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Developmental and Cognitive Outcomes in 342 Patients With Different Types of Hyperphenylalaninemia. 342例不同类型高苯丙氨酸血症患者的发育和认知结局
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.09471
Sibel Oz Yildiz, Halise Neslihan Onenli Mungan, Deniz Kor, Fatma Derya Bulut, Berna Seker Yilmaz, Sebile Kilavuz, Gulsah Seydaoglu
<p><strong>Objectives: </strong>The aim of this study is to evaluate neurodevelopmental and cognitive outcomes in patients diagnosed with different types of hyperphenylalaninemia (HPA), identify the factors influencing these outcomes, and contribute to the debate regarding the thresold for initiating dietary treatment based on plasma phenylalanine (Phe) levels.</p><p><strong>Methods: </strong>Patients with hyperphenylalaninemia (HPA) who were followed up and had developmental and/or cognitive evaluations at the Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, between 1984 and 2018, were retrospectively assessed. The study included patients with mild (Phe:360-600 μmol/L), moderate (Phe:600-1200 μmol/L), or classic Phenylketonuria (PKU) (Phe ≥1200 μmol/L) treated with diet and/or tetrahydrobiopterin (BH4), along with untreated HPA patients (Phe:240-360 μmol/L). This classification was based on plasma Phe levels measured at the time of diagnosis. Denver Developmental Screening Test (DDST), Stanford-Binet test, and Wechsler Intelligence Scale for Children (WISC-R) adapted for Turkish children were applied for developmental and cognitive evaluation. Intellectual disability or developmental delay (ID/DD) was defined as a full-scale intelligence quotient (IQ) <70 on the Stanford-Binet or WISC-R, or as delay in two or more developmental domains on the DDST, with children meeting any of these criteria classified as having ID/DD. The relationships between ID/DD, age at diagnosis, diagnostic methods, plasma Phe levels, and brain MRI findings were analyzed.</p><p><strong>Results: </strong>A total of 342 patients were included in the study, comprising 182 (53.2%) females and 160 (46.8%) males. Of these, 53 (15.5%) had mild PKU, 97 (28.4%) had moderate PKU, 102 (29.8%) had classic PKU, and 90 (26.3%) were diagnosed with HPA. A significant association was found between ID/DD and both the age at diagnosis and diagnostic method in patients treated with diet and/or BH4 (p < 0.001 and p < 0.01, respectively). In patients with ID/DD, the median plasma Phe levels at the first, third, and last years of follow-up were significantly higher compared to patients without ID/DD (p < 0.024). White matter abnormalities observed on brain MRI were significantly associated with PKU severity, the presence of ID/DD, and the median plasma Phe levels in the last year of follow-up (p = 0.01, p < 0.001, and p < 0.001, respectively). Notably, 9 (10%) of untreated HPA patients exhibited ID/DD, despite regular follow-up and the absence of known risk factors.</p><p><strong>Conclusion: </strong>In addition to early diagnosis and treatment, lifelong adherence and regular follow-up are essential for achieving normal neurodevelopmental and cognitive outcomes in individuals with PKU. However, clinical management remains heterogeneous across centers. The presence of developmental delay in 10% of untreated HPA patients underscores the need to urgently re-evaluate current
目的:本研究的目的是评估诊断为不同类型高苯丙氨酸血症(HPA)患者的神经发育和认知结果,确定影响这些结果的因素,并为基于血浆苯丙氨酸(Phe)水平开始饮食治疗阈值的争论做出贡献。方法:回顾性评估1984年至2018年在儿科代谢与营养科随访并进行发育和/或认知评估的高苯丙氨酸血症(HPA)患者。该研究包括轻度(Phe:360-600 μmol/L)、中度(Phe:600-1200 μmol/L)或经典苯丙酮尿(PKU) (Phe≥1200 μmol/L)患者,这些患者接受饮食和/或四氢生物蝶呤(BH4)治疗,以及未经治疗的HPA患者(Phe:240-360 μmol/L)。这种分类是基于诊断时测量的血浆Phe水平。采用适用于土耳其儿童的丹佛发育筛选测验(DDST)、斯坦福-比奈测验(Stanford-Binet Test)和韦氏儿童智力量表(WISC-R)进行发育和认知评价。结果:共纳入342例患者,其中女性182例(53.2%),男性160例(46.8%)。其中53例(15.5%)为轻度PKU, 97例(28.4%)为中度PKU, 102例(29.8%)为典型PKU, 90例(26.3%)为HPA。在饮食和/或BH4治疗的患者中,ID/DD与诊断年龄和诊断方法均有显著相关性(p < 0.001和p < 0.01)。在ID/DD患者中,随访第一年、第三年和最后一年的血浆Phe中位数水平显著高于无ID/DD患者(p < 0.024)。脑MRI观察到的白质异常与PKU严重程度、ID/DD的存在以及随访最后一年的血浆Phe中位数水平显著相关(p = 0.01, p < 0.001和p < 0.001)。值得注意的是,9(10%)未经治疗的HPA患者表现出ID/DD,尽管有定期随访和缺乏已知的危险因素。结论:除了早期诊断和治疗外,终身坚持和定期随访对于实现PKU患者正常的神经发育和认知结果至关重要。然而,各中心的临床管理仍然存在差异。10%未经治疗的HPA患者存在发育迟缓,这强调了迫切需要重新评估当前治疗开始和随访时的血浆Phe阈值。
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引用次数: 0
Perceptions of Patients with Respiratory Disorders About Environmental Smoke. 呼吸系统疾病患者对环境烟雾的认知。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.59568
Mufide Arzu Ozkarafakili, Metin Yangin, Aslihan Calim

