Takakuwa Teruhito, Nakane Takahiko, Ohsawa Masahiko, Nagasaki Joji, Aoyama Yasutaka, Nishimoto Mistutaka, Hayashi Yoshiki, Kuwae Yuko, Hino Masayuki, Nakamae Hirohisa
Hematology, Graduate School of Medicine, Osaka City University, Japan.
Diagnostic Pathology, Graduate School of Medicine, Osaka City University, Japan.
Intern Med. 2018 Apr 15;57(8):1155-1158. doi: 10.2169/internalmedicine.9144-17. Epub 2017 Dec 21.
Isolated sarcoma with features of mixed-phenotype acute leukemia (MPAL) is an extremely rare disease and it can be easily misdiagnosed as lymphoma or other malignancies. We herein report the case of a 61-year-old woman with non-leukemic sarcoma of the right pleura, pretracheal lymph node, and supraclavicular lymph node with features of MPAL, B/myeloid, not otherwise specified, which was first misdiagnosed as diffuse large B cell lymphoma. After performing a detailed re-examination of the biopsy specimens, few scattered eosinophilic myelocytes allowed us to reach a correct diagnosis of MPAL and the patient was thereafter successfully treated by intensified chemotherapy followed by cord blood transplantation.
具有混合表型急性白血病(MPAL)特征的孤立性肉瘤是一种极其罕见的疾病,很容易被误诊为淋巴瘤或其他恶性肿瘤。我们在此报告一例61岁女性病例,其右胸膜、气管前淋巴结和锁骨上淋巴结发生非白血病性肉瘤,具有MPAL、B/髓系(未另行指定)的特征,最初被误诊为弥漫性大B细胞淋巴瘤。在对活检标本进行详细复查后,发现少数散在的嗜酸性髓细胞,从而使我们能够正确诊断为MPAL,此后患者通过强化化疗继以脐血移植成功得到治疗。