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What Has Changed in the 2025 American Thyroid Association Management Guidelines for Adult Patients with Differentiated Thyroid Cancer? Part 2: Postoperative Initial Treatment. 2025年美国甲状腺协会成年分化型甲状腺癌患者管理指南有何变化?第2部分:术后初始治疗。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.30906
Mehmet Uludag, Mehmet Taner Unlu, Isik Cetinoglu, Ozan Caliskan, Nurcihan Aygun

American Thyroid Association (ATA) guidelines for the management of thyroid nodules and differentiated thyroid cancer (DTC) were first published in 1996 and subsequently updated in 2006, 2009, and 2015. In 2025, the ATA released a revised version focusing exclusively on DTC and excluding thyroid nodules from its scope. In our previous review, we summarized the updates regarding preoperative evaluation, diagnosis, and surgical management of DTC. In this second part of the series, we aimed to compare the 2015 and 2025 ATA guidelines in terms of initial postoperative management. The main changes are evaluated at the level of recommendations, with a particular emphasis on recurrence risk stratification, postoperative risk-adapted surveillance, adjuvant radioactive iodine (RAI) use, postoperative imaging, and radiation safety. This review provides a comprehensive comparison of the 2015 and 2025 ATA guidelines, outlining the key changes in early postoperative management of DTC and highlighting their potential impact on individualized patient care.

美国甲状腺协会(ATA)关于甲状腺结节和分化型甲状腺癌(DTC)治疗的指南于1996年首次发布,随后于2006年、2009年和2015年更新。2025年,ATA发布了一个修订版,专门针对DTC,并将甲状腺结节排除在其范围之外。在我们之前的综述中,我们总结了关于DTC的术前评估、诊断和手术治疗的最新进展。在本系列的第二部分中,我们旨在比较2015年和2025年ATA指南在初始术后管理方面的差异。主要变化在建议水平上进行评估,特别强调复发风险分层、术后风险适应监测、辅助放射性碘(RAI)使用、术后成像和辐射安全性。本综述对2015年和2025年ATA指南进行了全面比较,概述了DTC术后早期管理的关键变化,并强调了它们对个体化患者护理的潜在影响。
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引用次数: 0
The Role of Preoperative CHA2DS2-VASc Score in Predicting Late Saphenous Vein Graft Failure in Non-STEMI Patients with Prior Coronary Artery Bypass Grafting: A Retrospective Study. 术前CHA2DS2-VASc评分在预测非stemi患者既往冠状动脉搭桥术晚期隐静脉移植失败中的作用:一项回顾性研究
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.14377
Cemalettin Yilmaz, Ahmet Karaduman, Muhammed Mucahit Tiryaki, Regayip Zehir

Objectives: Despite the prevalence of saphenous vein graft (SVG) failure following coronary artery bypass graft (CABG) surgery, SVGs continue to be widely used. This study aimed to investigate the value of the CHA2DS2-VASc score, originally developed for predicting thromboembolic events in atrial fibrillation, in predicting SVG failure post-CABG.

Methods: This retrospective study analyzed data from 526 patients with a history of CABG who presented with non-ST-elevation myocardial infarction between January 2017 and April 2024. SVG failure was defined as exhibiting stenosis of 70% or greater, or complete occlusion. Preoperative CHA2DS2-VASc scores were calculated for each patient. Multivariable analysis was conducted to identify independent predictors of SVG failure.

Results: Among the 526 patients, 242 (46%) experienced SVG failure. Patients with SVG failure exhibited higher CHA2DS2-VASc scores. Multivariable analysis identified the CHA2DS2-VASc score (OR: 2.203, 95% CI: 1.672-2.902, p<0.001), time interval after CABG (OR: 1.167, 95% CI: 1.081-1.259, p<0.001), and number of SVGs (OR: 2.378, 95% CI: 1.745-3.241, p<0.001) as independent predictors of SVG failure. Of those parameters, the CHA2DS2-VASc score demonstrated a higher AUC value (AUC=0.796, AUC=0.724, AUC=0.641, respectively).

