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[Multifocal motor neuropathy. Report of three cases at a reference hospital in Mexico]. [多灶性运动神经病。墨西哥一家参考医院的三例病例报告]。
Pub Date : 2024-03-05 DOI: 10.5281/zenodo.10713055
Crhistian Alejandro Aguilar-Vázquez, Nallely Denisse Ruvalcaba-Sánchez, Luis Carlos Reyes-Sosa, Carlos César Reyes-Hernández, Sergio de Jesús Aguilar-Castillo

Background: Motor multifocal neuropathy is an immunemediated neuropathy characterized by progressive and asymmetric weakness of the distal extremities, without sensory symptoms, and an important feature of conduction blocks. The objective of this study is to comprehensively describe the nosological and pathogenic implications of this neurodegenerative disorder, given the unclear diagnosis of MMN and the significant challenges it poses.

Clinical cases: We present three clinical cases with a chronic clinical presentation, in which neuroconduction studies were performed, revealing the presence of anti-IgM GM1 antibodies, consistent with the diagnosis of motor multifocal neuropathy. Although the treatment administered in these cases was successful, it is important to note that the diagnosis of MMN experienced some delay, emphasizing the need for greater awareness and understanding of this disease.

Conclusion: The diagnosis of motor multifocal neuropathy is often delayed, and an incorrect treatment can worsen symptoms, especially due to its similarity to other neuropathies and nerve and muscle diseases. Despite a generally favorable prognosis, the lack of early diagnosis can lead to severe motor sequelae. In this study, we provide detailed descriptions of three clinical cases from a reference center in Mexico, presenting their clinical manifestations, observed neurophysiological patterns, and treatment response.

背景:运动性多灶性神经病是一种免疫介导的神经病,其特征是四肢远端进行性和非对称性无力,无感觉症状,其重要特征是传导阻滞。本研究的目的是全面描述这种神经退行性疾病的命名和致病意义,因为多灶性运动性神经病的诊断并不明确,而且具有很大的挑战性:我们介绍了三个临床病例,这些病例临床表现为慢性,在神经传导研究中发现了抗 IgM GM1 抗体,与运动性多灶性神经病的诊断一致。虽然这些病例的治疗取得了成功,但必须指出的是,运动多灶性神经病的诊断经历了一定的延迟,这强调了提高对这种疾病的认识和理解的必要性:结论:运动性多灶神经病的诊断往往被延误,不正确的治疗会加重症状,特别是由于它与其他神经病、神经和肌肉疾病相似。尽管预后一般良好,但缺乏早期诊断可能会导致严重的运动后遗症。在本研究中,我们详细描述了来自墨西哥参考中心的三个临床病例,介绍了他们的临床表现、观察到的神经电生理模式和治疗反应。
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引用次数: 0
Incidence of advanced chronic disease, need for palliative care and in-hospital mortality 晚期慢性病发病率、姑息治疗需求和院内死亡率
José Luis Canizal-Oñate, Drusila Tovar-Rodríguez, Norma León-Armas, Gabriela Martínez-Díaz, Berenice López-Zamora, María Del Pilar Cruz-Domínguez, Michelle Arrucha-Cozaya, Olga Lidia Vera-Lastra, Gabriela Medina-García

Background: There is a continuing increase in the prevalence of people affected with progressive chronic diseases. Palliative care is another form of care and organization of health problems that improve quality.

Objective: To determine the incidence of patients with advanced chronic illness and need of palliative care (NPC) and intrahospital mortality in a reference hospital.

Methods: Prospective observational study in hospitalized patients over 18 years of age in the internal medicine department who met at least one criterion of the NECPAL CCOMS-ICO tool. They were followed until death or discharge to determine intrahospital mortality. We used descriptive and inferential statistics.

