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Epileptic Seizure Provoked by Bone Metastasis of Chronic Lymphoid Leukemia and Merkel Cell Carcinoma.
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.
Afiliação
  • Folyovich A; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Majoros A; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Jarecsny T; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Pánczél G; National Institute of Oncology, Budapest, Hungary.
  • Pápai Z; Military Hospital, Budapest, Hungary.
  • Rudas G; MR Research Centre, Semmelweis University, Budapest, Hungary.
  • Kozák L; MR Research Centre, Semmelweis University, Budapest, Hungary.
  • Barna G; First Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
  • Béres-Molnár KA; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Vadasdi K; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Liszkay G; National Institute of Oncology, Budapest, Hungary.
  • Horváth E; Department of Neurology and Stroke, Szent János Hospital, Budapest, Hungary.
  • Toldi G; Department of Laboratory Medicine, Semmelweis University, Budapest, Hungary.
Case Rep Med ; 2020: 4318638, 2020.
Article em En | MEDLINE | ID: mdl-33178284
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. Case Presentation. 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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article