Posterior reversible encephalopathy syndrome - An underrecognized manifestation of systemic lupus erythematosus

被引:1
|
作者
Kur, Jason K. [1 ]
Esdaile, John M. [1 ]
机构
[1] Univ British Columbia, Vancouver Gen Hosp, Dept Med, Div Rheumatol, Vancouver, BC V5Z 1M9, Canada
关键词
systemic lupus erythematosus; seizures; encephalopathy; hypertension;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Posterior reversible encephalopathy syndrome (PRES) is a rare, recently described neurologic condition identifiable by clinical presentation and magnetic resonance image (MRI) appearance. It is associated with renal insufficiency, hypertension, and rheumatologic diseases. Patients present with headache, seizures, loss of vision and altered mental function, and a pattern on imaging studies of predominantly transient, posterior cerebral hyperintensities on T2-weighted MRI. There is a high likelihood of presentation of this syndrome to a rheumatologist. Methods. Three recent cases of systemic lupus erythematosus (SLE) with PRES, along with 9 previously reported cases, are reviewed. Results. All 3 patients presented with seizures and subacute visual changes in association with lupus nephritis. The first presented with hypertension, complete visual field loss, and status epilepticus 2 weeks after starting oral cyclosporine therapy for refractory lupus nephritis. The second patient was normotensive and presented with seizures and visual symptoms while in hospital with SLE-related pancreatitis and nephritis. The third patient had headache and seizures with severe lupus disease activity including nephritis, pancytopenia, and pulmonary hemorrhage. Cranial MRI showed predominantly posterior signal abnormalities on T2-weighted images, which resolved after cessation of cyclosporine in the first case, treatment with IV cyclophospharmide in the second case, and treatment with cyclophosphamide and plasmapheresis in the final case. Literature review showed that PRES is a manifestation of SLE or a consequence of therapy with calcineurin inhibitors or rituximab. The hallmark features are visual loss and seizures. Severe hypertension (> 170/110 mm Hg) and renal failure were present in the majority of previously identified cases of SLE and PRES. Our second case was normotensive but had marked lupus disease activity. PRES can lead to cerebral infarction. Conclusion. With increasing availability of MRI, PRES will be identified more frequently. Swift action to identify potential offending agents, controlling hypertension, and treating active disease can lead to reversal of radiologic and neurologic findings.
引用
收藏
页码:2178 / 2183
页数:6
相关论文
共 50 条
  • [41] "Highlighting" red nuclei by atypical posterior reversible encephalopathy syndrome in a patient with systemic lupus erythematosus
    Vaysman, Tetyana
    Xu, Prissilla
    Vartanian, Tara
    Michalak, Peter
    Pike, Kesley
    Liu, Antonio
    CLINICAL CASE REPORTS, 2019, 7 (07): : 1404 - 1408
  • [42] MR imaging findings suggestive of posterior reversible encephalopathy syndrome in adolescents with systemic lupus erythematosus
    Eyal Muscal
    Elfrides Traipe
    Marietta M. de Guzman
    Barry L. Myones
    Robin L. Brey
    Jill V. Hunter
    Pediatric Radiology, 2010, 40 : 1241 - 1245
  • [43] Differential serum cytokine profile in patients with systemic lupus erythematosus and posterior reversible encephalopathy syndrome
    Merayo-Chalico, J.
    Barrera-Vargas, A.
    Juarez-Vega, G.
    Alcocer-Varela, J.
    Arauz, A.
    Gomez-Martin, D.
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2018, 192 (02): : 165 - 170
  • [44] Central-variant posterior reversible encephalopathy syndrome in a young patient with systemic lupus erythematosus
    Maier, Smaranda
    Monica, Copotoiu
    Romaniuc, Andreea
    Andone, Sebastian
    Balasa, Rodica
    ACTA NEUROLOGICA BELGICA, 2019, 119 (02) : 269 - 271
  • [45] Central-variant posterior reversible encephalopathy syndrome in a young patient with systemic lupus erythematosus
    Smaranda Maier
    Copotoiu Monica
    Andreea Romaniuc
    Sebastian Andone
    Rodica Bălaşa
    Acta Neurologica Belgica, 2019, 119 : 269 - 271
  • [46] Neuropsychiatric Systemic Lupus Erythematosus and Posterior Reversible Encephalopathy Syndrome in a Young Woman: A Case Report
    Bawazir, Yasser Mohammed
    Anshasi, Neda'a Wasim
    CURRENT RHEUMATOLOGY REVIEWS, 2023, 19 (04) : 508 - 514
  • [47] Posterior reversible encephalopathy syndrome in a patient with systemic lupus erythematosus after cessation of oral prednisone
    Qi Li
    Fajin Lv
    Youdong Wei
    Bernard Yan
    Peng Xie
    Neurological Sciences, 2013, 34 : 2241 - 2242
  • [48] Posterior reversible encephalopathy syndrome as the first clinical manifestation of lupus nephritis
    Frederico Carvalho de Medeiros
    Bárbara Márcia Rocha Sousa
    Dandara Noária Cruz Santos
    Gisele Novais Matias Sion
    Cibele Fontes Alves
    Acta Neurologica Belgica, 2022, 122 : 219 - 221
  • [49] Posterior reversible encephalopathy syndrome as the first clinical manifestation of lupus nephritis
    de Medeiros, Frederico Carvalho
    Rocha Sousa, Barbara Marcia
    Cruz Santos, Dandara Noaria
    Novais Matias Sion, Gisele
    Fontes Alves, Cibele
    ACTA NEUROLOGICA BELGICA, 2022, 122 (01) : 219 - 221
  • [50] Posterior reversible encephalopathy syndrome during systemic lupus erythematosus:: four new cases and review of the literature
    Leroux, G.
    Sellam, J.
    Costedoat-Chalumeau, N.
    Huong, D. Le Thi
    Combes, A.
    Tieulie, N.
    Haroche, J.
    Amoura, Z.
    Nieszkowska, A.
    Chastre, J.
    Dormont, D.
    Piette, J-C
    LUPUS, 2008, 17 (02) : 139 - 147