scholarly journals Patient with COVID – 19 infection presenting with acute 6th cranial nerve palsy: A case report

2020 ◽  
Vol 8 (2) ◽  
pp. 129-130
Author(s):  
SM Sanayet Bin Mustafiz Srijon ◽  
Rawshan Arra Khanam ◽  
Al Fateha Rahman Mimi

We present a case of a 55 year old lady, hypertensive and diabetic who was infected with COVID-19 presenting with acute 6th cranial nerve palsy. The patient was diagnosed with COVID-19 on Sept 01 2020. Seven days later she developed double vision and headache. At that point on complete neurological examination including examination of cranial nerves she was found to have 6th cranial nerve (Abducens) palsy with convergent squint. As the patients cranial nerves were all intact initially it is suspected that her 6th nerve palsy was related to the viral illness. She was assessed by ophthalmologist and neurologist. She underwent MRI scan of the brain to look for other causes of 6th nerve palsy and it was unremarkable. After almost one week of continued inpatient management her diplopia improved but she still complained of intermittent diplopia with convergent squint. Bangladesh Crit Care J September 2020; 8(2): 129-130

2018 ◽  
pp. bcr-2018-225544 ◽  
Author(s):  
Shruti Heda ◽  
Davala Krishna Karthik ◽  
Erigaisi Srinivas Rao ◽  
Anirudda Deshpande

A 40-year-old woman presented with insidious onset, gradually progressive dysarthria and inability to manoeuvre bolus of food in her mouth while eating. The duration of her symptoms was 3 months. On evaluation, the left half of her tongue was wasted. The tongue deviated to the left on protrusion. There were no clinical features suggestive of involvement of the ipsilateral 9th, 10th or 11th cranial nerves. MRI of the brain showed a large, fusiform lesion in the left hypoglossal canal, extending into the jugular canal. The lesion was surgically excised and found to be a schwannoma.


Author(s):  
J.A. Espinosa ◽  
M. Giroux ◽  
K. Johnston ◽  
T. Kirkham ◽  
J.G. Villemure

ABSTRACT:Over a period of 12 years, 80 patients underwent ventricular shunting for normal pressure hydrocephalus. Three developed sixth cranial nerve palsy in the first two weeks after surgery. This uncommon complication is usually transitory following the same pattern of abducens palsy after lumbar puncture or spinal anesthesia. Traction on the nerve with local ischemia has been involved as the responsible mechanism in both instances.


2020 ◽  
Vol 13 (6) ◽  
pp. e232490
Author(s):  
Divya Natarajan ◽  
Suresh Tatineni ◽  
Srinivasa Perraju Ponnapalli ◽  
Virender Sachdeva

We report a case of isolated unilateral complete pupil involving third cranial nerve palsy due to pituitary adenoma with parasellar extension into the right cavernous sinus. The patient was referred to us from neurosurgery with sudden onset binocular vertical diplopia with complete ptosis, and mild right-sided headache of 5-day duration. Ocular examination revealed pupil involving third cranial nerve palsy in right eye while rest of the examination including automated perimetry was normal. MRI brain with contrast revealed a mass lesion with heterogenous enhancement in the sella suggestive of a pituitary macroadenoma with possible internal haemorrhage (apoplexy). In addition, the MRI showed lateral spread to the right cavernous sinus which was causing compression of the right third cranial nerve. The patient was systemically stable. This report highlights a unique case as the lesion showed a lateral spread of pituitary adenoma without compression of the optic chiasm or other cranial nerves.


1990 ◽  
Vol 72 (5) ◽  
pp. 818-820 ◽  
Author(s):  
Nicolette C. Notermans ◽  
Rob H. J. M. Gooskens ◽  
Cees A. F. Tulleken ◽  
Lino M. P. Ramos

✓ A child suffered a sixth and seventh cranial nerve palsy due to intracerebral insertion of a stylet. The stylet was introduced through the anterior fontanel, most probably in an attempt at infanticide. The migration of the stylet through the brain was monitored because the child was first examined 6 years earlier. At operation, the cranial part of the stylet lay in the fourth ventricle, compressing the facial nerve as well as the nucleus of the abducens nerve. The lower part of the stylet had reached the C-5 level.


