Sordia-Ramírez José, Infante-Valenzuela Adrián, Hernández-Galarza Iván de Jesús, Costilla-Esquivel Antonio
Department of Psychiatry, University Hospital "Dr. José E. González", Autonomous University of Nuevo León, Monterrey, Nuevo León, México.
Neurology Service, Internal Medicine Department, University Hospital "Dr. José E. González", Autonomous University of Nuevo León, Monterrey, Nuevo León, México.
J Med Case Rep. 2019 Apr 29;13(1):111. doi: 10.1186/s13256-019-2039-2.
Dyke-Davidoff-Masson syndrome is an uncommon constellation of radiological and clinical findings. Few reports describe co-occurring psychiatric manifestations. Systemic lupus erythematosus is a systemic disease with vascular, neurologic, and psychiatric involvement. To the best of our knowledge, no case reports have been made associating these entities.
We present the case of a 21-year-old Mexican mestizo woman with a history of systemic lupus erythematosus diagnosed at 4 years of age, who developed focal impaired awareness seizures when she was 8-years old, which became treatment-resistant at age 15. Two years prior to our evaluation, she developed deep vein thrombosis; clinical and laboratory criteria were met to diagnose secondary antiphospholipid syndrome. After being treated with anticonvulsants, glucocorticoids, and immunosuppressants with only a partial response, she developed a severe major depressive episode 1 year prior to our assessment, including two suicide attempts. She was referred to the out-patient clinic of our department for evaluation; intellectual disability, depressive symptoms, and behavioral symptoms were documented. Imaging studies revealed structural abnormalities in the left cerebral hemisphere: cortical atrophy, enlargement of sulci and cisternal spaces, and hyperpneumatization of the frontal sinus. Treatment with an antidepressant was initiated and maintained for 1 year, added to anticonvulsants and immunosuppressants. Depressive and behavioral symptoms diminished and no suicidal ideation has been noted at follow-up.
Dyke-Davidoff-Masson syndrome was diagnosed, accompanied by clinical symptoms previously reported as epilepsy and intellectual disability. This case report illustrates the complexity of syndrome presentation in an adult female, constituting a diagnostic and therapeutic challenge. This constellation of symptoms and structural brain abnormalities should be kept in mind in patients with neuropsychiatric manifestations and systemic diseases with central nervous system involvement, especially when diagnosed at a young age.
戴克-戴维多夫-马森综合征是一组罕见的影像学和临床症状。很少有报告描述其同时出现的精神症状。系统性红斑狼疮是一种累及血管、神经和精神系统的全身性疾病。据我们所知,尚无将这两种疾病相关联的病例报告。
我们报告一例21岁的墨西哥混血女性,4岁时被诊断为系统性红斑狼疮,8岁时出现局灶性意识障碍性癫痫发作,15岁时癫痫发作变得难以治疗。在我们评估前两年,她发生了深静脉血栓形成;符合继发性抗磷脂综合征的临床和实验室标准。在接受抗惊厥药、糖皮质激素和免疫抑制剂治疗但仅部分有效后,在我们评估前1年,她出现了严重的重度抑郁发作,包括两次自杀未遂。她被转诊至我们科室的门诊进行评估;记录到有智力障碍、抑郁症状和行为症状。影像学检查显示左脑半球存在结构异常:皮质萎缩、脑沟和脑池间隙增宽以及额窦气化过度。开始使用抗抑郁药治疗并持续了1年,同时继续使用抗惊厥药和免疫抑制剂。抑郁和行为症状减轻,随访时未再出现自杀意念。
诊断为戴克-戴维多夫-马森综合征,伴有先前报告的癫痫和智力障碍等临床症状。本病例报告说明了成年女性综合征表现的复杂性,构成了诊断和治疗挑战。对于有神经精神症状且患有累及中枢神经系统的全身性疾病的患者,尤其是年轻时被诊断出的患者,应牢记这组症状和脑结构异常。