Inoue Morihiro, Hagihara Masao, Uchida Tomoyuki, Hua Jian, Nakajima Takeshi, Tajima Shogo, Ota Yasunori
Depatment of Hematology, Eiju General Hospital, Japan.
Department of Opthalmology, Eiju General Hospital, Japan.
Intern Med. 2017 Dec 15;56(24):3341-3346. doi: 10.2169/internalmedicine.8617-16. Epub 2017 Oct 11.
A 48-year-old man was admitted due to marked leukocytosis. Bone marrow examinations resulted in a diagnosis of Philadelphia (Ph) chromosome-positive chronic myeloid leukemia. One month later, massive muscle and bone invasion by leukemic cells was detected. After induction chemotherapy, he complained of a headache and visual loss, which was caused by a leukemic infiltration in the central nervous system. After temporary remission in response to chemotherapy, the disease relapsed in the form of an intracranial tumor. The unusual t(14;22)(q24;q11.2) translocation of the Ph-chromosome and the significant increase in monocytes observed might have contributed to the unique and aggressive clinical course.
一名48岁男性因明显的白细胞增多症入院。骨髓检查确诊为费城(Ph)染色体阳性慢性髓性白血病。一个月后,检测到白血病细胞大量侵袭肌肉和骨骼。诱导化疗后,他出现头痛和视力丧失,这是由中枢神经系统的白血病浸润引起的。化疗后短暂缓解后,疾病以颅内肿瘤的形式复发。观察到的Ph染色体不寻常的t(14;22)(q24;q11.2)易位以及单核细胞的显著增加可能导致了独特且侵袭性的临床病程。