Astall E, Yarranton H, Arno J, Marcus R
Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.
J Clin Pathol. 1999 Sep;52(9):705-7. doi: 10.1136/jcp.52.9.705.
Granulocytic sarcoma with no demonstrable abnormalities in the peripheral blood or bone marrow is a rare but recognised initial manifestation of acute myeloid leukaemia and has led to diagnostic difficulties in some cases. A lymph node excisional biopsy from a patient presenting with cervical lymphadenopathy, a mediastinal mass, and a normal peripheral blood picture was reported to have features suggesting a T cell non-Hodgkin lymphoma, for which she was subsequently treated. However, 10 months later the patient developed acute myeloid leukaemia, FAB classification M0. The initial lymph node biopsy was reviewed and further immunohistochemical studies using antibodies against CD34 led to a revised diagnosis of primary granulocytic sarcoma.
外周血或骨髓无明显异常的粒细胞肉瘤是急性髓系白血病一种罕见但已被认识的初始表现,在某些病例中导致了诊断困难。据报道,一名表现为颈部淋巴结病、纵隔肿块且外周血象正常的患者接受了淋巴结切除活检,其特征提示为T细胞非霍奇金淋巴瘤,随后她接受了相应治疗。然而,10个月后该患者发展为急性髓系白血病,FAB分类为M0。对最初的淋巴结活检进行了复查,并使用抗CD34抗体进行了进一步的免疫组化研究,从而将诊断修正为原发性粒细胞肉瘤。