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Lupus
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Devic's neuromyelitis optica during pregnancy in a patient with systemic lupus erythematosus

F Bonnet

Services de médecine interne et maladies infectieuses, Hôpital Haut Lévêque et Hôpital Saint-André

P Mercié

Services de médecine interne et maladies infectieuses, Hôpital Haut Lévêque et Hôpital Saint-André; Clinique de médecine interne et maladies infectieuses, Centre François Magendie, Hôpital Haut Lévêque, Centre Hospitalier Universitaire de Bordeaux, 33604 Pessac, France

P Morlat

Services de médecine interne et maladies infectieuses, Hôpital Haut Lévêque et Hôpital Saint-André

C Hocke

Service de gynécologie-obstétrique, Hôpital Saint-André

C Vergnes

Laboratoire d'hématologie, Hôpital Haut Lévêque, Centre Hospitalier Universitaire de Bordeaux, 33075 Bordeaux, France

E Ellie

Services de médecine interne et maladies infectieuses, Hôpital Haut Lévêque et Hôpital Saint-André

J-F Viallard

I Faure

J-L Pellegrin

J Beylot

B Leng

Services de médecine interne et maladies infectieuses, Hôpital Haut Lévêque et Hôpital Saint-André

Neuropsychiatric forms of systemic lupus erythematosus (SLE) vary, most commonly consisting of seizures, psychiatric disturbances, or focal central nervous deficits. This is a new case of neuromyelitis optica or Devic's syndrome during the course of SLE. Few reports of this association exist in the literature. Our objective is to report this unique case of Devic's neuromyelitis optica during pregnancy in a patient with systemic lupus erythematosus. A 28-year-old woman had been diagnosed as having SLE with cutaneous and articular involvement in 1987 when she was 17 years old. She was treated with a synthetic antimalarial agent associated with corticosteroids. In 1994, during the fourth month of pregnancy, she had signs of transverse myelitis with a sensory level at T6 associated with an optic neuropathy suggesting a Devic's syndrome. The patient was managed by plasmapheresis sessions and intravenous corticosteroids. Transverse myelitis recurred postpartum and three years later at the same thoracic level. Management by bolus administration of a steroid and cyclophosphamide resulted in remission again. There have only been around a dozen reports in the literature of patients who had both Devic's neuromyelitis optica and SLE. Magnetic resonance imaging is contributive to diagnosis and therapeutic follow-up, showing spinal cord lesions with increased intensity on T2-weighted sequences. Although the clinical course of the present patient has been favourable so far, the prognosis of this neurologic disease is generally considered to be poor with elevated mortality.

Key Words: systemic lupus erythematosus • neuromyelitis optica

Lupus, Vol. 8, No. 3, 244-247 (1999)
DOI: 10.1191/096120399678847696


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