Polycythemia secondary to cerebellar hemangioblastoma
Polycythemia secondary to cerebellar hemangioblastoma
复制标题
小脑血管母细胞瘤继发的红细胞增多症
DOI:
10.1002/ajh.10196
复制
发表时间:
2002
影响因子:
12.8
通讯作者:
L. Ho
中科院分区:
文献类型:
--
作者:
C. So;L. Ho
A 49-year-old man presented with facial flushing and headache. His general practitioner had initially attributed these symptoms to his elevated blood pressure and prescribed anti-hypertensive therapy. However, the headaches failed to improve. In addition, the patient developed increasing difficulty walking and a variety of other neurological symptoms. He was therefore admitted to the hospital. His past medical history revealed that a craniotomy had been performed 20 years earlier, at which time a “brain tumor” had been resected. On physical examination, the patient was found to have unequal pupil size, bilateral papilloedema, sensorineural deafness, and upper motor neuron signs in both lower limbs.