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Bilateral Accessory Clavicular Heads of Sternocleidomastoid Stenosing Supraclavicular Fossa in Human: Case Report. 人类双侧副锁骨头锁骨上窝狭窄1例。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.39
Dibakar Borthakur, Harisha Kusuma, Mohammed Ahmed Ansari

The sternocleidomastoid muscle (SCM) is an important landmark for many clinical procedures performed in the neck. Typically, the SCM consists of two heads of origin, sternal and clavicular. We came across bilateral accessory clavicular fibers of the SCM having extended attachment up to the middle third of the clavicle in an elderly cadaver. On the right side, the accessory fibers formed a distinct, separate belly in the form of cleidooccipital muscle. On the left side, four clavicular heads of SCM were observed, which were partially separated from each other. The presence of accessory clavicular fibers may stenose supraclavicular fossa. Additionally, the SCM with accessory clavicular fibers is not a reliable surface landmark and hence may pose difficulties in important procedures in the region such as central venous catheterization.

胸锁乳突肌(SCM)是许多临床颈部手术的重要标志。典型地,SCM由两个起头组成,胸骨和锁骨。我们在一具老年尸体上发现双侧锁骨副纤维延伸到锁骨中间的三分之一处。在右侧,副纤维以锁枕肌的形式形成了一个明显的、独立的腹部。左侧观察到4个SCM锁骨头,彼此部分分离。锁骨副纤维的存在可能使锁骨上窝狭窄。此外,具有副锁骨纤维的SCM并不是一个可靠的表面标记,因此可能会给该区域的重要手术(如中心静脉导管置入术)带来困难。
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引用次数: 0
Eccrine Hidrocystoma of Eyelid Masquerading as Epidermal Inclusion Cyst: A Rare Case Report with Review of Literature. 眼睑汗液囊肿伪装表皮包涵性囊肿1例并文献复习。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.7
Gyanendra Singh, Mamta Singh, Palak Thakkar, Parth Goswami

Eccrine hidrocystomas are rare, benign cystic lesions that usually affect the scalp, cheeks, and eyelids. They are thought to originate from the sweat glands. These lesions can be single or many in nature and frequently worsen in the summer from increased perspiration. They are caused by dilated ducts of eccrine sweat glands. Clinically, they seem like small, transparent cystic lesions that are painless, and they usually affect middle-aged or older people. However, a histological study is necessary to make a final diagnosis. We present a case of a 35-year-old woman who had an epidermal inclusion cyst first identified as a single, painless cystic growth on her right lower eyelid.

汗腺囊肿是一种罕见的良性囊性病变,通常影响头皮、脸颊和眼睑。它们被认为起源于汗腺。这些病变可以是单一的,也可以是许多性质的,并且经常在夏季因出汗增加而恶化。它们是由汗腺导管扩张引起的。临床上,它们看起来像小的、透明的、无痛的囊性病变,通常发生在中年或老年人身上。然而,组织学研究是做出最终诊断的必要条件。我们提出一个病例35岁的妇女谁有表皮包涵囊肿首先确定为一个单一的,无痛性囊性生长在她的右下眼睑。
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引用次数: 0
A Comprehensive Guide to Typhoidal Anemia. 伤寒性贫血综合指南。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.10
Jayanta Deb, Suddha Sattwa Bandyopadhyay, Sanjit Debnath, Saurabh Gupta

Typhoid fever, caused primarily by Salmonella Typhi and Paratyphi, stands as a significant global health concern, with complications extending beyond the typical gastrointestinal manifestations. This review systematically examines the intricate relationship between typhoid fever and hematologic complications, collectively referred to as typhoidal anemia. Hematological abnormalities, including changes in blood profiles and bone marrow responses, are scrutinized, providing a comprehensive understanding of the disease's impact on physiological systems. Specific populations, such as immunocompromised individuals, sickle cell anemia patients, and children in resource-limited settings, reveal varied susceptibilities and outcomes. Complications, such as psoas abscess and secondary hemophagocytic lymphohistiocytosis, are explored, highlighting the multifaceted nature of the disease. The distinct contributions of Salmonella Typhi and Paratyphi to anemia are elucidated, shedding light on the pathophysiological mechanisms involved. Global prevalence and epidemiological variations offer valuable perspectives, underscoring the importance of regional nuances in disease manifestation. Challenges in accurate diagnosis and treatment limitations are acknowledged, emphasizing the need for continued research to enhance diagnostic precision and therapeutic strategies. Insights into long-term effects, prognosis, and the influence of host factors contribute to a holistic understanding of typhoidal anemia. The review concludes by identifying critical gaps in knowledge, advocating for ongoing research initiatives and heightened awareness campaigns. The synthesis of diverse findings provides a comprehensive overview of typhoidal anemia, underscoring the imperative of continued research and awareness for improved patient care and global public health.

