Nowakowska-Kopera Alicja, Wójcik Małgorzata, Rudzki Zbigniew, Gałazka Krystyna, Skotnicki Aleksander B
Uniwersytet Jagielloński w Krakowie, Collegium Medicum, Katedra i Klinika Hematologii.
Pol Merkur Lekarski. 2007 Aug;23(134):120-3.
A 65-year-old male patient initially presented with a penile tumour, identified as myeloid sarcoma. Subsequent bone marrow investigation revealed the presence of a synchronous plasma cell myeloma, without any evidence of a bone marrow-based myeloproliferative disorder. Although the course of both neoplasms was progressive, with increasing bone marrow involvement by the plasma cell myeloma and cutaneous dissemination of the myeloid sarcoma, both neoplasms remained confined to their original tissue compartments. Different biology of both tumours, including markedly divergent response to therapies, contributed to a significant clinical dilemma and finally to the patient demise 16 months after the presentation. While the association of plasma cell myeloma and various myeloid leukaemias is well documented, this is a first report of simultaneous occurrence of a myeloma and a myeloid sarcoma.
一名65岁男性患者最初表现为阴茎肿瘤,经鉴定为髓系肉瘤。随后的骨髓检查发现同时存在浆细胞骨髓瘤,且无任何基于骨髓的骨髓增殖性疾病证据。尽管两种肿瘤的病程均呈进行性,浆细胞骨髓瘤导致骨髓受累增加,髓系肉瘤出现皮肤播散,但两种肿瘤仍局限于其原始组织区域。两种肿瘤的生物学特性不同,包括对治疗的显著不同反应,这导致了严重的临床困境,最终患者在就诊16个月后死亡。虽然浆细胞骨髓瘤与各种髓系白血病的关联已有充分记录,但这是首例同时发生骨髓瘤和髓系肉瘤的报告。