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Archives of neurology 2011-Nov

Whipple limbic encephalitis.

Solo gli utenti registrati possono tradurre articoli
Entra registrati
Il collegamento viene salvato negli appunti
Frédéric Blanc
Kaouther Ben Abdelghani
Frédéric Schramm
Benoit Jaulhac
Emmanuel Chatelus
Christelle Sordet
Jacques-Eric Gottenberg
Jean Sibilia

Parole chiave

Astratto

OBJECTIVE

To describe a relapse of Whipple disease revealed by isolated limbic encephalitis with no other signs of systemic involvement.

METHODS

Case report.

METHODS

University Hospital of Strasbourg, Strasbourg, France. Patient A 41-year-old patient.

METHODS

Cognitive functions and results of cerebrospinal fluid analysis and brain magnetic resonance imaging.

RESULTS

A 41-year-old patient was hospitalized for headache associated with anterograde amnesia and temporospatial disorientation. Whipple disease with systemic manifestations was diagnosed 4 years previously and insufficiently treated. The neuropsychological evaluation showed impaired episodic memory and executive functions. Analysis of the cerebrospinal fluid showed increased lymphocytes and a positive Tropheryma whipplei polymerase chain reaction result. Cerebral magnetic resonance imaging revealed a typical pattern of limbic encephalitis with an intense signal in the amygdalae and hippocampi. The outcome under antibiotic treatment was marked by partial improvement of the cognitive disorders, disappearance of the positive T whipplei polymerase chain reaction result in cerebrospinal fluid, and a clear decrease of inflammation on brain magnetic resonance imaging.

CONCLUSIONS

Whipple disease can present as limbic encephalitis. Few cases have been previously described in the literature. Such diagnosis is of importance because of the specific treatment.

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