Cutaneous Rosai-Dorfman Disease Confused with Vascular Mass
Archives of Craniofacial Surgery
;
: 31-34, 2016.
Article
Dans Anglais
| WPRIM
| ID: wpr-220415
ABSTRACT
Rosai-Dorfman disease is a rare histiocytic disorder, clinically characterized by massive, bilateral painless cervical lymphadenopathy with potential for extranodal manifestations. We report a 45-year-old male patient who presented with a slowly growing erythematous nodule of the left chin. The mass appeared non-vascular on computed tomography study, but ultrasonogram was suggestive of a vascular lesion. The lesion was excised with presumptive diagnosis of a hemangioma. However, histopathologic examination of the surgical biopsy revealed histiocytic infiltration with emperipolesis, which was pathognomic for Rosai-Dorfman disease. Additional imaging studies did not reveal lymph node enlargement or other extranodal manifestation. The patient was diagnosed with cutaneous form of the Rosai-Dorfman disease and was discharged home. He remains free of local recurrence at 8 months.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Récidive
/
Biopsie
/
Histiocytose sinusale cytophagique
/
Échographie
/
Menton
/
Diagnostic
/
Empéripolèse
/
Hémangiome
/
Noeuds lymphatiques
/
Maladies lymphatiques
Type d'étude:
Etude diagnostique
Limites du sujet:
Humains
/
Mâle
langue:
Anglais
Texte intégral:
Archives of Craniofacial Surgery
Année:
2016
Type:
Article
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