Literature DB >> 9931537

Intermittent hemophagocytic lymphohistiocytosis is a regular feature of lysinuric protein intolerance.

M Duval1, O Fenneteau, V Doireau, A Faye, D Emilie, P Yotnda, J C Drapier, N Schlegel, G Sterkers, H O de Baulny, E Vilmer.   

Abstract

We describe 4 cases of lysinuric protein intolerance, which all fulfilled the diagnostic criteria for hemophagocytic lymphohistiocytosis. Mature histiocytes and neutrophil precursors participated in hemophagocytosis in the bone marrow. Moreover, serum levels of ferritin and lactate dehydrogenase were elevated, hypercytokinemia was present, and soluble interleukin-2 receptor levels were increased up to 18.6-fold. The diagnosis of lysinuric protein intolerance should therefore be considered in any patient presenting with hemophagocytic lymphohistiocytosis.

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Year:  1999        PMID: 9931537     DOI: 10.1016/s0022-3476(99)70423-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  23 in total

1.  Langerhans histiocytosis, haemophagocytic syndrome and Epstein-Barr virus infection.

Authors:  Lucien Corbeel
Journal:  Eur J Pediatr       Date:  2004-07-09       Impact factor: 3.183

2.  A novel mutation of the transcobalamin II gene in an infant presenting with hemophagocytic lymphohistiocytosis.

Authors:  Selma Unal; Ozlem Tezol; Yesim Oztas
Journal:  Int J Hematol       Date:  2014-02-22       Impact factor: 2.490

3.  Wolman disease associated with hemophagocytic lymphohistiocytosis: attempts for an explanation.

Authors:  Roberta Taurisano; Arianna Maiorana; Fabrizio De Benedetti; Carlo Dionisi-Vici; Renata Boldrini; Federica Deodato
Journal:  Eur J Pediatr       Date:  2014-05-21       Impact factor: 3.183

Review 4.  Pediatric hemophagocytic lymphohistiocytosis.

Authors:  Scott W Canna; Rebecca A Marsh
Journal:  Blood       Date:  2020-04-16       Impact factor: 22.113

5.  Continuous Renal Replacement Therapy for Treatment of Severe Attacks of Inborn Errors of Metabolism.

Authors:  Ayse Filiz Yetimakman; Selman Kesici; Murat Tanyildiz; Benan Bayrakci
Journal:  J Pediatr Intensive Care       Date:  2019-03-27

6.  Occurrence of haemophagocytic lymphohistiocytosis at less than 1 year of age: analysis of 96 patients.

Authors:  Shinsaku Imashuku; Ikuyo Ueda; Tomoko Teramura; Kanako Mori; Akira Morimoto; Masahiro Sako; Eiichi Ishii
Journal:  Eur J Pediatr       Date:  2005-02-25       Impact factor: 3.183

7.  Secondary Hemophagocytic Syndrome Associated with COG6 Gene Defect: Report and Review.

Authors:  Nouf Althonaian; Abdulrahman Alsultan; Eva Morava; Majid Alfadhel
Journal:  JIMD Rep       Date:  2018-02-15

Review 8.  Congenital neutropenia: diagnosis, molecular bases and patient management.

Authors:  Jean Donadieu; Odile Fenneteau; Blandine Beaupain; Nizar Mahlaoui; Christine Bellanné Chantelot
Journal:  Orphanet J Rare Dis       Date:  2011-05-19       Impact factor: 4.123

Review 9.  Diagnosis of inherited disorders of liver metabolism.

Authors:  P T Clayton
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 10.  Inborn errors of metabolism underlying primary immunodeficiencies.

Authors:  Nima Parvaneh; Pierre Quartier; Parastoo Rostami; Jean-Laurent Casanova; Pascale de Lonlay
Journal:  J Clin Immunol       Date:  2014-08-01       Impact factor: 8.317

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