伤寒主要由伤寒沙门氏菌和副伤寒沙门氏菌引起,是一个重大的全球卫生问题,其并发症超出了典型的胃肠道表现。这篇综述系统地检查了伤寒和血液学并发症之间复杂的关系,统称为伤寒性贫血。血液学异常,包括血液谱和骨髓反应的变化,被仔细检查,提供对疾病对生理系统影响的全面了解。特定人群,如免疫功能低下的个体、镰状细胞性贫血患者和资源有限的儿童,显示出不同的易感性和结果。并发症,如腰肌脓肿和继发性噬血细胞淋巴组织细胞增多症,被探讨,突出疾病的多面性。伤寒沙门氏菌和副伤寒沙门氏菌对贫血的独特贡献被阐明,阐明了所涉及的病理生理机制。全球流行率和流行病学变化提供了有价值的视角,强调了疾病表现的区域细微差别的重要性。在准确诊断和治疗限制方面的挑战得到承认,强调需要继续研究以提高诊断精度和治疗策略。深入了解长期影响、预后和宿主因素的影响有助于全面了解伤寒性贫血。报告的结论是确定了知识方面的关键差距,倡导正在进行的研究活动和加强认识运动。综合各种研究结果提供了伤寒性贫血的全面概述,强调了为改善患者护理和全球公共卫生而继续进行研究和提高认识的必要性。
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引用次数: 0
Correlation of Ki-67 Expression with the Stage of Disease in Patients of Colorectal Carcinoma. 结直肠癌患者Ki-67表达与疾病分期的关系
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.12
Ashutosh Nagpal, Poras Chaudhary

Colorectal carcinoma (CRC) is a multifactorial disease process with several factors influencing prognosis. CRC is associated with the expression of multiple cell proliferating markers such as Ki-67/MIB-1. This study was aimed to examine possible correlations between Ki-67 expression and the stage of colorectal carcinoma. This was a single centre prospective study including 93 patients who underwent surgery for colorectal carcinoma. Expression of Ki-67 was assessed by immunohistochemistry on formalin-fixed paraffin-embedded tumour tissue blocks. Categorical variables data were presented as number with corresponding percentage. Continuous data were analysed using parametric tests as applicable and categorical data using nonparametric tests. The level of significance α = 0.05 and P-value < 0.05 was considered statistically significant. The average Ki-67 expression was 77.66% (SD [standard deviation] = 9.68%) with a range of 60 to 90%. Patients with nodal involvement and larger size had a higher Ki-67 expression. To assess statistical significance, the cut-off for Ki-67 expression was set at 70%. Of 66, 48 (72.7%) adenocarcinomas and 12/18 (66.66%) mucinous adenocarcinomas had Ki-67 expression above cut-off as compared to signet ring cell variety. Ki-67 expression in colorectal carcinoma signifies mitotic activity of the tumour. Thus, it could be used as an adjunct to the existing diagnostic arsenal to help overcome its limitation in gauging the functional status of tissues.

结直肠癌(CRC)是一种多因素疾病,影响预后的因素很多。结直肠癌与多种细胞增殖标志物如Ki-67/MIB-1的表达有关。本研究旨在探讨Ki-67表达与结直肠癌分期之间的可能相关性。这是一项单中心前瞻性研究,包括93名接受结直肠癌手术的患者。免疫组化法检测Ki-67在福尔马林固定石蜡包埋肿瘤组织块上的表达。分类变量数据以数字和相应的百分比表示。使用参数检验分析连续数据,使用非参数检验分析分类数据。显著性水平α = 0.05, p值<;0.05认为有统计学意义。Ki-67的平均表达量为77.66% (SD[标准差]= 9.68%),范围为60 ~ 90%。淋巴结受累和淋巴结体积较大的患者Ki-67表达较高。为了评估统计学意义,Ki-67表达的临界值设为70%。在66例腺癌中,48例(72.7%)腺癌和12/18例(66.66%)粘液腺癌的Ki-67表达高于切值。Ki-67在结直肠癌中的表达表明肿瘤有丝分裂活性。因此,它可以作为一种辅助现有的诊断武器库,以帮助克服其局限性,以衡量组织的功能状态。
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引用次数: 0
Freeman-Sheldon Syndrome: A Rare Case Report with Dental Perspective. 弗里曼-谢尔登综合征:一个罕见的病例报告与牙科的角度。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.37
Sahil Mustafa Kidwai, Suman Sen, Nikil Kumar Jain, Sudhir Ramesh Maheshkar

