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Familial erythrophagocytic lymphohistiocytosis in infancy

✍ Scribed by Eva Gross-Kieselstein; Paulina Navon; D. Branski; A. Abrahamov; Lea Dollberg


Book ID
104775461
Publisher
Springer
Year
1981
Tongue
English
Weight
792 KB
Volume
136
Category
Article
ISSN
0340-6997

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✦ Synopsis


A 21/2-month-old infant suffering from pyrexia, purpura, hepatosplenomegaly, pancytopenia and hyperlipidemia is reported. Liver and spleen biopsies revealed mononuclear histiocytic infiltration with marked erythrophagocytosis. The girl died at 7I/2 months of age. Her brother died in infancy with an analogous clinical picture. The parents were first cousins. The clinical presentation and laboratory findings are consistent with the diagnosis of familial erythrophagocytic lymphohistiocytosis.


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