Conclusion: Pre-operative CHA2DS2-VASc score may be predictive of late SVG failure after CABG.

目的:尽管冠状动脉旁路移植术(CABG)术后隐静脉移植(SVG)存在失败率,但SVG仍被广泛应用。CHA2DS2-VASc评分最初用于预测房颤血栓栓塞事件,本研究旨在探讨CHA2DS2-VASc评分在预测cabg后SVG失效中的价值。方法:本回顾性研究分析了2017年1月至2024年4月期间526例有CABG病史的非st段抬高型心肌梗死患者的数据。SVG失败定义为狭窄70%或更大,或完全闭塞。计算每位患者术前CHA2DS2-VASc评分。进行多变量分析以确定SVG失效的独立预测因素。结果:526例患者中有242例(46%)出现SVG失败。SVG失败患者CHA2DS2-VASc评分较高。多变量分析确定CHA2DS2-VASc评分(OR: 2.203, 95% CI: 1.672-2.902)。结论:术前CHA2DS2-VASc评分可预测CABG术后晚期SVG失效。
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引用次数: 0
A Case of Button Battery Ingestion Mimicking Inferior Myocardial Ischemia and Atypical Chest Pain. 吞下纽扣电池致下段心肌缺血及不典型胸痛1例。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.63004
Galib Bairamovi, Hasan Ozkan Gezer, Cankat Erdogan, Alev Arslan, Abdulkerim Temiz

With the increasing use of electronic toys, the number of cases involving battery ingestion has risen significantly in recent years. This case report presents a child who attended the emergency department with sudden chest pain and crying episodes. The electrocardiogram (ECG) revealed signs of myocardial ischemia in inferior leads, despite completely normal cardiac function. A chest X-ray detected a button battery lodged in the esophagus. A 4-year-old boy presented to the emergency department with sudden, intense chest pain and crying while playing with his toys. An electrocardiogram showed prolonged corrected QT interval (cQT 0.56), marked ST depression, and negative T waves in leads DII, DIII and aVF. Echocardiography (ECHO) revealed normal cardiac function. Cardiac enzyme and biochemical tests returned normal results (troponin-I ≤ 3.2 ng/L, CK-MB 29.8 U/L). A disc-shaped battery was detected on chest radiography, and electrocardiographic findings completely normalized after the battery was removed endoscopically. In the literature, rare adult cases of multiple cylindrical battery ingestion have been reported with ECG findings that mimic myocardial ischemia or infarction. Our case is notable as it presents a single disc battery lodged in the esophagus of a pediatric patient that mimicked an inferior myocardial infarction.

随着使用电子玩具的人数不断增加,近年涉及误食电池的个案大幅上升。这个病例报告提出了一个孩子谁出席了急诊科突然胸痛和哭泣的情节。尽管心功能完全正常,但心电图显示下导联有心肌缺血的迹象。胸部x光检查发现一个纽扣电池卡在食道里。一名4岁的男孩在玩玩具时突然出现剧烈的胸痛和哭泣,被送往急诊室。心电图显示校正QT间期延长(cQT 0.56), ST段明显下降,DII、DIII和aVF导联T波呈负。超声心动图(ECHO)显示心功能正常。心肌酶、生化检查正常(肌钙蛋白i≤3.2 ng/L, CK-MB 29.8 U/L)。在胸片上发现一个盘状电池,在内窥镜下取出电池后,心电图结果完全正常化。在文献中,有罕见的成人摄入多个圆柱形电池的病例,其心电图表现类似心肌缺血或梗死。我们的病例是值得注意的,因为它提出了一个单一的磁盘电池卡在食管的儿科患者,模仿下位心肌梗死。
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引用次数: 0
First Paediatric Case of mRNA COVID-19 Vaccine Associated New Onset Systemic Myasthenic Crisis. 首例小儿mRNA - COVID-19疫苗相关新发全身性肌无力危象
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.34119
Serkan Kirik, Mehmet Agar, Hadice Gurkan Akyol, Yasemin Kirik

