今年16岁的越越(化名)本该在校园里读书，却被一种罕见的怪病击垮。去年3月份开始，越越出现头痛、呕吐等症状，后来逐渐失去行动能力。医生称，越越的病在医院领域非常罕见，在全国屈指可数。

The more the 16 years old of this year(alias)Should be read in the campus,But a rare kind of strange disease eat up.Beginning march last year,The more the more appear have a headache/Symptoms such as vomiting,Then gradually lose action ability.Doctors say,The more the disease in the hospital field is very rare,In the national can be counted on one's fingers.

　　“去年3月份，越越突发头痛，刚开始以为只是感冒，但反反复复一直没好，之后我们去了多家医院，都不能确诊”，越越的母亲说，去年11月底，女儿在北京协和医院被确诊患上了“黏液性毛细胞星形细胞瘤”，该病在全国仅出现过3例。从此，越越离开了校园。

"In march last year,The more the sudden headache,Just began to think that just a cold,But repeated hasn't been good,Then we went to many hospitals,Can diagnose",The more the mother said,By the end of November last year,Daughter at Beijing union hospital was diagnosed with the"Mucus sex hair cell astrocytoma",The disease in the national only appeared in 3 patients.From now on,The more the left the campus.

　　昨天，北京协和医院神经外科医生介绍，“黏液性毛细胞星形细胞瘤”在医院领域非常罕见，在全国屈指可数。目前软脑膜已经播散合并脑积水，“经过治疗后她的病情已得到缓解，坚持治疗是完全有机会好转的。由于病情较复杂，一个月医疗费至少得一万元。”

yesterday,Beijing union medical college hospital neurosurgery doctor introduction,"Mucus sex hair cell astrocytoma"In the hospital field is very rare,In the national can be counted on one's fingers.At present pia mater has spread merger hydrocephalus,"After treatment after her illness has eased,Adhere to the treatment is completely have the chance to get better.Due to the illness is complicated,A month medical treatment at least ten thousand yuan."

　　为了维持越越的生命，一年来，在家务农的父母将家里所有的积蓄都花光了，还欠下了19万元的外债，“现在实在没办法了，希望好心人能帮忙给我女儿生存下去的机会。”(记者潘珊菊)

In order to maintain the life more,A year,Home soil parents will be home all spent all his savings,Still owe 190000 yuan RMB,"Now there is no way out,Hope good intention can help to my daughter's chance of survival."(Reporter PanShanJu)