| Literature DB >> 17724571 |
M R Becker1, T Gaiser, R Rompel, P Middel.
Abstract
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, painless lymphoproliferative disorder of unknown origin with a usually benign course. About 40% of the patients show an extranodal involvement with skin being the most common site in 27% of these patients. We describe a patient with widespread disease involving the respiratory tract, kidneys and skin. Histopathology revealed the characteristic features of SHML with emperipolesis and immunohistochemical positivity of histiocytes for S100 and macrophage-associated antigens.Entities:
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Year: 2008 PMID: 17724571 DOI: 10.1007/s00105-007-1385-y
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751