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Primary sellar lymphoma of T-cell type radiologic and pathologic findings

机译:T细胞型原发性蝶鞍淋巴瘤的影像学和病理学发现

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摘要

We present the clinical, imaging and pathological findings of a case of primary sellar lymphoma of T-cell type with aggressive bony destruction. While reports of primary sellar lymphoma have been exceedingly rare, most of these are cases of B-cell lymphoma. Only two cases of sellar lymphoma of T-cell have been described in the literature. While evaluating an invasive sellar mass with extensive bone destruction, this diagnosis should be considered particularly in elderly or immunocom-promized patients.A 60-year-old female presented with progressively increasing history of headache which was initially localized and later became generalized. Associated symptoms were vomiting, facial weakness on the left side and ptosis of the right eye. There was no history of fever. Past medical history was significant only for hypertension. The patient was immunocompetent with no history of HIV.
机译:我们目前的临床,影像学和病理发现一例侵袭性骨破坏的T细胞型原发性蝶鞍淋巴瘤。尽管原发性蝶鞍淋巴瘤的报道极为罕见,但其中大多数是B细胞淋巴瘤。文献中仅描述了2例T细胞鞍状淋巴瘤。在评估具有广泛骨破坏的侵袭性蝶鞍肿块时,尤其应考虑对老年患者或免疫功能低下的患者进行诊断。一名60岁女性的头痛病史逐渐增多,最初是局部性的,后来逐渐普及。相关症状包括呕吐,左侧面部无力和右眼上睑下垂。没有发烧史。既往病史仅对高血压有意义。该患者具有免疫能力,无HIV病史。

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