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Late Intracerebral Hemorrhage After Successful Endovascular Closure of a Carotid-Cavernous Fistula: A Case Report and Updated Review. 血管内成功封闭颈动脉-海绵窦瘘后的晚期脑出血:1例报告和最新综述。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-13 DOI: 10.3390/reports8040234
Karol Uscamaita, Marta García Pla, Mikel Terceño, Adrià Arboix, Yolanda Silva

Background and Clinical Significance: Intracerebral hemorrhage (ICH) is a very rare complication following endovascular closure of direct carotid-cavernous fistulas (CCFs). When reported, ICH typically appears within the first 48 h after CCF closure. We performed an extensive literature review, starting from the case of a 48-year-old patient presenting with an intracerebral hemorrhage after CCF closure. Case Presentation: A 48-year-old woman with arterial hypertension developed an intracerebral hemorrhage in the right frontal lobe 12 days after successful closure of a traumatic CCF. The patient exhibited acute neurological deterioration in a previously hypoperfused territory. A narrative review identifies the classical molecular theory of hemodynamic dysregulation, known as Normal Perfusion Pressure Breakthrough (NPPB), as the principal pathophysiological mechanism. Other mechanisms such as oxidative stress, microglial activation, blood-brain barrier disruption, metalloproteinase expression, and possible genetic alterations such as ICA1L variants are also implicated. Conclusions: This case underscores the importance of considering molecular mechanisms in the pathophysiology of delayed post-endovascular treatment of ICH, as well as the need for hemodynamic monitoring and follow-up in patients with vascular comorbidities.

背景与临床意义:脑出血是直接颈动脉-海绵窦瘘(CCFs)血管内闭合后非常罕见的并发症。当报告时,ICH通常在CCF关闭后的头48小时内出现。我们进行了广泛的文献回顾,从一名48岁的患者在CCF关闭后出现脑出血的病例开始。病例介绍:一名48岁女性动脉高血压患者在成功关闭创伤性CCF后12天发生右额叶脑出血。患者在先前的低灌注区表现出急性神经退化。一篇叙述性的综述确定了血流动力学失调的经典分子理论,即正常灌注压突破(NPPB),作为主要的病理生理机制。其他机制,如氧化应激、小胶质细胞激活、血脑屏障破坏、金属蛋白酶表达和可能的遗传改变,如ICA1L变异也有牵连。结论:该病例强调了考虑脑出血后延迟血管内治疗的病理生理学分子机制的重要性,以及对血管合并症患者进行血流动力学监测和随访的必要性。
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引用次数: 0
Comment on Mavroudis et al. Post-Traumatic Epilepsy After Mild and Moderate Traumatic Brain Injury: A Narrative Review and Development of a Clinical Decision Tool. Reports 2025, 8, 193. 对Mavroudis等人的评论。轻、中度创伤性脑损伤后的创伤后癫痫:一种临床决策工具的叙述回顾和发展。报告2025、8、193。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-13 DOI: 10.3390/reports8040233
Roy G Beran

The paper by Mavroudis et al [...].

Mavroudis等人的论文[…]。
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引用次数: 0
Chest Wound Gunshot Management Aided by Cardiopulmonary Bypass: Interdisciplinary Teamwork or "Serendipity"? 体外循环辅助的胸部枪伤管理:跨学科团队合作还是“偶然发现”?
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-13 DOI: 10.3390/reports8040236
Valentina Tassi, Roland Peraj, Roberto Cirocchi, Valentino Borghetti, Mark Ragusa

Background and clinical significance. Penetrating cardiothoracic wounds require prompt treatment in order to decrease mortality and morbidity. Surgical therapy, aimed at bleeding control and removal of damaged tissue, varies widely from the direct suture of parenchymal lacerations to pneumonectomy, which is characterized by high mortality rates. We report our experience with a patient in hemorrhagic shock due to a gunshot wound to the chest, successfully treated by pneumorrhaphy under cardiopulmonary bypass (CPB). Case presentation. A 53-year-old man with a gunshot wound to the chest was admitted to our Emergency Department. A bedside ultrasonography revealed left pleural and pericardial effusion. He was hemodynamically instable, so he was immediately transferred to the operating room by the cardiac and Thoracic Surgery teams. Through a median sternotomy approximately 2 L of blood were evacuated and a deep laceration of the left upper lobe was discovered. The massive bleeding could not be controlled, leading to pleural cavity flooding. The surgical team decided to institute emergency CPB and perform lung repair by pneumorrhaphy, under circulatory support. The patient survived and was discharged on p.o. day 20. Conclusions. Clinical expertise, adequate instrumental equipment and a high level of interdisciplinary team-work favorably affected the patient's outcome.

