Hale Daniel A, Krause John R
Department of Pathology (Hale) and the Division of Hematopathology (Krause), the Charles A. Sammons Cancer Center, Dallas, Texas, and Baylor University Medical Center at Dallas.
Proc (Bayl Univ Med Cent). 2017 Apr;30(2):192-194. doi: 10.1080/08998280.2017.11929581.
The genetic complexity of multiple myeloma is due in part to the accumulation of mutations, with primary and secondary events. One such secondary event is the development of a gene mutation that may result in overexpression of cyclin D1. The pathway involving cyclin D1 is intricately involved in cell cycle regulation from the G1 to S phase, and alterations may contribute to tumorigenesis. We present a case of cyclin D1-positive multiple myeloma with lymphoplasmacytic morphology and discuss potential diagnostic pitfalls and effects on prognosis.
多发性骨髓瘤的遗传复杂性部分归因于突变的积累,包括原发性和继发性事件。其中一个这样的继发性事件是基因突变的发生,这可能导致细胞周期蛋白D1的过表达。涉及细胞周期蛋白D1的通路在从G1期到S期的细胞周期调控中错综复杂地发挥作用,其改变可能有助于肿瘤发生。我们报告一例具有淋巴浆细胞形态的细胞周期蛋白D1阳性多发性骨髓瘤病例,并讨论潜在的诊断陷阱及其对预后的影响。