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脑 MRI 显示头痛和伴有脑脊液淋巴细胞增多的神经功能缺损(HaNDL)综合征,伴有胼胝体细胞毒性病变(CLOCC)可逆性损害。

Headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL) syndrome with reversible cytotoxic lesion of the corpus callosum (CLOCC) on MRI of the brain.

机构信息

Nuclear Medicine and PET, Nepean Hospital, Kingswood, New South Wales, Australia.

Neurology, Nepean Hospital, Kingswood, New South Wales, Australia.

出版信息

BMJ Case Rep. 2024 Jul 23;17(7):e259463. doi: 10.1136/bcr-2023-259463.

Abstract

Headache and neurological deficits with cerebrospinal fluid (CSF) lymphocytosis (HaNDL) is a rare condition characterised by recurrent episodes of headache and transient neurological deficits. This case report presents a young patient initially diagnosed with hemiplegic migraine, having a normal brain CT, with focal cerebral perfusion mismatch not restricted to a single vascular territory on CT angiography. Brain MRI revealed a cytotoxic lesion of the splenium in the corpus callosum (CLOCC), a feature also reported in migraine. However, recurrent headaches with neurological deficits prompted further investigations with CSF analysis and brain MRI, confirming HaNDL and demonstrating reversibility of CLOCC. Recognising HaNDL as a differential diagnosis is essential in patients with recurrent headaches with focal neurological deficits, given the differences in therapeutic approach. The relationship between migraine and HaNDL is not fully understood, but they may share a pathophysiological link. Awareness of this is crucial for accurate diagnosis.

摘要

头痛伴脑脊液淋巴细胞增多和神经功能缺损(HaNDL)是一种罕见的疾病,其特征为反复发作的头痛和短暂性神经功能缺损。本病例报告介绍了一位年轻患者,最初被诊断为偏瘫性偏头痛,脑 CT 正常,CT 血管造影显示局限性脑灌注不匹配,不限于单一血管区域。脑 MRI 显示胼胝体压部(CLOCC)细胞毒性病变,这在偏头痛中也有报道。然而,反复头痛伴神经功能缺损促使进一步进行脑脊液分析和脑 MRI 检查,确诊 HaNDL,并显示 CLOCC 可逆性。鉴于治疗方法的不同,在反复发作头痛伴局灶性神经功能缺损的患者中,将 HaNDL 作为鉴别诊断非常重要。偏头痛和 HaNDL 之间的关系尚未完全清楚,但它们可能具有共同的病理生理学联系。了解这一点对于准确诊断至关重要。

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