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Chapter 52 Histiocytic Disorders 739

lymphohistiocytosis and not as X-linked lymphoproliferative disease. Risma K, Jordan MB: Hemophagocytic lymphohistiocytosis: updates and
Blood 116:1079, 2010. evolving concepts. Curr Opin Pediatr 24:9, 2012.
Marsh RA, Vaughn G, Kim MO, et al: Reduced-intensity conditioning Simko SJ, McClain KL, Allen CE: Up-front therapy for LCH: is it time to test
significantly improves survival of patients with hemophagocytic lympho- an alternative to vinblastine/prednisone? Br J Haematol 169(2):299–301,
histiocytosis undergoing allogeneic hematopoietic cell transplantation. 2015. doi: 10.1111/bjh.13208. [Epub 2014 Nov 16].
Blood 116:5824, 2010. Simko SJ, Tran HD, Jones J, et al: Clofarabine salvage therapy in refractory
Minkov M: Multisystem Langerhans cell histiocytosis in children: current multifocal histiocytic disorders, including Langerhans cell histiocytosis,
treatment and future directions. Paediatr Drugs 13:75, 2011. juvenile xanthogranuloma and Rosai-Dorfman disease. Pediatr Blood
Minkov M, Steiner M, Pötschger U, et al: International LCH Study Group: Cancer 61(3):479–487, 2014. doi: 10.1002/pbc.24772. [Epub 2013 Sep
reactivations in multisystem Langerhans cell histiocytosis: data of the 18].
international LCH registry. J Pediatr 153:700, 705, e701-702, 2008. Stepp SE, Dufourcq-Lagelouse R, Le Deist F, et al: Perforin gene defects in
Nelson DS, Quispel W, Badalian-Very G, et al: Somatic activating ARAF familial hemophagocytic lymphohistiocytosis. Science 286:1957, 1999.
mutations in Langerhans cell histiocytosis. Blood 123(20):3152–3155, Trottestam H, Horne A, Aricò M, et al: Histiocyte Society: Chemoimmuno-
2014. therapy for hemophagocytic lymphohistiocytosis: long-term results of the
Phillips M, Allen C, Gerson P, et al: Comparison of FDG-PET scans to HLH-94 treatment protocol. Blood 118:4577, 2011.
conventional radiography and bone scans in management of Langerhans Weitzman S, Jaffe R: Uncommon histiocytic disorders: the non-Langerhans
cell histiocytosis. Pediatr Blood Cancer 52:97, 2009. cell histiocytoses. Pediatr Blood Cancer 45:256, 2005.
Ravelli A, Grom AA, Behrens EM, et al: Macrophage activation syndrome Zhang K, Jordan MB, Marsh RA, et al: Hypomorphic mutations in PRF1,
as part of systemic juvenile idiopathic arthritis: diagnosis, genetics, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.
pathophysiology and treatment. Genes Immun 13:289, 2012. Blood 118:5794, 2011.
Rigaud S, Fondanèche MC, Lambert N, et al: XIAP deficiency in humans zur Stadt U, Schmidt S, Kasper B, et al: Linkage of familial hemophagocytic
causes an X-linked lymphoproliferative syndrome. Nature 444:110, lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identifica-
2006. tion of mutations in syntaxin 11. Hum Mol Genet 14:827, 2005.