Myasthenia gravis (MG) is an autoimmune disorder characterized by abnormal neuromuscular conduction. The thymus is believed to play a key role in the pathogenesis of MG; therefore, thymectomy is an important treatment option for the disease. As MG exacerbations and new-onset MG cases following Coronavirus Disease 2019 (COVID-19) vaccinations have been previously reported in the literature, various complications highly related to autoimmunity, such as Guillain-Barré syndrome, have also been described after vaccination. A previously healthy girl developed her first life-threatening systemic MG attack following administration of the messenger RNA (mRNA) BNT162b2 COVID-19 vaccine. Despite receiving treatment targeting MG, her clinical status did not show significant improvement, which led to the decision to perform thymectomy via the video-assisted thoracoscopic surgery (VATS) approach. After the procedure, a significant improvement was observed in her clinical condition. We aimed to contribute to the literature on this rarely encountered condition by reporting the first paediatric case in our country presenting with BNT162b2 vaccination-associated generalized weakness and severe respiratory distress, who was diagnosed with MG and thymoma during follow-up, in the light of contemporary literature. This case also serves as a warning for other mRNA vaccines.

重症肌无力(MG)是一种以神经肌肉传导异常为特征的自身免疫性疾病。胸腺被认为在MG的发病机制中起关键作用;因此,胸腺切除术是一种重要的治疗选择。由于此前已有文献报道冠状病毒病2019 (COVID-19)疫苗接种后MG加重和新发MG病例,疫苗接种后也报道了各种与自身免疫高度相关的并发症,如格林-巴罗综合征。一名先前健康的女孩在接种了信使RNA (mRNA) BNT162b2 COVID-19疫苗后出现了首次危及生命的系统性MG发作。尽管接受了针对MG的治疗,但她的临床状况没有明显改善,这导致决定通过视频辅助胸腔镜手术(VATS)方法进行胸腺切除术。手术后,观察到她的临床状况有明显改善。我们的目的是通过报道我国第一例出现与BNT162b2疫苗相关的全身性虚弱和严重呼吸窘迫的儿科病例,并结合当代文献,在随访期间被诊断为MG和胸腺瘤,从而为这一罕见疾病的文献做出贡献。该病例也为其他mRNA疫苗提供了警告。
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引用次数: 0
Intra-Articular PRP for Grade 2 Degenerative Meniscus Lesions; Radiological and Clinical Outcomes. 关节内PRP治疗2级退行性半月板病变放射学和临床结果。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.40359
Yigit Atalay, Osman Tugrul Eren, Raffi Armagan

Objectives: This study was conducted to evaluate the radiological and clinical results of platelet-rich plasma (PRP) therapy in degenerative meniscal lesions.

Methods: Seventy patients with pain and grade 2 degenerative meniscal lesions on MRI (Magnetic Resonance Imaging) were included in the study. All patients underwent Knee Injury and Osteoarthritis Score (KOOS), Tegner-Lysholm, International Knee Documentation Committee Score (IKDC), Visual Analog Scale (VAS) clinical scores, and MRI scans before and 6 months after the injection.

Results: There was a statistically significant increase in Tegner-Lysholm, KOOS, and IKDC scores after the procedure (p=0.001; p<0.01), and a statistically significant decrease in VAS score after the procedure (p=0.001; p<0.01). However, no statistically significant difference was observed in MRI parameters (p>0.05).

Conclusion: It has been shown that the use of intra-articular PRP in painful degenerative meniscal lesions improves knee functions and helps reduce pain. However, no significant difference was observed in MRI controls. The results of our study indicate that the use of intra-articular PRP injection in patients with grade 2 meniscus degeneration improves clinical scores but does not result in significant improvement in degeneration as measured by MRI.

