1.
Ann Pathol
; 33(4): 278-82, 2013 Aug.
Artigo
em Francês
| MEDLINE
| ID: mdl-23954124
RESUMO
We report the case of a 16-year-old girl with an anaplastic large cell lymphoma of lymphohistiocytic pattern revealed by a hemophagocytic syndrome. Histologically, the lymphomatous population was concealed by clusters of histiocytes. Immunohistochemical study allowed the diagnosis. The combination of these two entities is rarely described and may be a source of delay in diagnosis of a life-threatening condition.