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1.
Arq. bras. neurocir ; 40(1): 91-96, 29/06/2021.
Article in English | LILACS | ID: biblio-1362249

ABSTRACT

Schwannomas are the fourth most common primary neoplasms affecting the brain and cranial nerves. Central lesions commonly arise from sensory nerve roots, and a common intracranial site is the vestibular branch of the 8th nerve (>85%). We present the case report of a patient who has a schwannoma extending from the pterygopalatine fossa to the orbit, complaining about facial pain in the trajectory of the trigeminal ophthalmic branch. Schwannomas represent 1 to 2% of all neoplasms of the orbit, and trigeminal schwannomas are extremely rare, accounting for less than 0.5% of all intracranial tumors.


Subject(s)
Humans , Female , Middle Aged , Cranial Nerve Neoplasms/surgery , Trigeminal Nerve Diseases/surgery , Neurilemmoma/surgery , Orbit , Cranial Nerve Neoplasms/radiotherapy , Cranial Nerve Neoplasms/diagnostic imaging , Neurilemmoma/pathology , Neurilemmoma/diagnostic imaging
2.
Arq. bras. neurocir ; 39(4): 306-310, 15/12/2020.
Article in English | LILACS | ID: biblio-1362343

ABSTRACT

Paracoccidioidomycosis is a systemicmycosis caused by the Paracoccidioides brasiliensis fungus, which is endemic in Latin America. Brazil is the country with the highest number of cases. The affection of the central nervous system (CNS), a potentially fatal condition, occurs in 12% of the cases. The following forms of presentation are identified:meningeal, which is unusual;meningoencephalitic; and pseudotumoral, the latter two being more frequent. Imaging tests are essential for the diagnosis, but the histological identification of the fungus is required for confirmation of the pathology. The clinical picture depends on the neuraxial location.We present a case of amale rural worker, with expansive lesions in the CNS compatible with paracoccidioidomycosis.


Subject(s)
Humans , Male , Middle Aged , Paracoccidioidomycosis/surgery , Paracoccidioidomycosis/drug therapy , Paracoccidioidomycosis/epidemiology , Central Nervous System Fungal Infections/therapy , Paracoccidioides/pathogenicity , Paracoccidioidomycosis/diagnostic imaging , Central Nervous System Fungal Infections/mortality , Central Nervous System Fungal Infections/diagnostic imaging
3.
Arq. bras. neurocir ; 39(3): 232-234, 15/09/2020.
Article in English | LILACS | ID: biblio-1362423

ABSTRACT

Lhermitte-Duclos disease (LDD), or cerebellar dysplastic gangliocytoma, is a rare type of cerebellar tumor, from unknown origin. Patients can be asymptomatic for several years, but there are usually imprecise neurological signs for long periods.


Subject(s)
Humans , Female , Aged , Hamartoma Syndrome, Multiple/diagnosis , Hamartoma Syndrome, Multiple/therapy , Ganglioneuroma/surgery , Ganglioneuroma/diagnosis , Hamartoma Syndrome, Multiple/pathology , Cerebellar Neoplasms/diagnosis , Ganglioneuroma/pathology
4.
Arq. bras. neurocir ; 39(2): 142-145, 15/06/2020.
Article in English | LILACS | ID: biblio-1362532

ABSTRACT

Tuberculosis (TB) of the central nervous system (CNS) is considered one of the most severe forms of presentation of the disease. Although only 1% of TB cases involve the CNS, these cases represent around between 5 and 15% of extrapulmonary forms.1,2 Tuberculous meningitis (TBM) is the most frequent form of CNS TB. The granulomas formed in the cerebral tuberculoma may cause hydrocephalus and other symptoms indicative of a CNS mass lesion. In the absence of active TB or TBM, the symptoms may be interpreted as indicative of tumors.3,4 The prognosis is directly related to the early diagnosis and proper treatment installation.5 We report the case of a patient with intracranial hypertension syndrome, expansive mass in the parieto-occipital region, accompanied by a lesion in the rib, initially thought to be a metastatic lesion, although posteriorly diagnosed as a cerebral tuberculoma.


Subject(s)
Humans , Male , Aged, 80 and over , Tuberculoma/diagnosis , Tuberculoma/therapy , Tuberculoma, Intracranial/pathology , Tuberculosis, Central Nervous System , Microsurgery/methods , Antitubercular Agents/therapeutic use
5.
Arq. bras. neurocir ; 37(1): 47-49, 13/04/2018.
Article in English | LILACS | ID: biblio-911364

ABSTRACT

Vestibular schwannomas (VSs) account for 70% of all tumors of the cerebellopontine angle (CPA). Their clinical presentation is often insidious, with progressive hearing loss and involvement of other cranial nerves. Spontaneous hemorrhage in those tumors is very unusual, and generally presents with acute clinical features such as nausea, vomiting, headache and altered consciousness, usually with marked dysfunction of the cranial nerve involved, and with new deficits of neighboring cranial nerves. Asymptomatic patients are extremely rare. We present a case report of an incidental VS with asymptomatic bleeding, which evolved to death after surgery.


Schwannomas vestibulares (SVs) são responsáveis por cerca de 70% de todos os tumores do ângulo pontocerebelar. Sua apresentação costuma ser insidiosa, com perda auditiva progressiva e envolvimento de outros nervos cranianos. Hemorragia espontânea nesses tumores é incomum, e geralmente apresenta-se agudamente, com náusea, vômitos, cefaleia e alterações de consciência, normalmente com disfunção importante dos nervos cranianos envolvidos e com novos déficits dos nervos próximos. Pacientes assintomáticos são extremamente raros. Apresentamos um relato de caso de um SV incidental com sangramento assintomático que evoluiu para o óbito após cirurgia.


Subject(s)
Humans , Female , Aged , Hemorrhage , Neurilemmoma
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