Results 11 to 20 of about 4,160 (263)

Polyneuritis cranialis combined with Horner’s syndrome: a rare variant of Guillain Barré syndrome [PDF]

BMC Neurology
Background Polyneuritis cranialis (PNC), a rare variant of Guillain-Barré syndrome (GBS), is usually characterized by ocular and pharyngeal weakness without obvious numbness or weakness of the limbs or ataxia.
Xiangtao Nie, Wei He, Wenjing Qi, Yongbo Ma, Geke Zhu, Lei Hao, Xiuming Guo   +6 more
doaj   +2 more sources

A Case of Horner's Syndrome following Ultrasound-Guided Infraclavicular Brachial Plexus Block [PDF]

Case Reports in Anesthesiology, 2012
Horner’s syndrome results from paralysis of the ipsilateral sympathetic cervical chain (stellate ganglion) caused by surgery, drugs (mainly high concentrations of local anesthetics), local compression (hematoma or tumor), or inadequate perioperative ...
Trabelsi Walid, Belhaj Amor Mondher, Lebbi Mohamed Anis, Ferjani Mustapha   +3 more
doaj   +2 more sources

Ectopic thymus as a cause of Horner's syndrome [PDF]

Radiology Case Reports, 2020
Ectopy of the thymus is a rare anomaly arising during fetal development, where the thymus does not make a complete decent into the thoracic cavity where it should involute in adolescence.
Margeaux L. Berroth, AB, Lyudmila V. Morozova, MD, Jeffery M. Pollock, MD   +2 more
doaj   +2 more sources

Unveiling the Uncommon: A Case Report of Horner’s Syndrome as a Rare Glimpse Into Giant Cell Arteritis [PDF]

Case Reports in Neurological Medicine
Giant cell arteritis (GCA) is an inflammatory vasculitis affecting large and medium-sized arteries, leading to complications such as arterial dissection, blindness, and stroke.
Emily Barr, Justine Levesque, John Badir, Randall Dunston, Tamra Ranasinghe   +4 more
doaj   +2 more sources

Horner syndrome [PDF]

Current Opinion in Ophthalmology, 2003
Horner syndrome refers to the constellation of signs resulting from the interruption of sympathetic innervation to the eye and ocular adnexae. Classically, the clinical findings include a triad of ipsilateral blepharoptosis, pupillary miosis, and facial anhidrosis.
Kelly A, Walton, Lawrence M, Buono
openaire   +3 more sources

An unusual case of Brown-Sequard syndrome associated with Horner’s syndrome after a penetrating injury with a (Bhutanese dart) to the neck: A case report

SAGE Open Medical Case Reports, 2022
The occurrence of Brown-Sequard syndrome with Horner’s syndrome in a child with spinal trauma is a very rare and unusual entity. Brown-Sequard syndrome results from hemisection injury of the spinal cord, mostly in the cervical cord region.
Kuenzang Wangdi
doaj   +1 more source

The role of apraclonidine in Horner’s syndrome: A case report [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2016
Introduction. Horner’s syndrome is an interruption of the sympathetic nervous system at any point along its course between the hypothalamus and the orbit.
Karadžić Jelena, Kovačević Igor, Ljikar Jelena   +2 more
doaj   +1 more source

Unilateral Horner's Syndrome following supraclavicular brachial plexus block [PDF]

Kosin Medical Journal, 2018
Supraclavicular brachial plexus block, due to its wide range of indications, is the most widely practiced procedure in anesthesiology. We experienced the case of a 45-year-old female patient who developed unilateral Horner's Syndrome after the use of ...
Dawoon Oh
doaj   +1 more source

Vertebral artery dissection presenting as Pancoast's syndrome: A case report

Interdisciplinary Neurosurgery, 2021
Pancoast’s syndrome due to vascular lesions is extremely rare. We report a 73-year-old man with right arm paresthesia and Horner’s syndrome caused by a right proximal vertebral artery dissecting aneurysm.
Youngseok Kwak
doaj   +1 more source

Iatrogenic Horner’s syndrome after insertion of a central venous catheter: recommendations for clinical practice

The Egyptian Journal of Internal Medicine, 2022
Background Horner’s syndrome is a rare complication of central venous catheter (CVC) insertion. It comprises a triad of unilateral ptosis, ipsilateral meiosis with a normally reactive pupil, and ipsilateral facial anhidrosis of variable spread.
Taimoor Ashraf Khan, Sheharyar Zameer, Umar Ijaz, Muhammad Abdullah Zahid, Noor Ul Ain Zameer   +4 more
doaj   +1 more source