Sanders Daniel Steven, Fennell Thomas, Chisti Mohammad Muhsin
Department of Internal Medicine, McLaren-Oakland Hospital, Pontiac, Michigan, USA.
Department of Pathology, Oakland University William Beaumont Hospital, Royal Oak, Michigan, USA.
BMJ Case Rep. 2019 Apr 20;12(4):e227768. doi: 10.1136/bcr-2018-227768.
A patient with a diagnosis of myelodysplastic syndrome (MDS) with isolated 5q deletion underwent repeat bone marrow biopsy to assess haematological response after 6 months of initial lenalidomide therapy. Subsequent bone marrow biopsies revealed persistent MDS with del(5q) in addition to a small atypical mast cell population with >25% of mast cells with spindle-shaped morphology and immunohistochemistry characteristics consistent with mastocytosis. Molecular testing on the bone marrow was positive for D816V and the patient was diagnosed with systemic mastocytosis (SM) with an associated haematological neoplasm. MDS with SM is well known to be associated; however, to the best of our knowledge, only one prior case report identifies MDS with del(5q) and associated D816V positive mastocytosis. While the exact clonal origin of both chromosomal aberrations is unclear, this case illustrates the therapeutic efficacy of lenalidomide in a patient with MDS with del(5q) and rarely associated positive SM.
一名诊断为孤立性5q缺失的骨髓增生异常综合征(MDS)患者在接受来那度胺初始治疗6个月后,进行了重复骨髓活检以评估血液学反应。随后的骨髓活检显示持续性MDS伴del(5q),此外还有一小群非典型肥大细胞,其中>25%的肥大细胞具有纺锤形形态且免疫组化特征与肥大细胞增多症一致。骨髓的分子检测显示D816V呈阳性,该患者被诊断为系统性肥大细胞增多症(SM)伴相关血液肿瘤。MDS与SM相关是众所周知的;然而,据我们所知,之前仅有一例病例报告鉴定出伴有del(5q)和相关D816V阳性肥大细胞增多症的MDS。虽然两种染色体异常的确切克隆起源尚不清楚,但该病例说明了来那度胺对一名伴有del(5q)且很少伴有阳性SM的MDS患者的治疗效果。