研究背景及临床意义。穿透性心胸伤口需要及时治疗,以降低死亡率和发病率。手术治疗旨在控制出血和切除受损组织,从直接缝合实质撕裂伤到肺切除术,其特点是死亡率高。我们报告我们的经验,病人失血性休克,由于胸部枪伤,成功地治疗下肺体外循环(CPB)。例演示。一名胸部中枪的53岁男子被急诊科收治。床边超声检查显示左胸膜及心包积液。他的血流动力学不稳定,所以他立即被心外科和胸外科小组转移到手术室。通过正中胸骨切开术,排出约2l的血液,发现左上肺叶有深撕裂伤。大出血无法控制,导致胸腔积水。手术小组决定实施紧急CPB,并在循环支持下进行肺修补术。患者存活并于第20天出院。结论。临床专业知识、充足的仪器设备和高水平的跨学科团队合作对患者的预后有积极影响。
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引用次数: 0
A Mucosal Change like Hypertrophic Gastritis Following Zolbetuximab-Based Therapy in a Conversion Surgery Case of Advanced Gastric Cancer. 1例晚期胃癌转换手术患者佐仑妥昔单抗治疗后粘膜改变类似肥厚性胃炎。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-13 DOI: 10.3390/reports8040235
Soshi Oyama, Shuhei Suzuki, Takanobu Kabasawa, Takumi Kanauchi, Shotaro Akiba

Background and Clinical Significance: Zolbetuximab, a claudin 18.2-targeted monoclonal antibody, has demonstrated efficacy in advanced gastric cancer. Hypoalbuminemia has emerged as a notable adverse effect, but its underlying mechanism remains unclear. Case Presentation: A 53-year-old male with unresectable advanced gastric cancer received zolbetuximab-based combination therapy, achieving tumor regression enabling conversion surgery. During six cycles of treatment, serum albumin levels decreased from 4.3 g/dL to 3.5-3.6 g/dL (grade 1 hypoalbuminemia). A histopathological examination of the surgical specimen revealed hypertrophic gastritis characterized by marked foveolar hyperplasia, increased mucus secretion, and pyloric gland metaplasia on the lesser curvature. These findings suggest that zolbetuximab-induced mucosal alterations may contribute to hypoalbuminemia through enhanced protein loss. Conclusions: This is the first pathological documentation of hypertrophic gastritis associated with zolbetuximab therapy. Clinicians should monitor albumin levels during treatment and consider nutritional support when indicated. These findings provide important insights for optimizing patient management and ensuring safe conversion surgery planning.

背景及临床意义:Zolbetuximab是一种claudin 18.2靶向单克隆抗体,已被证实对晚期胃癌有疗效。低白蛋白血症已成为一种显著的不良反应,但其潜在机制尚不清楚。病例介绍:一名53岁晚期胃癌患者接受以唑苯妥昔单抗为基础的联合治疗,肿瘤消退,可进行转化手术。在6个治疗周期中,血清白蛋白水平从4.3 g/dL降至3.5-3.6 g/dL(1级低白蛋白血症)。手术标本的组织病理学检查显示肥厚性胃炎,其特征是明显的小窝增生,粘液分泌增加,幽门腺小弯化生。这些发现表明,唑苯妥昔单抗诱导的粘膜改变可能通过增加蛋白质损失导致低白蛋白血症。结论:这是第一个与唑仑妥昔单抗治疗相关的肥厚性胃炎的病理记录。临床医生应在治疗期间监测白蛋白水平,必要时考虑营养支持。这些发现为优化患者管理和确保安全的转换手术计划提供了重要的见解。
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引用次数: 0
Spontaneous Intracranial Hypotension in Pregnancy with Aggravated Comorbidity: A Case Report and Review of Diagnostic and Management Challenges. 妊娠期自发性颅内低血压伴加重合并症:一例报告及诊断和管理挑战的回顾。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-11 DOI: 10.3390/reports8040231
Taruna Agrawal, Jhia Jiat Teh, Konstantinos S Kechagias, Zak Jefferson-Pillai, Kanwaljeet Kaur Sandhu, Sarah-Jane Lam

