%0 Generic
%A B., Egenlauf
%A M., Schuhmann
%A T., Giese
%A T., Junghanss
%A M., Stojkovic
%A K., Tintelnot
%A S., deHoog
%A J., Greil
%A E., Richter
%A M., Vehresschild
%A C.P., Heussel
%A F.J.F., Herth
%A M., Kreuter
%D 2019
%T Supplementary Material for: Disseminated Mycosis by Arthrocladium fulminans Jeopardizing a Patient with GATA2 Deficiency
%U https://karger.figshare.com/articles/dataset/Supplementary_Material_for_Disseminated_Mycosis_by_b_i_Arthrocladium_i_b_b_i_fulminans_i_b_Jeopardizing_a_Patient_with_GATA2_Deficiency/7916417
%R 10.6084/m9.figshare.7916417.v1
%2 https://karger.figshare.com/ndownloader/files/14740130
%K Arthrocladium fulminans
%K Melanized fungus
%K MonoMAC
%K Immunodeficiency syndrome
%K GATA2
%K Mycobacterium sherrisii
%X GATA2 deficiency is characterized by monocytopenia, deficiency of dendritic cells, and a variable degree of lymphocytopenia affecting B cells and NK cells, leading to an enhanced risk of mycobacterial, viral, and fungal infections. Here we present a patient with a heterozygous intronic GATA2 mutation who acquired a fatal disseminated mycosis due to the black yeast-like fungus Arthrocladium fulminans following an infection with Mycobacterium sherrisii. This case illustrates that in patients with severe uncommon infections, immunodeficiency syndromes must be ruled out.
%I Karger Publishers