Girardot P M, Mathiot C, Validire P, Klijanienko J, Saidi A, Bessa E, Quintana E, Vielh P
Département de Pathologie, Institut Curie, Paris, France.
Diagn Cytopathol. 1996 Sep;15(3):237-40. doi: 10.1002/(SICI)1097-0339(199609)15:3<237::AID-DC12>3.0.CO;2-H.
The diagnosis of a case of childhood orbital granulocytic sarcoma, initially classified as a poorly-differentiated malignant tumor, was finally considered at the time of relapse following primary treatment with chemotherapy and local irradiation. At this time, systematic cerebrospinal fluid examination showed numerous blast cells with Auer rods, consistent with the diagnosis of meningeal acute myeloid leukemia of M2 type, and concomitant biopsy of the tumor indicated the diagnosis of chloroma. Reevaluation of the primary biopsy confirmed this diagnosis.
一名儿童眼眶粒细胞肉瘤病例,最初被归类为低分化恶性肿瘤,在接受化疗和局部放疗的初始治疗后复发时,最终得以确诊。此时,系统性脑脊液检查显示有大量带有奥氏小体的原始细胞,符合M2型脑膜急性髓系白血病的诊断,同时肿瘤活检表明为绿色瘤。对初次活检的重新评估证实了这一诊断。