Byrd J C, Edenfield W J, Dow N S, Aylesworth C, Dawson N
Division of Hematology-Oncology, Department of Internal Medicine, Walter Reed Army Medical Center and the Uniformed Services University of the Health Sciences, Washington, DC 20307, USA.
Leuk Lymphoma. 1996 Mar;21(1-2):153-9. doi: 10.3109/10428199609067593.
The purpose of this report is to record a patient with myelodysplastic syndrome (MDS) associated acute myelogenous leukemia (AML) and leukemia cutis who had blast expression of the neural cell adhesion molecule (NCAM) and to review the world literature on prognostic implications of extramedullary myeloid cell tumors (granulocytic sarcoma, myeloblastoma, chloroma and leukemia cutis) in MDS and MDS associated AML. Case report and world literature from January 1965-January 1994 for all cases of MDS-associated extramedullary myeloid cell tumors (EMT) is reviewed, and the first patient with EMT, MDS associated AML and blast expression of NCAM is described. There have been 46 cases of MDS associated EMT previously reported. 32 cases occurred in the absence of AML. AML developed in 47% of these patients at a mean of 38 weeks from initial EMT. Of the patients not developing AML, median survival from initial EMT was 11 weeks. Nine patients received chemotherapy at the time of EMT and had a median survival of 36 weeks. The median survival for patients receiving conservative therapy for EMT was 48 weeks. Patients (n = 15) with EMT and MDS associated AML had a poor outcome regardless of therapy with a median survival of 11 weeks. Unlike other forms of isolated EMT, MDS associated EMT is not always a forerunner of AML. Premature induction therapy for MDS associated EMT does not appear to prolong survival. EMT in the setting of MDS associated AML is associated with a poor prognosis despite aggressive chemotherapy. Blast expression of NCAM may prove to be a risk factor for EMT in MDS associated AML.
本报告旨在记录一名患有骨髓增生异常综合征(MDS)相关急性髓系白血病(AML)和白血病性皮肤浸润且具有神经细胞黏附分子(NCAM)原始细胞表达的患者,并回顾世界文献中关于髓外髓样细胞瘤(粒细胞肉瘤、成髓细胞瘤、绿色瘤和白血病性皮肤浸润)在MDS及MDS相关AML中的预后意义。回顾了1965年1月至1994年1月期间所有MDS相关髓外髓样细胞瘤(EMT)病例的病例报告及世界文献,并描述了首例患有EMT、MDS相关AML且具有NCAM原始细胞表达的患者。此前已报道46例MDS相关EMT病例。32例发生于无AML的情况下。这些患者中有47%在初次发生EMT后平均38周时发生AML。未发生AML的患者,从初次EMT起的中位生存期为11周。9例患者在发生EMT时接受了化疗,中位生存期为36周。接受EMT保守治疗的患者中位生存期为48周。患有EMT及MDS相关AML的患者(n = 15)无论接受何种治疗,预后均较差,中位生存期为11周。与其他形式的孤立性EMT不同,MDS相关EMT并不总是AML的先兆。对MDS相关EMT进行过早诱导治疗似乎并不能延长生存期。尽管进行了积极化疗,但MDS相关AML背景下的EMT预后较差。NCAM原始细胞表达可能被证明是MDS相关AML中EMT的一个危险因素。