Cutaneous Rosai-Dorfman Disease (RDD) Mimicking Primary Cutaneous Marginal Zone B-cell Lymphoma / 대한피부과학회지
Korean Journal of Dermatology
; : 809-813, 2013.
Article
de Ko
| WPRIM
| ID: wpr-204072
Bibliothèque responsable:
WPRO
ABSTRACT
Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is an idiopathic, benign, histiocytic proliferative disease involving lymph nodes and extranodal sites. A 52-year-old woman presented with a 2-year history of multiple non-tender, erythematous nodules on her face. The initial punch biopsy showed lymphoid follicle-like aggregation of CD20 positive lymphocytes in the papillary dermis consisting of primary cutaneous marginal zone B-cell lymphoma. She underwent a 3-month course of radiotherapy, but the lesions progressed. The re-biopsy specimen revealed marked histiocytes with positive CD68 and S-100 proteins. The patient was treated with prednisolone and isotretinoin to which she responded slightly. Repeated histopathologic examinations enable us to make a definite diagnosis. Differentiating these two disorders as early as possible is crucial for appropriate treatment.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Radiothérapie
/
Biopsie
/
Prednisolone
/
Lymphocytes
/
Isotrétinoïne
/
Protéines S100
/
Histiocytose sinusale cytophagique
/
Lymphome B de la zone marginale
/
Derme
/
Diagnostic
Type d'étude:
Diagnostic_studies
Limites du sujet:
Female
/
Humans
langue:
Ko
Texte intégral:
Korean Journal of Dermatology
Année:
2013
Type:
Article