Objectives: Environmental smoke exposure is a poorly understood issue and might be a potential source of long-term respiratory exposure to toxic pollutants. Both secondhand and thirdhand smoke (THS) exposure are important matters of public health. We aimed to document the knowledge about smoke exposure of vulnerable groups with respiratory diseases.

Methods: A total of 911 currently smoking patients admitted to the outpatient clinics between October 2023 - October 2024 enrolled in our study. Following a medical examination and pulmonary function assessment, individuals were asked to complete the BATHS questionnaire on thirdhand smoking exposure.

Results: Of the 911smoker participants who comprised our sample, 322 (35.3%) had COPD, 227 (24.9%) had asthma and 570 (62.5%) experienced moderate to severe secondhand exposure. Patients with COPD had the lowest BATHS total and persistence scores (3.61±0.58 and 3.77±0.69, respectively), while asthmatics had the lowest BATHS health scores (3.41±0.46) (p<0.05). Total and subdimension scores were significantly higher among individuals aged 18-30, university graduates, employed in the workforce, and earning exceeds minimum wage (p <0.05). No gender difference was noted (p>0.05). BATHS total scores had significant negative correlation with secondhand smoke exposure and disease duration (p<0.05) whereas positively correlated with better pulmonary function values, attending a smoking cessation clinic, and living at home with children under sixteen (p<0.05).

Conclusion: This study identifies the knowledge gap about the detrimental effects of smoke exposure in patients with respiratory diseases. It underscores the importance of focusing initiatives to reduce both active and passive smoking through educational programs targeting active smokers at risk of lung illnesses.

目的:环境烟雾暴露是一个知之甚少的问题,可能是长期呼吸道暴露于有毒污染物的潜在来源。二手烟和三手烟暴露都是重要的公共卫生问题。我们的目的是记录呼吸系统疾病易感人群的烟雾暴露知识。方法:在2023年10月至2024年10月期间,共有911名目前在门诊就诊的吸烟患者加入我们的研究。在医学检查和肺功能评估之后,要求个人完成关于三手烟暴露的bath问卷。结果:在构成我们样本的911名吸烟者参与者中,322名(35.3%)患有COPD, 227名(24.9%)患有哮喘,570名(62.5%)经历过中度至重度二手暴露。COPD患者的bath总分和持久性评分最低(分别为3.61±0.58和3.77±0.69),哮喘患者的bath健康评分最低(3.41±0.46)(p0.05)。bath总分与二手烟暴露和疾病持续时间呈显著负相关(p)。结论:本研究确定了呼吸系统疾病患者对二手烟暴露有害影响的认识差距。它强调了通过针对有肺部疾病风险的主动吸烟者的教育项目来减少主动和被动吸烟的重要性。
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引用次数: 0
Intralesional Platelet-Rich Plasma Injection in Patients with Recalcitrant Alopecia Areata. 顽固性斑秃斑内富血小板血浆注射治疗。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.63444
Mert Aydogan, Nermin Karaosmanoglu, Pinar Ozdemir Cetinkaya

Objectives: Alopecia areata (AA) is a common, chronic autoimmune disease that causes non-cicatricial hair loss. Its relapsing and remitting nature leads to the search for new, effective treatment options. The study aimed to evaluate the therapeutic efficacy of intralesional platelet-rich plasma (PRP) and intralesional steroid (ILS) injections in patients with AA.