Background and Clinical Significance: Spontaneous intracranial hypotension (SIH) is a rare cause of headache characterised by cerebrospinal fluid (CSF) leakage, with an estimated incidence of 3.7 to 5 cases per 100,000 per year, peaking around the age of 40 years. Its diagnosis and management are particularly challenging in pregnancy due to overlapping symptoms and limited diagnostic options. Case Presentation: We report the case of a 42-year-old pregnant woman at 14 weeks of gestation presenting with a history of orthostatic headache and facial sinus tenderness, later diagnosed as spontaneous intracranial hypotension. Conclusions: Headache is a common clinical symptom that may be associated with a wide spectrum of underlying conditions, ranging from benign causes such as migraine or tension-type headache to potentially life-threatening pathologies, including subarachnoid haemorrhage. This case illustrates the diagnostic complexity of SIH in pregnancy and the importance of a multidisciplinary approach and vigilance for neurological symptoms during pregnancy.

背景和临床意义:自发性颅内低血压(SIH)是一种罕见的头痛病因,其特征是脑脊液(CSF)渗漏,估计发病率为每年每10万人3.7至5例,在40岁左右达到高峰。由于症状重叠和诊断选择有限,其诊断和管理在妊娠期尤其具有挑战性。病例介绍:我们报告一例42岁妊娠14周的孕妇,表现为直立性头痛和面部鼻窦压痛,后来诊断为自发性颅内低血压。结论:头痛是一种常见的临床症状,可能与广泛的潜在疾病有关,从良性原因如偏头痛或紧张性头痛到潜在的危及生命的病理,包括蛛网膜下腔出血。本病例说明了妊娠期SIH诊断的复杂性和多学科方法的重要性以及对妊娠期神经系统症状的警惕。
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引用次数: 0
Mesonephric Hyperplasia and Adenocarcinoma of the Cervix: A Rare Evolution, Case Report, and Review of the Literature. 子宫颈中肾增生与腺癌:罕见的演变、病例报告及文献回顾。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-11 DOI: 10.3390/reports8040230
Angel Yordanov, Diana Strateva, Albena Baicheva, Ivan Baichev, Stoyan Kostov, Vasilena Dimitrova

Background and Clinical Significance: Mesonephric adenocarcinoma (MA) of the uterine cervix is an exceptionally uncommon and aggressive cancer that arises from remnants of the mesonephric duct. It was first classified by the World Health Organization (WHO) in the 2020 WHO Classification of Female Genital Tumors as a type of cervical adenocarcinoma, also referred to as Gartner's duct carcinoma. Due to its rarity, both detection and treatment pose significant challenges, and there is little information on its clinical manifestations and prognosis. Mesonephric hyperplasia (MH) in the uterine cervix is an uncommon condition that is often misdiagnosed as adenocarcinoma. Case Presentation: We present the case of a 49-year-old, asymptomatic, perimenopausal woman diagnosed with cervical mesonephric adenocarcinoma following a routine Pap smear, performed by Papanicolaou test, with a III A-B result; however, a cone biopsy revealed stage IB1 mesonephric adenocarcinoma. The patient underwent a radical hysterectomy type C (Querleu-Morrow 2017 classification). The final pathology confirmed stage IB2 of the cancer (2018 classification) according to The International Federation of Gynecology and Obstetrics (FIGO), with previous evidence of mesonephric hyperplasia from a trial abrasion performed three years earlier. Conclusions: This case highlights the challenges in recognizing and managing mesonephric hyperplasia and adenocarcinoma of the cervix. Given the uncommon nature of this cancer, clinicians should consider it when treating patients with ambiguous cervical pathology and mesonephric hyperplasia. Optimizing patient outcomes relies on early detection, accurate staging, and radical surgical treatment.

