Aims: This retrospective study aims to emphasize clinicopathological data and diagnosis of an uncommon myeloid neoplasm;
myeloid sarcoma. Methods: Data of all patients from 2000-2019 were retrieved from the archives of Trakya University School
of Medicine Hematology and Pathology Departments. Patients’ charts were examined retrospectively by collecting data including age, gender, anatomic site, history of hematological malignancy, blood count, pathological characteristics and treatments
administered. Results: There were 8 patients; 6 male and 2 female. The median age was 42.5 years (range: 29-69 years). The
most prevalently involved sites were skin, lymph node and bone/soft tissue. There were six patients as myeloid sarcoma with
preexisting or concurrent acute myeloid leukemia, one patient as de novo and one patient as acute myeloid leukemia with myelodysplasia related changes. One of the concurrent acute myeloid leukemia patients was Down syndrome related acute myeloid
leukemia with myeloid sarcoma. Immunohistochemically, out of 8 patients, 4 were of myelomonocytic, 2 were of the myelocytic
and 2 were of the monocytic differentiation. Conclusion: Myeloid sarcoma is a tumor mass made up of immature myeloid blasts
appearing at an anatomical site other than bone marrow. Taking into account of having a challenging diagnosis, unusual cellular
infiltration at any site on a patient especially with a history of acute myeloid leukemia should have myeloid sarcoma in their
differential diagnosis. Keywords: Myeloid sarcoma, acute myeloid leukemia, myeloid neoplasia
Birincil Dil | İngilizce |
---|---|
Konular | Klinik Tıp Bilimleri |
Bölüm | Olgu Sunumu |
Yazarlar | |
Yayımlanma Tarihi | 29 Şubat 2020 |
Gönderilme Tarihi | 9 Şubat 2020 |
Yayımlandığı Sayı | Yıl 2020 Cilt: 7 Sayı: 1 |