目的:本研究旨在评价富血小板血浆(PRP)治疗退行性半月板病变的放射学和临床结果。方法:选取70例MRI表现为疼痛和退行性半月板2级病变的患者作为研究对象。所有患者在注射前和注射后6个月分别进行了膝关节损伤和骨关节炎评分(oos)、Tegner-Lysholm评分、国际膝关节文献委员会评分(IKDC)、视觉模拟评分(VAS)临床评分和MRI扫描。结果:术后Tegner-Lysholm、kos、IKDC评分均有统计学意义的升高(p=0.001; p0.05)。结论:在疼痛的退行性半月板病变中使用关节内PRP可改善膝关节功能并有助于减轻疼痛。然而,在MRI对照中没有观察到显著差异。我们的研究结果表明,在2级半月板退变患者中使用关节内PRP注射可以提高临床评分,但MRI测量的退变并没有显著改善。
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引用次数: 0
An Alternative Route for the Treatment of Hypothyroidism in Neonates with Intestinal Disorders: Buccal Administration of Levothyroxine. 治疗伴有肠道疾病的新生儿甲状腺功能减退的另一种途径:左旋甲状腺素口腔给药。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.36690
Gulay Sonmez Demir, Musa Turgut, Didem Yildirim Cakar, Murat Ocal, Osman Uzunlu, Bayram Ozhan, Ozmert M A Ozdemir, Hacer Ergin

Iodine-containing antiseptics and contrast agents used in neonates can lead to hypothyroidism, which, although often transient, may require prolonged treatment in some cases. Untreated hypothyroidism, even if temporary, can negatively impact neurodevelopment, particularly in preterm infants. In addition, gastrointestinal disorders such as short bowel syndrome or ileus may hinder oral levothyroxine absorption, necessitating alternative administration routes. Here, we present a late preterm neonate who developed hypothyroidism after iodine-containing contrast agent use for diagnosing total intestinal aganglionosis. The patient failed to respond to oral and rectal levothyroxine administration due to functional ileus and persistent gastrointestinal drainage. Subsequently, levothyroxine was administered via the buccal route by diluting the tablet form. The treatment resulted in rapid normalization of thyroid function tests, with no adverse effects observed. In our case, buccal administration of diluted levothyroxine tablets was found to be a beneficial treatment approach for managing hypothyroidism in a patient unable to tolerate oral therapy due to intestinal dysmotility and malabsorption, particularly in the absence of alternative formulations. Furthermore, it highlights the importance of monitoring thyroid function in neonates exposed to iodine-containing agents, especially those with gastrointestinal motility disorders. Buccal levothyroxine may provide a practical solution for managing hypothyroidism in similar clinical scenarios.

新生儿使用含碘防腐剂和造影剂可导致甲状腺功能减退,虽然通常是短暂的,但在某些情况下可能需要长期治疗。未经治疗的甲状腺功能减退,即使是暂时的,也会对神经发育产生负面影响,尤其是早产儿。此外,胃肠道疾病如短肠综合征或肠梗阻可能阻碍口服左旋甲状腺素的吸收,需要其他给药途径。在这里,我们提出一个晚期早产儿谁发展甲状腺功能减退后,含碘造影剂用于诊断全肠神经节病。由于功能性肠梗阻和持续的胃肠道引流,患者口服和直肠左甲状腺素治疗无效。随后,通过稀释片剂形式通过口腔途径给药左甲状腺素。治疗导致甲状腺功能检查迅速正常化,未观察到不良反应。在我们的病例中,对于由于肠道运动障碍和吸收不良而无法耐受口服治疗的患者,特别是在没有替代配方的情况下,口服稀释左甲状腺素片被发现是一种有益的治疗方法。此外,它强调了监测暴露于含碘剂的新生儿甲状腺功能的重要性,特别是那些有胃肠运动障碍的新生儿。在类似的临床情况下,口腔左旋甲状腺素可能为治疗甲状腺功能减退症提供一个实用的解决方案。
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引用次数: 0
Abnormal Blood Pressure Dipping Pattern in Women with Hypopituitarism Secondary to Sheehan Syndrome: A Case-Control Study. 希恩综合征继发垂体功能低下妇女血压异常下降模式:一项病例对照研究。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.45793
Ibtissem Oueslati, Salma Salhi, Emna Talbi, Moncef Feki, Meriem Yazidi, Melika Chihaoui

Objectives: The aims of this study were to assess the 24-hour ambulatory BP levels and to determine the prevalence of abnormal circadian BP dipping patterns in women with hypopituitarism secondary to Sheehan syndrome.

