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Reply to sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease)

✍ Scribed by M. Pérez-Guillermo; J. Sola-Pérez


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
8 KB
Volume
16
Category
Article
ISSN
8755-1039

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✦ Synopsis


published in Diagnostic Cytopathology concerning the cytologic findings in a case of Rosai-Dorfman disease (RDD) with nodal and nasal involvement. The authors mentioned that there are few reports about cytologic findings of RDD, and they refer to only four articles, dated 1990-1992.

In an issue of Diagnostic Cytopathology published in 1993, we reported on a case of extranodal RDD involving both breasts in a 71-yr-old female diagnosed by fine-needle aspiration (FNA). 2 Our cytologic findings were very similar to those referred to by Alvarez Alegret et al., 1 i.e., poor showing of centroblasts and immunoblasts, frequent plasma cells together with lymphohistiocytic aggregates, numerous histiocytes with broad cytoplasm, and a vesicular nucleus that occasionally showed a prominent nucleolus and slight atypia. Lymphocytophagocytosis (emperipolesis) was seen more easily in Pap-stained smears than in Diff-Quik-stained smears.

We believe that the cytologic pattern of RDD as seen in FNA aspirates is unmistakable, and permits a confident diagnosis of this entity.


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## Sinus histiocytosis with massive lymphadenopathy (SHML) is a benign, self-limiting condition of unknown etiology, which generally presents as massive bilateral cervical lymphadenopathy. It is important to distinguish SHML from other causes of histiocytosis because of the different treatment modal