3岁免疫正常儿童急性播散性脑脊髓炎伴脑脓肿1例报告

Pamela Cherfan, Marianne Touma Boulos, Doris Elia, C. Geagea, Patricia Kaldany
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引用次数: 0

摘要

急性播散性脑脊髓炎(ADEM)是一种单相免疫介导的炎症性脱髓鞘疾病,主要影响脑和脊髓白质。在磁共振成像(MRI)上,病变通常是弥漫性的,界限不清,在T2上显示高信号区,周围有水肿。另一方面,颅内脓肿是罕见的、严重的、危及生命的感染。MRI上,环状增强病变中水扩散受限是脑脓肿的典型表现。我们报告一个具有挑战性的情况下,一个3岁的男孩提出发烧,严重的头痛,嗜睡和颈部僵硬。脑脊液(CSF)显示白细胞计数高,脑MRI显示两个病变引起脓肿,并伴有多区血管源性水肿。六天后,尽管抗生素治疗,但由于嗜睡和步态障碍的持续存在,后续MRI显示血管源性水肿的更好描绘,现在引起ADEM病变,两个病变引起脓肿消退。诊断考虑是脑干脓肿或ADEM或两者之间的关联。然而,在文献中没有报道这两个实体之间的关联。由于第一次MRI病变是典型的脓肿,因此保留了脑脓肿与ADEM之间关联的诊断。患者接受高剂量类固醇治疗,病情迅速得到显著改善,尽管脑脊液培养未见细菌生长,但抗生素治疗仍持续了4周。总之,我们在这里报告了第一例脑脓肿与ADEM之间的关联,在治疗后进展良好的儿童。鉴别诊断可能是类似脓肿的非典型ADEM MRI图像。中华临床儿科杂志,2019;8(2):41-44 doi: https://doi.org/10.14740/ijcp339
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Disseminated Encephalomyelitis With Brain Abscess in a 3-Year-Old Immunocompetent Child: A Case Report
Acute disseminated encephalomyelitis (ADEM) is a monophasic immune-mediated inflammatory demyelinating condition that predominately affects the white matter of the brain and spinal cord. On magnetic resonance imaging (MRI), lesions are usually diffuse, poorly demarcated, and demonstrate regions of high signal on T2 with surrounding edema. On the other hand, intracranial abscesses are uncommon, serious and life-threatening infections. On MRI, restricted water diffusion, in ring-enhancing lesions, is typical of brain abscesses. We report a challenging case of a 3-year-old boy presenting with fever, severe headache, somnolence and neck stiffness. The cerebrospinal fluid (CSF) showed high white blood cell count and the brain MRI showed two lesions evoking abscesses with multiple areas of vasogenic edema. Six days later and due to the persistence of the somnolence with a gait disturbance despite antibiotic therapy, a follow-up MRI showed a better delineation of the vasogenic edema that now evokes ADEM lesions with regression of the two lesions evoking abscesses. Diagnostic considerations were brainstem abscesses or ADEM or an association between them. However, no association between these two entities has been reported in the literature. Because first MRI lesions were typical of abscesses, the diagnosis of an association between brain abscesses and ADEM was retained. The patient was treated with high doses of steroids that drastically and promptly improved his condition and the antibiotic therapy was continued for 4 weeks despite the absence of bacterial growth on CSF culture. In conclusion, we report here a first case of an association between brain abscesses and ADEM in a child with a good evolution after treatment. The differential diagnosis could be atypical MRI images of ADEM that resembled abscesses. Int J Clin Pediatr. 2019;8(2):41-44 doi: https://doi.org/10.14740/ijcp339
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