Methods: This was a cross-sectional study including 35 women with complete anterior hypopituitarism secondary to Sheehan syndrome and 47 age- and body-mass index-matched control women. Subjects receiving treatment for hypertension were not included. All participants underwent clinical examination, laboratory tests, and BP measurement using ambulatory 24-hour monitoring.

Results: The mean age was 61.3±10.6 years in patients vs 60.5±8.5 years in controls (p=0.720). Compared to controls, women with Sheehan syndrome had a higher prevalence of dyslipidemia (p=0.032) and metabolic syndrome (p=0.028). The prevalence of hypertension was 68% in patients and 62% in controls (p=0.520). Altered day-night BP variation was more frequent in patients (85%) than in controls (54%) (p=0.004). Additionally, patients had a significantly higher prevalence of nocturnal hypertension (38% versus 3%; p=0.002). Sheehan syndrome was positively associated with a non-dipper and riser BP profile (Odds Ratio=4.7, 95% confidence interval: 1.54-14.33, p=0.004).

Conclusion: Women with hypopituitarism secondary to Sheehan syndrome had a higher disruption of the circadian BP rhythm than controls. Although the prevalence of newly diagnosed hypertension was comparable between patients and controls, women with Sheehan syndrome had a higher prevalence of nocturnal hypertension.

目的:本研究的目的是评估24小时动态血压水平,并确定继发于希恩综合征的垂体功能低下女性中异常昼夜血压下降模式的患病率。方法:这是一项横断面研究,包括35名继发于希恩综合征的完全性垂体前叶功能低下的女性和47名年龄和体重指数匹配的对照女性。接受高血压治疗的受试者不包括在内。所有参与者都接受了临床检查、实验室检查和24小时动态监测的血压测量。结果:患者平均年龄为61.3±10.6岁,对照组为60.5±8.5岁(p=0.720)。与对照组相比,患有Sheehan综合征的女性血脂异常(p=0.032)和代谢综合征(p=0.028)的患病率更高。患者高血压患病率为68%,对照组为62% (p=0.520)。患者(85%)比对照组(54%)更频繁出现昼夜血压变化(p=0.004)。此外,患者夜间高血压的患病率明显更高(38%对3%;p=0.002)。Sheehan综合征与非下沉和上升血压谱呈正相关(优势比=4.7,95%可信区间:1.54-14.33,p=0.004)。结论:与对照组相比,希恩综合征继发垂体功能低下患者的昼夜血压节律紊乱程度更高。虽然新诊断的高血压患病率在患者和对照组之间相当,但患有希恩综合征的女性夜间高血压患病率更高。
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引用次数: 0
A Rare Presentation of A Common Dermatosis; Unilateral Blaschko-Linear Erythema Multiforme. 一种常见皮肤病的罕见表现单侧多形blaschko -线状红斑。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.20688
Birgul Ozkesici Kurt, Ilknur Kıvanc Altunay, Aysegul Oz, Seyhan Ozakkoyunlu Hascicek, Pinar Ozdemir Cetinkaya, Asli Aksu

Erythema multiforme (EM) is a self-limiting, immune-mediated condition characterized by target-like lesions, often triggered by infections, with herpes simplex virus (HSV) being the most common agent. In rare cases, EM may present following Blaschko's lines, a pattern of cutaneous mosaicism. We report a unique case of EM in a 17-year-old male with lesions distributed along Blaschko's lines across his arm, trunk, and leg, marking the most extensive presentation of EM in this pattern to date. The patient had no history of HSV infection or drug use, except for cannabis consumption, which was considered a probable trigger based on the Naranjo Adverse Drug Reaction Probability Scale. Histopathological analysis confirmed the diagnosis of EM, and the lesions resolved with topical clobetasol propionate. This case highlights the rare occurrence of EM along Blaschko's lines in a young patient and suggests cannabis as a potential trigger, contributing to the understanding of atypical presentations and etiology in EM.

