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骨髓血管生成及巨核细胞c-Mpl表达在原发性血小板增多症中的诊断和预后价值

Diagnostic and prognostic value of bone marrow angiogenesis and megakaryocyte c-Mpl expression in essential thrombocythemia.

作者信息

Mesa Ruben A, Hanson Curtis A, Li Chin-Yang, Yoon Soo-Young, Rajkumar S Vincent, Schroeder Georgene, Tefferi Ayalew

机构信息

Division of Hematology and Internal Medicine, the Division of Hematopathology, and the Cancer Center Statistics Unit, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Blood. 2002 Jun 1;99(11):4131-7. doi: 10.1182/blood.v99.11.4131.

Abstract

The lack of diagnostic certainty in some patients makes it difficult to distinguish between primary and secondary forms of thrombocytosis. To augment current diagnostic studies for thrombocytosis, we retrospectively evaluated clinical records and bone marrow trephine specimens of 183 patients with thrombocytosis-164 with essential thrombocythemia (ET), 19 with reactive thrombocytosis (RT)-for bone marrow angiogenesis, bone marrow megakaryocyte c-Mpl staining, and morphologic evidence of megakaryocyte proliferation. Angiogenesis was increased in patients with ET compared with healthy controls (P <.0001) and patients with RT (P =.006). In addition, an increase in angiogenesis was associated with certain disease features such as splenomegaly (P =.004) and reticulin fibrosis (P =.005). Decreased megakaryocyte c-Mpl staining was observed in a heterogeneous pattern in ET compared with healthy controls (P <.0001) and RT (P <.0001). Histologic stratifying criteria incorporating increased angiogenesis, decreased megakaryocyte c-Mpl expression, and marked megakaryocyte proliferation in the bone marrow was highly sensitive (97%) and specific (95%) for distinguishing ET from RT (P <.0001). However, with the current duration of follow-up available on the patients, none of the histologic features evaluated have yet demonstrated prognostic value for subsequent clinical course, vascular events, or survival.

摘要

一些患者缺乏明确的诊断,这使得区分原发性和继发性血小板增多症变得困难。为了加强目前对血小板增多症的诊断研究,我们回顾性评估了183例血小板增多症患者的临床记录和骨髓活检标本,其中164例为原发性血小板增多症(ET),19例为反应性血小板增多症(RT),评估指标包括骨髓血管生成、骨髓巨核细胞c-Mpl染色以及巨核细胞增殖的形态学证据。与健康对照组(P <.0001)和RT患者(P =.006)相比,ET患者的血管生成增加。此外,血管生成增加与脾肿大(P =.004)和网状纤维增生(P =.005)等某些疾病特征相关。与健康对照组(P <.0001)和RT患者(P <.0001)相比,ET患者巨核细胞c-Mpl染色呈异质性降低。结合骨髓血管生成增加、巨核细胞c-Mpl表达降低和骨髓中显著的巨核细胞增殖的组织学分层标准,对区分ET和RT具有高度敏感性(97%)和特异性(95%)(P <.0001)。然而,根据目前患者的随访时间,所评估的组织学特征均未显示出对后续临床病程、血管事件或生存率的预后价值。

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