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Horner Syndrome Secondary to Thyroid Surgery.
Meliha Demiral1, Ciğdem Binay1, Enver Simsek1
1Department of Pediatric Endocrinology, School of Medicine, Eskişehir Osmangazi University, Eskişehir, Turkey.
Case Reports in Endocrinology
|January 31, 2017
Summary
Horner syndrome (HS), a rare complication of thyroidectomy, can cause eye and facial changes. This case highlights HS in a 15-year-old female post-thyroidectomy, emphasizing awareness of this surgical complication.
Area of Science:
- Ophthalmology
- Endocrinology
- Neurosurgery
Background:
- Horner syndrome (HS) results from oculosympathetic pathway disruption, presenting with myosis, ptosis, and anhydrosis.
- HS is an infrequent but significant complication following thyroidectomy procedures.
- Thyroid nodules requiring surgical intervention necessitate careful consideration of potential iatrogenic complications.
Observation:
- A 15-year-old female presented with a large right thyroid lobe nodule.
- Following total thyroidectomy, the patient developed ipsilateral myosis and upper eyelid ptosis on postoperative day 2.
- The clinical presentation was an incomplete Horner syndrome, notably lacking vasomotor symptoms.
Findings:
- The patient was diagnosed with Horner syndrome post-thyroidectomy.
- Potential etiologies include ischemic nerve damage or sympathetic chain stretching during surgery.
- This case represents a rare instance of HS in a pediatric patient after thyroid surgery.
Implications:
- Clinicians must maintain a high index of suspicion for HS after thyroidectomy.
- Early recognition and diagnosis of HS are crucial for appropriate patient management.
- Understanding the mechanisms of HS can inform surgical techniques to minimize risk during thyroid procedures.
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