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Chronic Monteggia in pediatric population: A narrative literature review. 儿童慢性蒙氏病:叙述性文献综述。
Q3 Medicine Pub Date : 2022-10-28 DOI: 10.4081/pmc.2022.289
Chiara Arrigoni, Nunzio Catena

Monteggia lesion is a traumatic condition that affects the forearm and is characterized by the association of an ulna fracture with a dislocation of the radius capitellar and proximal radius ulnar joints in the majority of cases. Although several authors have contributed to the understanding of this pathology over the years, it remains a challenge for orthopedists, and if not recognized and treated properly, it can have serious consequences. In these cases, a chronic injury develops, which is even more difficult to manage in terms of timing and treatment options. A narrative review of the literature on missed elbow injuries in children was conducted, and chronic Monteggia was the most frequently encountered injury. The analysis of the articles attempts to clarify some points and draw general conclusions on which to reflect.

Monteggia损伤是一种影响前臂的创伤性疾病,其特征是在大多数情况下,尺骨骨折伴有桡骨小头关节脱位和桡骨尺近端关节脱位。尽管几位作者多年来对这种病理的理解做出了贡献,但它仍然是骨科医生的一个挑战,如果不能正确认识和治疗,它可能会产生严重的后果。在这些情况下,慢性损伤发展,这在时间和治疗选择方面更加难以管理。对儿童肘部损伤漏诊的文献进行了叙述回顾,慢性蒙氏病是最常见的损伤。文章的分析试图澄清一些观点,并得出值得反思的一般性结论。
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引用次数: 0
Slipped capital femoral epiphysis: Diagnostic pitfalls and therapeutic options. 股骨骨骺滑动:诊断陷阱和治疗选择。
Q3 Medicine Pub Date : 2022-10-28 DOI: 10.4081/pmc.2022.296
Elena Panuccio, Daniele Priano, Valerio Caccavella, Antonio Memeo

One of the most prevalent hip pathologies that develops during adolescence is Slipped Capital Femoral Epiphysis (SCFE), and over the past few decades, its incidence has been rising. To ensure an early diagnosis and prompt intervention, orthopedic surgeons should be aware of this entity. Review of recent developments in clinical examination and imaging diagnostic procedures. The presentation includes commonly used imaging methods, slippage measurement techniques, and classification schemes that are pertinent to treatment. An overview of SCFE surgery based on pertinent study findings and knowledge gained from ongoing clinical practice. The gold standard treatment for stable SCFE cases- those in which the continuity of the metaphysis and epiphysis is preserved-is pinning in situ using a single cannulated screw without reduction. However, there are disagreements over the best course of action for stable moderate/severe SCFE. On the best surgical strategy for unstable epiphysiolysis, no universal agreement has been reached. Finding the surgical procedure that will improve the long-term outcomes of a slipped capital femoral epiphysis is the question at hand.

在青春期发生的最常见的髋关节疾病之一是股骨头骨骺滑动(SCFE),在过去的几十年里,其发病率一直在上升。为了确保早期诊断和及时干预,骨科医生应该意识到这个实体。回顾临床检查和影像诊断程序的最新进展。介绍了常用的成像方法、滑移测量技术和与治疗相关的分类方案。基于相关的研究结果和从正在进行的临床实践中获得的知识,对SCFE手术进行概述。稳定SCFE病例的金标准治疗方法是使用单个空心螺钉原位固定,不复位,即保持干骺端和骺端连续性。然而,对于稳定的中/重度SCFE的最佳治疗方案存在分歧。对于不稳定骨骺松解的最佳手术策略,尚未达成普遍共识。找到一种可以改善股骨骨骺滑动的长期预后的手术方法是当前的问题。
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引用次数: 1
Intestinal twin-to-twin transplant for short gut: Review of the literature and discussion of a complex case. 短肠的双胞移植:文献回顾和一个复杂病例的讨论。
Q3 Medicine Pub Date : 2022-10-18 DOI: 10.4081/pmc.2022.287
Sara Ugolini, Riccardo Coletta, Antonino Morabito

Paediatric Intestinal Transplantation (IT) presents the highest mortality on the waiting-list due to anatomical disproportion. Living-Donor IT (LDIT) offers the best advantages and when performed among identical monozygotic twins, it also benefits from unique immunology. According to MEDLINE/Pubmed, twin-to-twin LDIT has been performed in seven cases (6:7 males, median age of 32 years). None of the patients received immunosuppression postoperatively. Only one paediatric twinto- twin LDIT was carried out with a 160-cm mid-ileum tract: an interposed 4/5-cm arterial graft was required to ensure a tensionfree anastomosis to the anterior wall of the infra-renal abdominal aorta. In contrast, venous anastomosis was done directly to the inferior cava vein. We present a case for debate of a 13- month-old SBS patient where a twin-LDIT was discussed with parents, who decided to wait after careful analysis and ethical considerations.

