Granular cell tumor (GCT) at Sella turcica region is seldom reported, those with clinic symptom is even rare, there are altogether less than50 cases so far.
鞍区颗粒细胞瘤非常罕见，至今报道有症状的颗粒细胞瘤还不足50例。
According to these, this tumor can be differentiated from granular renal cell carcinoma, mixed renal cell carcinoma and chromophobe renal cell carcinoma.
据此，可与颗粒型肾细胞癌、混合型肾细胞癌及肾嫌色细胞癌鉴别。
Uneven expression was noted in tumor cell membrane, usually in granular shape.
在肿瘤细胞膜上表达分布不均，呈粗颗粒状。
Conclusion: Paraneoplastic neurological syndromes may appear in the patients with tumor or acute granular cell leukemia, and commonly signifies a poor prognosis.
结论：副肿瘤综合征可出现在实体肿瘤或白血病患者，它的出现几乎均预示着预后不良。
Conclusion: Paraneoplastic neurological syndromes may appear in the patients with tumor or acute granular cell leukemia, and commonly signifies a poor prognosis.
结论：副肿瘤综合征可出现在实体肿瘤或白血病患者，它的出现几乎均预示着预后不良。
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