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Table 1 Clinical and laboratory characteristics

From: Posterior reversible encephalopathy syndrome could be an underestimated variant of “reversible neurological deficits” in Systemic Lupus Erythematosus

 

10 episodes, no. (%)

Demographics

 

Age at onset (years)

22.93 ± 2.48 *

Female

10 (100)

SLE characteristics

 

Duration (months)

20.8 ± 12.8*

Fever

8 (80)

Rash

8 (80)

Photosensitive

6 (60)

Ulcers

5 (50)

Arthritis/arthralgia

10 (100)

Serositis

5 (50)

Lymphadenopathy

5 (50)

Vasculitis

4 (40)

Reynaud’s phenomena

4 (40)

SLEDAI

25.8 ± 5.7*

Associated risk factors

 

Acute hypertension

8 (80)

<160/100 mmHg

5 (50)

≥170/110 mmHg

3 (30)

Renal failure (cr. ≥1.5 mg/dl) b

2 (20)

Neurological manifestations

 

Seizures

8 (80)

Coma

6 (60)

Headache

3 (30)

Vomiting

3 (30)

Cortical blindness

2 (20)

Stupor

1(10)

Laboratory findings

 

Leucopenia

6 (60)

Lymphopenia

2 (20)

Anemia

5 (50)

Thrombocytopenia

3 (30)

Proteinuria

8 (80)

Hypoproteinemia

8 (80)

Hypocomplementemia

8 (80)

Anti-SSA

7 (70)

Anti-SSB

2 (20)

Anti-dsDNA

6 (60)

Anti-RNP/Sm

3 (30)

Anti- Sm

2 (20)

Anti-Nucleosomes

2 (20)

aPL

4 (40)

Treatmentb

 

Methylprednisolone pulses

8 (80)

Cyclophosphamide

8 (80)

Outcome

 

Complete neurological recovery

8 (80)

Residual neurological deficit

1(10)

Death

1(10)

  1. SLEDAI: Systemic Lupus Erythematosus Disease Activity Index [23] aPL: antiphospholipid antibodies. Mean and S.D.
  2. b.At clinical onset.