Results: We studied 370 admissions from April to August 2021, including 110 patients, 59 women (55.3%) and 51 men (44.7%), age 65.5 ± 15.85 years. The incidence of NPC was 29.7%. The most frequent comorbidity was oncologic in 39 patients (35.5%), followed by chronic heart disease in 17 patients (15.5%); 38 patients were classified as NECPAL grade I (34.5%), 44 NECPAL II (40%) and 28 NECPAL III (25.5%). Twenty-five patients died during their in-hospital stay, with a mortality of 22.7%.

Conclusions: The incidence of hospitalized patients in need of palliative care is considerable, more than half of them for non-oncologic pathology. More effective care strategies are required for external referral and multidisciplinary in-hospital care.

背景:受渐进性慢性疾病影响的人越来越多。姑息治疗是提高医疗质量的另一种治疗和组织形式:方法:对一家参照医院的晚期慢性病患者、需要姑息治疗的患者(NPC)的发病率和院内死亡率进行前瞻性观察研究:方法:前瞻性观察研究,对象为内科住院的 18 岁以上患者,他们至少符合 NECPAL CCOMS-ICO 工具中的一项标准。对这些患者进行随访,直至死亡或出院,以确定院内死亡率。我们采用了描述性和推论性统计方法:我们对 2021 年 4 月至 8 月的 370 例入院患者进行了研究,其中包括 110 名患者,59 名女性(55.3%)和 51 名男性(44.7%),年龄为 65.5 ± 15.85 岁。鼻咽癌发病率为 29.7%。39名患者(35.5%)最常见的合并症是肿瘤,其次是17名患者(15.5%)的慢性心脏病;38名患者被划分为NECPALⅠ级(34.5%),44名NECPALⅡ级(40%)和28名NECPALⅢ级(25.5%)。25名患者在住院期间死亡,死亡率为22.7%:需要姑息治疗的住院病人人数众多,其中一半以上是非肿瘤性病变。需要更有效的外部转诊和多学科院内护理策略。
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引用次数: 0
[Dual kidney transplantation, report of a case and review of the literature]. [双肾移植,病例报告和文献综述]。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10713079
Diana Fabiola Fernández-Ánge, Luis García-Covarrubias, Héctor Hinojosa-Heredia, Ma Virgilia Soto, Aldo García-Covarrubias, Héctor Santiago Díliz-Pérez

Background: Kidney transplant is the best replacement therapy for kidney function; However, donors are insufficient, so extended criteria donors (ECD) are needed, which, in well-selected recipients, provide better survival than being on dialysis. Dual kidney transplantation (DRT) should be offered to elderly patients with lower immunological risk and with a lower body mass index. DCE are considered donors who died due to stroke, ≥ 60 years old or aged between 50 and 59 years, with diabetes or previous hypertension, clinical proteinuria, estimated glomerular filtration rate (eGFR) between 30 and 60 mL/min, or Terminal serum creatinine > 2.5 mg/dL.

Clinical case: 57-year-old male patient undergoing TRD of a 67-year-old DCE, with creatinine of 2 mg/dL at the time of extraction, without previous pathologies, with eGFR: 34 mL/min, KDPI: 92% , KDRI: 1.64, Remuzzi pre-implantation biopsy 5, with 14-hour cold ischemia. He was discharged on the eighth day with a creatinine of 1 mg/dL. At 45 months with creatinine of 0.9 mg/dL, and eGFR by CKD-EPI of 91 mL/min/ 1.73m2.

Conclusion: TRD is an alternative for ECD grafts. The "old for old" strategy allows TRD in older recipients a better survival than being on replacement treatment. The correlation with the KDRI, KDPI scales and the preimplantation biopsy according to the Remuzzi score improves transplant results by discarding kidneys with severe histopathological alterations, this can help reduce the rate of discarding SCAD and kidneys.

