[Pituitary metastases: a diagnostic and therapeutic challenge].

IF 0.6 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Medicina-buenos Aires Pub Date : 2024-01-01
Mónica G Loto, Amelia Rogozinski, Analia Alfieri, María C Ballarino, María F Battistone, Alberto Chervin, Karina D Danilowicz, Sabrina Diez, Patricia Fainstein Day, Alejandra Furioso, Mariela Glerean, Mariana Gonzalez Pernas, Débora Katz, María S Mallea Gil, Marcela Martinez, Karina A Miragaya, Maria I Sabate, Patricia Slavinsky, Soledad Sosa, Gabriela Szuman, Julieta Tkatch, Marcelo N Vitale, Mirtha Guitelman
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引用次数: 0

Abstract

Introduction: Sellar metastases (SM) are rare manifestations of malignancy. Breast and lung cancer are the most common primary tumors. Most cases are diagnosed in patients with advanced malignant disease; however, symptoms of pituitary involvement can precede the diagnosis of the primary tumor.

Methods: Retrospective analysis of symptoms at presentation, hormonal, radiological and histological findings, management, and outcome of patients with SM from 2009 to 2020.

Results: Eighteen patients'cases were included, 11 with histological confirmation. Median (m) age was 53 years (range 35-75), 53% male. Primary malignant tumors: 8 lungs, 6 breast, 1 follicular thyroid carcinoma, 1 Hodgkin lymphoma, and 2 clear cell renal carcinomas. The m time between the diagnosis of the primary neoplasm and the occurrence of the SM was 108 months (range: 11-180). In 8 patients the diagnosis of the primary neoplasm was made after the finding of the symptomatic sellar mass. Insipidus diabetes, adenohypophysis deficit, visual disorders, headache, and cranial nerve deficits were evident in 78, 77, 61, 39 and 39% of the cases, respectively. Fifteen patients harbored supra / parasellar masses, in three a lesion was limited to the pituitary gland, and stalk. Eleven out of 18 (61.1%) of the patients were operated on by the trans-sphenoidal approach, for diagnostic and / or decompressive purposes. Eighteen died, with a median survival time of 6 months (1-36).

Discussion: In the presence of a pituitary lesion with diffuse gadolinium uptake, associated with insipidus diabetes and / or visual disorder SM should be suspected even in patients without a history of oncological disease.

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[垂体转移瘤:诊断和治疗的挑战]。
简介Sellar转移瘤(SM)是恶性肿瘤的罕见表现。乳腺癌和肺癌是最常见的原发肿瘤。大多数病例是在晚期恶性疾病患者中确诊的;然而,垂体受累的症状可能出现在原发肿瘤确诊之前:方法:回顾性分析2009年至2020年间SM患者的发病症状、激素、放射学和组织学检查结果、处理方法和预后:结果:共纳入18例患者,其中11例经组织学证实。中位(m)年龄为53岁(35-75岁),53%为男性。原发恶性肿瘤:8 例肺癌、6 例乳腺癌、1 例甲状腺滤泡癌、1 例霍奇金淋巴瘤和 2 例透明细胞肾癌。从诊断出原发性肿瘤到发生 SM 的最长时间为 108 个月(范围:11-180 个月)。8例患者是在发现有症状的蝶窦肿块后才确诊原发肿瘤的。分别有78%、77%、61%、39%和39%的病例有明显的脂溢性糖尿病、腺嗜酸不足、视力障碍、头痛和颅神经障碍。15例患者的垂体上/旁肿块,3例患者的病变局限于垂体和垂体柄。18名患者中有11名(61.1%)是通过经蝶窦方法进行手术的,目的是诊断和/或减压。18人死亡,中位生存时间为6个月(1-36):讨论:如果垂体病变伴有弥漫性钆摄取,并伴有尿崩症、糖尿病和/或视力障碍,即使患者没有肿瘤病史,也应怀疑是SM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicina-buenos Aires
Medicina-buenos Aires 医学-医学:内科
CiteScore
1.30
自引率
12.50%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Information not localized
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