Methods: A retrospective chart review was carried out from 2020-2021. A total of 75 patients with AA were included in the study. Thirty-six patients were treated with intralesional PRP, and 39 patients were treated with ILS injections for three sessions. The patients were evaluated with a hair pull test and SALT scores at months 0, 3, and 6.

Results: Of 75 patients, the mean age of the PRP group was 34.33±10.61, and the mean age of the ILS group was 33.82±13.31 years. After three PRP or ILS therapy sessions, at 3. and 6. months, SALT 3 and SALT 6 scores were statistically significantly lower in the PRP group than in the ILS group (p=0.038, p<0.001, respectively). When the treatment response was evaluated at the end of the 6th month in the PRP group, there was no response in 2 (5.5%) patients, partial response in 1 (2.7%) patient, good response in 3 (8.4%) patients, and very good response in 30 (83.4%) patients. Only 2 (5.9%) patients had a clinical relapse in a 6-month period. Side effects were seen in 16 (44.4%) patients in the PRP group and 8 (20.5%) patients in the ILS group, and the frequency of side effects in the PRP group was statistically significantly higher than in the ILS group (p=0.026). However, the side effects of both groups were minor, such as itching, pain, burning, ecchymosis, and folliculitis.

Conclusion: PRP seems to be an effective and safe treatment option for limited patchy alopecia areata, but its superiority over ILS has not been fully demonstrated, making ILS still the first-line treatment.

目的:斑秃(AA)是一种常见的慢性自身免疫性疾病,引起非瘢痕性脱发。它的复发和缓解的性质导致寻找新的,有效的治疗方案。本研究旨在评价斑块内富血小板血浆(PRP)和斑块内类固醇(ILS)注射对AA患者的治疗效果。方法:对2020-2021年进行回顾性图表复习。共有75例AA患者纳入研究。36例患者接受病灶内PRP治疗,39例患者接受三次ILS注射治疗。在第0、3、6个月时,通过拔毛试验和SALT评分对患者进行评估。结果:75例患者中,PRP组平均年龄为34.33±10.61岁,ILS组平均年龄为33.82±13.31岁。三次PRP或ILS治疗后,3点。和6。结论:PRP似乎是治疗局限性斑秃的一种有效、安全的治疗方案,但其优于ILS的优势尚未得到充分证明,因此仍是ILS治疗的一线选择。
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引用次数: 0
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
Gastrointestinal Kaposi Sarcoma: Histopathological Features and Diagnostic Challenges - Insights from a Single Center. 胃肠道卡波西肉瘤:组织病理学特征和诊断挑战-来自单一中心的见解。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.32457
Melek Buyuk, Neslihan Berker, Leman Damla Ercan, Cemil Burak Kulle, Gizem Dagci, Mine Gulluoglu

Objectives: Gastrointestinal Kaposi sarcoma (GI-KS) is a rare vascular neoplasm associated with human herpesvirus 8 (HHV 8), most often emerging in immunosuppressed individuals. Its endoscopic appearance-ranging from nodular and polypoid lesions to ulcerations-can be subtle. In addition, histopathological features of KS may mimic benign inflammatory conditions or other mesenchymal tumors, delaying accurate diagnosis. This study aimed to evaluate the histopathological features of GI-KS and to clarify the neoplastic and non-neoplastic diagnostic challenges in a single-center cohort.

Methods: We retrospectively reviewed 13 GI-KS cases diagnosed between 2005 and 2025. Clinical data and endoscopic findings were retrieved from the hospital's electronic medical records. Hematoxylin and eosin-stained sections, along with HHV-8 immunohistochemistry (IHC) slides, were retrospectively evaluated.