背景:肾移植是肾功能的最佳替代疗法;然而,供体不足,因此需要扩展标准供体(ECD)。双肾移植(DRT)应提供给免疫风险较低、体重指数较低的老年患者。因中风而死亡、年龄≥ 60 岁或 50 至 59 岁、患有糖尿病或既往高血压、临床蛋白尿、估计肾小球滤过率(eGFR)介于 30 至 60 毫升/分钟之间或终端血清肌酐 > 2.5 毫克/分升的供体均可视为双肾移植供体:57岁男性患者,接受67岁DCE的TRD治疗,拔管时肌酐为2 mg/dL,既往无病变,eGFR:34 mL/min,KDPI:92% ,KDRI:1.64,Remuzzi植入前活检5,冷缺血14小时。他于第八天出院,血肌酐为 1 毫克/分升。45 个月后,他的肌酐为 0.9 mg/dL,根据 CKD-EPI 计算,eGFR 为 91 mL/min/ 1.73m2:结论:TRD 是 ECD 移植的替代方案。结论:TRD 是 ECD 移植的替代方案,"以旧换新 "的策略使年龄较大的受者在 TRD 中的存活率高于替代治疗。与KDRI、KDPI量表和根据Remuzzi评分进行的移植前活检相关联,可通过放弃组织病理学改变严重的肾脏来改善移植结果,这有助于降低SCAD和肾脏的放弃率。
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引用次数: 0
[Answer to "Comment on article: "Risk factors associated with cognitive impairment in older adults: cross-sectional study""]. [回答 "对文章的评论:"与老年人认知障碍相关的风险因素:横断面研究"]。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10711253
Moises Moreno-Noguez

In the design of cross-sectional studies, the measurement of the components of the architectural design (baseline state, maneuver, and outcome) are measured simultaneously, for this reason it is relevant to try to respect that the maneuver is prior to the outcome, in this way, in the present study it was considered to exclude subjects with a history of alterations that generate alterations of cognitive function. However, the presence of conditions such as dependence on basic activities of daily living has not been shown to be a condition related to impaired cognitive function, which is why it was included as one of the factors studied.

在横断面研究的设计中,对建筑设计各组成部分(基线状态、操作和结果)的测量是同时进行的,因此,尽量尊重操作先于结果是有意义的,这样,在本研究中,就考虑了排除有导致认知功能改变的病史的受试者。然而,日常生活基本活动依赖等情况并未被证明是与认知功能受损有关的条件,这也是将其作为研究因素之一的原因。
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引用次数: 0
COVID-19 and type 2 diabetes mellitus: implications in pancreatic beta cells. COVID-19 与 2 型糖尿病:对胰腺β细胞的影响。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10712093
Ivonne Grisel Sánchez-Cervantes, Ignacio González-Sánchez, Irma Elena López-Martínez, Elsa Liliana Aguirre-Benítez, Cristina Coronel-Cruz

The prevalence of chronic metabolic diseases in Mexico is high, being type 2 Diabetes mellitus (T2DM) as the most common disease. Several studies have shown that, compared with healthy individuals, patients with T2DM suffer a higher severity and mortality of Coronavirus disease 2019 (COVID-19). Therefore, it is important to the knowledge of the bidirectional relationship between these diseases. T2DM can increase SARS-CoV-2 virus pathogenicity in part due to metabolic disturbance. As a result, COVID-19 susceptibility and severity rise in diabetic individuals, which makes them a high-risk population. On the other hand, the infection caused by SARS-CoV-2 can lead individuals to hyperglycemia or new-onset diabetes. In order to understand the relationship between COVID-19 and T2DM, this review aims to emphasize the tropism of the SARS-CoV-2 virus to pancreatic beta-cells, as well as the physiologic effects of these.

