Literature DB >> 11992871

Isolated Horner syndrome and syrinx of the cervical spinal cord.

Howard Pomeranz1.   

Abstract

PURPOSE: To alert ophthalmologists to the possibility of a spinal cord lesion in individuals with Horner syndrome and no neurologic symptoms.
DESIGN: Observational case report.
METHODS: Neuro-ophthalmic and neuroimaging assessment of a 16-year-old man with an isolated Horner syndrome localizing to a first- or second-order neuron.
RESULTS: With magnetic resonance imaging, a syrinx of the cervical spinal cord extending from C5 to C7 was found. No Chiari malformation was present.
CONCLUSION: Patients with an isolated Horner syndrome localizing to a first- or second-order sympathetic neuron should undergo magnetic resonance imaging of the head, neck, spinal cord, and chest to investigate for possible origins. An isolated Horner syndrome may be the presenting manifestation of a cervical syrinx.

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Mesh:

Year:  2002        PMID: 11992871     DOI: 10.1016/s0002-9394(02)01340-5

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  5 in total

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3.  Cervicothoracic epidural hematoma in a toddler with miosis, ptosis, nonspecific symptoms, and no history of major trauma: case report.

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Review 4.  Horner syndrome: clinical perspectives.

Authors:  Sivashakthi Kanagalingam; Neil R Miller
Journal:  Eye Brain       Date:  2015-04-10

5.  Post-operative Horner's Syndrome: A Rare Complication Following Posterior Scoliosis Surgery in a Patient With Syringomyelia.

Authors:  Isaac J May; Andrew J Berg; David Dillon
Journal:  Cureus       Date:  2022-05-23
  5 in total

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