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Editorial
. 2023 Apr;70(4):e30060.
doi: 10.1002/pbc.30060. Epub 2022 Nov 1.

Concurrence of a kinase-dead BRAF and an oncogenic KRAS gain-of-function mutation in juvenile xanthogranuloma

Markus G Seidel  1   2 , Luka Brcic  3 , Gerald Hoefler  3 , Caroline Hutter  4   5 , Milen Minkov  4   6 , Laura Sophie Steffen  1 , Armin Zebisch  7   8 , Martin Benesch  1
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Editorial

Concurrence of a kinase-dead BRAF and an oncogenic KRAS gain-of-function mutation in juvenile xanthogranuloma

Markus G Seidel et al. Pediatr Blood Cancer. 2023 Apr.
No abstract available

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References

REFERENCES

    1. Weitzman S, Jaffe R. Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses. Pediatr Blood Cancer. 2005;45(3):256-264.
    1. Büttgen K, Levy M. Juvenile xanthogranuloma (JXG). In: Corona R, ed. UpToDate ®. Wolters Kluwer; 2021.
    1. Rajendra B, Duncan A, Parslew R, Pizer BL. Successful treatment of central nervous system juvenile xanthogranulomatosis with cladribine. Pediatr Blood Cancer. 2009;52(3):413-415.
    1. Maintz L, Wenzel J, Irnich M, Reinhard H, Bieber T. Successful treatment of systemic juvenile xanthogranulomatosis with cytarabine and 2-chlorodeoxyadenosine: case report and review of the literature. Br J Dermatol. 2017;176(2):481-487.
    1. Histiocyte_Society, Histiocytosis NACf, Minkov M. NCT02205762: LCH-IV, International Collaborative Treatment Protocol for Children and Adolescents With Langerhans Cell Histiocytosis. Vol. 2022. U.S. National Library of Medicine: National Institutes of Health; 2014.

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