Freeman-Sheldon syndrome is a rare form of multiple congenital contracture syndromes (arthrogryposes) and is the most severe form of distal arthrogryposis. The main skeletal malformations include camptodactyly with ulnar deviation and talipes equinovarus while facial characteristics include deep-sunken eyes with hypertelorism, increased philtrum length, small nose and nostrils, and a small mouth. Here we report a rare case of Freeman-Sheldon syndrome (FSS) in an 8-years-old patient giving emphasis on the dental management of FSS.

弗里曼-谢尔登综合征是一种罕见的多发性先天性挛缩综合征(关节挛缩),是远端关节挛缩最严重的形式。主要的骨骼畸形包括掌状畸形伴有尺偏和马蹄内翻,而面部特征包括深凹的眼睛伴远视、中骨长度增加、鼻子和鼻孔小、嘴巴小。在此,我们报告一个罕见的弗里曼-谢尔登综合征(FSS)的病例,一个8岁的病人,强调FSS的牙科管理。
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引用次数: 0
Navigating the Risks of Dental Aspiration in Older Adults: A Case Study of Prompt Diagnosis and Intervention. 引导老年人误吸牙的风险:及时诊断和干预的案例研究。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.13
Louise Cardoso Fava Ferreira Dos Santos, Marcelo de Queiroz Pereira da Silva, Márcio Luís Duarte

Foreign body aspiration is a significant cause of respiratory distress in geriatric patients, often leading to severe complications if not promptly identified and treated. Dental materials account for approximately 15-20% of foreign body aspirations in adults, with symptoms that can include dyspnea, localized wheezing, and, in some cases, cyanosis and pneumonia. We report the case of a 60-year-old man who aspirated a dental crown, resulting in shortness of breath. A computed tomography scan revealed the crown lodged in the left main bronchus. The patient underwent successful bronchoscopy for foreign body removal and experienced a full recovery without complications. Neurological conditions, such as epilepsy or Parkinson's disease, increase the risk of aspiration, particularly in elderly patients, in which symptoms may be misdiagnosed due to their nonspecific presentation. While the right bronchus is more commonly affected due to anatomical structure, foreign body aspiration in the left bronchus also warrants attention. This case underscores the importance of rapid imaging and bronchoscopy to reduce the risk of morbidity and mortality from aspiration events. Increased awareness and timely intervention are essential for improving patient outcomes in cases of dental and other foreign body aspirations in older populations.

异物吸入是老年患者呼吸窘迫的一个重要原因,如果不及时发现和治疗,往往会导致严重的并发症。牙科材料约占成人异物呼入的15-20%,其症状包括呼吸困难、局部喘息,在某些情况下还会出现发绀和肺炎。我们报告的情况下,60岁的男子谁吸牙冠,导致呼吸短促。计算机断层扫描显示冠状动脉卡在左主支气管内。该患者成功接受了支气管镜检查以清除异物,并经历了完全恢复,无并发症。神经系统疾病,如癫痫或帕金森氏病,会增加误吸的风险,特别是在老年患者中,这些患者的症状可能因其非特异性表现而被误诊。由于解剖结构的原因,右支气管更常受到影响,而左支气管的异物吸入也值得注意。该病例强调了快速成像和支气管镜检查对于降低误吸事件的发病率和死亡率的重要性。提高认识和及时干预是必要的,以改善患者的结果,在牙科和其他异物的情况下,老年人的愿望。
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引用次数: 0
Ormond's Disease - 26 Years of Experience at One Centre. 奥蒙德病-在一个中心26年的经验。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.1
Miroslav Průcha, Pavel Zdráhal, Radek Kříž, Alena Šnajdrová, Luděk Voska

