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成人及青少年甲状旁腺腺瘤。18例病例的批判性评估与手术策略

Parathyroid Adenomas in Adults and Adolescents. Critical Appraisal and Surgical Strategy in 18 Cases.

作者信息

Diaconescu Mihai Radu, Costea Ioan, Glod Mihai, Terinte Radu, Diaconescu Smaranda

出版信息

Chirurgia (Bucur). 2017 Jan-Feb;112(1):18-24. doi: 10.21614/chirurgia.112.1.18.

Abstract

UNLABELLED

Our study underline scarcity of isolated case reports or small case series of parathyroid adenoma (PA) published in autochthonous medical literature,their variable clinical expression among the "historic" varieties but also the diagnostic difficulties and delays of diagnosis as well consecration of surgery as the golden therapeutic standard of this disorder.

PATIENTS AND METHOD

Demographic, clinical presentations, laboratory and imaging data, operative findings and procedures together with pathology account and outcome from the case reports of 18 patients with documented PHP were retrospectively analyzed. The male/female ratio was 1/5, with ages ranging from 16 to 58 (mean 46) years. Renal stones (n=9) and bone sufferings (n=6) were the most common modes of presentation. To these were added psychiatric and neuromuscular complaints, digestive disorders (pancreatitis and peptic ulcer) arterial hypertension and presence of a palpable nodule. Mean serum calcium and phospho-rus, alkaline phosphatase and PTH dosage together with parathyroid ultrasound and 99m Tc sestamibi scintigraphy are the most useful parameters for diagnosis. Eighteen adenomectomies were performed of which bilateral neck exploration was done in 16 patients and minimally invasive approach in the remaining two cases. In 9 situations concomitant thyroid exeresis for associated lesions or tactical purpose were done. Pathology revealed single adenoma consisting of main and oxyphil cells in 17 cases. In one case an atypical adenoma was identified and in another case three years after removal of a benign adenoma the subject presented a clinical ipsilateral recurrence which provided to be a carcinoma. Postoperative clinical and humoral outcome was favorable in all situations less the case of carcinoma which died after 14 months. Despite the rarity and difficulties of diagnosis in cases of PA, practitioners must be aware of potential existence of these lesions in order to apply as early and appropriate treatment where surgery is the gold standard.

摘要

未标注

我们的研究强调了国内医学文献中发表的甲状旁腺腺瘤(PA)孤立病例报告或小病例系列的稀缺性,其在“历史”类型中的临床表达多变,以及诊断困难和诊断延迟,同时也强调了手术作为这种疾病黄金治疗标准的地位。

患者与方法

回顾性分析了18例记录在案的甲状旁腺功能亢进症患者病例报告中的人口统计学、临床表现、实验室和影像学数据、手术发现及操作,以及病理报告和结果。男女比例为1/5,年龄范围为16至58岁(平均46岁)。肾结石(n = 9)和骨骼病变(n = 6)是最常见的表现形式。此外还有精神和神经肌肉症状、消化系统疾病(胰腺炎和消化性溃疡)、动脉高血压以及可触及结节。平均血清钙、磷、碱性磷酸酶和甲状旁腺激素水平测定,以及甲状旁腺超声和99m锝甲氧基异丁基异腈闪烁扫描是最有用的诊断参数。共进行了18例腺瘤切除术,其中16例患者进行了双侧颈部探查,其余2例采用微创方法。9例因相关病变或策略性目的同时进行了甲状腺切除术。病理显示17例为主要由主细胞和嗜酸细胞组成的单发性腺瘤。1例为非典型腺瘤,另1例在切除良性腺瘤三年后出现同侧临床复发,结果为癌。除癌患者在14个月后死亡外,所有情况下术后临床和体液结果均良好。尽管PA病例罕见且诊断困难,但从业者必须意识到这些病变的潜在存在,以便在手术为黄金标准的情况下尽早进行适当治疗。

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