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Pearls and pitfalls of cuffless blood pressure monitoring devices 无袖血压监测设备的优点和缺陷
Pub Date : 2023-09-30 DOI: 10.37897/rmj.2023.3.2
Radu-Alexandru Iacobescu, Bogdan-Danut Florescu, Alina-Mihaela Dimache, Luiza-Elena Corneanu, Elena Adorata Coman
Cuffless blood pressure measuring devices are emerging as alternatives for out-of-office assessment of patients with hypertension. This novel technology promises to deliver continuous or beat-to-beat blood pressure measurement and resolve some of the inconveniences associated with conventional cuff-based devices such as improper cuff fit, discomfort, low adherence to monitoring, and technical challenges. Blood pressure can be estimated based on phenomena related to cardiovascular activity: pulse wave velocity, pulse wave analysis, tonometry, and volume clamping. In this narrative review, we seek to summarize current approaches for nontraditional measurement of blood pressure and discuss some of the benefits and limitations of this technology.
无袖带血压测量装置正在成为高血压患者外出评估的替代方案。这项新技术有望提供连续或连续的血压测量,并解决传统袖带设备带来的一些不便,如袖带不合适、不舒服、监测依从性低以及技术挑战。血压可以根据与心血管活动相关的现象来估计:脉搏波速度、脉搏波分析、血压计和容量夹紧。在这篇叙述性综述中,我们试图总结目前非传统血压测量的方法,并讨论该技术的一些优点和局限性。
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引用次数: 0
Red cell distribution width as a prognostic marker in ovarian cancer patients 红细胞分布宽度作为卵巢癌患者的预后指标
Pub Date : 2023-09-30 DOI: 10.37897/rmj.2023.3.3
Nicolae Bacalbasa, Irina Balescu, Mihaela Vilcu, Claudia Stoica, Tarig Massawi, Sorin Petrea, Cristina Martac, Adriana Ciuvica, Andrei Voichitoiu, Iulian Brezean, Victor Cauni, Bogdan Gaspar
Red cell distribution width [RDW] represents a new prognostic marker which has been widely studied in malignant tumors including ovarian cancer patients. Therefore, it has been stipulated that RDW can be also used as a prognostic marker and a follow up tool for these patients. The aim of the current paper was to analyze the variations of this parameter on a study group of 31 patients diagnosed with advanced stage ovarian cancer and respectively 48 cases with benign ovarian lesions submitted to surgery between 2017-2020 in “Cantacuzino” Clinical Hospital.
红细胞分布宽度(RDW)作为一种新的预后指标,在包括卵巢癌在内的恶性肿瘤患者中得到了广泛的研究。因此,已经规定RDW也可以作为这些患者的预后标志物和随访工具。本论文的目的是分析该参数在2017-2020年在Cantacuzino临床医院进行手术的31例晚期卵巢癌患者和48例卵巢良性病变患者的研究组中的变化。
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引用次数: 0
Diagnosis of exclusion in Burning Mouth Syndrome (BMS) 灼口综合征的排除诊断
Pub Date : 2023-09-30 DOI: 10.37897/rmj.2023.3.1
Elena Claudia Coculescu, Bogdan-Ioan Coculescu
Internationally, relatively few studies have been undertaken regarding research on non-specific oral burning pain, especially regarding the identification of possible causal factors. Knowledge in this field from a physiopathological and therapeutic perspective is recent, which supports the need for further study and the definition of the disease as an interdisciplinary syndrome. Deepening the research on the etiopathogenesis of burning mouth syndrome (BMS) would be beneficial to medical practice, as it would allow for appropriate therapy and an increased healing rate.