背景和临床意义:子宫颈中肾腺癌(MA)是一种罕见的侵袭性癌症,起源于中肾管的残余。世界卫生组织(WHO)在2020年《世界卫生组织女性生殖器肿瘤分类》中首次将其分类为一种宫颈腺癌,也称为高德纳导管癌。由于其罕见性,无论是发现还是治疗都面临着巨大的挑战,而且关于其临床表现和预后的信息很少。摘要子宫颈中肾增生是一种罕见的疾病,常被误诊为腺癌。病例介绍:我们提出一个病例,49岁,无症状,围绝经期妇女诊断为子宫颈间肾腺癌常规巴氏涂片后,进行巴氏涂片检查,与III a - b结果;然而,椎体活检显示IB1期中肾腺癌。患者接受了C型根治性子宫切除术(Querleu-Morrow 2017分类)。根据国际妇产科学联合会(FIGO),最终病理证实癌症为IB2期(2018年分类),此前有证据表明,三年前进行的试验性磨损导致中肾增生。结论:本病例强调了识别和处理子宫颈中肾增生和腺癌的挑战。鉴于这种癌症的罕见性质,临床医生在治疗宫颈病理不明确和中肾增生的患者时应考虑到这一点。优化患者预后依赖于早期发现、准确分期和根治性手术治疗。
{"title":"Mesonephric Hyperplasia and Adenocarcinoma of the Cervix: A Rare Evolution, Case Report, and Review of the Literature.","authors":"Angel Yordanov, Diana Strateva, Albena Baicheva, Ivan Baichev, Stoyan Kostov, Vasilena Dimitrova","doi":"10.3390/reports8040230","DOIUrl":"10.3390/reports8040230","url":null,"abstract":"<p><p><b>Background and Clinical Significance</b>: Mesonephric adenocarcinoma (MA) of the uterine cervix is an exceptionally uncommon and aggressive cancer that arises from remnants of the mesonephric duct. It was first classified by the World Health Organization (WHO) in the 2020 WHO Classification of Female Genital Tumors as a type of cervical adenocarcinoma, also referred to as Gartner's duct carcinoma. Due to its rarity, both detection and treatment pose significant challenges, and there is little information on its clinical manifestations and prognosis. Mesonephric hyperplasia (MH) in the uterine cervix is an uncommon condition that is often misdiagnosed as adenocarcinoma. <b>Case Presentation</b>: We present the case of a 49-year-old, asymptomatic, perimenopausal woman diagnosed with cervical mesonephric adenocarcinoma following a routine Pap smear, performed by Papanicolaou test, with a III A-B result; however, a cone biopsy revealed stage IB1 mesonephric adenocarcinoma. The patient underwent a radical hysterectomy type C (Querleu-Morrow 2017 classification). The final pathology confirmed stage IB2 of the cancer (2018 classification) according to The International Federation of Gynecology and Obstetrics (FIGO), with previous evidence of mesonephric hyperplasia from a trial abrasion performed three years earlier. <b>Conclusions</b>: This case highlights the challenges in recognizing and managing mesonephric hyperplasia and adenocarcinoma of the cervix. Given the uncommon nature of this cancer, clinicians should consider it when treating patients with ambiguous cervical pathology and mesonephric hyperplasia. Optimizing patient outcomes relies on early detection, accurate staging, and radical surgical treatment.</p>","PeriodicalId":74664,"journal":{"name":"Reports (MDPI)","volume":"8 4","pages":""},"PeriodicalIF":0.8,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12643449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145590122","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multimodality Imaging of Moyamoya Disease: A Practical Guide for Neuroradiologists Based on a Case Report. 烟雾病的多模态成像:基于病例报告的神经放射科医师实用指南。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-11 DOI: 10.3390/reports8040232
Elisa Ferraro, Agata Amaduri, Corrado Ini', Mario Travali, Francesco Tiralongo, Pietro Valerio Foti, Concetto Cristaudo, Antonio Basile

