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1.
Korean Journal of Clinical Neurophysiology ; : 77-80, 2014.
Artículo en Inglés | WPRIM | ID: wpr-208476

RESUMEN

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.


Asunto(s)
Adolescente , Adulto , Femenino , Humanos , Diagnóstico Diferencial , Herpes Simple , Herpesvirus Humano 2 , Meningitis , Madres , Parto , Simplexvirus
2.
Journal of the Korean Child Neurology Society ; (4): 213-217, 2004.
Artículo en Coreano | WPRIM | ID: wpr-205925

RESUMEN

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.


Asunto(s)
Preescolar , Humanos , Masculino , Encéfalo , Quiste Epidérmico , Células Epiteliales , Glucosa , Leucocitosis , Imagen por Resonancia Magnética , Meningitis , Meningitis Aséptica , Remisión Espontánea , Rotura , Rotura Espontánea
3.
Journal of the Korean Pediatric Society ; : 122-127, 1999.
Artículo en Coreano | WPRIM | ID: wpr-140423

RESUMEN

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.


Asunto(s)
Adolescente , Niño , Femenino , Humanos , Líquido Cefalorraquídeo , Citoplasma , Células Endoteliales , Europa (Continente) , Meningitis , Meningitis Aséptica , Cuello , Neutrófilos
4.
Journal of the Korean Pediatric Society ; : 122-127, 1999.
Artículo en Coreano | WPRIM | ID: wpr-140422

RESUMEN

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.


Asunto(s)
Adolescente , Niño , Femenino , Humanos , Líquido Cefalorraquídeo , Citoplasma , Células Endoteliales , Europa (Continente) , Meningitis , Meningitis Aséptica , Cuello , Neutrófilos
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