[Acidophil stem cell pituitary neuroendocrine tumors/adenoma: a clinicopathological analysis of five cases].

L Lou, S X Du, Y T Fu, Q Q Shao, W L Guo, Y P Zong, M M Qin, X X Tian, Y H Li
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Abstract

Objective: To investigate the clinicopathological characteristics of acidophil stem cell pituitary neuroendocrine tumors (PitNET)/adenoma. Methods: Five cases of acidophil stem cell PitNET/adenoma were diagnosed between May 2022 and July 2023 at the Second Hospital of Hebei Medical University, Shijiazhuang, China. The clinicopathological features of the tumor were analyzed by using histology, immunohistochemistry, and electron microscopy. The relevant literature was reviewed. Results: There were 1 male and 4 females, aged from 23 to 69 years. Patient 3 was 55 years old at the time of diagnosis and first surgery, and relapsed 5 years later. The patients' median age was 32 years. Patients 1 and 5 showed elevated blood prolactin, with various degrees of hormonal symptoms except Patient 3, who showed only tumor compression symptoms. Imaging studies showed that all cases involved the sellar floor. The tumors of Patients 1, 2 and 5 were closely related to the cavernous sinus segment of the internal carotid artery. The tumors exhibited a diffuse growth pattern with chromophobic to slightly acidophilic cytoplasm. A few of tumor cells showed chromophobic cytoplasm. The nucleoli were conspicuous. Intranuclear inclusion bodies and variably-sized clear vacuoles were observed occasionally. Under electron microscope, marked mitochondrial abnormalities were observed, including increased mitochondria number, expanded hypertrophy, and absence of mitochondrial ridge fracture. Some mitochondrial matrices were dense, while some were vacuolated. Conclusions: Acidophil stem cell PitNET/adenoma is a rare type of pituitary adenomas/PitNETs. It often has a more clinically aggressive manner with immature cells, diffuse expression of PIT1, prolactin, and varying degrees of growth hormone expression. Because of the obvious diversity of their clinical hormone status and hormone immune expression, the diagnosis of this type tumor is still a challenge.

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[嗜酸性干细胞垂体神经内分泌肿瘤/腺瘤:五例病例的临床病理分析]。
研究目的研究嗜酸性干细胞垂体神经内分泌肿瘤(PitNET)/腺瘤的临床病理特征。方法2022年5月至2023年7月在河北医科大学第二医院确诊的5例嗜酸性干细胞垂体神经内分泌肿瘤(PitNET)/腺瘤。通过组织学、免疫组化和电子显微镜分析了肿瘤的临床病理特征。并查阅了相关文献。结果:患者中有 1 名男性和 4 名女性,年龄从 23 岁到 69 岁不等。患者 3 在确诊和首次手术时 55 岁,5 年后复发。患者的中位年龄为 32 岁。除患者 3 仅表现出肿瘤压迫症状外,患者 1 和患者 5 均表现出血泌乳素升高,并伴有不同程度的激素症状。影像学检查显示,所有病例均累及蝶窦底。患者1、2和5的肿瘤与颈内动脉海绵窦段密切相关。肿瘤呈弥漫性生长,细胞质嗜色至微嗜酸。少数肿瘤细胞表现为嗜铬细胞质。核小体明显。偶尔可观察到核内包涵体和大小不一的透明空泡。在电子显微镜下,可观察到明显的线粒体异常,包括线粒体数量增加、膨大肥厚和线粒体脊断裂缺失。部分线粒体基质致密,部分呈空泡状。结论:嗜酸性干细胞PitNET/腺瘤是垂体腺瘤/PitNET的一种罕见类型。它在临床上通常具有较强的侵袭性,细胞未成熟,弥漫表达 PIT1、催乳素和不同程度的生长激素。由于其临床激素状态和激素免疫表达的明显多样性,这类肿瘤的诊断仍是一个难题。
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中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
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1.00
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10377
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