Rosai-Dorfman Disease: Report of a Case Associated with IgG4-Related Sclerotic Lesions
Korean Journal of Pathology
; : 583-586, 2012.
Article
en En
| WPRIM
| ID: wpr-45637
Biblioteca responsable:
WPRO
ABSTRACT
We describe a rare case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) associated with a six-year history of autoimmune pancreatitis, which was controlled by steroid treatment. The patient presented with multiple, cervical and thoracic lymphadenopathy and abnormal, nodular opacities in the lung. Histologically, Rosai-Dorfman disease with numerous IgG4-positive cells was identified in a subcutaneous lymph node in the patient's left forearm. The patient recovered uneventfully with steroid treatment.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Pancreatitis
/
Histiocitosis Sinusal
/
Antebrazo
/
Pulmón
/
Ganglios Linfáticos
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Enfermedades Linfáticas
Límite:
Humans
Idioma:
En
Revista:
Korean Journal of Pathology
Año:
2012
Tipo del documento:
Article