Background and Clinical Significance: Moyamoya disease is a rare, progressive cerebrovascular disease characterized by steno-occlusion of the terminal internal carotid arteries and the arteries around the circle of Willis, with the formation of abnormal collateral vessels. Early clinical manifestations include recurrent hemodynamic transient ischemic attacks (TIAs), especially in young subjects. Multimodality imaging, including computed tomography, magnetic resonance, and digital subtraction angiography, is necessary to reach a correct diagnosis in young patients with stroke-like symptoms. Various radiological findings are crucial for early diagnosis, staging, and management of moyamoya disease. Case Presentation: We describe the case of a 31-year-old male presenting with acute focal neurological deficits and a history of recurrent TIAs. Neuroimaging was performed to assess vascular pathology, parenchymal injury, and collateral circulation and to provide critical information on vascular anatomy and the extent of ischemic damage. Conclusions: The purpose of this case report is to illustrate the main specific radiological signs and the diagnostic value of multimodality neuroimaging in the evaluation of moyamoya disease, providing a practical imaging-based diagnostic approach for neuroradiologists.

背景及临床意义:烟雾病是一种罕见的进行性脑血管疾病,以颈内动脉终末及威利斯圈周围动脉狭窄闭塞为特征,伴异常侧支血管形成。早期临床表现包括复发性血流动力学短暂性脑缺血发作(tia),特别是在年轻受试者中。多模态成像,包括计算机断层扫描、磁共振和数字减影血管造影,对于有卒中样症状的年轻患者的正确诊断是必要的。各种影像学表现对烟雾病的早期诊断、分期和治疗至关重要。病例介绍:我们描述的情况下,31岁的男性表现为急性局灶性神经功能障碍和复发性TIAs的历史。神经影像学用于评估血管病理、实质损伤和侧支循环,并提供血管解剖和缺血性损伤程度的关键信息。结论:本病例报告旨在阐述烟雾病的主要特异性影像学征象及多模态神经影像学在烟雾病评价中的诊断价值,为神经放射医师提供一种实用的基于影像学的诊断方法。
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引用次数: 0
Second Trimester Interstitial Ectopic Pregnancy. 中期间质性异位妊娠。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-10 DOI: 10.3390/reports8040229
Daniel Reyes, Amanda Key, Zachary LeBaron, Samantha Matz, Daniel Gridley

Background and Clinical Significance: Interstitial ectopic pregnancy is a rare but potentially life-threatening type of ectopic gestation that carries high risk of rupture and hemorrhage due to its vascular location and predisposition for delayed presentation. Case Presentation: We present a 33-year-old female with acute abdominal pain and elevated β-hCG, with transvaginal ultrasound demonstrating a live left adnexa ectopic pregnancy dated at approximately 14 weeks. MRI confirmed the gestational sac as tubal ectopic, but poorly localized within the interstitial fallopian tube. Exploratory laparoscopy revealed the gestational sac mainly in the interstitial left fallopian tube without rupture or distal involvement. Conclusions: This case demonstrates absent classic imaging findings associated with tubal, interstitial, and ovarian ectopic gestations including tubal ring sign, interstitial line sign, endo-myometrial mantle measurement, or claw sign due to location and advanced gestational age. Familiarity with these challenges and recognition that interstitial ectopic pregnancy may present atypically are important for timely recognition and management.

背景和临床意义:间质性异位妊娠是一种罕见但可能危及生命的异位妊娠,由于其血管位置和延迟表现的倾向,具有破裂和出血的高风险。病例介绍:我们报告了一位33岁的女性,急性腹痛和β-hCG升高,经阴道超声显示左附件异位妊娠约14周。MRI证实妊娠囊为输卵管异位,但在输卵管间质内定位不良。腹腔镜探查显示妊娠囊主要位于左输卵管间质,未见破裂或远端受累。结论:本病例未表现出输卵管、间质和卵巢异位妊娠的典型影像学表现,包括输卵管环征、间质线征、子宫内膜套膜测量或因位置和孕龄而引起的爪征。熟悉这些挑战并认识到间质性异位妊娠可能表现为非典型性,对于及时识别和处理是重要的。
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引用次数: 0
Safe Crestal Sinus Elevation Below 3 mm Residual Bone with Tissue-Level Implant Placement: A Case Report. 安全嵴窦抬高低于3mm残余骨与组织水平植入:1例报告。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-07 DOI: 10.3390/reports8040228
Carola Di Frischia, Marco Tallarico, Marco Gargari, Edoardo Magnifico, Francesco Cecchetti, Francesco Mattia Ceruso

