Lemierre's Syndrome as a Trigger for Secondary Hemophagocytic Lymphohistiocytosis.

J Pediatr Hematol Oncol

*Department of Pediatrics †Division of Pediatric Hematology-Oncology ‡Department of Pathology §Division of Pediatric Infectious Diseases, University of Virginia, Charlottesville, VA.

Published: August 2017

Secondary hemophagocytic lymphohistiocytosis (sHLH) is a rare hyperinflammatory disorder caused by an aberrant immune response to a number of infectious or inflammatory conditions. Successful treatment of this potentially fatal condition requires early recognition and prompt therapy directed at the underlying trigger. In this report, we describe the clinical presentation, diagnostic findings, management, and outcome of a child with Lemierre's syndrome-associated sHLH. This is the first reported association of these 2 rare conditions and expands the number of known triggers for sHLH.

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Source
http://dx.doi.org/10.1097/MPH.0000000000000755DOI Listing

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