多形性红斑(EM)是一种自限性、免疫介导的疾病,以靶样病变为特征,通常由感染引发,单纯性疱疹病毒(HSV)是最常见的病原体。在极少数情况下,EM可能表现为遵循Blaschko线,一种皮肤嵌合的模式。我们报告一例独特的EM病例,患者为17岁男性,其病变沿Blaschko线分布在其手臂、躯干和腿部,标志着迄今为止该模式中最广泛的EM表现。患者无HSV感染史或药物使用史,除了吸食大麻,根据Naranjo药物不良反应概率量表,大麻被认为是可能的触发因素。组织病理学分析证实了EM的诊断,病灶局部用丙酸氯倍他索解决。该病例强调了EM在年轻患者中沿Blaschko线的罕见发生,并提示大麻是潜在的触发因素,有助于理解EM的非典型表现和病因。
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引用次数: 0
Clinical, Radiological and Hormonal Characteristics of Our Patients with Primary Empty Sella: A Single-Centre Experience. 原发性空蝶鞍患者的临床、放射学和激素特征:单中心经验。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.54022
Adem Kilinc, Betul Kizildag, Adem Doganer, Kamile Gul, Ayten Oguz

Objectives: A common incidental radiological finding in asymptomatic adults is primary empty sella (PES). We examined the clinical, radiological and hormonal features of patients with PES to identify risk factors and guide follow-up strategies.

Methods: The study included 120 patients with PES. Data on patients was obtained retrospectively and included details on symptoms, diseases, as well as radiological, biochemical and hormonal findings. Patients were divided into two groups (partial and total) according to sella turcica cerebrospinal fluid volume and pituitary height. They were also classified as having isolated hormone deficiency (HD), hypopituitarism or panhypopituitarism according to the severity of pituitary insufficiency.

Results: HD was found in 83.3% of the study group. The most common causes were growth hormone deficiency and central hypogonadism. The two groups were indistinguishable with regard to pituitary insufficiency; however, panhypopituitarism was more prevalent in the total PES group (60.5% vs 30.5%). PES was more common in women, while both general and severe HD were more common in men. Pituitary height was positively correlated with thyroid stimulating hormone, free T4, insulin-like growth factor-1, testosterone, estradiol, adrenocorticotropic hormone and cortisol (r=0.275, p=0.002; r=0.277, p=0.002; r=0.394, p<0.001; r=0.319, p<0.001; r=0.195, p=0.032; r=0.220, p=0.016; r=0.310, p=0.001). Low pituitary height and male gender were associated with an increased risk of panhypopituitarism (p=0.002 vs p=0.015).

Conclusion: Pituitary insufficiency is common in PES, but panhypopituitarism is more common in total PES. Low pituitary height and male gender are risk factors for panhypopituitarism. Patients with these characteristics should be monitored more closely.

目的:无症状成人常见的偶发放射学发现是原发性空鞍(PES)。我们检查了PES患者的临床、放射学和激素特征,以确定危险因素并指导随访策略。方法:选取120例PES患者作为研究对象。回顾性获取患者数据,包括症状、疾病以及放射学、生化和激素检查结果的细节。根据蝶鞍脑脊液容量和垂体高度将患者分为部分组和全部组。根据垂体功能不全的严重程度,将其分为孤立性激素缺乏症(HD)、垂体功能减退症或全垂体功能减退症。结果:研究组HD发生率为83.3%。最常见的原因是生长激素缺乏和中枢性性腺功能减退。两组在垂体功能不全方面无明显差异;然而,全垂体功能减退症在全PES组中更为普遍(60.5%对30.5%)。PES在女性中更常见,而一般和严重的HD在男性中更常见。垂体高度与促甲状腺激素、游离T4、胰岛素样生长因子-1、睾酮、雌激素、促肾上腺皮质激素、皮质醇呈正相关(r=0.275, p=0.002; r=0.277, p=0.002; r=0.394)。结论:垂体功能不全在PES中常见,而全垂体功能低下在全PES中更为常见。低垂体高度和男性是全垂体功能低下的危险因素。具有这些特征的患者应更密切地监测。
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引用次数: 0
Analysis of the Risk of Neoplasm and Malignancy of Salivary Gland Neoplasm of Uncertain Malignant Potential (SUMP): From the Perspective of Cytomorphological Subgroups. 涎腺恶性潜能不确定肿瘤(SUMP)的肿瘤与恶性风险分析:从细胞形态学亚群的角度。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.95580
Enver Yarikkaya, Senay Erdogan Durmus, Elis Kangal, Selma Sengiz Erhan, Cem Comunoglu

