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SHML
Wednesday 5 October 2005
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease, is a disorder of unknown cause.
Synopsis
bilateral cervical lymphadenopathy, fever, leukocytosis and polyclonal gammopathy
nodal histiocytosis
bilateral cervical lymphadenopathy
emperipolesis
S100+ CD1a- macrophages
Etiology
rare germline mutations TNFRSF6 coding for FAS protein (CD95/ApoI)
autoimmune lymphoproliferative syndrome (ALPS) (15958855)
Localization
lymph node (nodal SHML)
extranodal SHML
- uveitis and subconjunctival masses (12479625)
- breast (10740798, 10740798)
- pancreas (10370692)
- cutaneous SHML (10494712) and diffuse muco-cutaneous SHML (9870677)
- intramedullary spinal cord SHML (9067506)
- renotesticular SHML (9031615)
Associations
autoimmune lymphoproliferative syndrome (ALPS) (15958855)
HIV infection (9818538, 1926767)
HHV6 infection (1321861)
malignant lymphoma (15468978) +/- same lymph node (10786808)
- diffuse large B-cell lymphoma (15468978)
- follicular lymphoma
- nodular lymphocyte predominant type Hodgkin lymphoma (NLPHL) (8522313)
generalized AA amyloidosis (10836304)
rare occurrence in identical twins (ALPS ?) (3345128)
idiopathic hypereosinophilic syndrome (3606023)
Differential diagnosis
autoimmune lymphoproliferative syndrome (ALPS) (15958855)
Toxoplasma lymphadenitis (nodal toxoplasmosis) (15291364)
References
Foucar E, Rosai J, Dorfman R. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Semin Diagn Pathol. 1990 Feb;7(1):19-73. PMID: 2180012