Ormond's disease is a systemic autoimmune disease with serious complications. We present our retrospective analysis of 83 patients diagnosed with and treated for idiopathic retroperitoneal fibrosis (Ormond's disease) in our department from 1997 to 2023. In this retrospective study, we analysed the diagnostic approaches, the clinical history and surgical and immunosuppressive therapies, and their subsequent effects on our patients. Patients with established disease activity were given immunosuppressive treatment, using corticosteroids alone or in combination with azathioprine, in patients with exacerbation of the disease mycophenolate mofetil. Three patients with Ormond's disease and systemic complications (IgG4-related disease) were treated with rituximab. In the entire cohort, 83 patients received immunosuppressive therapy; the next 5 patients did not receive this treatment because they did not present inflammatory activity from the disease. In these 83 patients, computed tomography showed that immunosuppressive treatment resulted in partial or complete regression of the inflammatory infiltrate. Out of the 83 patients, 10 patients experienced disease exacerbation 7 and 24 months after the immunosuppressive treatment was discontinued. The follow-up ranged from 24 months to 26 years.

奥蒙德氏病是一种具有严重并发症的全身性自身免疫性疾病。我们对 1997 年至 2023 年在我科确诊并接受治疗的 83 例特发性腹膜后纤维化(奥蒙德氏病)患者进行了回顾性分析。在这项回顾性研究中,我们分析了诊断方法、临床病史、手术和免疫抑制疗法及其对患者的后续影响。已确诊的疾病活动期患者接受免疫抑制治疗,单用皮质类固醇或联合硫唑嘌呤,病情加重的患者则接受霉酚酸酯治疗。三名患有奥蒙德氏病和全身并发症(IgG4 相关疾病)的患者接受了利妥昔单抗治疗。在整个队列中,有 83 名患者接受了免疫抑制治疗;其后的 5 名患者没有接受这种治疗,因为他们没有出现疾病的炎症活动。计算机断层扫描显示,在这 83 名患者中,免疫抑制治疗导致炎症浸润部分或完全消退。在 83 名患者中,有 10 名患者在停止免疫抑制治疗 7 个月和 24 个月后病情加重。随访时间从 24 个月到 26 年不等。
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引用次数: 0
Dual Roots of Origin of Inferior Alveolar Nerve and "Vagal Ansa" Cervicalis: Surgical and Anaesthetic Implications. 下肺泡神经和颈神经“迷走神经袢”的双重根:手术和麻醉意义。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.28
Dibakar Borthakur, Arthi Ganapathy, Kamalesh Saravanan, Jayanta Biswas, Saroj Kaler Jhajhria

During routine cadaveric dissection for undergraduate medical teaching, we observed dual roots of origin of the inferior alveolar nerve (IAN) on the right infratemporal fossa in an elderly male cadaver. The IAN originated by two roots encircling the second part of the maxillary artery (MA). The superior root of the ansa cervicalis (AC) originated from the ipsilateral vagus nerve and two independent muscular branches of the right vagus provided additional innervations to the anterior neck muscles. Awareness about the dual roots of origin of IAN is imperative for anaesthesiologists and dentists, while administering local anaesthesia. A prior knowledge about the vagal origin of AC is essential to prevent iatrogenic damage during surgeries.

在本科医学教学的常规解剖过程中,我们观察了一具老年男性尸体右侧颞下窝的下肺泡神经(IAN)的双根起源。下颌动脉起源于环绕上颌动脉(MA)第二部分的两根。颈袢上根起源于同侧迷走神经,右迷走神经的两个独立的肌肉分支为颈前肌提供了额外的神经支配。麻醉师和牙医在进行局部麻醉时,必须意识到IAN的双重起源。事先了解AC的迷走神经起源对于预防手术中医源性损伤至关重要。
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引用次数: 0
Unveiling the Enigma: Plasma Cell Leukaemia Presenting with Flower-like Cells, Mimicking Adult T-cell Leukaemia - A Rare Diagnostic Conundrum. 揭开谜团:浆细胞白血病呈现花状细胞,模仿成人t细胞白血病-一个罕见的诊断难题。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.25
Anurag Singh, Gyanendra Singh

Peripheral plasma cell leukaemia (PCL) is a rare hematologic malignancy that can pose diagnostic challenges due to its resemblance to other conditions such as adult T-cell leukaemia/lymphoma (ATLL) or dissemination lymphoma in peripheral blood. We present a case report of a 40-year-old male with symptoms of fatigue, irregular heartbeat, weight loss, and bone pain, whose peripheral blood examination revealed hyperleukocytosis with atypical lymphoid cells exhibiting flower-shaped nuclei, reminiscent of adult T-cell leukaemia/lymphoma. Further investigations including bone marrow aspiration and biopsy confirmed the diagnosis of primary PCL. Immunophenotyping revealed expression of plasma cell antigens CD38 and CD138. This case underscores the importance of recognizing morphological variants and employing comprehensive immunophenotypic analysis for accurate diagnosis of PCL, especially when atypical nuclear features mimic other hematologic malignancies.

