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[Hemophagocytic lymphohistiocytosis associated with a lymphohistiocytic pattern anaplastic large cell lymphoma: a
Damien Sizaret1, Claire Lecointre, Rémy Kerdraon
1Service d'anatomie et de cytologie pathologiques, hôpital de la Source, Orléans cedex 2, France. dsizaret@gmail.com
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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