Neurosarcoidosis Associated with Psychiatric Symptoms: Case Report

Author:

Neves Maick1,Aguiar Paulo2,Belsuzarri Telmo3,Zeviani Wolnei3,Mattos João3,Navarro Juliano3,Marques Renata45,Francisco Letícia4

Affiliation:

1. Pontifícia Universidade Católica de Campinas (PUC-Campinas), Campinas, São Paulo, Brazil

2. Department of Neurosurgery, Hospital Santa Paula, São Paulo, São Paulo, Brazil

3. Department of Neurosurgery, Hospital Celso Pierro, PUC Campinas, Campinas, São Paulo, Brazil

4. Hospital Celso Pierro, Pontifícia Universidade Católica de Campinas (PUC-Campinas), Campinas, São Paulo, Brazil

5. Centro de Atenção Integral à Saúde da Mulher (Caism), Universidade Estadual de Campinas (Unicamp), Campinas, São Paulo, Brazil

Abstract

Background Sarcoidosis is a granulomatous disease predominant in women and black men that has inflammatory origin of unknown etiology; neurosarcoidosis is a rare and critical presentation of the disease. Case description A 26-year-old black female presented frontal headache for 1 year, as well as behavioral and mood changes for 15 days. Skull tomography and nuclear magnetic imaging of the skull revealed damaged meninges, a right frontal bone lesion, and an intraparenchymal contrast-enhancing lesion. Screening with computed tomography (CT) scans was performed, and it showed signs of bronchiectasis in the lower third of the right lung, but it was asymptomatic. The biopsy showed signs of reactional lesion with the presence of non-caseating granulomas. After the treatment with corticosteroids, the patient presented progressive improvement. Conclusions Neurosarcoidosis is a rare and critical pathology of sarcoidosis that presents a lytic bone lesion and clinical psychiatric symptoms; neurosarcoidosis is also rare in the literature.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,Surgery

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