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Tubercular Mediastinal Lymphadenopathy Presenting as an Isolated Unilateral Vocal Cord Palsy and the "Sail" Sign.
Saluja, Alvee; Anees, Shahbaz; Abbey, Pooja; Ghotekar, L H; Dhamija, Rajinder K.
Afiliação
  • Saluja A; Neurology, Lady Hardinge Medical College, New Delhi, IND.
  • Anees S; Neurology, Lady Hardinge Medical College, New Delhi, IND.
  • Abbey P; Radio-diagnosis, Lady Hardinge Medical College, New Delhi, IND.
  • Ghotekar LH; Internal Medicine, Lady Hardinge Medical College, New Delhi, IND.
  • Dhamija RK; Neurology, Institute of Human Behavior and Allied Sciences, New Delhi, IND.
Cureus ; 16(1): e51950, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38333460
ABSTRACT
Tuberculosis continues to remain a major public health challenge, especially in low- and middle-income countries. Unilateral vocal cord palsy in adults as the sole manifestation of tubercular mediastinal lymphadenopathy has been rarely reported. A 22-year-old lady presented with a history of hoarseness of voice for the past month. The general physical examination revealed palpable lymph nodes in the left axilla. Axial CT sections at the level of the vocal cords demonstrated dilation of the right laryngeal ventricle and mild anteromedial deviation of the ipsilateral arytenoid cartilage ("sail" sign) suggestive of a right vocal cord palsy. Contrast-enhanced CT chest revealed right paratracheal, right hilar, and subcarinal lymph nodes with areas of central necrosis. She was started on anti-tubercular therapy and her voice completely improved after three months of treatment. The "Sail" sign on axial CT scans is a useful radiological sign for diagnosing unilateral vocal cord palsy. Rarely, compression of the recurrent laryngeal nerve by enlarged mediastinal lymph nodes due to tuberculosis can present with unilateral vocal cord palsy as the sole manifestation in adults.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article