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OPTHALMOPLEGIA +/- II
Yasser Alzainy
Neurology Resident
AL-AZHAR UNIVERSITY
Faculty of Medicine
Neurology Department
CLINICAL APPROACH
What is the
presentation?
 History
 Examination
 Binocular diplopia +/-
deminution of vision
 III, IV, VI, V1
 +/- II
 +/- V2
CLINICAL APPROACH
Where is the Lesion? (diplopia)
 Supranuclear
 Nuclear / Internuclear
 Infranuclear
 Neuronal
 Neuromuscular junction
 Orbital pathology
What is the Lesion?
 History
 Onset, course, duration
 Asccoiated symptoms
 Investigation
 Lab
 Imaging
INTRODUCTION
DIFFERENTIAL
Cavernous sinus syndrome
 III, IV, VI, V1
 V2
 +/- II
Orbital Apex syndrome
 III, IV, VI, V1
 II
CAUSES
Cavernous sinus syndrome
 Cavernous sinus thrombosis
 Carotid-cavernous fistula / aneurysm
 Pituitary disorders
 Pituitary adenoma
 Craniopharyngioma
 Pituitary Apoplexy
Orbital Apex syndrome
 Orbital infection
 Orbital Neoplasm (metastases,
lymphoma)
 Thyroid eye disease
 Orbital pseudo tuomor / Idiopathic
orbital myositis
 Tolosa Hunst syndrome+ Ocular myesthenia
+ Miller Fischer syndrome
GENERAL WORK-UP
 Routine Lab.
 Brain & orbital MRI.
 Systemic search for malignancy.
 Myasthenia & thyroid testing: AChR-Ab, TSH, T4, thyroid-stimulating
Ab, antithyroid Abs.
 some selected cases: LP + CSF cytology
CAVERNOUS SINUS THROMBOSIS
Suggestive Findings
 sinusitis; facial, dental or orbital
infection
 severe retrobulbar pain, isolated VI,
ptosis: early sx
 progress to become bilateral
 ocular bruits
 papilloedema and retinal
hemorrhages > deminution of vision
Work-Up
 MRI brain and Orbit
 Coagulopathy profile (aseptic CST)
 Leukocytosis in CBC
CAROTID-CAVERNOUS FISTULA / ANEURYSM
Suggestive Findings
 throbbing retro-orbital pain
 orbital bruits
 severe conjunctival injection
 pulsating exophtahlmos
Work-Up
 Angiography
PITUITARY DISORDERS (PITUITARY ADENOMA,
CRANIOPHARYNGIOMA)
Suggestive Findings
 endocrine dysfunction
 bitemporal hemanopia earlier than
ophthalmoplegia
 monocular deminution of vision may occur
 personlaity changes / seizures (frontal
lobe)
Work-Up
 MRI brain + C
 hormonal work-up
Pituitary adenoma
Craniopharyngioma
ORBITAL INFECTION
Suggestive Findings
 similar to CST
 prominent optic affection
 purulent discharge
Work-Up
 MRI braind and orbit
 exclude CST
 CBC
 Blood culture
ORBIRAL NEOBLASM
Suggestive Findings
 prominent proptosis
 early optic affection
Work-Up
 MRI brand and orbit + C
 Metastatic work-up
THYROID EYE DISEAE
Suggestive Findings
 associated hyper > hypo- thyroidism
 may precede / co-exist / follow
Work-Up
 MRI brain and Orbit
 regular enlargment of extraocular muscles
with tendon sparing
ORBITAL PSEUDO TUOMOR (IDIOPATHIC INFLAMMATORY
ORBITAL DZ)
Suggestive Findings
 Dx of exclusion
 almost strictly unilateral
 associated other autoimmune /
inflammatory condition
 dramatic response to steroids
Work-Up
 MRI brain and orbit + C
 enlargement of extraocular muscle (one
or more) with tendon involvement
 avid enhancement
TOLOSA HUNST SYNDROME
Suggestive Findings
 Diagnosis of exclusion
 duration: days to weeks
 II involvement in 25%
 Highly responsive to steroids
Work-Up
 MRI brain and orbit +C
 enhancing lesion
 Biopsy
Thank you

