Lencastre André, Cabete Joana, João Alexandre, Farinha Pedro, Ferreira Gilda, Lestre Sara
Centro Hospitalar de Lisboa Central, EPE, Hospital de Santo António dos Capuchos, Dermatology Service, Lisbon, Portugal.
Hospital Center of Central Lisbon, EPE, Santo António dos Capuchos Hospital, Dermatology Service, Lisbon, Portugal.
An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):158-61. doi: 10.1590/abd1806-4841.20132388.
Blastic plasmacytoid dendritic cell neoplasm is a rare and aggressive hematodermic neoplasia with frequent cutaneous involvement and leukemic dissemination. We report the case of a 76-year-old man with a 2 month history of violaceous nodules and a tumor with stony consistency, located on the head, and mandibular, cervical and supraclavicular lymphadenopathies. Multiple thoracic and abdominal adenopathies were identified on computerized tomography. Flow cytometry analysis of the skin, lymph node and bone marrow biopsies demonstrated the presence of plasmocytoid dendritic cell neoplastic precursor cells (CD4+, CD45+, CD56+ and CD123+ phenotype). After initial clinical and laboratorial complete remission with chemotherapy, the patient died due to relapse of the disease associated with the appearance of a cervical mass with medullary compromise.
母细胞性浆细胞样树突状细胞肿瘤是一种罕见且侵袭性的血液系统肿瘤,常累及皮肤并发生白血病播散。我们报告一例76岁男性患者,有2个月的紫罗兰色结节病史,头部有一个质地坚硬的肿瘤,伴有下颌、颈部和锁骨上淋巴结肿大。计算机断层扫描发现多个胸腹部淋巴结肿大。对皮肤、淋巴结和骨髓活检进行流式细胞术分析,显示存在浆细胞样树突状细胞肿瘤前体细胞(CD4+、CD45+、CD56+和CD123+表型)。患者经化疗后最初达到临床和实验室完全缓解,但因疾病复发伴颈部肿块出现并累及骨髓而死亡。