Background and Clinical Significance: Maxillary sinus augmentation is a well-established surgical procedure for dental implant placement in the posterior maxilla when the residual alveolar bone height is insufficient. Traditionally, the lateral approach has been preferred in cases with less than 4 mm of bone; however, the crestal approach has emerged as a less invasive alternative, particularly with the advent of advanced techniques and tools such as hydraulic pressure systems and dedicated osteotomy kits. Case Presentation: This case report presents the clinical management of a 68-year-old female patient requiring rehabilitation of the right maxillary molars, where the residual bone height measured only 3.6 mm (in position 1.6) and 2.5 mm (in position 1.7). Using the CAS kit system with rounded drills and hydraulic pressure, a controlled crestal sinus elevation was performed, followed by simultaneous implant placement. Despite the extremely limited bone height, a final insertion torque of 30 Ncm was achieved for both implants, likely due to favorable sinus floor anatomy, under-preparation of the implant sites, and the use of tapered, macro-textured implants. Postoperative follow-up over three years showed stable bone levels and successful prosthetic rehabilitation with single crowns. Conclusions: This case report highlights the potential of the crestal approach in anatomically challenging scenarios. Proper planning, technique, and implant selection are mandatory to achieve predictable and long-lasting outcomes, even in cases previously considered contraindicated for this method. Further randomized controlled trials are needed to confirm this preliminary result.

背景与临床意义:上颌窦提升术是上颌后牙槽骨高度不足时种植体植入的一种成熟的手术方法。传统上,对于骨量小于4毫米的病例,外侧入路是首选;然而,嵴入路已成为一种侵入性较小的替代方法,特别是随着液压系统和专用截骨工具等先进技术和工具的出现。病例报告:本病例报告了一名68岁女性患者的临床处理,需要修复右侧上颌磨牙,其残余骨高度仅为3.6 mm(位置1.6)和2.5 mm(位置1.7)。使用CAS套件系统与圆钻和液压,进行一个可控的冠窦抬高,然后同时种植体放置。尽管骨高度非常有限,但两种种植体的最终插入扭矩均达到30 Ncm,这可能是由于良好的窦底解剖结构、种植体部位准备不足以及使用锥形、宏观纹理的种植体所致。术后随访3年多,显示骨水平稳定,单冠修复成功。结论:本病例报告强调了嵴入路在解剖学上具有挑战性的情况下的潜力。正确的计划、技术和种植体的选择是必须的,以达到可预测和持久的结果,即使在以前被认为是禁忌的病例中也是如此。需要进一步的随机对照试验来证实这一初步结果。
{"title":"Safe Crestal Sinus Elevation Below 3 mm Residual Bone with Tissue-Level Implant Placement: A Case Report.","authors":"Carola Di Frischia, Marco Tallarico, Marco Gargari, Edoardo Magnifico, Francesco Cecchetti, Francesco Mattia Ceruso","doi":"10.3390/reports8040228","DOIUrl":"10.3390/reports8040228","url":null,"abstract":"<p><p><b>Background and Clinical Significance</b>: Maxillary sinus augmentation is a well-established surgical procedure for dental implant placement in the posterior maxilla when the residual alveolar bone height is insufficient. Traditionally, the lateral approach has been preferred in cases with less than 4 mm of bone; however, the crestal approach has emerged as a less invasive alternative, particularly with the advent of advanced techniques and tools such as hydraulic pressure systems and dedicated osteotomy kits. <b>Case Presentation:</b> This case report presents the clinical management of a 68-year-old female patient requiring rehabilitation of the right maxillary molars, where the residual bone height measured only 3.6 mm (in position 1.6) and 2.5 mm (in position 1.7). Using the CAS kit system with rounded drills and hydraulic pressure, a controlled crestal sinus elevation was performed, followed by simultaneous implant placement. Despite the extremely limited bone height, a final insertion torque of 30 Ncm was achieved for both implants, likely due to favorable sinus floor anatomy, under-preparation of the implant sites, and the use of tapered, macro-textured implants. Postoperative follow-up over three years showed stable bone levels and successful prosthetic rehabilitation with single crowns. <b>Conclusions:</b> This case report highlights the potential of the crestal approach in anatomically challenging scenarios. Proper planning, technique, and implant selection are mandatory to achieve predictable and long-lasting outcomes, even in cases previously considered contraindicated for this method. Further randomized controlled trials are needed to confirm this preliminary result.</p>","PeriodicalId":74664,"journal":{"name":"Reports (MDPI)","volume":"8 4","pages":""},"PeriodicalIF":0.8,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12643441/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145590299","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical and Sociodemographic Characterization of Mexican Cohort with Pseudoarthrosis: A Retrospective, Cross-Sectional, and Descriptive Study. 墨西哥假关节队列的临床和社会人口学特征:回顾性、横断面和描述性研究。
IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-11-05 DOI: 10.3390/reports8040227
Emilio Ignacio Pérez Jiménez, Félix Gustavo Mora Ríos, Brian Misael Muñoz Hernández, Josué Ramos Texta, Roberto Carlos Domínguez González, Joan Artemio Pérez Figueroa, Pedro García-Benavides, Carlos Alberto Castro-Fuentes