墨西哥的慢性代谢疾病发病率很高,其中最常见的疾病是 2 型糖尿病(T2DM)。多项研究表明,与健康人相比,T2DM 患者患 2019 年冠状病毒病(COVID-19)的严重程度更高,死亡率也更高。因此,了解这些疾病之间的双向关系非常重要。T2DM 可增加 SARS-CoV-2 病毒的致病性,部分原因是新陈代谢紊乱。因此,糖尿病患者对 COVID-19 的易感性和严重程度都会升高,成为高危人群。另一方面,SARS-CoV-2 病毒感染可导致高血糖或新发糖尿病。为了了解 COVID-19 与 T2DM 之间的关系,本综述旨在强调 SARS-CoV-2 病毒对胰腺 beta 细胞的滋养作用及其生理影响。
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引用次数: 0
Macular edema in retinal fundus images by a computational algorithm 通过计算算法分析视网膜眼底图像中的黄斑水肿
César Augusto Garrido-Pino, Luis Miguel López-Montero, Leonel López-Lozano, Martha Alicia Hernández-González, Iván Cruz-Aceves

Background: Diabetes is a metabolic disease highly prevalent in our country that ends in disabling complications such as diabetic retinopathy and macular edema. As a high-impact socioeconomic issue, it is important to look for an early diagnostic test that also allows us to introduce a telemedicine service for the population with little access to specialized health services.

Objective: To describe the performance in discrimination of macular edema of a feature detection algorithm on retinal fundus images from diabetic patients.

Material and methods: We use a database of 266 retinal fundus images of diabetic patients and were classified in Macular Edema or Without Macular Edema by ophthalmologists' assessment and we test if the algorithm was capable of establish the presence or not of macular edema.

Results: We made 3 tests in which the standards of sensitivity, specificity and efficiency of the algorithm were increasing according to the amount of retinal fundus images in the training phase, reaching specificity values of 100%, sensitivity 84% and efficiency 91.30%.

Conclusions: Our study lays the foundation of a reliable screening method due to its high specificity value and allows not only a binary reply in the presence or not of macular edema but the clinical and topographic classification favoring the onset of treatment.

背景:糖尿病是一种代谢性疾病,在我国发病率很高,最终会导致糖尿病视网膜病变和黄斑水肿等致残性并发症。作为一个影响巨大的社会经济问题,寻找一种早期诊断测试非常重要,这种测试还能让我们为很少有机会获得专业医疗服务的人群提供远程医疗服务:目的:描述一种特征检测算法在糖尿病患者视网膜眼底图像上判别黄斑水肿的性能:我们使用了一个包含 266 幅糖尿病患者视网膜眼底图像的数据库,通过眼科医生的评估将这些图像分为黄斑水肿和无黄斑水肿两种,并测试该算法是否能够确定黄斑水肿的存在:我们进行了 3 次测试,根据训练阶段视网膜眼底图像的数量,算法的灵敏度、特异性和效率标准不断提高,特异性达到 100%,灵敏度达到 84%,效率达到 91.30%:我们的研究为一种可靠的筛查方法奠定了基础,因为这种方法具有很高的特异性,不仅能对是否存在黄斑水肿做出二元回答,还能进行有利于开始治疗的临床和地形分类。
{"title":"Macular edema in retinal fundus images by a computational algorithm","authors":"César Augusto Garrido-Pino, Luis Miguel López-Montero, Leonel López-Lozano, Martha Alicia Hernández-González, Iván Cruz-Aceves","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Diabetes is a metabolic disease highly prevalent in our country that ends in disabling complications such as diabetic retinopathy and macular edema. As a high-impact socioeconomic issue, it is important to look for an early diagnostic test that also allows us to introduce a telemedicine service for the population with little access to specialized health services.</p><p><strong>Objective: </strong>To describe the performance in discrimination of macular edema of a feature detection algorithm on retinal fundus images from diabetic patients.</p><p><strong>Material and methods: </strong>We use a database of 266 retinal fundus images of diabetic patients and were classified in Macular Edema or Without Macular Edema by ophthalmologists' assessment and we test if the algorithm was capable of establish the presence or not of macular edema.</p><p><strong>Results: </strong>We made 3 tests in which the standards of sensitivity, specificity and efficiency of the algorithm were increasing according to the amount of retinal fundus images in the training phase, reaching specificity values of 100%, sensitivity 84% and efficiency 91.30%.</p><p><strong>Conclusions: </strong>Our study lays the foundation of a reliable screening method due to its high specificity value and allows not only a binary reply in the presence or not of macular edema but the clinical and topographic classification favoring the onset of treatment.</p>","PeriodicalId":94200,"journal":{"name":"Revista medica del Instituto Mexicano del Seguro Social","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Partial trisomy 9p syndrome: Expanding the phenotype]. [部分 9p 三体综合征:扩展表型]。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10713116
José Abel Pérez-Castillo, Mariana Reyes-Rosales, Héctor Rodrigo Cardoso-Enciso, José Luis Rodríguez-Cuevas

