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Temporal kemiğin dev hücreli tümörü
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1279648
Hatice Kaplanoğlu, A. Turan, Veysel Kaplanoğlu
Giant cell tumor (GCT) arises from undifferentiated mesenchymal cells of the bone marrow. GCT, a benign and locally aggressive tumor, is more commonly seen in the metaphysis of long bones. It may cause local bone destruction, recurrence, and pulmonary metastases (~1%). A 15-year-old male patient was admitted with complaints of swelling on the right face, a headache that has persisted for one year and progressively worsened in the last three months, and hearing loss. Craniotomy and total tumor excision were performed. Histopathological examination revealed a giant cell tumor of the bone. We present a case of temporal bone GCT with its clinical and radiologic features.
巨细胞瘤(GCT)起源于未分化的骨髓间充质细胞。GCT是一种良性的局部侵袭性肿瘤,常见于长骨干骺端。可引起局部骨破坏、复发和肺转移(约1%)。15岁男性患者入院,主诉右脸肿胀,头痛持续一年,近三个月逐渐加重,听力下降。行开颅和全肿瘤切除术。组织病理学检查显示骨巨细胞瘤。我们报告一例颞骨GCT的临床及影像学表现。
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引用次数: 0
Pramipeksolün mevsimsel depresyon üzerindeki etkinliği: olgu sunumu
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1276024
O. Ozdemi̇r
The efficacy and safety of pramipexole have been reported both in the treatment of unipolar/bipolar depression and anxiety/depression in patients with Parkison disease. But, there is no evidence for its clinical effect in seasonal depressive disorder. In this case report, the patient with seasonal depression responded to pramipexole is presented.
普拉克索在治疗帕金森病患者的单极/双相抑郁和焦虑/抑郁方面的有效性和安全性均有报道。但目前尚无证据表明其对季节性抑郁症的临床疗效。在这个病例报告中,有季节性抑郁症的患者对普拉克索有反应。
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引用次数: 0
Kruppel benzeri faktör 2 polimorfizmlerinin koroner arter hastalığı riski ile ilişkisi
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1283236
Ulaş Deği̇rmenci̇, Metin Yildirim, Merih Akkapulu, Ali Yalin, Dilek çiçek DİLEK ÇİÇEK, Ragıp Onur Öztornaci, Bahar Taşdelen, Serap Yalin
Purpose: Coronary artery disease is defined as complications that develop in proportion to the prevalence of ischemia due to occlusion of the coronary arteries and the resulting cell death. The development of atherosclerosis is significantly influenced by endothelial cell dysfunction. Kruppel-like factor 2, a transcription factor, has been shown to regulate critical biological events in endothelial biology, such as vascular tone, migration, proliferation, vasoreactivity, and angiogenesis. In our study, it was aimed to clarify the relationship between coronary artery disease and Kruppel-like factor 2 protein levels and C1239A polymorphisms. Materials and Methods: 191 individuals who underwent coronary angiography at Mersin University Faculty of Medicine, Department of Cardiology, Health, Research and Application Center were included in the study. Measurements of serum fasting blood glucose, HDL cholesterol, total cholesterol, and triglyceride levels were performed on the AU5800 (Beckman Coulter, United States) autoanalyzer. Serum LDL levels were calculated using the Friedwald equation. Serum Kruppel-like factor 2 protein levels were measured by sandwich enzyme-linked immunoassay method on the Multiskan GO (Thermo Scientific, Finland) device. Kruppel-like factor 2 C1239A variations were detected on the Applied Biosystem VIIA™ 7 Real-Time PCR (Life Technologies Co., United States) device by TaqMan® single nucleotide polymorphism (SNP) genotyping method. Results: Men had a 3.8-fold higher risk of CAD than women. (Odd’s ratio 3.83, 95% Confidence interval 1.98-7.39; p
目的:冠状动脉疾病被定义为与冠状动脉闭塞引起的缺血发生率及由此导致的细胞死亡成比例的并发症。动脉粥样硬化的发生与内皮细胞功能障碍密切相关。kruppel样因子2是一种转录因子,已被证明可调节内皮生物学中的关键生物学事件,如血管张力、迁移、增殖、血管反应性和血管生成。本研究旨在阐明冠状动脉疾病与kruppel样因子2蛋白水平及C1239A多态性的关系。材料与方法:在梅尔辛大学医学院、心内科、健康、研究与应用中心接受冠状动脉造影的191例患者纳入研究。在AU5800 (Beckman Coulter,美国)自动分析仪上测量空腹血糖、高密度脂蛋白胆固醇、总胆固醇和甘油三酯水平。使用Friedwald方程计算血清LDL水平。在Multiskan GO (Thermo Scientific, Finland)设备上,采用三明治酶联免疫分析法检测血清克虏伯样因子2蛋白水平。采用TaqMan®单核苷酸多态性(SNP)基因分型方法,在Applied Biosystem VIIA™7 Real-Time PCR (Life Technologies Co., United States)设备上检测kruppel样因子2 C1239A变异。结果:男性患冠心病的风险是女性的3.8倍。(奇数比3.83,95%置信区间1.98-7.39;p
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引用次数: 0
Executive functions and psychiatric disorders in adults with iron deficiency anemia 成人缺铁性贫血的执行功能和精神障碍
