Cutaneous Leukemic Infiltrates Successfully Treated With Biomodulatory Therapy in a Rare Case of Therapy-Related High Risk MDS/AML
Overview
Authors
Affiliations
Cutaneous manifestations in hematologic malignancies, especially in leukemia, are not common and may be very variable. Here we report a very unusual case of a patient (female, 70 years old) who was admitted to the hospital in 2016 because of skin lesions on the face, the trunk of the body and the extremities. She had a history of breast cancer in the year 2004 (pT1b, pN0, cM0, L0, V0, R0) which had been resected and treated with adjuvant radiation and chemotherapy (cyclophosphamide, methotrexate, 5-fluorouracile) as well as psoriasis treated with methotrexate and cyclosporine. Because of mild cytopenia a bone marrow aspirate/biopsy was performed showing myelodysplastic syndrome (MDS) with multilineage dysplasia. Cytogenetic review revealed a complex aberrant karyotype denoting adverse outcome. Simultaneously, a skin biopsy could confirm leukemic skin infiltration. Consequently, a therapy with azacitidine was started. After the first cycle the patient developed severe pancytopenia with a percentage of 13% peripheral blasts (previously 0-2%) as well as fever without evidence for infection which was interpreted as progressive disease. Therefore, the therapeutic regimen was changed to a biomodulatory therapy consisting of low-dose azacitidine 75 mg/day (given sc d1-7 of 28), pioglitazone 45 mg/day per os, and all-trans-retinoic acid (ATRA) 45 mg/m2/day per os. After cycle 1 of this combined biomodulatory therapy the patient showed hematologic recovery; besides a mild anemia (hemoglobin 11.1 g/dl) she developed a normal blood count. Moreover, the cutaneous leukemic infiltrates which had been unaffected by the azacitidine ameliorated tremendously after 2 cycles resulting in a complete remission of the skin lesions after cycle 6. In conclusion, we report a very unusual case with cutaneous infiltrates being the first clinical manifestation of hematologic disease, preceding the development of acute myeloid leukemia. While azacitidine alone was ineffective, a combined biomodulatory approach resulted in a complete remission of the cutaneous manifestation.
Harrer D, Luke F, Pukrop T, Ghibelli L, Reichle A, Heudobler D Cancers (Basel). 2024; 16(1).
PMID: 38201607 PMC: 10778239. DOI: 10.3390/cancers16010180.
Heudobler D, Luke F, Hahn J, Grube M, Schlosser P, Kremers S Haematologica. 2023; 109(4):1274-1278.
PMID: 37881883 PMC: 10985427. DOI: 10.3324/haematol.2023.283864.
Kleszcz R Cancers (Basel). 2023; 15(17).
PMID: 37686523 PMC: 10486994. DOI: 10.3390/cancers15174247.
Drug Repurposing by Tumor Tissue Editing.
Luke F, Harrer D, Pantziarka P, Pukrop T, Ghibelli L, Gerner C Front Oncol. 2022; 12:900985.
PMID: 35814409 PMC: 9270020. DOI: 10.3389/fonc.2022.900985.
Clinical characteristics, treatment, and prognosis of 118 cases of myeloid sarcoma.
Zhao H, Dong Z, Wan D, Cao W, Xing H, Liu Z Sci Rep. 2022; 12(1):6752.
PMID: 35474239 PMC: 9042854. DOI: 10.1038/s41598-022-10831-7.