Background: Trisomy of the short arm of chromosome 9 (9p) is the fourth most common chromosomopathy. It is a partial or complete autosomal structural anomaly of the short arm of chromosome 9. It is generally caused by a reciprocal parental translocation between chromosome 9 and another autosome; spontaneous genetic alteration (de novo) is rare. It presents great phenotypic variability due to the variable size of the chromosome fragment involved.

Clinical case: We present the case of a patient diagnosed with trisomy of the short arm of chromosome 9 with a karyotype with a chromosomal complement 46,XX,add(9)(p24), interpreted as an additional chromosome fragment on chromosome 9p. A microarray study was carried out, which reported that the 9p24.3-p13.1 region is found in triple dose, which corresponds to a partial trisomy 9p or Rethoré syndrome, which is a low prevalence entity, with an expressiveness and variable prognosis. In the present case, the finding of a murmur and diagnosis of pulmonary valve stenosis was the initial approach; The heart disease described in our patient has not been reported in the literature as part of the clinical picture, meaning that it was not an initial diagnostic suspicion.

Conclusion: Despite having described an already defined phenotype, other clinical data that are not documented should be considered, and when new clinical evidence is found, report it and thereby expand the phenotype for a timely diagnosis.

背景:9 号染色体短臂三体综合征(9p)是第四大常见染色体病。它是第 9 号染色体短臂的部分或完全常染色体结构异常。它通常是由父母第 9 号染色体与另一个常染色体之间的互变引起的;自发的基因改变(从头开始)很少见。由于涉及的染色体片段大小不一,其表型变异很大:本例患者被诊断为 9 号染色体短臂三体综合征,核型为染色体补体 46,XX,add(9)(p24),可解释为 9p 染色体上有一个额外的染色体片段。一项微阵列研究显示,9p24.3-p13.1 区域存在三倍剂量,这相当于 9p 部分三体综合征或雷霍雷综合征,该综合征发病率低,具有表现性,预后不一。在本病例中,最初的诊断方法是发现杂音并诊断为肺动脉瓣狭窄;我们的患者所描述的心脏病作为临床表现的一部分在文献中还没有报道过,这意味着它并不是最初的诊断怀疑因素:结论:尽管已经描述了已定义的表型,但仍应考虑其他未记录的临床数据,当发现新的临床证据时,应及时报告,从而扩大表型,以便及时诊断。
{"title":"[Partial trisomy 9p syndrome: Expanding the phenotype].","authors":"José Abel Pérez-Castillo, Mariana Reyes-Rosales, Héctor Rodrigo Cardoso-Enciso, José Luis Rodríguez-Cuevas","doi":"10.5281/zenodo.10713116","DOIUrl":"https://doi.org/10.5281/zenodo.10713116","url":null,"abstract":"<p><strong>Background: </strong>Trisomy of the short arm of chromosome 9 (9p) is the fourth most common chromosomopathy. It is a partial or complete autosomal structural anomaly of the short arm of chromosome 9. It is generally caused by a reciprocal parental translocation between chromosome 9 and another autosome; spontaneous genetic alteration (de novo) is rare. It presents great phenotypic variability due to the variable size of the chromosome fragment involved.</p><p><strong>Clinical case: </strong>We present the case of a patient diagnosed with trisomy of the short arm of chromosome 9 with a karyotype with a chromosomal complement 46,XX,add(9)(p24), interpreted as an additional chromosome fragment on chromosome 9p. A microarray study was carried out, which reported that the 9p24.3-p13.1 region is found in triple dose, which corresponds to a partial trisomy 9p or Rethoré syndrome, which is a low prevalence entity, with an expressiveness and variable prognosis. In the present case, the finding of a murmur and diagnosis of pulmonary valve stenosis was the initial approach; The heart disease described in our patient has not been reported in the literature as part of the clinical picture, meaning that it was not an initial diagnostic suspicion.</p><p><strong>Conclusion: </strong>Despite having described an already defined phenotype, other clinical data that are not documented should be considered, and when new clinical evidence is found, report it and thereby expand the phenotype for a timely diagnosis.</p>","PeriodicalId":94200,"journal":{"name":"Revista medica del Instituto Mexicano del Seguro Social","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Obscure gastrointestinal bleeding secondary to ectopic pancreas. Case report]. [继发于异位胰腺的隐匿性消化道出血。病例报告]。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10713031
Citlalli Guadalupe Hernández-Guzmán, Martha Gabriela Rojas-Loureiro, Guillermo Jesús Carmona-Aguilera, Mabel Leyva-Camacho, Juan Pablo Menindez-Cruz, Jesús Noé Bailón-Contreras, Manuel Eduardo Cárdenas Muñóz

