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1.
Korean Journal of Clinical Neurophysiology ; : 77-80, 2014.
Artigo em Inglês | WPRIM | ID: wpr-208476

RESUMO

Herpes simplex virus type 2 (HSV2) meningitis primarily develops during or following a primary genital HSV2 infection that was acquired from sexual contact or through the birth canal during delivery from mother. We describe a 15 year old virgin without history of previous herpes simplex infection who developed 2 episodes of HSV2 meningitis. Although recurrent meningitis due to HSV is primarily seen in young or sexually active adults. HSV2 meningitis should be in the differential diagnosis of recurrent meningitis in adolescent patients.


Assuntos
Adolescente , Adulto , Feminino , Humanos , Diagnóstico Diferencial , Herpes Simples , Herpesvirus Humano 2 , Meningite , Mães , Parto , Simplexvirus
2.
Journal of the Korean Child Neurology Society ; (4): 213-217, 2004.
Artigo em Coreano | WPRIM | ID: wpr-205925

RESUMO

Mollaret's meningitis is a recurrent aseptic meningitis with characteristic clinical features and Mollaret cells in cerebrospinal fluid(CSF). We describe a case of Mollaret's meningitis in a 3-year-old boy who presented with three episodes of aseptic meningitis within a 4-month period. Each episode was characterized by sudden onset of meningeal irritation followed by spontaneous remission in several days. He was free of neurological symptoms between the episodes. In the acute phase of each episode, his CSF showed polymorphonuclear pleocytosis with normal protein and glucose concentrations. In addition, some epithelial cell clusters in the CSF were evident during the third episode. No pathogenic microorganisms were identified in the CSF or the blood cultures. Brain MRI revealed a benign pineal cyst, 0.8 cm in diameter, and epithelial cell clusters were supposed to represent ruptured cystic walls and recurrent episodes of aseptic meningitis were triggered by spontaneous rupture of the cyst. Our case appears to support "spontaneous rupture of epidermoid cysts in the central nervous system" as one of the etiologies of Mollaret's meningitis.


Assuntos
Pré-Escolar , Humanos , Masculino , Encéfalo , Cisto Epidérmico , Células Epiteliais , Glucose , Leucocitose , Imageamento por Ressonância Magnética , Meningite , Meningite Asséptica , Remissão Espontânea , Ruptura , Ruptura Espontânea
3.
Journal of the Korean Pediatric Society ; : 122-127, 1999.
Artigo em Coreano | WPRIM | ID: wpr-140423

RESUMO

Mollaret meningitis is a recurrent aseptic meningitis with characteristic clinical features and Mollaret cells in cerebrospinal fluid. Since Mollaret first reported Mollaret meningitis in 1944, further reports had been made mainly in Europe. The syndrome consists of brief attacks of meningitis that recur at regular intervals and alternate with a symptom-free period lasting for weeks or months. The symptoms subside as quickly as they develop, and the patient is completely asymptomatic until the next episode, without any residual neurologic abnormalities. Specific changes in the cytologic pattern of the cerebrospinal fluid occur over the course of an attack. In the early stages, polymorphonuclear leukocytes and endothelial cells appear in the cerebrospinal fluid, called Mollaret cell. We experienced a case of Mollaret meningitis in a 15-year-old female child who had 5 episodes of recurrent aseptic meningitis, always accompanied by vesicles on the face and anterior neck. We observed Mollaret cells which had faint, finely vacuolated cytoplasm, eccentrically located nuclei show on Papanicolau stain. We present a case of Mollaret meningitis with a brief review of related literatures.


Assuntos
Adolescente , Criança , Feminino , Humanos , Líquido Cefalorraquidiano , Citoplasma , Células Endoteliais , Europa (Continente) , Meningite , Meningite Asséptica , Pescoço , Neutrófilos
4.
Journal of the Korean Pediatric Society ; : 122-127, 1999.
Artigo em Coreano | WPRIM | ID: wpr-140422

RESUMO

Mollaret meningitis is a recurrent aseptic meningitis with characteristic clinical features and Mollaret cells in cerebrospinal fluid. Since Mollaret first reported Mollaret meningitis in 1944, further reports had been made mainly in Europe. The syndrome consists of brief attacks of meningitis that recur at regular intervals and alternate with a symptom-free period lasting for weeks or months. The symptoms subside as quickly as they develop, and the patient is completely asymptomatic until the next episode, without any residual neurologic abnormalities. Specific changes in the cytologic pattern of the cerebrospinal fluid occur over the course of an attack. In the early stages, polymorphonuclear leukocytes and endothelial cells appear in the cerebrospinal fluid, called Mollaret cell. We experienced a case of Mollaret meningitis in a 15-year-old female child who had 5 episodes of recurrent aseptic meningitis, always accompanied by vesicles on the face and anterior neck. We observed Mollaret cells which had faint, finely vacuolated cytoplasm, eccentrically located nuclei show on Papanicolau stain. We present a case of Mollaret meningitis with a brief review of related literatures.


Assuntos
Adolescente , Criança , Feminino , Humanos , Líquido Cefalorraquidiano , Citoplasma , Células Endoteliais , Europa (Continente) , Meningite , Meningite Asséptica , Pescoço , Neutrófilos
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