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pubmed-article:21649574pubmed:dateCreated2011-6-8lld:pubmed
pubmed-article:21649574pubmed:abstractTextHemophagocytic lymphohistiocytosis is a rare and often fatal disease that may occur in solid organ transplant recipients. Here, we describe 2 patients who developed hemophagocytic lymphohistiocytosis after having a lung transplant and present a review of all cases of hemophagocytic lymphohistiocytosis occurring in solid organ transplant recipients. Diagnosis of hemophagocytic lymphohistiocytosis relies on the association of clinical findings and the presence of hemophagocytosis. Clinical presentation is nonspecific and patients may present with unexplained sepsis or multiple organ failure. Management consists of treating the underlying process; but unfortunately, the prognosis is poor.lld:pubmed
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pubmed-article:21649574pubmed:authorpubmed-author:DongBeiBlld:pubmed
pubmed-article:21649574pubmed:authorpubmed-author:HayesDonDJrlld:pubmed
pubmed-article:21649574pubmed:authorpubmed-author:HobbsStephen...lld:pubmed
pubmed-article:21649574pubmed:authorpubmed-author:Diaz-GuzmanEn...lld:pubmed
pubmed-article:21649574pubmed:authorpubmed-author:KeslerMelissa...lld:pubmed
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pubmed-article:21649574pubmed:year2011lld:pubmed
pubmed-article:21649574pubmed:articleTitleHemophagocytic lymphohistiocytosis after lung transplant: report of 2 cases and a literature review.lld:pubmed
pubmed-article:21649574pubmed:affiliationDepartment of Internal Medicine, University of Kentucky College of Medicine, Lexington, KY, USA. enriquedgz@uky.edulld:pubmed
pubmed-article:21649574pubmed:publicationTypeJournal Articlelld:pubmed
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