Prystowsky J H, Johnson B L, Bolwell B J, Lazarus G S
Department of Dermatology, University of Pennsylvania, School of Medicine, Philadelphia.
Am J Med. 1989 Apr;86(4):477-80. doi: 10.1016/0002-9343(89)90351-3.
In this report, we have presented our experience with a patient with a rare cutaneous granulocytic sarcoma. In addition to hematoxylin and eosin, myeloperoxidase stain and specific stains for lysozyme and esterase were helpful in confirming the histologic diagnosis of granulocytic sarcoma. Despite multiple attempts to control this patient's tumor by conservative surgery, radiation therapy, and chemotherapy, we eventually had to resort to limb amputation. This procedure restored a meaningful quality of life to this patient for one and a half years prior to the development of acute leukemia. Treatment with corticosteroids at the time of surgery may have prevented a local recurrence of granulocytic sarcoma despite positive tissue margins. Our experience underscores the importance of directing treatment toward the granulocytic sarcoma whereas the myelodysplasia concurrently present may not require therapy for several years.
在本报告中,我们介绍了我们对一名患有罕见皮肤粒细胞肉瘤患者的治疗经验。除苏木精和伊红染色外,髓过氧化物酶染色以及溶菌酶和酯酶的特异性染色有助于确诊粒细胞肉瘤的组织学诊断。尽管多次尝试通过保守手术、放射治疗和化疗来控制该患者的肿瘤,但我们最终不得不采取截肢手术。在急性白血病发生前的一年半时间里,这一手术为该患者恢复了有意义的生活质量。手术时使用皮质类固醇治疗可能预防了粒细胞肉瘤的局部复发,尽管手术切缘组织呈阳性。我们的经验强调了针对粒细胞肉瘤进行治疗的重要性,而同时存在的骨髓发育异常可能在数年内无需治疗。