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Horner Syndrome Secondary to Thyroid Surgery.
Demiral, Meliha; Binay, Cigdem; Simsek, Enver; Ilhan, Hüseyin.
Afiliação
  • Demiral M; Department of Pediatric Endocrinology, School of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
  • Binay C; Department of Pediatric Endocrinology, School of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
  • Simsek E; Department of Pediatric Endocrinology, School of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
  • Ilhan H; Department of Pediatric Surgery, School of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.
Case Rep Endocrinol ; 2017: 1689039, 2017.
Article em En | MEDLINE | ID: mdl-28133554
ABSTRACT
Horner syndrome (HS), caused by an interruption in the oculosympathetic pathway, is characterised by myosis, ipsilateral blepharoptosis, enophthalmos, facial anhydrosis, and vascular dilation of the lateral part of the face. HS is a rare complication of thyroidectomy. A 15-year-old female patient presented with solitary solid and large nodule in the right thyroid lobe. Ultrasound-guided fine-needle aspiration was performed and the cytological examination results were undefined. The patient underwent a total thyroidectomy. On postoperative day 2, she developed right-sided myosis and upper eyelid ptosis. HS was diagnosed. Interestingly, the patient exhibited an incomplete clinical syndrome with the absence of vasomotor symptoms. We herein report a case of HS in a 15-year-old female patient after total thyroidectomy. The possible causes of HS were ischaemia-induced nerve damage and stretching of the cervical sympathetic chain by the retractor during thyroidectomy. Clinicians should be aware of the possibility of this rare but important surgical complication.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Endocrinol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Endocrinol Ano de publicação: 2017 Tipo de documento: Article