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1252790
Yavuz Yilmaz, Hatice Terzi, Burak Taşova
Purpose: The focus has been on the hematological complications of iron deficiency, while the nonhematological complications have been less studied. Its effects on cognitive functions were mostly investigated in children and adolescents. The purpose of this study is to compare the executive functioning of persons with iron deficiency anemia to healthy controls in order to determine whether they have any comorbid psychiatric disorders. Materials and Methods: 42 patients with iron deficiency anemia and 44 healthy controls participated in this study. To investigate whether any psychiatric disorders existed, the individuals were given a Structured Clinical Interview for DSM-5 Clinician's Version. Executive functioning was assessed using the Stroop Test and the Number Sequence Learning Test. Results: When compared to the control group, the IDA group took longer on average to complete parts 1–5 of the Stroop Test. There was no difference between the groups with regards to the results of number sequence learning test. Psychiatric illnesses were more common (43%) in the IDA group than they were in the control group (13.6%). The difference was significant when the groups were compared in terms of psychiatric disorders. Conclusion: According to the study's findings, those with iron deficiency anemia have worse executive functioning scores than healthy controls and are more likely to have psychiatric disorders. An extensive assessment of the health consequences of iron deficiency anemia is extremely important.
目的:缺铁的血液学并发症是目前研究的重点,而对缺铁的非血液学并发症研究较少。其对认知功能的影响主要研究于儿童和青少年。本研究的目的是比较缺铁性贫血患者与健康对照者的执行功能,以确定他们是否有任何共病性精神疾病。材料与方法:42例缺铁性贫血患者和44例健康对照者参加本研究。为了调查是否存在任何精神疾病,对这些个体进行了DSM-5临床医生版的结构化临床访谈。使用Stroop测试和数字序列学习测试评估执行功能。结果:与对照组相比,IDA组完成Stroop Test第1-5部分的平均时间更长。在数列学习测试结果方面,两组间无显著差异。精神疾病在IDA组(43%)比对照组(13.6%)更常见。当两组在精神疾病方面进行比较时,差异是显著的。结论:根据这项研究的发现,缺铁性贫血患者的执行功能得分比健康对照组更差,而且更有可能患有精神疾病。对缺铁性贫血的健康后果进行广泛评估是极其重要的。
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引用次数: 0
Sekiz yaşında bir çocukta risperidona bağlı enürezis
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1244903
Nur Seda GÜLCÜ ÜSTÜN
Risperidone is an antipsychotic commonly used in children and adolescents. The use of risperidone is mostly safe in children, but it can cause some side effects. Few cases of enuresis with risperidone have been reported in the literature so far, some of these cases have been associated with the use of antidepressants or other antipsychotics in combination with risperidone. We present an 8.5-year-old patient with enuresis with risperidone.
利培酮是一种常用于儿童和青少年的抗精神病药物。利培酮在儿童中的使用基本上是安全的,但它可能会产生一些副作用。到目前为止,文献中很少报道利培酮引起遗尿的病例,其中一些病例与抗抑郁药或其他抗精神病药物与利培酮联合使用有关。我们报告一例8.5岁的遗尿患者,利培酮治疗。
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引用次数: 0
Şizofrenide gen ifadeleri ve mutasyon analizleri
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1278390
Serdar Kalemci̇, Huriye Gülistan BOZDAĞ BAŞKAYA, Arife Zeybek
Dear Editor; We read with interest the article titled “CYB mtDNA mutations and the expression status of genes in the PI3K/AKT/mTOR signaling pathway in patients with schizophrenia” published in Cukurova Medical Journal by Dirican et al.
亲爱的编辑器;我们饶有兴趣地阅读了Dirican等人在Cukurova Medical Journal上发表的题为“精神分裂症患者中CYB mtDNA突变和PI3K/AKT/mTOR信号通路中基因的表达状态”的文章。
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引用次数: 0
A neonatal lupus syndrome with pericardial tamponade due to maternal Sjögren’s syndrome 新生儿狼疮综合征与心包填塞由于产妇Sjögren综合征
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1241756
H. Yapicioğlu, M. Özdemir, Tugay Tepe, Tolga Akbaş, F. Özlü, Sevcan Erdem
Neonatal lupus syndrome (NLS) is a rare disease with dermatological, cardiac, hepatic and hematologic involvement due to placental transfer of anti-Ro/ SSA and anti-La/ SSB antibodies in infants of mothers with autoimmune diseases. Multisystemic involvement is common in infants. Here we present a baby with neonatal lupus syndrome whose mother had Sjögren's syndrome. He presented with thrombocytopenia, then convulsion and cardiac arrest due to pericardial tamponade. So, the risk of NLS should be kept in mind in infants of mothers with autoimmune diseases.