Background: Ectopic pancreas is a benign subepithelial tumor with an abnormal anatomical position, typically diagnosed incidentally as it does not produce symptoms and is challenging to identify in paraclinical studies. The incidence is very low, so our objective is to present the case of a patient with ectopic pancreas as a rare cause of obscure gastrointestinal bleeding.

Clinical case: A 70-year-old man presented with melena, anemia, and weight loss. The initial approach involved endoscopic studies (panendoscopy, colonoscopy, enteroscopy), a tagged red blood cell scan and computed tomography, none of which identified the bleeding site. Therefore, an exploratory laparoscopy was performed, revealing a 3 x 3 cm exophytic lesion in the proximal jejunum, which was completely resected. Histopathology confirmed an ectopic pancreas.

Conclusions: This condition is an uncommon but potentially serious cause of gastrointestinal bleeding, as the definitive diagnosis is often delayed. Therefore, clinical suspicion is crucial for early diagnosis and timely treatment, involving a multidisciplinary team of specialists in gastroenterology, radiology, pathology, and general surgery. In this manuscript, we present one of the few reported cases of ectopic pancreas as the cause of mid-intestinal bleeding.

背景:异位胰腺是一种解剖位置异常的良性上皮下肿瘤,由于不产生症状,通常是偶然诊断出来的,在临床旁研究中很难发现。其发病率非常低,因此我们的目的是介绍一例异位胰腺患者的病例,这是导致不明显消化道出血的罕见原因:临床病例:一名 70 岁的男性患者出现血便、贫血和体重减轻。初步检查包括内镜检查(全景镜、结肠镜、肠镜)、标记红细胞扫描和计算机断层扫描,但均未发现出血部位。因此,医生进行了探查性腹腔镜检查,发现空肠近端有一个 3 x 3 厘米的外生病灶,并将其完全切除。组织病理学证实为异位胰腺:结论:这种情况并不常见,但可能是导致消化道出血的严重原因,因为明确诊断往往被延误。因此,由消化内科、放射科、病理科和普外科专家组成的多学科团队参与临床怀疑对于早期诊断和及时治疗至关重要。在本手稿中,我们介绍了为数不多的胰腺异位导致中肠出血的病例。
{"title":"[Obscure gastrointestinal bleeding secondary to ectopic pancreas. Case report].","authors":"Citlalli Guadalupe Hernández-Guzmán, Martha Gabriela Rojas-Loureiro, Guillermo Jesús Carmona-Aguilera, Mabel Leyva-Camacho, Juan Pablo Menindez-Cruz, Jesús Noé Bailón-Contreras, Manuel Eduardo Cárdenas Muñóz","doi":"10.5281/zenodo.10713031","DOIUrl":"https://doi.org/10.5281/zenodo.10713031","url":null,"abstract":"<p><strong>Background: </strong>Ectopic pancreas is a benign subepithelial tumor with an abnormal anatomical position, typically diagnosed incidentally as it does not produce symptoms and is challenging to identify in paraclinical studies. The incidence is very low, so our objective is to present the case of a patient with ectopic pancreas as a rare cause of obscure gastrointestinal bleeding.