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Unilateral ophthalmoplegia

  • 1. OPTHALMOPLEGIA +/- II Yasser Alzainy Neurology Resident AL-AZHAR UNIVERSITY Faculty of Medicine Neurology Department
  • 2. CLINICAL APPROACH What is the presentation?  History  Examination  Binocular diplopia +/- deminution of vision  III, IV, VI, V1  +/- II  +/- V2
  • 3. CLINICAL APPROACH Where is the Lesion? (diplopia)  Supranuclear  Nuclear / Internuclear  Infranuclear  Neuronal  Neuromuscular junction  Orbital pathology What is the Lesion?  History  Onset, course, duration  Asccoiated symptoms  Investigation  Lab  Imaging
  • 4.
  • 6. DIFFERENTIAL Cavernous sinus syndrome  III, IV, VI, V1  V2  +/- II Orbital Apex syndrome  III, IV, VI, V1  II
  • 7. CAUSES Cavernous sinus syndrome  Cavernous sinus thrombosis  Carotid-cavernous fistula / aneurysm  Pituitary disorders  Pituitary adenoma  Craniopharyngioma  Pituitary Apoplexy Orbital Apex syndrome  Orbital infection  Orbital Neoplasm (metastases, lymphoma)  Thyroid eye disease  Orbital pseudo tuomor / Idiopathic orbital myositis  Tolosa Hunst syndrome+ Ocular myesthenia + Miller Fischer syndrome
  • 8. GENERAL WORK-UP  Routine Lab.  Brain & orbital MRI.  Systemic search for malignancy.  Myasthenia & thyroid testing: AChR-Ab, TSH, T4, thyroid-stimulating Ab, antithyroid Abs.  some selected cases: LP + CSF cytology
  • 9. CAVERNOUS SINUS THROMBOSIS Suggestive Findings  sinusitis; facial, dental or orbital infection  severe retrobulbar pain, isolated VI, ptosis: early sx  progress to become bilateral  ocular bruits  papilloedema and retinal hemorrhages > deminution of vision Work-Up  MRI brain and Orbit  Coagulopathy profile (aseptic CST)  Leukocytosis in CBC
  • 10. CAROTID-CAVERNOUS FISTULA / ANEURYSM Suggestive Findings  throbbing retro-orbital pain  orbital bruits  severe conjunctival injection  pulsating exophtahlmos Work-Up  Angiography
  • 11.
  • 12. PITUITARY DISORDERS (PITUITARY ADENOMA, CRANIOPHARYNGIOMA) Suggestive Findings  endocrine dysfunction  bitemporal hemanopia earlier than ophthalmoplegia  monocular deminution of vision may occur  personlaity changes / seizures (frontal lobe) Work-Up  MRI brain + C  hormonal work-up
  • 15. ORBITAL INFECTION Suggestive Findings  similar to CST  prominent optic affection  purulent discharge Work-Up  MRI braind and orbit  exclude CST  CBC  Blood culture
  • 16.
  • 17. ORBIRAL NEOBLASM Suggestive Findings  prominent proptosis  early optic affection Work-Up  MRI brand and orbit + C  Metastatic work-up
  • 18.
  • 19. THYROID EYE DISEAE Suggestive Findings  associated hyper > hypo- thyroidism  may precede / co-exist / follow Work-Up  MRI brain and Orbit  regular enlargment of extraocular muscles with tendon sparing
  • 20. ORBITAL PSEUDO TUOMOR (IDIOPATHIC INFLAMMATORY ORBITAL DZ) Suggestive Findings  Dx of exclusion  almost strictly unilateral  associated other autoimmune / inflammatory condition  dramatic response to steroids Work-Up  MRI brain and orbit + C  enlargement of extraocular muscle (one or more) with tendon involvement  avid enhancement
  • 21.
  • 22. TOLOSA HUNST SYNDROME Suggestive Findings  Diagnosis of exclusion  duration: days to weeks  II involvement in 25%  Highly responsive to steroids Work-Up  MRI brain and orbit +C  enhancing lesion  Biopsy
  • 23.

Editor's Notes

  1. Images 5.1A–5.1C: Postcontrast axial, sagittal, and coronal T1-weighted images demonstrate a large complex multilobulated mass in the sellar/suprasellar area. The sella turcica is massively expanded. The tumor shows the characteristic “snowman” appearance. Image 5.1D: Postcontrast sagittal T1-weighted image of a normal MRI. The pituitary gland (yellow arrow) and stalk normally enhance and are seen below the optic chiasm (red arrow)
  2. Images 5.2A–5.2C: Postcontrast sagittal T1-weighted, axial T2-weighted, and non-contrast axial T1-weighted images demonstrate an enormous, hyperintense cystic pituitary mass, which has expanded the sella turcica, with mass effect on the brainstem and both medial temporal lobes. Image 5.2D: Gross pathology of a craniopharyngioma (image credit The Armed Forces Institute of Pathology).
  3. Axial FLAIR and coronal T1-weighted images demonstrate hyperintensity and enlargement of the right lateral rectus muscle (red arrows)
  4. Postcontrast, fat-suppressed axial and coronal T1-weighted images demonstrate an enhancing lesion (red arrows) in the left cavernous sinus.