Recurrent Vocal Fold Paralysis and Parsonage-Turner Syndrome

المؤلفون المشاركون

Pinto, Marcus Vinicius
Vincent, Maurice Borges
Joffily, Lucia

المصدر

Case Reports in Otolaryngology

العدد

المجلد 2013، العدد 2013 (31 ديسمبر/كانون الأول 2013)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2013-10-31

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الأمراض

الملخص EN

Background.

Parsonage-Turner syndrome, or neuralgic amyotrophy (NA), is an acute brachial plexus neuritis that typically presents with unilateral shoulder pain and amyotrophy but also can affect other peripheral nerves, including the recurrent laryngeal nerve.

Idiopathic vocal fold paralysis (VFP) represents approximately 12% of the VFP cases and recurrence is extremely rare.

Methods and Results.

We report a man with isolated recurrent unilateral right VFP and a diagnosis of NA years before.

Conclusions.

We emphasize that shoulder pain and amyotrophy should be inquired in any patient suffering from inexplicable dysphonia, and Parsonage-Turner syndrome should be considered in the differential diagnosis of idiopathic VFP.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Pinto, Marcus Vinicius& Joffily, Lucia& Vincent, Maurice Borges. 2013. Recurrent Vocal Fold Paralysis and Parsonage-Turner Syndrome. Case Reports in Otolaryngology،Vol. 2013, no. 2013, pp.1-4.
https://search.emarefa.net/detail/BIM-496866

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Pinto, Marcus Vinicius…[et al.]. Recurrent Vocal Fold Paralysis and Parsonage-Turner Syndrome. Case Reports in Otolaryngology No. 2013 (2013), pp.1-4.
https://search.emarefa.net/detail/BIM-496866

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Pinto, Marcus Vinicius& Joffily, Lucia& Vincent, Maurice Borges. Recurrent Vocal Fold Paralysis and Parsonage-Turner Syndrome. Case Reports in Otolaryngology. 2013. Vol. 2013, no. 2013, pp.1-4.
https://search.emarefa.net/detail/BIM-496866

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-496866