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Original Contribution |

Long-term Outcomes of CLIPPERS (Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids) in a Consecutive Series of 12 Patients

Guillaume Taieb, MD; Claire Duflos, MD; Dimitri Renard, MD; Bertrand Audoin, MD, PhD; Elsa Kaphan, MD; Jean Pelletier, MD, PhD; Nadège Limousin, MD; Christine Tranchant, MD, PhD; Stephane Kremer, MD; Jérome de Sèze, MD, PhD; Romain Lefaucheur, MD; David Maltête, MD, PhD; David Brassat, MD, PhD; Michel Clanet, MD, PhD; Patrice Desbordes, MD; Eric Thouvenot, MD, PhD; Laurent Magy, MD, PhD; Thierry Vincent, MD, PhD; Jean-Luc Faillie, MD; Nicolas de Champfleur, MD; Giovanni Castelnovo, MD; Sandrine Eimer, MD; Dominique Figarella Branger, MD, PhD; Emmanuelle Uro-Coste, MD, PhD; Pierre Labauge, MD, PhD
Arch Neurol. 2012;69(7):847-855. doi:10.1001/archneurol.2012.122.
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Background  Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) is a central nervous system inflammatory disease.

Objective  To describe the disease course of CLIPPERS.

Design  A nationwide study was implemented to collect clinical, magnetic resonance imaging, cerebrospinal fluid, and brain biopsy specimen characteristics of patients with CLIPPERS.

Setting  Academic research.

Patients  Twelve patients with CLIPPERS.

Main Outcome Measures  The therapeutic management of CLIPPERS was evaluated.

Results  Among 12 patients, 42 relapses were analyzed. Relapses lasted a mean duration of 2.5 months, manifested frequent cerebellar ataxia and diplopia, and were associated with a mean Expanded Disability Status Scale (EDSS) score of 4. Besides typical findings of CLIPPERS, magnetic resonance imaging showed brainstem mass effect in 5 patients, extensive myelitis in 3 patients, and closed ring enhancement in 1 patient. Inconstant oligoclonal bands were found on cerebrospinal fluid investigation in 4 patients, with an increased T-cell ratio of CD4 to CD8. Among 7 available brain biopsy specimens, staining was positive for perivascular CD4 T lymphocytes in 5 samples. Thirty-eight of 42 relapses were treated with pulse corticosteroid therapy, which led to improvement, with a mean residual EDSS score of 1.9 (range, 0-7). In 1 patient with untreated relapses, scores on the EDSS progressively increased to a score of 10 at death. Among 5 patients without long-term corticosteroid therapy, the mean annualized relapse rate was 0.5 (range, 0.25-2.8). Among 7 patients taking oral corticosteroids, no relapses occurred in those whose daily dose was 20 mg or higher. No progressive course of CLIPPERS was observed. Four patients with a final EDSS score of 4 or higher had experienced previous severe relapses (EDSS score, ≥5) and brainstem and spinal cord atrophy.

Conclusions  CLIPPERS is a relapsing-remitting disorder without progressive forms. Long-term disability is correlated with the severity of previous relapses. Further studies are needed to confirm that prolonged corticosteroid therapy prevents further relapses.

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Figures

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Figure 1. Clinical characteristics of patients during relapses. A, Duration of relapses, with corresponding Expanded Disability Status Scale (EDSS) scores. Treated relapses are indicated by diamonds and untreated relapses by squares. B, Individual patient clinical characteristics during the cumulative relapses. INO indicates internuclear ophthalmoplegia.

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Figure 2. Clinical course of 5 patients having chronic lymphocytic inflammation with pontine perivascular enhancement responsive to corticosteroids who did not receive long-term corticosteroid therapy. EDSS indicates Expanded Disability Status Scale.

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Figure 3. Clinical course of 7 patients having chronic lymphocytic inflammation with pontine perivascular enhancement responsive to corticosteroids who received long-term corticosteroid therapy. EDSS indicates Expanded Disability Status Scale.

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Figure 4. Relevant magnetic resonance imaging in 12 patients having chronic lymphocytic inflammation with pontine perivascular enhancement responsive to corticosteroids using gadolinium-enhanced T1-weighted and T2-weighted imaging. Gadolinium-enhanced T1-weighted images show a homogeneous gadolinium-enhancing lesion greater than 3 mm (A) and a gadolinium-enhancing pattern as a closed ring (B). Increased T2-weighted signal is confluent (C) and exceeds the size of the corresponding punctuate gadolinium-enhancing lesions (D). Axial (E) and sagittal (F) gadolinium-enhanced T1-weighted images show juxtacortical lesions. Gadolinium-enhanced T1-weighted (G) and T2-weighted (H) images show a large confluent spinal cord lesion. Pons swelling (I), brainstem atrophy (J), spinal cord atrophy (K), and black hole (L) are shown.

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Figure 5. Neuropathological findings in patients 1, 3, 5, 6, and 9, show marked perivascular infiltrates. Infiltrates were predominantly composed of CD4 T cells, associated with few CD8 T cells and very low or absent granzyme B. Original magnification ×100 for patient 3; all others are original magnification ×400.

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