Chang H, Shih L-Y, Kuo T-T
Division of Hematology-Oncology and Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University, 199 Tung Hwa North Road, Taipei, Taiwan, R.O.C.
Ann Hematol. 2003 Jul;82(7):435-9. doi: 10.1007/s00277-003-0673-6. Epub 2003 May 24.
Aleukemic myeloid leukemia cutis is extremely rare and is usually associated with early marrow relapse and poor treatment outcome. We report a 39-year-old man presenting with generalized cutaneous nodules. The initial diagnosis was cutaneous malignant lymphoma. New skin lesions and a nasopharyngeal mass developed during phototherapy. Biopsy of the cutaneous and nasopharyngeal lesions revealed monotonous blast cell infiltration. Cytochemical stain and immunophenotypic analysis of the fresh cell suspension made from another skin biopsy specimen identified that the neoplastic cells belonged to the monocytic lineage. A diagnosis of primary aleukemic leukemia cutis was established. The leukemic cells expressed CD56 but did not carry AML-1/ETO, CBFbeta/MYH11, or common MLL fusion transcripts. He received standard induction therapy for acute myeloid leukemia, followed by high-dose postremission chemotherapy and has been disease-free for more than 30 months. To the best of our knowledge, the current case has the longest disease-free survival among those reported.
无白血病性髓细胞性白血病皮肤表现极为罕见,通常与早期骨髓复发及不良治疗结果相关。我们报告一名39岁男性,表现为全身性皮肤结节。初始诊断为皮肤恶性淋巴瘤。光疗期间出现新的皮肤病变及鼻咽部肿物。皮肤及鼻咽部病变活检显示单一性原始细胞浸润。对另一皮肤活检标本制成的新鲜细胞悬液进行细胞化学染色及免疫表型分析,确定肿瘤细胞属于单核细胞系。确诊为原发性无白血病性白血病皮肤表现。白血病细胞表达CD56,但不携带AML-1/ETO、CBFβ/MYH11或常见的MLL融合转录本。他接受了急性髓细胞白血病的标准诱导治疗,随后进行了大剂量缓解后化疗,目前已无病生存超过30个月。据我们所知,该病例是已报道病例中无病生存期最长的。