Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Absent radius

Missing radius bone associated with congenital failure of development.


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PMID (PMCID)
31006900
 OTHER
Langerhans cell histiocytosis and multiple reticulohistiocytomas in a patient with TAR syndrome: An association not previously described.
Hipolito LN, Mendoza-Cembranos MD, Villaescusa MT, Jo-Velasco M, Requena L, Alegria-Landa V.
J Cutan Pathol. 2019;:.
We describe a patient with thrombocytopenia-absent radius (TAR) syndrome, multisystemic Langerhans cell histiocytosis and multiple reticulohistiocytomas.
21428712
 MALE Child
Langerhans cell histiocytosis in a pediatric patient with thrombocytopenia-absent radius syndrome and 1q21.1 deletion: case report and proposal of a rapid molecular diagnosis of 1q21.1 deletion.
Giordano P, Cecinati V, Grassi M, Giordani L, De Mattia D, Santoro N.
Immunopharmacol Immunotoxicol. 2011;33(4):754-8.
We describe a child with thrombocytopenia-absent radius (TAR) syndrome in whom a refractory Langerhans cell histiocytosis (LCH) developed at 9 years.