Yilmaz Asu Fergun, Soyer Nur, Ozsan Nazan, Cagirgan Seckin, Gunes Ajda, Comert Melda, Sahin Fahri, Saydam Guray, Gunel Nur Selvi, Vural Filiz
Hematology Department, Ataturk Training and Research Hospital, İzmir Katip Celebi University Hospital, İzmir, Turkey.
Hematology Department, Ege University Hospital, İzmir, Turkey.
Case Rep Hematol. 2017;2017:6350267. doi: 10.1155/2017/6350267. Epub 2017 Mar 21.
Myeloid or granulocytic sarcoma (GS) is a tumoral lesion consisting of immature granulocytic cells. It is a rare entity during the course of CML patients especially after allogeneic stem cell transplantation (SCT). Relapse without bone marrow involvement is much rarer. We report a case of CML patient who relapsed with isolated granulocytic sarcoma after allogeneic SCT during cytogenetic and molecular remission. 28-year-old male was diagnosed as CML and allogeneic SCT was performed because of refractory disease to tyrosine kinase inhibitors. Complete cytogenetic and molecular response was achieved after allogeneic SCT followed by dasatinib treatment. Approximately 5 years after the transplantation, very rapidly progressive lesion was documented and diagnosed as GS although he was at molecular and cytogenetic remission. The patient died during chemotherapy due to sepsis. GS relapse after allogeneic SCT is a very rare type of relapse in CML patients with molecular and cytogenetic remission. Since it is a very aggressive disease with a poor prognosis, combined chemoradiotherapies with other possible options like DLI or second allogeneic SCT should be considered as soon as the diagnosis is confirmed.
髓系或粒细胞肉瘤(GS)是一种由未成熟粒细胞组成的肿瘤性病变。在慢性粒细胞白血病(CML)患者病程中,尤其是异基因造血干细胞移植(SCT)后,它是一种罕见的情况。无骨髓受累的复发更为罕见。我们报告一例CML患者,在异基因SCT后处于细胞遗传学和分子学缓解期时,出现孤立性粒细胞肉瘤复发。一名28岁男性被诊断为CML,因对酪氨酸激酶抑制剂耐药而接受异基因SCT。异基因SCT后联合达沙替尼治疗,实现了完全的细胞遗传学和分子学缓解。移植后约5年,尽管患者处于分子学和细胞遗传学缓解期,但记录到一个进展非常迅速的病变,诊断为GS。患者在化疗期间因败血症死亡。异基因SCT后GS复发是分子学和细胞遗传学缓解的CML患者中一种非常罕见的复发类型。由于它是一种侵袭性很强、预后很差的疾病,一旦确诊,应尽快考虑联合放化疗以及其他可能的选择,如供者淋巴细胞输注(DLI)或第二次异基因SCT。