Clonal cytopenia of undetermined significance and atypical Behcet's: the importance of zinc

被引:1
作者
Leonard, Patricia [1 ]
Louw, Alison [2 ]
Prentice, David [3 ]
Cirillo, Melita [4 ,5 ]
机构
[1] Curtin Univ, Sch Med, Bentley, WA, Australia
[2] PathWest Lab Med WA, Mol Haematol, Murdoch, WA, Australia
[3] Perron Inst Neurol & Translat Sci, Neurol, Nedlands, WA, Australia
[4] Royal Perth Hosp, Haematol, Perth, WA, Australia
[5] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA, Australia
关键词
Inflammatory bowel disease; Haematology (incl blood transfusion); Immunology; Malignant and Benign haematology; Vitamins and supplements; COPPER DEFICIENCY MYELONEUROPATHY; T-CELLS; DISEASE; RISK; NUMBER; LOCI;
D O I
10.1136/bcr-2021-247154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atypical Behcet's is recognised in myelodysplastic syndrome (MDS) cases and is associated with trisomy 8. Clonal cytopenia of undetermined significance (CCUS) is recognised as a precursor to MDS. Our case describes the presentation of atypical Behcet's, in association with CCUS, post a Streptococcal infection. A mutation of a zinc finger RNA spliceosome, ZRSR2, is also described. Our patient initially presented with macrocytic anaemia, together with neutropenia and lymphocytopenia on routine monitoring. Later gastrointestinal symptoms together with oral and anal ulcerations developed. He was treated with oral zinc therapy and had resolution of recurrent oral ulcerations and significant reduction in severity of anal ulcerations. The functional impact of ZRSR2 mutation on spliceosome assembly is yet to be defined, but has been previously reported in CCUS with a clinical phenotype of macrocytic anaemia.
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