新生儿狼疮综合征(NLS)是一种罕见的疾病,由于抗ro / SSA和抗la / SSB抗体在自身免疫性疾病母亲的婴儿胎盘转移而累及皮肤、心脏、肝脏和血液系统。多系统受累在婴儿中很常见。这里我们提出一个婴儿与新生儿狼疮综合征,其母亲有Sjögren综合征。他先是出现血小板减少,然后是惊厥和心包填塞引起的心脏骤停。因此,对于患有自身免疫性疾病的母亲所生的婴儿,NLS的风险应牢记在心。
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引用次数: 0
Oral mukosel: olgu sunumu 口服mukosel, olgu sunmu
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1240546
Shreyas Shah, Rahul RAVİRAJ SHETTY
Mucocele is a commonly occurring pathology in the oral cavity and especially found on labial mucosa. It is commonly seen in the younger population peaking in the 10–20-year age group. In most cases the patient will give a positive history of recent trauma caused due to lip biting. The clinical picture will be of a soft, clear swelling with a bluish color. The size can vary from a few mm to few centimeters at times. A diagnosis can be reached many times just on the basis of a proper history and the clinical features alone. This report depicts the successful management of a case of mucocele which in turn would assist the dental practitioner for diagnosing and managing this condition.
黏液囊肿是口腔常见病,尤其常见于唇黏膜。它常见于10 - 20岁年龄组的年轻人。在大多数情况下,患者会给出由于咬唇引起的近期创伤的积极历史。临床表现为柔软、清晰、带蓝色的肿胀。大小有时从几毫米到几厘米不等。很多时候,仅仅根据病史和临床特征就可以做出诊断。本报告描述了成功的管理情况下粘液囊肿,这反过来将有助于牙科医生诊断和管理这种情况。
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引用次数: 0
Hipofizer disfonksiyonu olan Fabry hastası: alışılmadık bir görünüm 伴有垂体功能障碍的法布里患者:一种不寻常的表现
Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1219901
Gamze AKKUŞ, Saime PAYDAS
Fabry is a multisystemic disease mainly affecting heart, kidney, central nervous system and endocrine system with intralysosomal glycolipid accumulation. Although thyroid and adrenal gland involvement has been demonstrated in limited studies, glycolipid accumulation in the pituitary could not be exhibited. A 66-year-old female patient diagnosed with Fabry Disease revealed a low level of pituitary hormone levels. Moreover, an empty sella was found in pituitary MRI. We argued that pituitary function seems impaired due to Fabry Disease, and endocrine workup should be periodically performed in patients with Fabry Disease
Fabry是一种多系统疾病,主要影响心脏、肾脏、中枢神经系统和内分泌系统,伴有溶酶体内糖脂积累。虽然在有限的研究中已证实甲状腺和肾上腺受累,但垂体中的糖脂积累尚未表现出来。一位66岁的女性患者被诊断为法布里病,其垂体激素水平较低。此外,垂体MRI显示空蝶鞍。我们认为,垂体功能似乎受损,由于法布里病,和内分泌检查应定期进行法布里病患者
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引用次数: 0
COVID-19 pandemisinin Çin Hindi'ndeki rutin doğum öncesi idrar iyot tarama programına etkisi
IF 0.2 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-07-02 DOI: 10.17826/cumj.1241109
Pathum Sookaromdee, V. Wi̇wani̇tki̇t
The healthcare sector has been impacted by the COVID-19 outbreak. The prevention of COVID-19 infections was given priority, and personnel and resources for the healthcare industry were reassigned. How the COVID-19 pandemic might impact common screening practices in public healthcare is an intriguing subject. Prior studies have amply demonstrated the value of regular cancer screening and cervical cancer screening1-2. Alternative cancer screening methods are used in addition to the standard public health laboratory tests in different parts of the world, depending on the problem that is present at that area.
医疗保健行业受到了COVID-19疫情的影响。重点做好疫情防控工作,重新调配医疗卫生人力资源。COVID-19大流行如何影响公共医疗保健中的常见筛查做法是一个有趣的话题。先前的研究充分证明了定期癌症筛查和宫颈癌筛查的价值1-2。在世界不同地区,除了标准的公共卫生实验室测试外,还根据该地区存在的问题使用其他癌症筛查方法。
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引用次数: 0
期刊
Cukurova Medical Journal
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