Massier Anamaria, Scheithauer Bernd W, Taylor Harris C, Clark Christopher, Llerena Luis
Fairview Hospital, Cleveland Clinic Health System, 18101 Lorain Avenue, Cleveland, OH 44111, USA.
Endocr Pathol. 2007 Winter;18(4):233-8. doi: 10.1007/s12022-007-9010-2.
Primary pituitary sarcoma in the absence of previous radiation therapy is very rare, only eight cases having been reported. We present the first reported case of sclerosing epithelioid fibrosarcoma of the pituitary, a 56-year-old woman presenting with diplopia and panhypopituitarism. Magnetic resonance imaging showed a 1.2 x 0.4 x 0.5-cm sellar mass invading the right cavernous sinus. Despite surgery and radiation therapy, our patient developed intracranial metastases and died 2 years after the initial diagnosis. Sclerosing epithelioid fibrosarcoma is an infrequently occurring, distinct variant of soft tissue fibrosarcoma. Its immunophenotype includes vimentin and occasionally CD-34, B cell lymphoma-2, S-100 protein, or keratin expression. Although initially thought to be a low-grade lesion, sclerosing epithelioid fibrosarcomas may also behave in a high-grade manner.
在未接受过先前放射治疗的情况下,原发性垂体肉瘤非常罕见,仅报道过8例。我们报告了首例垂体硬化性上皮样纤维肉瘤病例,患者为一名56岁女性,表现为复视和全垂体功能减退。磁共振成像显示一个1.2×0.4×0.5厘米的鞍区肿块,侵犯右侧海绵窦。尽管进行了手术和放射治疗,我们的患者仍发生了颅内转移,并在初始诊断后2年死亡。硬化性上皮样纤维肉瘤是软组织纤维肉瘤中一种罕见的独特变体。其免疫表型包括波形蛋白,偶尔还有CD-34、B细胞淋巴瘤-2、S-100蛋白或角蛋白表达。尽管最初认为是低级别病变,但硬化性上皮样纤维肉瘤也可能表现为高级别病变。