2014 ◽  
Vol 27 (6) ◽  
pp. 782 ◽  
Author(s):  
Luís Almeida Dores ◽  
Marco Alveirinho Simão ◽  
Marta Canas Marques ◽  
Óscar Dias

Sphenoid sinus disease is particular not only for its clinical presentation, as well as their complications. Although rare, these may present as cranial nerve deficits, so it is important to have a high index of suspicion and be familiar with its diagnosis and management. Symptoms are often nonspecific, but the most common are headache, changes in visual acuity and diplopia due to dysfunction of one or more ocular motor nerves. The authors report a case of a 59 years-old male, who was referred to the ENT emergency department with frontal headaches for one week which had progressively worsened and were associated, since the last 12 hours, with diplopia caused by left third cranial nerve palsy. Neurologic examination was normal aside from the left third cranial nerve palsy. Anterior and posterior rhinoscopy excluded the presence of nasal masses and purulent rhinorrhea. The CT scan revealed a soft tissue component and erosion of the roof of the left sphenoid sinus. Patient was admitted for intravenous antibiotics and steroids treatment without any benefit after 48 hours. He was submitted to endoscopic sinus surgery with resolution of the symptoms 10 days after surgery. The authors present this case for its rarity focusing on the importance of differential diagnosis in patients with headaches and cranial nerves palsies.<br /><strong>Keywords:</strong> Sphenoid Sinusitis; Oculomotor Nerve Diseases.


2017 ◽  
Vol 1 (1) ◽  

Traumatic isolated sixth cranial nerve palsy is a rare condition that has been reported to be as low as 1% to 2, 7% following traumatic brain injury. The sixth nerve innervates the ipsilateral lateral rectus which abducts the eye. Isolated loss of lateral gaze with no other cranial nerve signs and muscular entrapment is thought to be resulted from an injury to the peripheral nerve along its course from the brain stem to the lateral rectus. We presented a case of traumatic isolated unilateral sixth cranial nerve palsy in a female patient with diplopia and restriction left eye movement to lateral following head trauma after accident. Head Computed Tomography (CT) scan showed left frontal bone fracture involving the lateral wall of the orbit and also left retro orbital hemorrhage with no other lesions noted in the brain. Eye examination revealed isolated sixth cranial nerve palsy with normal vision of both eyes. Here we discussed about the possible mechanism, differential diagnosis and also management of the patient.


2013 ◽  
Vol 04 (02) ◽  
pp. 210-212 ◽  
Author(s):  
Rajesh K. Ghanta ◽  
Perumallu Tangella ◽  
Kalyan Koti ◽  
Srinivas Dandamudi

ABSTRACTIntracranial extra‑axial cavernous angiomas are rare lesions. We report a rare case of extra‑axial cavernous angioma in the cerebellopontine angle (CPA) in a 50‑year‑old male, who presented with lower cranial nerve palsy and gait ataxia. Computed tomography (CT) scan of the brain showed a hyperdense lesion in the left cerebellopontine angle. The lesion was totally excised by the retrosigmoid approach and a pathological examination confirmed the lesion to be a cavernous angioma. Following surgery, the lower cranial nerve palsy recovered significantly


2015 ◽  
Vol 14 (1) ◽  
pp. 74-76
Author(s):  
Shahed Iqbal ◽  
Wahida Akter ◽  
M Badruddoza ◽  
Mahmood Ahmed Chowdhury

Tuberculoma is one of the manifestations of Central Nervous System (CNS) tuberculosis (TB). A tuberculoma is a tuberculous focus, which enlarges with in brain tissue, firm, avascular, spherical masses, with size varying between 2 cm to 10 cm in diameter and the compressed surrounding tissue shows edema and gliosis. Tuberculoma resuls from aggregation of caseous tubercle that usually manifest clinically as brain tumour. Tuberculomas account for upto 40% of brain tumours in some areas of the world. In adults tuberculomas are most often supratentorial, but in children they are often infratentorial, located at the base of the brain near the cerebellum. Lesions are most often singular but may be multiple. The most common symptoms are headache, fever & convulsion & also may give rise to signs of raised intracranial pressure or a hemiplegia, or cranial nerve palsy if in the brain stem. Here described a case of 4 years old female child who presented with the complants of high grade fever for 10 days duration followed by right sided weakness for 4 months. She had 6,sup>th and 7th cranial nerve palsy with exaggerated reflex on right side. Her tuberculin test was positive but Cerebro Spinal Fluid (CSF) study was normal & Magnetic Resonance Imaging (MRI) of brain showed rim enhancing lesion. Early recognition and timely treatment of CNS TB is critical if the considerable mortality and morbidity associated with the condition is to be prevented. DOI: http://dx.doi.org/10.3329/cmoshmcj.v14i1.22892 Chatt Maa Shi Hosp Med Coll J; Vol.14 (1); Jan 2015; Page 74-76


