| Literature DB >> 16462585 |
Antonio Ruggiero1, Giorgio Attinà, Palma Maurizi, Antonino Mulè, Elisabetta Tarquini, Giuseppe Barone, Ilaria Lazzareschi, Riccardo Riccardi.
Abstract
Rosai-Dorfman disease, or sinus histiocytosis with massive lymphadenopathy (SHML), is a rare and self-limiting benign disorder that most commonly involves the cervical lymph nodes. The authors describe two cases of SHML. Fine-needle aspiration of the lymphadenopathy was performed in both patients. Immunocytochemical and histologic features, as the evidence of emperipolesis and S100 protein positivity on immunostaining, were typical of SHML. Fine-needle aspiration cytology plays an important diagnostic role in SHML and may be conclusive in a typical clinical setting. The diagnosis of SHML should be considered in the differential diagnosis of massive, painless cervical lymphadenopathy. Long-term follow-up is necessary to observe the complete regression of the massive lymphadenopathy. However, specific therapy is available and should be limited to patients with compressive symptoms or extranodal disease.Entities:
Mesh:
Year: 2006 PMID: 16462585 DOI: 10.1097/01.mph.0000200686.33291.d1
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289