Results: Thirteen patients (11 male; mean age 47±18 years) were identified, of whom 84.6% were immunosuppressed (eight HIV-positive, two renal transplant recipients, and one receiving corticosteroids). Cutaneous or extraintestinal KS lesions were present in 11 cases. Endoscopic evaluation revealed nodular lesions (30.8%), polypoid lesions (23.1%), snake-skin-like hemorrhagic areas (7.7%), infiltrative lesions (7.7%), erythematous elevated lesions (7.7%), or nonspecific erythematous changes (7.7%). Suspicion of KS was documented in only three endoscopy reports. Lesions were most commonly located in the stomach (76.9%), followed by the rectum (15.4%) and colon (7.7%). Histologically, slit-like vascular channels and erythrocyte extravasation were observed in 84.6% of cases, hemosiderin deposits in 53.8%, chronic inflammatory infiltrates including plasma cells in 76.9%, and foveolar epithelial hyperplasia in 70% of gastric cases. The histologic spectrum included diagnostic pitfalls such as chronic gastritis-like features in three cases, reactive gastropathy-like changes in one case, granulation tissue-like appearance in one case, and GIST/leiomyoma-like spindle cell morphology in one case.

Conclusion: The histologic features of GI-KS can mimic both neoplastic and inflammatory conditions. Therefore, histopathological evaluation should be conducted alongside clinical information, as GI-KS may present with subtle or nonspecific findings. Given the potential for life-threatening complications such as obstruction, bleeding, or perforation, accurate diagnosis and timely treatment are critically important. Routine application of HHV-8 IHC -even in cases with minimal suspicion- is essential for ensuring diagnostic accuracy, guiding appropriate management, and preventing serious outcomes.

目的:胃肠道卡波西肉瘤(GI-KS)是一种罕见的与人类疱疹病毒8 (HHV 8)相关的血管肿瘤,最常见于免疫抑制个体。它的内窥镜表现——从结节和息肉样病变到溃疡——可能很微妙。此外,KS的组织病理学特征可能与良性炎症或其他间质肿瘤相似,从而延迟了准确诊断。本研究旨在评估GI-KS的组织病理学特征,并在单中心队列中阐明肿瘤和非肿瘤诊断挑战。方法:回顾性分析2005年至2025年间诊断的13例GI-KS病例。临床数据和内窥镜检查结果从医院的电子病历中检索。苏木精和伊红染色切片以及HHV-8免疫组织化学(IHC)切片进行回顾性评估。结果:13例患者(男性11例,平均年龄47±18岁),其中84.6%的患者免疫抑制(8例hiv阳性,2例肾移植患者,1例接受皮质类固醇)。11例出现皮肤或肠外KS病变。内镜检查显示结节性病变(30.8%)、息肉样病变(23.1%)、蛇皮样出血区(7.7%)、浸润性病变(7.7%)、红斑性升高病变(7.7%)或非特异性红斑性改变(7.7%)。怀疑KS仅在三份内窥镜报告中被记录。病变最常见于胃(76.9%),其次为直肠(15.4%)和结肠(7.7%)。组织学上,84.6%的胃病例有裂隙样血管通道和红细胞外渗,53.8%的胃病例有含铁血黄素沉积,76.9%的胃病例有慢性炎症浸润,包括浆细胞,70%的胃病例有小凹上皮增生。组织学谱包括诊断缺陷,如3例慢性胃炎样特征,1例反应性胃病样改变,1例肉芽组织样外观,1例GIST/平滑肌瘤样梭形细胞形态。结论:GI-KS具有类似肿瘤和炎症的组织学特征。因此,组织病理学评估应与临床信息一起进行,因为GI-KS可能表现出微妙或非特异性的发现。考虑到可能出现危及生命的并发症,如梗阻、出血或穿孔,准确的诊断和及时的治疗至关重要。常规应用HHV-8免疫连体检测——即使是在极少怀疑的病例中——对于确保诊断准确性、指导适当管理和防止严重后果至关重要。
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引用次数: 0
Cervical lymphadenopathies: A Retrospective Single-Center Analysis of Patients Undergoing Excisional Biopsy. 宫颈淋巴结病:接受切除活检患者的回顾性单中心分析。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.04657
Serdal Celik, Berina Slipcevic, Emirhan Ceviken, Osman Kilic, Mahmut Tayyar Kalcioglu

Objectives: The aim of this retrospective study was to evaluate and compare cervical ultrasound findings, fine needle aspiration biopsy (FNAB) results and excisional biopsy results in the diagnosis of patients presenting with cervical lymphadenopathy and to reveal the most common causes.

