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Transcript
Noon Report
8/23/16
Pooya Banankhah
HPI


33 F with no PMH presented with HA, R eye pain, and double vision x 4 days.

4 days prior to admission: R sided severe headache

2 days prior to admission: headache developed into sudden-onset R sided eye pain
10/10, radiating to her R jaw, associated with double vision, and worse with eye
movement.

Also notes periorbital swelling, nausea and chills
Social hx:


No alcohol, tobacco, drugs.
Currently not working. Lives at home with husband.
Family hx:

Non-contributory
Physical Exam

Presenting Vitals:
T: 36.7 °C (Oral) HR: 65 (Monitored) RR: 17 BP: 116 / 67 SpO2: 98%

Physical Exam:

Gen: Anxious but in NAD

HEENT: PERRLA, EOM notable for inability to abduct R eye past midline. Pain w/ lateral and
upward gaze noted in R eye.

Heart: rrr, no murmurs, rubs or gallops

Lungs: ctab, no w/r/c

Ext: warm, well perfused, w/o edema bilaterally

Skin: No lesions or rashes noted.

Neuro: A&Ox3, CN normal except for diplopia present in right eye but not left, EOMI intact
except for inability to abduct right eye past midline, Vision 20/20 in both right and left eye,
otherwise normal neuro exam.
Labs:

CBC: WBC:11.6/ Hgb:14.2/ Hct:42.9/ Plt:350

BMP: Na 136/ K 4.1/ Cl 102/ CO2 102/ BUN 7/ Cr 0.56/ Glu 104
More Labs

ESR 20, CRP 2.8

LDH 110

HgA1c 5.8%

TSH 3.24

UA: small blood, trace leuks, negative nitrites, 4WBC, 2RBC

HIV, RPR, Hep A/B/C panel negative

SPEP: Normal

Serum ACE: normal

SM ab, RNP Ab, Myeloper Ab negative
Imaging

CT Head:


No acute intracranial abnormality.
MRI Brain:

Some very subtle soft tissue thickening and enhancement along the R lateral
cavernous sinus margin extending through the region of R orbital apex

No evidence of demyelinating disease

No acute hemorrhage, mass, fluid collection, infarction

No abnormal parenchymal or leptomeningeal enhancement
Imaging

MRI Orbit:

Enhancing T1 isointense soft tissue extending toward the right orbital apex and to
the origin of the right lateral rectus muscle measuring approximately
8.9x6.8x14.8mm.

No dural tail observed to suggest meningioma

L cavernous sinus unremarkable
Differential Diagnosis
Differential diagnosis:

Tolosa Hunt Syndrome

Sarcoidosis

Lymphoma with meningioma

Periorbital cellulitis

TB

Ophthalmologic migraine

Poorly controlled DM

MS

Myositis

Duanes syndrome (congenital non-
progressive strabismus)

Orbital apex syndrome (CN deficit
due to mass lesion near apex)

Carotid-cavernous fistula or
thrombosis

ICA dissection

SCC

Abscess

Mucormycosis, actinomycosis

GCA

Wegner’s
Lumbar puncture:

RBC 192, WBC 0

Cytology: Rare mature lymphocytes and monocytes. Negative for malignant cells

Flow cytometry: Insufficient sample

CSF Cx and fungal cx negative
Work up

No biopsy done by ophtho:


Meningioma can be diagnosed on imaging and lymphoma can be identified on
cytology from LP
CT Abdomen and thorax:

No evidence of malignancy or lymphadenopathy
Diagnosis

Tolosa Hunt Syndrome:

Treated with Solumedrol 1000mg daily for 3 days followed by Medrol dose pack

Plan to repeat MRI in 4 weeks
Post-Discharge Follow up

Follow up in ophtho clinic:

On methylprednisone 20mg PO daily

No improvement noted per patient

No biopsy

Has neuro follow up
Tolosa Hunt Syndrome

Definition:




Episodic orbital pain associated with paralysis of one or more of the CN III, IV, VI due to
granulomatous inflammation of the cavernous sinus
Epidemiology:

One case per million per year

Same prevalence in men and women
Presentation:

Pain behind the eye followed by painful ophthalmoplegia

CN III,IV, VI palsy leading to diplopia

Unilateral 95% of time
Natural history:

Benign condition but permanent neurological deficits can occur, relapses occur in at
least 50% of patients and often requiring immunosuppressive therapy

May resolve spontaneously if left untreated
Tolosa Hunt Syndrome

Pathogenesis:



Inflammatory process of unknown etiology
Histopathology:

Nonspecific inflammation of the septa and wall of the cavernous sinus

Lymphocyte and plasma cell infiltration

Giant cell granulomas

Proliferation of fibroblasts
CN III, IV, VI and superior division of V palsy due to pressure from
inflammation
Tolosa Hunt Syndrome

Diagnostic Criteria:

95-100% sensitive, 50% specific

Unilateral HA

Granulomatous inflammation of cavernous sinus or orbit on MRI or biopsy

Paresis of CN III, IV, VI

Evidence of causation:


HA preceding oculomotor paresis

HA around ipsilateral eye
No alternative diagnosis
Imaging Findings

Axial imaging without (left) and with (right) enhancement demonstrates nonspecific fullness involving
the left cavernous sinus, consistent with Tolosa-Hunt syndrome within the context of the history.
Tolosa Hunt Syndrome


Treatment:

Glucocorticoids

Rapid resolution of pain in 24-72 hours (40%) and within 1 week (78%)

Improvement in MRI findings in 2-8 weeks
Caveat:

Lymphoma and vasculitis will also likely respond to steroids