</p><p><strong>Clinical case: </strong>A 70-year-old man presented with melena, anemia, and weight loss. The initial approach involved endoscopic studies (panendoscopy, colonoscopy, enteroscopy), a tagged red blood cell scan and computed tomography, none of which identified the bleeding site. Therefore, an exploratory laparoscopy was performed, revealing a 3 x 3 cm exophytic lesion in the proximal jejunum, which was completely resected. Histopathology confirmed an ectopic pancreas.</p><p><strong>Conclusions: </strong>This condition is an uncommon but potentially serious cause of gastrointestinal bleeding, as the definitive diagnosis is often delayed. Therefore, clinical suspicion is crucial for early diagnosis and timely treatment, involving a multidisciplinary team of specialists in gastroenterology, radiology, pathology, and general surgery. In this manuscript, we present one of the few reported cases of ectopic pancreas as the cause of mid-intestinal bleeding.</p>","PeriodicalId":94200,"journal":{"name":"Revista medica del Instituto Mexicano del Seguro Social","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Petersen's hernia after laparoscopic gastric bypass 腹腔镜胃旁路术后的彼得森疝
Francisco Javier Plascencia-Posada, Gilberto González-Pérez, Kriscia Vanessa Ascencio-Diaz, Fanny Yesenia González-Ponce, Natalia Guadalupe Barrera-López, Alejandro González-Ojeda, Clotilde Fuentes-Orozco

Background: RYDG is the second most prevalent bariatric operation worldwide in terms of surgical treatment for the management of obesity and its comorbidities; however, one of its complications is the development of Petersen's space hernia. Currently there is no specific cause for their development since, based on studies published worldwide, they have an unpredictable behavior in each individual.

Objective: To establish the prevalence of Petersen's hernia and risk factors for its development.

Material and methods: Retrospective cohort study that included patients who underwent laparoscopic gastric bypass from January 2015 to December 2020. All procedures were performed by a single surgeon using antecolic and retrogastric configuration. Study variables: weight, BMI, mesenteric gap closure, suture material used, post-surgical complications.

Results: 00 patients were included, 64 women and 36 men, age 40.33 ± 2.08 years. The prevalence of Petersen's space hernia was 3% with a mean presentation time of 18 ± 7.54 months. The variables related to its development in the 3 cases were closure of the mesenteric gap, height, body mass index (BMI) and weight after the surgical procedure. All patients underwent reoperation, reducing the content and closing the mesenteric gap with non-absorbable suture material.

Conclusion: The development of the hernia not only depends on the closure of the mesenteric gap, but also on the reduction of weight and loss of volume of the mesentery with the reopening of the space.