2020 ◽  
Vol 11 ◽  
pp. 102
Author(s):  
Miguel Angel Lopez-Gonzalez ◽  
Timothy Marc Eastin ◽  
Dinesh Ramanathan ◽  
Song Minwoo ◽  
Baishakhi Choudhury

Background: Petroclival lesions pose a significant neurosurgical challenge due to involvement or close proximity to important neurovascular structures. Chondrosarcomas are rare lesions that can affect these areas. Case Description: A 24-year-old male with 3 months history of poor coordination, imbalance, left-sided face hypoesthesia, facial palsy House-Brackmann Grade 2, and 6th cranial nerve palsy with diplopia. Hearing was preserved. Preoperative images showed a 5.5 cm multilobulated enhancing extra-axial mass centered in the left petroclival region with extension into middle and posterior fossa causing severe (Stage 3) brainstem compression.[1] After a lengthy discussion of treatment options, the patient consented for the procedure. We performed a presigmoid retrolabyrinthine combined petrosal approach. We used cranial nerves monitoring (VII, VIII, IX, X, XI, XII), frameless stereotaxy, and a lumbar drain. Due to the tumor size and location (petroclival region with extension into the posterior and middle cranial fossa), we chose this approach to achieve a maximal safe resection of the tumor and preserve hearing. Alternative approaches of use are expanded middle fossa with transcavernous extension or expanded endonasal approach. The selected approach achieved wide exposure of the tumor which was highly vascular. The tumor was carefully dissected off the brainstem, cranial nerves (IV, V, VI, VII, VIII), and basilar artery trunk. A gross total resection was achieved (Multimedia 1). The patient did well after surgery and was extubated on postoperative day (POD) 1 and the lumbar drain removed on POD 5. Pathology reported low-grade chondrosarcoma (WHO grade I). At 3 months follow-up, the patient improved neurologically, including facial nerve weakness (House-Brackmann Grade 1) except for his left 6th cranial nerve palsy which mildly improved. Conclusion: Petroclival chondrosarcomas are rare tumors that are usually treated with surgical resection followed by stereotactic radiosurgery. The tumor size, location, and extension dictate approach selection. For lesions involving the petroclival region with extension into the middle fossa and posterior fossa, the combined petrosal approach is reasonable.


Cephalalgia ◽  
2014 ◽  
Vol 34 (8) ◽  
pp. 624-632 ◽  
Author(s):  
Xingwen Zhang ◽  
Zhibing Zhou ◽  
Timothy J Steiner ◽  
Wei Zhang ◽  
Ruozhuo Liu ◽  
...  

Background Three editions of International Classification of Headache Disorders (ICHD) diagnostic criteria for Tolosa-Hunt syndrome (THS) have been published in 1998, 2004 and 2013; in ICHD-3 beta, there have been considerable changes. The validity of these new diagnostic criteria remains to be established. Methods We retrospectively identified 77 patients with non-traumatic painful ophthalmoplegia (PO) admitted between 2003 and 2013. We reviewed patients’ age at onset and gender, time courses between onset of pain and development of cranial nerve palsy, the cranial nerves involved, imaging findings, therapeutic efficacy of steroid treatment and recurrence of attacks. Results THS was the most frequent type of PO (46/77). In THS patients, the third cranial nerve was most commonly involved (76.3%). The median time interval between pain and cranial nerve palsy was two days, although in five patients (10.9%) the interval ranged from 16 to 30 days. Definitely abnormal MRI findings were found in 24 patients (52.2%). Conclusions It is essential to rule out other causes of PO in diagnosing THS, with MRI playing a crucial role in differential diagnosis. It may be helpful to understand and master the entity of THS for researchers and clinicians to adjust the gradation and ranking of the diagnostic criteria.


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