Objectives: This study aimed to investigate the risk of neoplasm (RON) and the risk of malignancy (ROM) in cases diagnosed as salivary gland neoplasm of uncertain malignant potential (SUMP), with subclassification based on cytomorphologic features.

Methods: A retrospective review was conducted on salivary gland fine-needle aspiration (FNA) specimens diagnosed as SUMP between 2018 and 2022 in a tertiary care setting. Each case was re-evaluated by two pathologists and subclassified into basaloid, oncocytic, or clear cell/other categories according to the dominant cytomorphologic pattern. RON and ROM were calculated for the overall SUMP category and for each cytomorphologic subgroup.

Results: Among 41 SUMP cases, the basaloid subtype was the most common (70.7%), followed by the oncocytic (19.5%) and the clear cell/others (9.8%). Histopathological confirmation was available in 65.9% of cases, all of which were neoplastic, resulting in a RON of 100%. The overall ROM was 29.6%. The ROMs by subgroup were 25% for basaloid, 40% for oncocytic, and 50% for clear cell/others. Pleomorphic adenoma was the most frequently encountered benign neoplasm (33.3%), and basal cell carcinoma was the most common malignant diagnosis (18.5%). The majority of malignant cases (87.5%) were located in the parotid gland.

Conclusion: This study confirms the consistently high neoplastic potential of SUMP lesions and highlights the variation in malignancy risk among different cytomorphologic subtypes. Although the ROM differed among the subgroups, they all demonstrated clinical relevance, supporting the utility of cytomorphologic subclassification in salivary gland cytopathology. These findings may contribute to more refined risk assessment and patient management within the Milan System framework.

目的:本研究旨在探讨涎腺不确定恶性潜能肿瘤(SUMP)的肿瘤发生风险(RON)和恶性肿瘤发生风险(ROM),并根据细胞形态学特征进行亚分类。方法:回顾性分析2018年至2022年在三级医疗机构诊断为SUMP的唾液腺细针抽吸(FNA)标本。每个病例由两名病理学家重新评估,并根据主要的细胞形态学模式将其细分为碱性细胞、嗜瘤细胞或透明细胞/其他类别。计算总体SUMP类别和每个细胞形态学亚组的RON和ROM。结果:在41例SUMP中,基底细胞亚型最常见(70.7%),其次是嗜瘤细胞亚型(19.5%)和透明细胞/其他亚型(9.8%)。65.9%的病例有组织病理证实,所有病例均为肿瘤性,RON为100%。总体ROM为29.6%。亚组ROMs为碱性细胞25%,嗜瘤细胞40%,透明细胞/其他50%。多形性腺瘤是最常见的良性肿瘤(33.3%),基底细胞癌是最常见的恶性肿瘤(18.5%)。绝大多数恶性肿瘤(87.5%)位于腮腺。结论:本研究证实了SUMP病变始终具有较高的肿瘤潜力,并强调了不同细胞形态亚型之间恶性风险的差异。虽然各亚组的ROM不同,但它们都显示出临床相关性,支持细胞形态学亚分类在唾液腺细胞病理学中的应用。这些发现可能有助于在米兰系统框架内进行更精细的风险评估和患者管理。
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Medical Bulletin of Sisli Etfal Hospital
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