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The Case
of Ms. SI
John Angelo Luigi S. Perez
June 19, 2015
St. Luke's College of Medicine
48/F
Right-Handed
Roman Catholic
Kasambahay
Old Balara, QC
Foot Numbness
History of Present Illness
2
weeks
Ascending extremity paresthesia
R then L
LE then UE
1
week
1
day
A
No headache, dizziness,
slurring of speech, pain. (+) pruritus, pain
History of Present Illness
2
weeks
Ascending extremity paresthesia
R > L
LE > UE
1
week
Ascending extremity weakness
R > L
LE > UE
● Tripping
● Steppage gait
1
day
A
No headache, dizziness,
slurring of speech, pain. (+) pruritus, pain
History of Present Illness
2
weeks
Ascending extremity paresthesia
R > L
LE > UE
1
week
● Tripping
● Steppage gait
Legs gave way
(+) Fall
1
day
A
No headache, dizziness,
slurring of speech, pain. (+) pruritus, pain
Ascending extremity weakness
R > L
LE > UE
● Hypertensive
 Amlodipine, uncompliant
● Non-diabetic
● Non-asthmatic
● No CA
● Unremarkable family history
Review of Systems
● Palpitations● Intermittent knee pains
● Pruritic rashes on legs
● Pruritic hands
Physical Examination
● Sallow skin
● Erythematous cheeks and
nose
● PPC, AS
● Moist mucosa, (+) ulcers
● No CLADs
● SLE, CBS
● AP, no murmurs, regularly regular
● Flat, soft
● Normoactive, non-tender
● Pulses full and equal
● Grade 2 bipedal edema
● Multiple, hyperpigmented,
lichenified lesions
MMSE
Cranial Nerves
I
II
III, IV, VI
V
VI
VII
VIII
IX
X
XI
XII
Neurologic Examination – Cranial Nerves
Neurologic Examination – Somatic Motor
55
54
44
55
33
0 2
Good tone and bulk
No fasciculations
Good irritability
Neurologic Examination – Tendon Reflexes
+++
+
++
0 0
(-) Toe extensor
+
Neurologic Examination – Somatic Sensory
90%
10%
60%
60%
10%
60%
100%
100%
30%
50%
50%
20%
(+) Romberg's sign
Cerebellum intact
Where do we localize the lesion?
Levelize?
Lateralize?
Localize?
Mononeuritis
Multiplex
● Asymmetric
● Asynchronous
● Painful
● Separate nerves
Salient Features
Subjective Objective
● 48/F
● 2 weeks
weakness and
numbness
● Palpitations
● Joint pains
● Pruritus
● Stable VS
● Sallow skin
● Facial erythema
● Rashes
● Buccal ulcers
● Bipedal edema
● Mononeuritis
multiplex
Mononeuritis Multiplex
+
Skin Lesions?
We have 3 differential diagnoses
● Diabetic Neuropathy
● Guillain-Barré Syndrome (AIDP)
● System Lupus Erythematosus
Diabetic Neuropathy
Guillain-Barré
Syndrome
(AIDP)
Systemic Lupus
Erythematosus
SLE is a multisystemic disease
Neuropsychiatric SLE (NPSLE) is
a recognized entity
62%
18%
8%
5%
5%1%
Headache
Seizures
CVD
Psychosis
Neuropathy
Movement
Muscal and Brey. Neurol. Clin. 28(1) 2010
Peripheral neuropathy attributed
to SLE is rare
96%
4%
SLE Related
Related
Florica et al. Semin. Arthritis Rheum. 41(2) 2011
Asymmetry 59%
Distal weakness 34%
Salient Features
Subjective Objective
● 48/F
● 2 weeks
weakness and
numbness
● Palpitations
● Joint pains
● Pruritus
● Stable VS
● Sallow skin
● Facial erythema
● Rashes
● Buccal ulcers
● Bipedal edema
● Mononeuritis
multiplex
Mononeuritis
Multiplex
secondary to
Systemic Lupus
Erythematosus
SLE is diagnosed using a set of
clinical and laboratory criteria
Various autoantibodies are useful
in the SLE workup
Harrison's Principles of Internal Medicine, 19th
Ed.
Complete Blood Count
Urinalysis
Renal Function and Electrolytes
Our patient's 2D echo showed
decreased heart function
● EF 43/39%
● Hypokinesia in inferior and
inferlateral wall of LV
Autoimmune Workup
Autoimmune Workup
EMG-NCV
Our patient satisfies the SLICC
criteria
The pathogenesis of SLE is
complex
Harrison's Principles of Internal Medicine, 19th
Ed.
SLE is managed according to the
severity of the disease
Course in the Wards
HD
1
D
Guillain-Barre
Syndrome
HD
11
HD
5
HD
3
HD
2
HD
4
HD
7
HD
6
HD
8
HD
9
HD
10
Course in the Wards
HD
1
D
Guillain-Barre
Syndrome
HD
11
HD
5
HD
3
HD
2
HD
4
HD
7
HD
6
HD
8
HD
9
HD
10
Given IVIg
Deficits fluctuated
(+) fever, pruritus
Course in the Wards
HD
1
D
Guillain-Barre
Syndrome
HD
11
HD
5
HD
3
HD
2
HD
4
HD
7
HD
6
HD
8
HD
9
HD
10
Given IVIg
Deficits fluctuated
(+) fever, pruritus
Rheuma: autoimmune workup
(+) Hematuria
Started on HCQ,
prednisone
Course in the Wards
HD
1
D
Guillain-Barre
Syndrome
HD
11
HD
5
HD
3
HD
2
HD
4
HD
7
HD
6
HD
8
HD
9
HD
10
Given IVIg
Deficits fluctuated
(+) fever, pruritus
Rheuma: autoimmune workup
(+) Hematuria
Started on HCQ,
prednisone
Cyclo-
phosphamide
QUIZ TIME!
A patient comes to your clinic complaining of
hematuria. He also admits to joint pains, reduced
appetite, fever and itchy arms. On PE, you note
reddish cheeks and a mouth sore. Your
impression is SLE.
1. What is the first immunologic test to confirm
your impression?
2. The autoantibody above turns out positive. How
will you manage your patient?
SLE is managed according to the
severity of the disease
Enumerate the following autoantibodies:
2. Correlates with disease activity
3. Associated with drug-induced SLE
4. Associated with lupus depression or
psychosis
Various autoantibodies are useful
in the SLE workup
Harrison's Principles of Internal Medicine, 19th
Ed.
5. What is the most common presentation of
NPSLE?
6. Give 4 SLICC criteria that permit the
diagnosis of SLE.
Headaches are the most common
presentation of NPSLE
62%
18%
8%
5%
5%1%
Headache
Seizures
CVD
Psychosis
Neuropathy
Movement
Muscal and Brey. Neurol. Clin. 28(1) 2010
SLE is diagnosed using a set of
clinical and laboratory criteria
Today's Learning Points
Questions?

