多发性骨髓瘤伴伴慢性特发性骨髓纤维化。

U Schmidt, M Ruwe, L D Leder
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引用次数: 0

摘要

多发性骨髓瘤偶尔表现出类似慢性特发性骨髓纤维化的骨髓病变。在本研究中,描述了这种“骨髓纤维化”骨髓瘤的穿刺活检组织学,并将其与慢性淋巴细胞白血病过程中发生的真正的慢性特发性骨髓纤维化病例进行了比较。骨髓纤维化骨髓瘤的特征是骨髓浆细胞浸润,伴有骨硬化、骨髓纤维化和局灶性巨核细胞增生。这些骨髓瘤与更常见的多发性骨髓瘤有单纯性骨髓纤维化和/或骨硬化。此外,“骨髓纤维化”骨髓瘤与真正的慢性特发性骨髓纤维化共存的骨髓瘤并不相同,后者似乎非常罕见,只有在明确证实局灶性巨核细胞增生伴非典型性时才应诊断。为了避免对“骨髓纤维化”骨髓瘤的误解,需要了解这些不同的骨髓瘤变体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple myeloma with bone marrow biopsy features simulating concomitant chronic idiopathic myelofibrosis.

Multiple myelomas occasionally exhibit bone marrow lesions simulating a concomitant chronic idiopathic myelofibrosis. In the present study, trephine biopsy histologies of such "myelofibrotic" myelomas are described and compared to those from a case of true chronic idiopathic myelofibrosis which developed in the course of chronic lymphocytic leukaemia. "Myelofibrotic" myeloma are characterized by osteosclerosis, marrow fibrosis and focal megakaryocytic hyperplasia in the presence of plasma cell infiltration of the bone marrow. These myelomas are to be distinguished from the more commonly occurring multiple myeloma with simple marrow fibrosis and/or osteosclerosis. Furthermore, "myelofibrotic" myelomas are not identical to myelomas coexisting with true chronic idiopathic myelofibrosis, a condition which would appear to be extremely rare and should only be diagnosed if focal megakaryocytic hyperplasia with atypia can be unequivocally demonstrated. Avoidance of misinterpretation of "myelofibrotic" myeloma requires a knowledge of these different myeloma variants.

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