Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4128374 | Annales de Pathologie | 2013 | 5 Pages |
Abstract
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.
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Authors
Damien Sizaret, Claire Lecointre, Rémy Kerdraon, Claire Bléchet, Carole Bonneau, Magda Alexis, François Camus, Patrick Michenet,