鼻窦异位垂体腺瘤的诊断

IF 0.1 Q4 PATHOLOGY AJSP: reviews & reports Pub Date : 2021-01-01 DOI:10.1097/PCR.0000000000000454
D. Berry, D. Ornan, M. Lopes
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引用次数: 0

摘要

补充的数字内容可在文本中找到。异位垂体腺瘤(EPAs)是一种罕见的鼻窦肿瘤,在实践中提出了诊断挑战。我们提出一个病例的病人表现为进行性头痛。检查发现前斜坡处有一个增强肿块,并延伸至蝶窦。手术切除肿瘤,镜检显示为神经内分泌肿瘤,单形细胞呈巢状排列。肿瘤表达synaptophysin、chromogranin、生长激素、催乳素、促甲状腺激素、促卵泡激素、α-糖蛋白亚基、转录因子steridogenic factor 1、Pit-1,诊断为多激素垂体腺瘤。鉴于放射学和手术的印象是一个完整的和未受累的垂体,病变被确定为垂体腺瘤产生于异位腺垂体组织。本病例显示多种可能的组织类型参与鼻腔肿瘤的组织形成。我们强调鼻窦垂体腺瘤的影像学、术中、细胞学和组织学特征,以强调扩大鉴别的作用,包括中枢神经系统病变,在这个解剖区域的肿瘤。
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Diagnosis of Sinonasal Ectopic Pituitary Adenomas
Supplemental digital content is available in the text. Abstract Ectopic pituitary adenomas (EPAs) are uncommon sinonasal neoplasms that present a diagnostic challenge in practice. We present a case of a patient presenting with progressive headache. Workup revealed an enhancing mass on magnetic resonance imaging at the anterior clivus with extension into the sphenoid sinus. Resection of the tumor was performed, and microscopic examination showed a neuroendocrine tumor composed of monomorphic cells arranged in nests. The tumor expressed synaptophysin, chromogranin, growth hormone, prolactin, thyroid-stimulating hormone, follicle-stimulating hormone, α-subunit of the glycoproteins, and transcription factors steroidogenic factor 1 and Pit-1, diagnosed as a plurihormonal pituitary adenoma. Given the radiologic and surgical impression of an intact and uninvolved pituitary gland, the lesion was identified as a pituitary adenoma arising in ectopic adenohypophyseal tissue. This case demonstrates the multitude of possible tissue types involved in tumor histogenesis in the sinonasal cavity. We highlight the radiographic, intraoperative, cytologic, and histologic features of sinonasal pituitary adenoma to emphasize the role of an expanded differential, including central nervous system lesions, for neoplasms in this anatomic region.
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