Methods: A total of 137 patients who underwent cervical ultrasonography and FNAB before excision were included in the study. Demographic data, cervical ultrasonographic findings, FNAB pathology results and final pathology results after excisional biopsy were analysed.

Results: The pathological results indicated that reactive follicular hyperplasia was diagnosed in 33.6% (n=46) of the patients. A diagnosis of non-Hodgkin lymphoma (NHL) was made in 27.7% (n=38) of cases, while 13.1% (n=18) were diagnosed with Hodgkin lymphoma. Malignant pathology was diagnosed in 66 patients. In the FNAB results of patients diagnosed as malignant, 57 were interpreted as non-diagnostic and suspicious, while 9 were interpreted as benign. Of these, 8 had a pathological examination of lymph node excision that revealed non-Hodgkin lymphoma (NHL), and in one patient with a benign FNAB result, the result of lymph node excision was reported as malignant.

Conclusion: Especially in cervical lymphadenopathies in patients over 40 years of age, the possibility of malignancy increases significantly. In lymphoproliferative diseases and in cases accompanied by clinical suspicion, it would be rational to use the direct excisional biopsy option. Although prior fine needle aspiration biopsy may provide significant guidance in metastatic diseases, it should be kept in mind that false negative rates may increase in the diagnosis and staging of lymphoma.

目的:本回顾性研究的目的是评估和比较宫颈超声检查结果,细针穿刺活检(FNAB)结果和切除活检结果对宫颈淋巴结病的诊断,并揭示最常见的原因。方法:选取术前行宫颈超声检查及FNAB检查的137例患者作为研究对象。分析人口统计学资料、宫颈超声检查结果、FNAB病理结果及切除活检后最终病理结果。结果:病理结果显示,33.6%(46例)的患者诊断为反应性滤泡增生。诊断为非霍奇金淋巴瘤(NHL)的病例占27.7% (n=38),而诊断为霍奇金淋巴瘤的病例占13.1% (n=18)。66例患者病理诊断为恶性。在诊断为恶性的患者FNAB结果中,57例被解释为无诊断性和可疑,9例被解释为良性。其中,8例淋巴结切除病理检查显示非霍奇金淋巴瘤(NHL), 1例FNAB结果为良性,淋巴结切除结果报告为恶性。结论:尤其在40岁以上的宫颈淋巴结病变患者中,恶性肿瘤的可能性明显增加。在淋巴细胞增生性疾病和伴有临床怀疑的病例中,使用直接切除活检是合理的选择。虽然先前的细针穿刺活检可以为转移性疾病提供重要的指导,但应该记住,假阴性率可能会增加淋巴瘤的诊断和分期。
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引用次数: 0
Fatigue, Insomnia, and Disability as Independent Predictors of Depressive Symptoms in Multiple Sclerosis: A Prospective Observational Study. 疲劳、失眠和残疾是多发性硬化症抑郁症状的独立预测因素:一项前瞻性观察研究
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.33407
Ceren Alis, Nuray Kose, Sibel Sen Kilic, Gencer Genc, Serpil Bulut

Objectives: This study aimed to identify the clinical factors independently associated with depressive symptoms in patients with multiple sclerosis (MS) and to evaluate the impact of depression on health-related quality of life (QoL).

Methods: In this prospective observational study, 90 patients with MS were evaluated. Age, sex, disease duration, MS subtype, and Expanded Disability Status Scale (EDSS) scores were recorded. The Fatigue Severity Scale (FSS), Insomnia Severity Index (ISI), Epworth Sleepiness Scale (ESS), Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS) scale, and the EuroQol 5-Dimension 3-Level (EQ-5D-3L) questionnaire were administered. The presence of restless legs syndrome (RLS) was also recorded. Depression severity was measured using the Patient Health Questionnaire-9 (PHQ-9). First, univariable associations were examined, and relevant variables were subsequently entered into a multivariable linear regression model using backward elimination.

Results: Higher FSS, ISI, and EDSS scores were independently associated with higher PHQ-9 scores. FSS and ISI scores showed the strongest correlations with depression (ρ=+0.52 and +0.57; p<0.001). EDSS showed a modest association (ρ=+0.23, p=0.031). Age, sex, and disease duration were not significant predictors. S-LANSS scores, MS subtype, and RLS were significant in univariate analysis but excluded from the final model. Depression scores were significantly associated with higher EQ-5D-3L scores, indicating poorer QoL (p<0.001).

