◽  
2001 ◽  
Vol 49 (4) ◽  
pp. 925-933 ◽  
Author(s):  
Ashkan Monfared ◽  
Daniel Kim ◽  
Sivakumar Jaikumar ◽  
Goutham Gorti ◽  
Andrew Kam

2015 ◽  
Vol 23 (3) ◽  
pp. 99-103
Author(s):  
Somesh Mozumder ◽  
Shirish Dubey ◽  
Aniruddha Dam ◽  
Anup Kumar Bhowmick

Introduction: Recurrent laryngeal nerves (RLN) are particularly prone to injury during thyroid surgeries due to its intimate relationship and proximity with the gland. Zuckerkandl’s tubercle (ZT) helps in preserving RLN intra operative. Material and Methods: A prospective study for identifying RLN in thyroid surgery using relationship with superior parathyroid gland and tubercle of Zuckerkandl was conducted on 50 thyroidectomy patients between August 2013 and February 2014. Results: In all cases ZT was identified. Temporary paralysis of RLN was seen in 3 (6%) cases and permanent paralysis in 2 (4%) of cases. Discussion: The site of greatest risk during thyroidectomy to the RLN is in the last 2-3 cm extralaryngeal course of the nerve. Relationship of recurrent laryngeal nerve with superior parathyroid gland and tubercle of Zukerkandl (ZT) is known. Conclusion: Use of ZT and superior parathyroids as a landmark allows safe dissection of RLN.


1981 ◽  
Vol 55 (1) ◽  
pp. 78-79 ◽  
Author(s):  
ANIS BARAKA ◽  
KAMAL HEMADY ◽  
FIRYAL YAMUT ◽  
WISAL YAZIGI ◽  
RINALDO F. CANALIS

2021 ◽  
Vol 14 (12) ◽  
pp. e245484
Author(s):  
David Vaughan ◽  
Adrinda Affendi ◽  
Patrick Sheahan ◽  
Brian Sweeney

Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.


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