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J Neurol Sci ; 163(2): 187-91, 1999 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-10371083

RESUMO

Histiocytic necrotizing lymphadenitis, or Kikuchi's disease (KD), is a self-limited clinicopathologic entity recognized increasingly worldwide. A 27-year-old man with cervical lymphadenopathy and fever who was diagnosed with KD developed mild headache with no nuchal rigidity. The cerebrospinal fluid (CSF) was sterile and contained 78 white blood cells/mm3 with lymphocytes predominating, accompanied by smaller numbers of monocytes and granulocytes. This abnormality normalized spontaneously over 5 weeks. Eleven similar cases have been reported, all but one from Japan. The development of meningitis in KD was observed in four (9.8%) of 41 KD patients we have treated, suggesting that the meningitis was related to KD and not merely coincidental.


Assuntos
Linfadenite Histiocítica Necrosante/complicações , Meningite Asséptica/complicações , Adulto , Cefaleia , Linfadenite Histiocítica Necrosante/líquido cefalorraquidiano , Linfadenite Histiocítica Necrosante/patologia , Linfadenite Histiocítica Necrosante/fisiopatologia , Humanos , Linfonodos/patologia , Masculino , Meningite Asséptica/patologia , Meningite Asséptica/fisiopatologia
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