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April 10, 2012; 78 (15) Articles

CNS involvement at the onset of primary hemophagocytic lymphohistiocytosis

K. Deiva, N. Mahlaoui, F. Beaudonnet, G. de Saint Basile, G. Caridade, D. Moshous, Y. Mikaeloff, S. Blanche, A. Fischer, M. Tardieu
First published March 14, 2012, DOI: https://doi.org/10.1212/WNL.0b013e31824f800a
K. Deiva
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N. Mahlaoui
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F. Beaudonnet
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G. de Saint Basile
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G. Caridade
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D. Moshous
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Y. Mikaeloff
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A. Fischer
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Citation
CNS involvement at the onset of primary hemophagocytic lymphohistiocytosis
K. Deiva, N. Mahlaoui, F. Beaudonnet, G. de Saint Basile, G. Caridade, D. Moshous, Y. Mikaeloff, S. Blanche, A. Fischer, M. Tardieu
Neurology Apr 2012, 78 (15) 1150-1156; DOI: 10.1212/WNL.0b013e31824f800a

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Abstract

Objectives: To differentiate onset of CNS involvement in primary hemophagocytic lymphohistiocytosis (HLH) from that of other CNS inflammatory diseases and to identify early symptoms linked to abnormal cognitive outcome.

Methods: Forty-six children with primary HLH who had neurologic evaluation within 2 weeks and brain MRI within 6 months of diagnosis were included. Initial symptoms, CSF study, brain MRI, and neurologic outcome were assessed. Brain MRIs were compared with those of 44 children with acute disseminated encephalomyelitis (ADEM).

Results: At disease onset, 29 children (63%) had neurologic symptoms and 7 (15%) had microcephaly. Twenty-three (50%) children had abnormal CSF study, but only 15 (33%) had abnormal brain MRI. The latter showed that patients with HLH, unlike patients with ADEM, had symmetric periventricular lesions, without thalamic and brainstem involvement and with infrequent hyposignal intensity on T1. At the end of follow-up (3.6 ± 3.6 years), 17 of the 28 (61%) surviving patients had normal neurologic status, 5 (18%) had a severe neurologic outcome, and 6 (21%) had mild cognitive difficulties. Abnormal neurologic outcome was not influenced by age or type of genetic defect, but by the presence of neurologic symptoms, MRI lesions, or abnormal CSF study at onset. Early clinical and MRI symptoms may regress after treatment.

Conclusion: Neurologic symptoms are frequent at the onset of primary HLH and are mostly associated with abnormal CSF findings, but with normal brain MRI. In cases of abnormal brain MRI, the observed lesions differ from those of ADEM.

GLOSSARY

ADEM=
acute disseminated encephalomyelitis;
CHS=
Chediak-Higashi syndrome;
CRF=
case report form;
FHLH=
familial hemophagocytic lymphohistiocytosis;
FLAIR=
fluid-attenuated inversion recovery;
GS=
Griscelli syndrome;
HLH=
hemophagocytic lymphohistiocytosis;
HPS=
Hermansky-Pudlak syndrome;
HSCT=
hematopoietic stem cell transplantation;
MTX=
methotrexate;
PID=
primary immunodeficiencies;
SE=
spin-echo;
WI=
weighted image;
XLP=
X-linked lymphoproliferative syndrome

Footnotes

  • Editorial, page 1114

  • Received June 8, 2011.
  • Accepted September 23, 2011.
  • Copyright © 2012 by AAN Enterprises, Inc.
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