Conclusion: Fatigue and insomnia were the strongest independent predictors of depression in MS, surpassing traditional clinical indicators. Routine screening for these symptoms may facilitate earlier detection and treatment of depression and improve QoL in clinical practice.

目的:本研究旨在确定与多发性硬化症(MS)患者抑郁症状独立相关的临床因素,并评估抑郁对健康相关生活质量(QoL)的影响。方法:在这项前瞻性观察研究中,对90例多发性硬化症患者进行评估。记录年龄、性别、病程、MS亚型和扩展残疾状态量表(EDSS)评分。采用疲劳严重程度量表(FSS)、失眠严重程度指数(ISI)、Epworth嗜睡量表(ESS)、利兹神经性症状和体征评估量表(S-LANSS)和EuroQol 5维3水平问卷(EQ-5D-3L)。不宁腿综合征(RLS)的存在也被记录。使用患者健康问卷-9 (PHQ-9)测量抑郁严重程度。首先,单变量关联被检查,相关变量随后进入一个多变量线性回归模型使用反向消去。结果:高FSS、ISI和EDSS评分与高PHQ-9评分独立相关。FSS和ISI评分与MS患者抑郁的相关性最强(ρ=+0.52和+0.57);结论:疲劳和失眠是MS患者抑郁的最强独立预测因子,优于传统临床指标。常规筛查这些症状有助于早期发现和治疗抑郁症,提高临床生活质量。
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引用次数: 0
What Has Changed in the 2025 American Thyroid Association Management Guidelines for Adult Patients with Differentiated Thyroid Cancer? Part 3: Long-Term Surveillance, Advanced and Novel Treatments. 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?第三部分:长期监测,先进和新颖的治疗方法。
IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-13 eCollection Date: 2025-01-01 DOI: 10.14744/SEMB.2025.67864
Mehmet Uludag, Ozan Caliskan, Mehmet Taner Unlu, Isik Cetinoglu, Nurcihan Aygun

American Thyroid Association (ATA) guidelines for the management of thyroid nodules and differentiated thyroid cancer (DTC) were first published in 1996 and updated in 2006, 2009, and 2015. In 2025, the ATA released a revised version that, for the first time, focuses exclusively on DTC. In our previous reviews, we summarized the updates on preoperative, diagnostic, surgical, and early postoperative management of DTC. In this third and final part, we compare the 2015 and 2025 ATA guidelines with respect to long-term follow-up, TSH suppression strategies, thyroglobulin monitoring, follow-up of low-risk patients. Diagnostic radioiodine whole-body scanning, FDG-PET/CT, dynamic risk stratification, and the management of recurrent or metastatic disease, including local therapies, radioiodine preparation and dosing, and systemic treatments were also highlighted in this part. Particular emphasis is placed on the expanded recommendations for kinase inhibitor therapy, sequencing of systemic agents, targeted therapies (NTRK, RET, ALK, BRAF), redifferentiation approaches, immunotherapy, and supportive care strategies addressing bone and brain metastases, financial toxicity and psychosocial needs. This review provides a comprehensive synthesis of these updates and discusses their implications for individualized long-term management of DTC.

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,并于2006年、2009年和2015年更新。在2025年,ATA发布了一个修订版,这是第一次,专门针对DTC。在我们之前的综述中,我们总结了DTC的术前、诊断、手术和术后早期治疗的最新进展。在第三部分也是最后一部分,我们比较了2015年和2025年ATA指南在长期随访、TSH抑制策略、甲状腺球蛋白监测、低风险患者随访方面的差异。该部分还重点介绍了放射性碘全身扫描诊断、FDG-PET/CT、动态风险分层以及复发或转移性疾病的管理,包括局部治疗、放射性碘制备和给药以及全身治疗。特别强调了激酶抑制剂治疗的扩展推荐,全身药物的测序,靶向治疗(NTRK, RET, ALK, BRAF),再分化方法,免疫治疗,以及针对骨和脑转移,经济毒性和社会心理需求的支持性护理策略。本文综述了这些最新进展,并讨论了它们对DTC个体化长期治疗的影响。
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Medical Bulletin of Sisli Etfal Hospital
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