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慢性淋巴细胞白血病和默克尔细胞癌骨转移引发的癫痫发作

Epileptic Seizure Provoked by Bone Metastasis of Chronic Lymphoid Leukemia and Merkel Cell Carcinoma.

作者信息

Folyovich András, Majoros Angéla, Jarecsny Tamás, Pánczél Gitta, Pápai Zsuzsanna, Rudas Gábor, Kozák Lajos, Barna Gábor, Béres-Molnár Katalin A, Vadasdi Károly, Liszkay Gabriella, Horváth Eszter, Toldi Gergely

机构信息

Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.

National Institute of Oncology, Budapest, Hungary.

出版信息

Case Rep Med. 2020 Oct 27;2020:4318638. doi: 10.1155/2020/4318638. eCollection 2020.

Abstract

BACKGROUND

Merkel cell carcinoma (MCC) is a rare primary neuroendocrine cutaneous tumor, rarely metastasizing to the brain. Chronic lymphoid leukemia (CLL) is a disease predisposing to MCC. According to previous reports, headache and focal neurological deficits suggest disease progression to the brain. We present a patient with MCC whose seizure was not elicited by a cerebral metastasis, but by bone metastases compressing the brain. . A 62-year-old female patient had a history of CLL. A lesion with the appearance of an atheroma was removed from the right upper arm. Histology confirmed the diagnosis of MCC. She was admitted to the neurology department with her first GM seizure. The cranial MRI/MRA showed bone metastases in the right parietal and both frontal areas, compressing the brain. Flow cytometry of CSF did not reveal metastasis of MCC.

CONCLUSIONS

The case history of the patient was unique even among the rare cases of MCC with neurological involvement. The seizure was not elicited by a cerebral metastasis, but by bone metastases compressing the brain. In addition to patient history, clinical presentation and radiological findings enabled a suspected diagnosis of skull metastasis of MCC compressing the brain, causing symptomatic epileptic seizures.

摘要

背景

默克尔细胞癌(MCC)是一种罕见的原发性神经内分泌皮肤肿瘤,很少转移至脑部。慢性淋巴细胞白血病(CLL)是一种易患MCC的疾病。根据既往报道,头痛和局灶性神经功能缺损提示疾病进展至脑部。我们报告一例MCC患者,其癫痫发作并非由脑转移引起,而是由压迫脑部的骨转移所致。一名62岁女性患者有CLL病史。从右上臂切除一个外观似动脉粥样硬化的病灶。组织学检查确诊为MCC。她因首次全身性强直阵挛发作入住神经内科。头颅MRI/MRA显示右侧顶叶和双侧额叶有骨转移,压迫脑部。脑脊液流式细胞术未发现MCC转移。

结论

即使在罕见的伴有神经受累的MCC病例中,该患者的病史也很独特。癫痫发作并非由脑转移引起,而是由压迫脑部的骨转移所致。除患者病史外,临床表现和影像学检查结果有助于疑似诊断为MCC颅骨转移压迫脑部,导致症状性癫痫发作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc24/7609155/f0fcb5a2b220/CRIM2020-4318638.001.jpg

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