Isolated Intracranial Rosai-Dorfman Disease: A Case Report
Korean Journal of Pathology
;
: 430-433, 2004.
Article
Dans Coréen
| WPRIM
| ID: wpr-112672
ABSTRACT
Rosai-Dorfman disease (RDD) is an idiopathic histioproliferative disorder of the lymph nodes and extranodal sites. Central nervous system involvement is extremely rare. Intracranial RDD, especially the isolated form, resembles meninigioma both clinically and radiologically. Here, we report a case of isolated, intracranial, dura-based RDD. The patient presented with headache and dizziness with no evidence of lymphadenopathy. Histologically, the lesion consisted of large histiocytes with emperipolesis and lymphoplasma cell infiltrates with a fibrotic background. We discuss the differential diagnosis of this lesion. To our knowledge, this is the first reported Korean case of intracranial RDD.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Histiocytose sinusale cytophagique
/
Système nerveux central
/
Diagnostic différentiel
/
Sensation vertigineuse
/
Empéripolèse
/
Céphalée
/
Histiocytes
/
Noeuds lymphatiques
/
Maladies lymphatiques
/
Méninges
Type d'étude:
Etude diagnostique
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Pathology
Année:
2004
Type:
Article
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