背景:就肥胖症及其并发症的外科治疗而言,RYDG 是全球第二大最流行的减肥手术;然而,其并发症之一是彼得森间隙疝的发生。目前还没有明确的发病原因,因为根据世界范围内发表的研究结果,每个人的发病情况都是不可预测的:确定彼得森疝的发病率及其风险因素:回顾性队列研究纳入了 2015 年 1 月至 2020 年 12 月期间接受腹腔镜胃旁路手术的患者。所有手术均由一名外科医生使用反结肠和反胃配置进行。研究变量:体重、体重指数、肠系膜间隙闭合情况、使用的缝合材料、术后并发症:共纳入 00 例患者,其中女性 64 例,男性 36 例,年龄(40.33±2.08)岁。彼得森间隙疝的发病率为 3%,平均发病时间为(18 ± 7.54)个月。在这 3 个病例中,与疝气发生有关的变量包括肠系膜间隙的闭合情况、身高、体重指数(BMI)以及手术后的体重。所有患者都接受了再次手术,用非吸收缝合材料缩小了肠内容物并关闭了肠系膜间隙:结论:疝气的发展不仅取决于肠系膜间隙的闭合,还取决于体重的减轻和肠系膜容积的减小,以及肠系膜间隙的重新开放。
{"title":"Petersen's hernia after laparoscopic gastric bypass","authors":"Francisco Javier Plascencia-Posada, Gilberto González-Pérez, Kriscia Vanessa Ascencio-Diaz, Fanny Yesenia González-Ponce, Natalia Guadalupe Barrera-López, Alejandro González-Ojeda, Clotilde Fuentes-Orozco","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>RYDG is the second most prevalent bariatric operation worldwide in terms of surgical treatment for the management of obesity and its comorbidities; however, one of its complications is the development of Petersen's space hernia. Currently there is no specific cause for their development since, based on studies published worldwide, they have an unpredictable behavior in each individual.</p><p><strong>Objective: </strong>To establish the prevalence of Petersen's hernia and risk factors for its development.</p><p><strong>Material and methods: </strong>Retrospective cohort study that included patients who underwent laparoscopic gastric bypass from January 2015 to December 2020. All procedures were performed by a single surgeon using antecolic and retrogastric configuration. Study variables: weight, BMI, mesenteric gap closure, suture material used, post-surgical complications.</p><p><strong>Results: </strong>00 patients were included, 64 women and 36 men, age 40.33 ± 2.08 years. The prevalence of Petersen's space hernia was 3% with a mean presentation time of 18 ± 7.54 months. The variables related to its development in the 3 cases were closure of the mesenteric gap, height, body mass index (BMI) and weight after the surgical procedure. All patients underwent reoperation, reducing the content and closing the mesenteric gap with non-absorbable suture material.</p><p><strong>Conclusion: </strong>The development of the hernia not only depends on the closure of the mesenteric gap, but also on the reduction of weight and loss of volume of the mesentery with the reopening of the space.</p>","PeriodicalId":94200,"journal":{"name":"Revista medica del Instituto Mexicano del Seguro Social","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Plants with antiviral properties used in Otorhinolaryngology. 耳鼻喉科使用的具有抗病毒特性的植物。
Pub Date : 2024-03-04 DOI: 10.5281/zenodo.10712138
Salomón Waizel-Haiat, José Waizel-Bucay, Juan Santiago Salas-Benito, Edgar Paul Salas-Lira

Viruses represent one of the main causes of human morbidity and mortality worldwide. Plants have been used since time immemorial to treat, cure or alleviate diseases. We present some of them that make compounds with antiviral action and are used in traditional medicine. The objective of this work was to contribute to the knowledge of plants popularly used for the treatment of respiratory diseases of viral origin. The parts or organs mainly used are: the stem, leaves and flowers, while the method of use is mainly in decoction or infusion and its administration route is orally. The chemical compounds contained in plants used with antiviral properties are very diverse in nature, and belong to the groups of: essential oils, phenolic acids, alkaloids, flavonoids, glycosides, gums and mucilages, oleoresins; pectins, lignans, saponins and tannins.

病毒是全球人类发病和死亡的主要原因之一。植物自古以来就被用来治疗、治愈或减轻疾病。我们介绍了其中一些能产生具有抗病毒作用的化合物并被用于传统医学的植物。这项工作的目的是增进人们对常用于治疗病毒性呼吸道疾病的植物的了解。主要使用的部位或器官是茎、叶和花,使用方法主要是煎煮或浸泡,给药途径是口服。具有抗病毒特性的植物所含的化学物质种类繁多,主要分为以下几类:精油、酚酸、生物碱、黄酮类、苷类、胶质和粘液质、油脂、果胶、木脂素、皂苷和鞣质。
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引用次数: 0
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Revista medica del Instituto Mexicano del Seguro Social
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