外周浆细胞白血病(PCL)是一种罕见的血液恶性肿瘤,由于其与其他疾病(如成人t细胞白血病/淋巴瘤(ATLL)或外周血播散性淋巴瘤)相似,可能带来诊断挑战。我们报告一个40岁男性的病例,其症状为疲劳、心跳不规则、体重减轻和骨痛,其外周血检查显示白细胞增多,非典型淋巴样细胞呈花状核,使人联想到成人t细胞白血病/淋巴瘤。进一步的检查包括骨髓穿刺和活检证实了原发性PCL的诊断。免疫表型分析显示浆细胞抗原CD38和CD138的表达。本病例强调了识别形态变异和采用全面的免疫表型分析对PCL准确诊断的重要性,特别是当非典型核特征与其他血液系统恶性肿瘤相似时。
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引用次数: 0
Biofilm-forming Ability of Anaerobic Bacterial Strains Isolated from Patients Diagnosed with Periodontitis. 牙周炎患者厌氧菌的生物膜形成能力。
Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2025-01-01 DOI: 10.14712/23362936.2025.22
Ivan Skliar, Maryna Kryvtsova, Yevhen Kostenko, Marianna Savenko

Bacterial biofilms represent the primary causative agents of pathogenic processes within the oral cavity. Biofilm microorganisms exhibit heightened resistance to adverse environmental factors. The objective of this study was to ascertain the biofilm-forming potential of clinical strains of anaerobic microorganisms isolated from the periodontal pocket of patients diagnosed with periodontitis. The study of biofilm formation was carried out by the method (Djordjevic et al., 2002) using flat-bottomed 96-well polystyrene microtitration plates. Biofilm formation was determined by staining with 0.1% crystal violet. The study utilised clinical strains isolated from the periodontal pocket of 61 patients diagnosed with grade III chronic periodontitis. Of these, 30 strains belonging to three bacterial species were selected for further analysis: Porphyromonas asaccharolytica, Slackia exigua, and Schaalia odontolytica. Among the Porphyromonas asaccharolytica strains, 80% formed biofilm; the figure for Slackia exigua was 90%, and for Schaalia odontolytica - 80%. In total, 25 strains were capable of biofilm formation. The results indicate that the isolated strains of Porphyromonas asaccharolytica, Slackia exigua, and Schaalia odontolytica exhibited a significant capacity for biofilm formation (83.3% of the strains formed biofilm), particularly Slackia exigua strains, which exhibited the highest number of strains with high biofilm formation ability - 5 (16.6%). It is also noteworthy that these microorganisms exhibited a moderate persistence frequency (16.4% each), of the total sample of microbial biocenoses from inflammatory periodontal soft tissue areas.

细菌生物膜是口腔内致病过程的主要病原体。生物膜微生物对不利环境因素表现出更高的抵抗力。本研究的目的是确定从诊断为牙周炎的患者的牙周袋中分离的临床菌株厌氧微生物的生物膜形成潜力。生物膜形成的研究方法(Djordjevic et al., 2002)采用96孔平板聚苯乙烯微滴定板。0.1%结晶紫染色测定生物膜形成。该研究利用从61例诊断为III级慢性牙周炎的患者的牙周袋中分离的临床菌株。其中,30株属于3种细菌,分别为:解糖卟啉单胞菌(Porphyromonas assacacchartica)、脱落菌(Slackia exigua)和溶牙沙利亚菌(Schaalia dotoltotica)。在溶糖卟啉单胞菌菌株中,80%形成生物膜;exigua的比例为90%,Schaalia的比例为80%。共有25株菌株能够形成生物膜。结果表明:溶糖卟啉单胞菌、绿僵菌和溶牙沙利菌的生物膜形成能力显著(83.3%的菌株形成生物膜),其中绿僵菌的生物膜形成能力最强,达到5株(16.6%);同样值得注意的是,这些微生物在来自炎症性牙周软组织区域的微生物群落样本中表现出中等的持久性频率(各16.4%)。
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引用次数: 0
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