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Case Reports
. 2021 Aug;62(3):e485-e487.
doi: 10.1111/ajd.13653. Epub 2021 Jun 22.

When histiocytoses are part of an ominous tetrad

Miguel Dominguez-Santas  1 , Irene Carretero-Barrio  2 , Ana Suarez-Valle  1 , Borja Diaz-Guimaraens  1 , Monica Garcia-Cosio  2 , Asuncion Ballester-Martínez  1 , Carmen Moreno-Garcia Del Real  2
Affiliations
Case Reports

When histiocytoses are part of an ominous tetrad

Miguel Dominguez-Santas et al. Australas J Dermatol. 2021 Aug.
No abstract available

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References

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    1. Classen C, Minkov M, Lehrnbecher T. The non-langerhans cell histiocytoses (rare histiocytoses) - Clinical aspects and therapeutic approaches. Klinische Pädiatrie. 2016; 228: 294-306.
    1. Wang K-H, Chen W-Y, Liu H-N et al. Cutaneous Rosai-Dorfman disease: clinicopathological profiles, spectrum and evolution of 21 lesions in six patients. Br J Dermatol. 2006; 154: 277-86.
    1. Hernández-San Martín MJ, Vargas-Mora P, Aranibar L. Juvenile xanthogranuloma: an entity with a wide clinical spectrum. Actas Dermo-Sifiliográficas 2020; 111: 725-33
    1. Zvulunov A, Barak Y, Metzker A. Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia. World statistical analysis. Arch Dermatol. 1995; 131: 904-8.

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