Horner syndrome as a manifestation of thyroid carcinoma: a rare association.
Arq Bras Endocrinol Metabol
; 57(6): 483-5, 2013 Aug.
Article
in En
| MEDLINE
| ID: mdl-24030189
ABSTRACT
An 82-year-old patient presented a progressively growing hard thyroid nodule, and left ptosis. Additionally, ophthalmologic evaluation revealed ipsilateral miosis, diagnostic findings of Horner syndrome. Computerized tomography revealed a 7.5-cm thyroid mass infiltrating the main neck vessels. Although clinical and imaging data were suggestive of poorly differentiated thyroid carcinoma, fine-needle aspiration led to the diagnosis of papillary carcinoma. Paliative care was proposed to the patient due to the advanced stage of the neoplasm and to significant comorbidities. Horner syndrome is an infrequent manifestation of thyroid disorders and benign etiologies are more often implied. Malignant thyroid neoplasms represent a rare cause of Horner syndrome. However, an appropriate and prompt diagnosis is paramount for timely treatment of rare thyroid malignancies.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thyroid Gland
/
Thyroid Neoplasms
/
Horner Syndrome
/
Carcinoma, Papillary, Follicular
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Limits:
Aged80
/
Female
/
Humans
Language:
En
Journal:
Arq Bras Endocrinol Metabol
Year:
2013
Document type:
Article