Abdou Asmaa Gaber, Seleit Iman, Bakry Ola Ahmed, Abdel-Wahed Moshira Mohammed
Dr. Asmaa Gaber Abdou , Department of Pathology, Faculty of medicine, Menofiya University, Shebein Elkom, Egypt;
Acta Dermatovenerol Croat. 2013;21(3):189-92.
Acute myeloid leukemia (AML) is a clonal expansion of myeloid blasts in peripheral blood, bone marrow, or other tissues. Cutaneous manifestations of leukemia are either specific or nonspecific. Specific lesions result from direct infiltration of the skin by leukemic cells. We present a case of myeloid leukemia cutis manifested by erythematous asymptomatic nodules and plaques distributed on the chest, abdomen and back. The clinical and histopathologic features of the cutaneous infiltrate were suggestive of hematolymphoid malignancy, more towards lymphoma. However, the immunohistochemical features were against the diagnosis of lymphoma and were highly suspicious of myeloid leukemia, which were concomitantly confirmed by bone marrow biopsy and blood smear. In any poorly differentiated malignant skin infiltrate of confirmed hematopoietic lineage, myeloid differentiation should be considered and excluded by an appropriate panel. CD56+ AML is a rare type of AML that has special features like the great liability of extramedullary involvement including skin, monocytic characteristic of leukemia cells, and absence of myeloperoxidase expression.
急性髓系白血病(AML)是外周血、骨髓或其他组织中髓系母细胞的克隆性增殖。白血病的皮肤表现可分为特异性或非特异性。特异性病变是由白血病细胞直接浸润皮肤所致。我们报告一例皮肤型髓系白血病,表现为分布于胸部、腹部和背部的无症状红斑性结节和斑块。皮肤浸润的临床和组织病理学特征提示血液淋巴系统恶性肿瘤,更倾向于淋巴瘤。然而,免疫组化特征不支持淋巴瘤的诊断,高度怀疑为髓系白血病,骨髓活检和血液涂片同时证实了这一诊断。在任何确诊为造血谱系的低分化恶性皮肤浸润中,都应考虑髓系分化,并通过适当的检测排除。CD56+ AML是一种罕见的AML类型,具有特殊特征,如髓外浸润(包括皮肤)的易感性高、白血病细胞具有单核细胞特征以及缺乏髓过氧化物酶表达。