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Malignant adenohypophysis spindle cell oncocytoma with repeating recurrences and a high Ki-67 index

机译:恶性腺垂体梭形细胞瘤重复复发Ki-67指数高

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摘要

Adenohypophysis spindle cell oncocytoma (ASCO) is a rare tumor recently reported by Roncaroli et al in 2002. This tumor is considered a grade I tumor by the World Health Organization.We report a rare case of malignant ASCO with repeating recurrences and a high Ki-67 index—a challenging diagnosis guided by clinical presentations, radiological signs, and postoperative pathological tests.We represent a 30-year-old man who had suffered from headaches, diplopia, and impaired visual field and acuity. His magnetic resonance imaging revealed an abnormal sellar mass and was originally misdiagnosed as a pituitary macroadenoma. We present detailed analysis of the patient's disease course and review relevant literature.When surgically treated, the specimen revealed a typical histopathology pattern of ASCO. The tumor recurred for several times and the patient underwent 3 surgeries and 1 γ-knife treatment, which was accompanied by a continuously increasing Ki-67 index.This is the first reported case of malignant ASCO (WHO III–IV grade). Despite its rarity, ASCO should be considered in the differential diagnosis of sellar lesions that mimic pituitary adenomas.
机译:腺垂体梭状细胞瘤细胞瘤(ASCO)是Roncaroli等人于2002年最近报道的一种罕见肿瘤。世界卫生组织将该肿瘤视为I级肿瘤。 67指数-以临床表现,放射学迹象和术后病理检查为指导的具有挑战性的诊断。我们代表一名30岁的男子,他患有头痛,复视,视野和视力受损。他的磁共振成像显示异常鞍状肿块,最初被误诊为垂体大腺瘤。我们对患者的病程进行了详细分析,并复习了相关文献。通过手术治疗后,标本显示出典型的ASCO病理组织学模式。肿瘤复发了几次,患者接受了3次手术和1次γ刀治疗,并伴有Ki-67指数的持续升高。这是第一例恶性ASCO(WHO III–IV级)报道。尽管罕见,但在鉴别垂体腺瘤的鞍状病变的鉴别诊断中应考虑使用ASCO。

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