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pubmed-article:907235pubmed:issue6-7lld:pubmed
pubmed-article:907235pubmed:dateCreated1977-11-25lld:pubmed
pubmed-article:907235pubmed:abstractTextA four-year old boy with familial erythrophagocytic lymphohistiocytosis is reported. The clinical picture was that of prolonged fever, hepato and splenomegaly, adenopathies and, in the terminal state, bleeding tendency and sligth jaundice. The laboratory data showed anemia, leucopenia and abnormal coagulation studies compatibles with disseminated intravascular clotting. The differential diagnosis with malignant histiocytosis is attempted from a histological point of view.lld:pubmed
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pubmed-article:907235pubmed:authorpubmed-author:Navarro...lld:pubmed
pubmed-article:907235pubmed:authorpubmed-author:González...lld:pubmed
pubmed-article:907235pubmed:authorpubmed-author:PinedaGGlld:pubmed
pubmed-article:907235pubmed:authorpubmed-author:Camacho...lld:pubmed
pubmed-article:907235pubmed:authorpubmed-author:Sosa AlamoRRlld:pubmed
pubmed-article:907235pubmed:authorpubmed-author:Alvarez...lld:pubmed
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pubmed-article:907235pubmed:volume10lld:pubmed
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pubmed-article:907235pubmed:pagination565-70lld:pubmed
pubmed-article:907235pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:907235pubmed:articleTitle[Familial erythrophagocytic lymphohistiocytosis (author's transl)].lld:pubmed
pubmed-article:907235pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:907235pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:907235pubmed:publicationTypeCase Reportslld:pubmed