Treaba Diana O, Khedr Salwa, Mangray Shamlal, Jackson Cynthia, Castillo Jorge J, Winer Eric S
Department of Pathology and Laboratory Medicine, Rhode Island Hospital, The Warren Alpert Medical School, Brown University, Providence, RI 02903, USA.
Case Rep Hematol. 2012;2012:875039. doi: 10.1155/2012/875039. Epub 2012 Aug 2.
Primary myelofibrosis (formerly known as chronic idiopathic myelofibrosis), has the lowest incidence amongst the chronic myeloproliferative neoplasms and is characterized by a rather short median survival and a risk of progression to acute myeloid leukemia (AML) noted in a small subset of the cases, usually as a terminal event. As observed with other chronic myeloproliferative neoplasms, the bone marrow biopsy may harbor small lymphoid aggregates, often assumed reactive in nature. In our paper, we present a 70-year-old Caucasian male who was diagnosed with primary myelofibrosis, and after 8 years of followup and therapy developed an AML. The small lymphoid aggregates noted in his bone marrow were neoplastic in nature and represented bone marrow involvement by a CD5-negative mantle cell lymphoma (MCL) that presented without any associated lymphadenopathy. We reviewed the English medical literature to identify a single case report of simultaneous association of AML and a MCL in the bone marrow. The unusual association presented here suggests an increase in observer awareness to apparently benign lymphoid aggregates in chronic myeloproliferative neoplasms.
原发性骨髓纤维化(以前称为慢性特发性骨髓纤维化)在慢性骨髓增殖性肿瘤中的发病率最低,其特征是中位生存期较短,在一小部分病例中存在进展为急性髓系白血病(AML)的风险,通常为终末期事件。与其他慢性骨髓增殖性肿瘤一样,骨髓活检可能有小的淋巴细胞聚集,通常认为其本质上是反应性的。在我们的论文中,我们报告了一名70岁的白种男性,他被诊断为原发性骨髓纤维化,经过8年的随访和治疗后发展为AML。在他骨髓中发现的小淋巴细胞聚集本质上是肿瘤性的,代表骨髓受CD5阴性套细胞淋巴瘤(MCL)累及,且无任何相关淋巴结病表现。我们查阅了英文医学文献,以确定一份关于AML与骨髓中MCL同时存在的单病例报告。这里呈现的这种不寻常关联提示临床医生应提高对慢性骨髓增殖性肿瘤中看似良性的淋巴细胞聚集的认识。