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The Case of Ms. SI

Notas do Editor

  1. Stable VS Multiple, brown to pink macular patches of varying size ranging 2-3cm on legs, arms and trunk Normal medical PE
  2. Stable VS Multiple, brown to pink macular patches of varying size ranging 2-3cm on legs, arms and trunk Normal medical PE
  3. MMSE: 30 CrN: Intact L: 4-5mm BRTL; R: 4-5 BRTL, irregular pupil Intact Intact Sensory deficit on the L, 70-80% Intact Left facial hemiparesis Intact gross hearing Uvula deviated to the L, weak palatal rise L No gag Weak shoulder shrug, L Tongue deviated to the L
  4. Good bulk and tone No fasciculations, fibrillations No spasticity Left arm drifts No dysmmetria, no ataxia No toe extensor
  5. Good bulk and tone No fasciculations, fibrillations No spasticity Left arm drifts No dysmmetria, no ataxia No toe extensor
  6. Good bulk and tone No fasciculations, fibrillations No spasticity Left arm drifts No dysmmetria, no ataxia No toe extensor
  7. Up to 40% of SLE patients develop neuropsychatric problems called NPSLE
  8. Asymmetry most common: 59% Distal weakness most common: 34%
  9. The proposed pathophysiologic in NPSLE is microangiopathy affecting nearby nerves. In biopsies, microinfarcts,large infarcts and hemorrhages have been noted.
  10. Hydroxychloroquine 200mg OD Prednisone 10mg 2tabs BID
  11. Cyclophosphamide 500mg in 250cc D5W