在国际上,对非特异性口腔灼痛的研究相对较少,特别是对可能的病因的确定。从生理病理和治疗的角度来看,这一领域的知识是最近的,这支持了进一步研究和将该疾病定义为跨学科综合征的必要性。深化对口腔灼烧综合征发病机制的研究,将有利于医学实践,有利于合理治疗,提高治愈率。
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引用次数: 0
Neutrophil to lymphocyte ratio as a prognostic marker for advanced stage ovarian cancer 中性粒细胞与淋巴细胞比值作为晚期卵巢癌的预后指标
Pub Date : 2023-09-30 DOI: 10.37897/rmj.2023.3.4
Irina Balescu, Nicolae Bacalbasa, Mihaela Vilcu, Claudia Stoica, Tarig Massawi, Sorin Petrea, Cristina Martac, Adriana Ciuvica, Andrei Voichitoiu, Victor Cauni, Bogdan Gaspar, Iulian Brezean
Ovarian cancer remains one of the most aggressive malignancies which is frequently diagnosed in advanced stages of the disease, when disseminated lesions are already present. In order to maximize the rates of complete debulking surgery, different prognostic markers have been investigated. The aim of the current paper is to investigate the prognostic value of neutrophil to lymphocyte ratio in advanced stage ovarian cancer patients submitted to debulking surgery.
卵巢癌仍然是最具侵袭性的恶性肿瘤之一,通常在疾病的晚期诊断出来,此时已经存在弥散性病变。为了最大限度地提高手术的完成率,研究了不同的预后指标。本文旨在探讨中性粒细胞/淋巴细胞比值对晚期卵巢癌减容手术患者预后的价值。
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引用次数: 0
Unsuspected paraganglioma of the urinary bladder with intraoperative hypertensive peak: A case report 伴有术中高血压高峰的膀胱副神经节瘤1例
Pub Date : 2023-06-30 DOI: 10.37897/rmj.2023.2.7
Maali Ben Nasr, Nizar Cherni, Abdallah Chaachouaa, Wassim El Ajmi, Arij Zouaoui, Ferjaoui Wael, Samir Ghozzi
Background. Bladder paraganglioma (BPG) is a very rare tumor. Case report: We report the case of a 48-year-old woman with a history of isolated hematuria. Cystoscopy showed a solid mass on the bottom of the bladder. During the intervention the patient experienced a severe hypertensive episode. BPG was then suspected. Pathology findings confirmed the diagnosis.123I-metaiodobenzylguanidine scan showed a pathological tracer accumulation in the left bladder wall consistent with BPG. The patient underwent a transurethral resection of the bladder after drug preparation. The postoperative course was uneventful and our patient was normotensive. Conclusion. Diagnosis of BPG is often made on histological examination of the tumor.
背景。摘要膀胱副神经节瘤是一种非常罕见的肿瘤。病例报告:我们报告的情况下,48岁的妇女与历史孤立血尿。膀胱镜检查显示膀胱底部有一个实性肿块。在干预期间,患者经历了严重的高血压发作。BPG随即被怀疑。病理结果证实了诊断。123I-metaiodobenzylguanidine扫描显示病理示踪剂在左膀胱壁积聚,与BPG一致。患者在药物制备后行经尿道膀胱切除术。术后过程顺利,患者血压正常。结论。BPG的诊断通常是通过肿瘤的组织学检查来确定的。
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引用次数: 0
Classic Hodgkin lymphoma-nodular sclerosis – case report 典型霍奇金淋巴瘤-结节硬化1例报告
Pub Date : 2023-06-30 DOI: 10.37897/rmj.2023.2.8
Mihaela Lebedenco, Nicoleta Berbec, Oana Stanca, Anca Roxana Lupu
Hodgkin's lymphoma is the third most common cancer in young people between 15 and 34 years of age, with a lower incidence in other age groups and slightly higher in males. The etiology of Hodgkin's lymphoma is still unknown - although various factors influencing the oncogenesis of the disease have been noted, the mechanism of their influence is poorly understood. This article will present the case of a 41-year-old patient with classic Hodgkin's lymphoma - nodular sclerosis histological subtype - chemorefractory.
