TY - JOUR
T1 - Cutaneous presentation of enteropathy-associated T-cell lymphoma masquerading as a DUSP22-rearranged CD30+ lymphoproliferation
AU - Bisig, Bettina
AU - Cairoli, Anne
AU - Gaide, Olivier
AU - Somja, Joan
AU - Bregnard, Cloé
AU - Gaulard, Philippe
AU - Xerri, Luc
AU - Lefort, Karine
AU - Missiaglia, Edoardo
AU - Gilliet, Michel
AU - Hohl, Daniel
AU - Guenova, Emmanuella
AU - de Leval, Laurence
N1 - © 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/10
Y1 - 2022/10
N2 - DUSP22 gene rearrangements are recurrent in systemic and cutaneous ALK-negative anaplastic large cell lymphomas, rarely encountered in other cutaneous CD30+ lymphoproliferations, and typically absent in other peripheral T-cell lymphomas. We report the case of a 51-year-old woman, with longstanding celiac disease and a rapidly enlarging leg ulcer, due to a DUSP22-rearranged CD30+ T-cell lymphoproliferation. Subsequent history revealed an intestinal enteropathy-associated T-cell lymphoma (EATL). Identical monoclonal TR gene rearrangements and mutations in STAT3 and JAK1 typical of EATL were present in the cutaneous and intestinal lesions. No DUSP22 rearrangement was detected in the patient's intestinal tumour, nor in 15 additional EATLs tested. These findings indicate that DUSP22 rearrangements are not entirely specific of ALCLs, may rarely occur as a secondary aberration in EATL, and expand the differential diagnosis of DUSP22-rearranged cutaneous CD30+ lymphoproliferative disorders.
AB - DUSP22 gene rearrangements are recurrent in systemic and cutaneous ALK-negative anaplastic large cell lymphomas, rarely encountered in other cutaneous CD30+ lymphoproliferations, and typically absent in other peripheral T-cell lymphomas. We report the case of a 51-year-old woman, with longstanding celiac disease and a rapidly enlarging leg ulcer, due to a DUSP22-rearranged CD30+ T-cell lymphoproliferation. Subsequent history revealed an intestinal enteropathy-associated T-cell lymphoma (EATL). Identical monoclonal TR gene rearrangements and mutations in STAT3 and JAK1 typical of EATL were present in the cutaneous and intestinal lesions. No DUSP22 rearrangement was detected in the patient's intestinal tumour, nor in 15 additional EATLs tested. These findings indicate that DUSP22 rearrangements are not entirely specific of ALCLs, may rarely occur as a secondary aberration in EATL, and expand the differential diagnosis of DUSP22-rearranged cutaneous CD30+ lymphoproliferative disorders.
KW - Female
KW - Humans
KW - Middle Aged
KW - Dual-Specificity Phosphatases/genetics
KW - Enteropathy-Associated T-Cell Lymphoma/diagnosis
KW - Ki-1 Antigen
KW - Lymphoma, Large-Cell, Anaplastic/diagnosis
KW - Lymphoma, T-Cell, Peripheral
KW - Mitogen-Activated Protein Kinase Phosphatases/genetics
KW - Receptor Protein-Tyrosine Kinases/genetics
KW - Skin Neoplasms/diagnosis
UR - https://www.scopus.com/pages/publications/85127395643
U2 - 10.1007/s00428-022-03309-4
DO - 10.1007/s00428-022-03309-4
M3 - Article
C2 - 35366115
SN - 1432-2307
VL - 481
SP - 653
EP - 657
JO - Virchows Archiv
JF - Virchows Archiv
IS - 4
ER -