AI Article Synopsis

  • Skin involvement in chronic myelomonocytic leukemia (CMML) has been categorized as either specific or non-specific, with recent studies using advanced molecular techniques revealing that skin lesions may actually share clonal mutations found in bone marrow cells.
  • A case study of a 77-year-old man showed treatment-resistant granulomatous skin lesions before his CMML diagnosis, with matching genetic mutations identified in both his skin and bone marrow.
  • The lesions improved following treatment with azacytidine, highlighting how granulomatous skin lesions can serve as early indicators for diagnosing CMML, supported by a review of similar existing cases and their genetic profiles.

Article Abstract

Traditionally, skin involvement in chronic myelomonocytic leukemia (CMML) has been considered to be either specific (leukemia cutis) or non-specific, with granulomatous dermatitis included in the latter group. More recently, the true nature of the myeloid cells present in the cutaneous infiltrates of this theoretically reactive dermatitis is being clarified with the use of new molecular techniques such as next-generation sequencing. The same mutations in bone marrow (BM) myeloid neoplastic cells and in the cells of cutaneous infiltrates have been found. We present the case of a 77-year-old man who presented with spread and treatment-resistant skin granulomatous lesions previous to the diagnosis of CMML. The same clonal mutations in SRSF2, IDH1, and RUNX1 were found in both skin and BM with resolution of the lesions after the initiation of azacytidine. In conclusion, we report an exceptional case in which specific granulomatous cutaneous lesions have preceded and allowed the earlier diagnosis of an underlying CMML and a review of all previous similar cases in the literature, including molecular alterations.

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Source
http://dx.doi.org/10.1111/cup.14638DOI Listing

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