霍奇金淋巴瘤是15至34岁年轻人的第三大常见癌症,其他年龄组发病率较低,男性发病率略高。霍奇金淋巴瘤的病因尚不清楚,尽管已经注意到影响该疾病发生的各种因素,但其影响机制尚不清楚。本文将介绍一例41岁的典型霍奇金淋巴瘤-结节硬化组织学亚型-化疗难治的病例。
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引用次数: 0
Diagnostic dilemma: Multiple Autoimmune Syndrome versus incomplete Graham-Little-Piccardi-Lassueur Syndrome overlap mixed connective tissue disease 诊断困境:多重自身免疫综合征与不完全graham - little - piccard - lassueur综合征重叠混合性结缔组织病
Pub Date : 2023-06-30 DOI: 10.37897/rmj.2023.2.6
Tudorel Poalelungi, Ana-Maria Olaru, Mihaela Mariuta
Objectives. We present a very rare case of incomplete Graham-Little-Piccardi-Lassueur syndrome (GLPLS) overlap with Mixed Connective Tissue Disease (MCTD) versus Multiple Autoimmune Syndrome (MAS). Case Presentation. A 53- year-old female with a long history of more than two years of patchy hair loss on scalp like “footprints in the snow”, partial loss of eyebrows' hair, face erythema, scaly atrophied red/brown patches on face, grouped follicular papules 2-3 mm in diameter with a pointed or hair-like horny spine extending approximately 1-2 mm around the tip of the follicle on lumbar area. The histopathological results from biopsies of scalp and lumbar areas confirmed the clinical diagnosis of cicatricial alopecia induced by lichen plan pilaris (LPP) and also presence of lichen spinulosus (LS) on lumbar area. The description provided by pathologist is however borderline regarding so called interface dermatosis like chronic cutaneous lupus erythematous (CCLE) or Pseudopelade of Brocq (PPB) as the end stage of CCLE or LPP. Blood tests showed both Antinuclear antibodies and U1-nRNP in high titers and the absence of anti-Sm, anti SS-A, anti SS-B and anti-dsDNA antibodies, and also peculiar antibody patterns of MCTD. Outcome. After thorough investigation, MCTD was proven by antibodies results. After one year of treatment a lot of clinical features dramatically responded under therapy. Conclusions. Clinical manifestations in the pathology with strictly cutaneous or systemic localization in conjunction or overlap with other autoimmune diseases (grouped in the MAS) represent a rare diagnostic in daily practice.
目标。我们报告一个非常罕见的不完全graham - little - piccard - lassueur综合征(GLPLS)与混合性结缔组织病(MCTD)和多发性自身免疫性综合征(MAS)重叠的病例。案例演示。女性,53岁,长有两年多的斑状脱发史,如“雪地上的脚印”,眉毛部分脱发,面部红斑,鳞状萎缩的红色/棕色斑块,成组的毛囊丘疹,直径2-3毫米,在腰部毛囊尖端周围延伸约1-2毫米的尖状或头发状角质棘。头皮及腰椎活检病理结果证实临床诊断为毛状苔藓(LPP)及腰椎棘状苔藓(LS)所致瘢痕性脱发。然而,病理学家提供的描述对于所谓的界面皮肤病,如慢性皮肤红斑狼疮(CCLE)或布罗克假性皮炎(PPB)作为CCLE或LPP的终末阶段是模棱两可的。血检显示抗核抗体和U1-nRNP均高滴度,无抗sm、抗SS-A、抗SS-B和抗dsdna抗体,且MCTD特有的抗体模式。结果。经过深入的研究,MCTD得到了抗体结果的证实。经过一年的治疗,许多临床特征在治疗下有显著的反应。结论。临床病理表现为与其他自身免疫性疾病(归类为MAS)合并或重叠的严格皮肤或全身定位,在日常实践中是一种罕见的诊断。
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引用次数: 0
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