scholarly journals Report of a rare case: Double recurrent laryngeal nerve

2016 ◽  
Vol 32 (4) ◽  
pp. 298-299
Author(s):  
Berke Manoglu ◽  
Eyup Murat Yilmaz ◽  
Ahmet Erdogan ◽  
Murat Bulut Ozkan ◽  
Vedat Menderes Ozciftci
Author(s):  
Mehmet ULUŞAHİN ◽  
Kadir TOMAS ◽  
Mithat Kerim ARSLAN

Head & Neck ◽  
1990 ◽  
Vol 12 (4) ◽  
pp. 355-356 ◽  
Author(s):  
Izhar Ben-Shlomo ◽  
Shmuel Zohar ◽  
Hanna Turani ◽  
Carlos Cozacov

2015 ◽  
Vol 4 ◽  
pp. 88 ◽  
Author(s):  
Kashif Naeem ◽  
Vinod Choondal

<p><span>Ortner</span><span>’</span><span>s (cardio-vocal) syndrome is a rare disease entity that involves compression of the left recurrent laryngeal nerve due to enlargement of cardiovascular structures. The syndrome was first described by Norbert Ortner (an Austrian physician) in 1897 and is usually reported to be associated with mitral stenosis. However, we report a rare case when a 20-year-old girl presented with hoarseness of voice and was found to have an enlarged main pulmonary trunk due to pulmonary hypertension that was compressing the left recurrent laryngeal nerve. The case highlights a rare presentation of a relatively common disease and stresses the importance of detailed cardiac workup in a patient with hoarseness of voice. We present the case and review the literature. </span></p>


1980 ◽  
Vol 45 (3) ◽  
Author(s):  
Frank B. Wilson ◽  
D. J. Oldring ◽  
Kathleen Mueller

On page 112 of the report by Wilson, Oldring, and Mueller ("Recurrent Laryngeal Nerve Dissection: A Case Report Involving Return of Spastic Dysphonia after Initial Surgery," pp. 112-118), the paraphrase from Cooper (1971), "if the patients are carefully selected and are willing to remain in therapy for a long period of time," was inadvertantly put in quotation marks.


1998 ◽  
Vol 23 (4) ◽  
pp. 377-377 ◽  
Author(s):  
Brok ◽  
Stroeve ◽  
Copper ◽  
B.W. Ongerboer De Visser ◽  
Schouwenburg

1990 ◽  
Vol 23 (3) ◽  
pp. 553-563 ◽  
Author(s):  
Roger L. Crumley

Swiss Surgery ◽  
2001 ◽  
Vol 7 (1) ◽  
pp. 20-24 ◽  
Author(s):  
Robert ◽  
Mariéthoz ◽  
Pache ◽  
Bertin ◽  
Caulfield ◽  
...  

Objective: Approximately one out of five patients with Graves' disease (GD) undergoes a thyroidectomy after a mean period of 18 months of medical treatment. This retrospective and non-randomized study from a teaching hospital compares short- and long-term results of total (TT) and subtotal thyroidectomies (ST) for this disease. Methods: From 1987 to 1997, 94 patients were operated for GD. Thirty-three patients underwent a TT (mostly since 1993) and 61 a ST (keeping 4 to 8 grams of thyroid tissue - mean 6 g). All patients had received propylthiouracil and/or neo-mercazole and were in a euthyroid state at the time of surgery; they also took potassium iodide (lugol) for ten days before surgery. Results: There were no deaths. Transient hypocalcemia (< 3 months) occurred in 32 patients (15 TT and 17 ST) and persistent hypocalcemia in 8 having had TT. Two patients developed transient recurrent laryngeal nerve palsy after ST (< 3 months). After a median follow-up period of seven years (1-15) with five patients lost to follow-up, 41 patients having had a ST are in a hypothyroid state (73%), thirteen are euthyroid (23%), and two suffered recurrent hyperthyroidism, requiring completion of thyroidectomy. All 33 patients having had TT - with follow-ups averaging two years (0.5-8) - are receiving thyroxin substitution. Conclusions: There were no instances of persistent recurrent laryngeal nerve palsy in either group, but persistent hypoparathyroidism occurred more frequently after TT. Long after ST, hypothyroidism developed in nearly three of four cases, whereas euthyroidy was maintained in only one-fourth; recurrent hyperthyroidy was rare.


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