Background/objectives: Pseudoarthrosis continues to be a public health problem; however, in our country, information is scarce, particularly when talking about the clinical and sociodemographic characterization of the Mexican population with pseudoarthrosis.

Methods: In this study, clinical and sociodemographic characteristics such as sex, age, educational level, nutritional status, comorbidities, affected bone, fracture characteristics, degree of exposure, and waiting time for the patient to undergo surgery were analyzed.

Results: A total of 267 patients were included in the present study. A higher frequency of men (53.6%) was identified compared to women, and the main age group was 46-75 years (50.1%). The main comorbidities identified in our population were smoking (n = 141; 52.8%) and osteoporosis (n = 84; 31.5%). When evaluating the clinical characteristics of pseudoarthrosis, the tibia (n = 65; 24.3%) and radius (n = 54; 20.2%) were the main bones affected. Fracture exposure could be identified in 17.65% (n = 47) of the population, and the main grade of involvement was II (46.8%). Regarding the prevalence of the affected bone, the tibia was the main one, with 13.5% (9.38-17.58%) female patients, 12.7% (8.73-16.73%) with overweight, 18.0% (13.37-22.59%) with osteoporosis, and 14.2% (10.04-18.42%) with a history of smoking.

Conclusions: In our cohort, we identified a high prevalence of the tibia as the affected bone, while overweight, obesity, osteoporosis, and smoking were the clinical and sociodemographic characteristics that characterized our population. The findings of this study lay the groundwork for understanding the clinical and sociodemographic context of a Mexican cohort with nonunion.

背景/目的:假关节仍然是一个公共卫生问题;然而,在我国,信息是稀缺的,特别是在谈论墨西哥人口与假关节的临床和社会人口学特征。方法:分析患者的临床及社会人口学特征,如性别、年龄、文化程度、营养状况、合并症、受累骨、骨折特征、暴露程度、手术等待时间等。结果:本研究共纳入267例患者。男性的发病率(53.6%)高于女性,主要年龄组为46-75岁(50.1%)。在我们的人群中发现的主要合并症是吸烟(n = 141, 52.8%)和骨质疏松症(n = 84, 31.5%)。在评估假关节的临床特征时,胫骨(n = 65, 24.3%)和桡骨(n = 54, 20.2%)是主要受影响的骨骼。17.65% (n = 47)的人群可识别骨折暴露,主要受累等级为II级(46.8%)。患骨患病率以胫骨为主,女性占13.5%(9.38 ~ 17.58%),超重占12.7%(8.73 ~ 16.73%),骨质疏松占18.0%(13.37 ~ 22.59%),有吸烟史占14.2%(10.04 ~ 18.42%)。结论:在我们的队列中,我们确定了胫骨作为受影响骨骼的高患病率,而超重、肥胖、骨质疏松症和吸烟是我们人群的临床和社会人口学特征。本研究的发现为了解墨西哥骨不连队列的临床和社会人口学背景奠定了基础。
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