儿科肠道移植(IT)由于解剖比例失调,在等待名单上死亡率最高。活体供体IT (LDIT)提供了最好的优势,当在同卵同卵双胞胎中进行时,它也受益于独特的免疫学。据MEDLINE/Pubmed报道,已在7例(男性6:7,中位年龄32岁)中进行了双胞LDIT。所有患者术后均未接受免疫抑制。只有一例小儿双胎LDIT采用160厘米的回肠中束:需要插入4/5厘米的动脉移植物,以确保与肾下腹主动脉前壁无张力吻合。静脉吻合术直接与下腔静脉吻合。我们提出了一个13个月大的SBS患者的案例,其中双胞胎ldit与父母进行了讨论,他们在仔细分析和伦理考虑后决定等待。
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引用次数: 0
Role of urinary NGAL and microalbuminuria in the detection of subclinical acute kidney injury in pediatric intensive care unit and diabetic children. 尿NGAL和微量白蛋白尿在儿科重症监护病房和糖尿病儿童亚临床急性肾损伤检测中的作用。
Q3 Medicine Pub Date : 2022-07-15 DOI: 10.4081/pmc.2022.285
Sally K I Ishak, Fayrouz El Aguizy, Eman H Elsebaie, Meray R L Youssef, Mohamed M Ismail, Fatma H Abdelraouf, Heba A Abdel Ghaffar, Nermine M Riad

Subclinical Acute Kidney Injury (AKI) describes patients who did not fulfill the classical criteria for AKI diagnosis but showed elevated levels of new biomarkers reflecting tubular injury. One of these biomarkers is Neutrophil Gelatinase-Associated Lipocalin (NGAL). The aim of this study is to investigate the role of urinary NGAL and microalbuminuria as non-invasive biomarkers in the detection of subclinical AKI. Analysis of urinary NGAL and microalbuminuria in 91 subjects [30 pediatric intensive care unit (PICU) patients, 31 diabetic patients and 30 healthy controls] recruited from Cairo University Pediatric Hospital was done. Our study revealed that urinary NGAL was significantly higher in the PICU group followed by the diabetic group and lowest in the controls group (p=0.022). A positive correlation was found between urinary NGAL and microalbuminuria in the PICU group (Rvalue= 0.585, p-value=0.001). In diabetic group, a positive correlation was found between urinary NGAL and fasting blood glucose, 2 hours post prandial and HbA1C (R-value=0.421; pvalue= 0.021; R-value=0.426; p-value=0.019; R-value=0.438; pvalue= 0.018 respectively). Urinary NGAL may be a potential biomarker to detect subclinical AKI before actual functional renal damage leading to early intervention and reduction of mortality.

亚临床急性肾损伤(AKI)描述了不符合AKI诊断的经典标准,但显示出反映肾小管损伤的新生物标志物水平升高的患者。这些生物标志物之一是中性粒细胞明胶酶相关脂钙蛋白(NGAL)。本研究的目的是探讨尿NGAL和微量白蛋白尿作为非侵入性生物标志物在亚临床AKI检测中的作用。对来自开罗大学儿科医院的91名受试者(30名儿童重症监护病房(PICU)患者、31名糖尿病患者和30名健康对照)的尿NGAL和微量白蛋白尿进行了分析。我们的研究显示,尿NGAL在PICU组显著增高,其次是糖尿病组,在对照组最低(p=0.022)。PICU组尿NGAL与微量白蛋白尿呈正相关(r值= 0.585,p值=0.001)。糖尿病组尿NGAL与空腹血糖、餐后2 h、HbA1C呈正相关(r值=0.421;pvalue = 0.021;热阻= 0.426;假定值= 0.019;热阻= 0.438;p值分别= 0.018)。尿NGAL可能是一种潜在的生物标志物,在实际功能性肾损害之前检测亚临床AKI,从而导致早期干预和降低死亡率。
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引用次数: 0
Achilles tendon surgery in clubfoot: Are long term sequelae predictable? 内翻足的跟腱手术:长期后遗症可预测吗?
Q3 Medicine Pub Date : 2022-05-03 DOI: 10.4081/pmc.2022.280
L. Pedrotti, B. Bertani, G. Tuvo, R. Mora, L. Marin, Federica De Rosa
Congenital Clubfoot (CCF) treatment involves a surgical procedure on the Achilles tendon most of the time, i.e. tenotomy or, in selected cases, Z-plasty lengthening. Many authors have studied the outcomes of Achilles tenotomy, describing complete clinical and ultrasound tendon fibers integrity restoration 3-6 weeks after surgery. Nevertheless, little is known about the mechanical properties of the operated tendon. Recently, cases of subcutaneous rupture of the Achilles tendon have been described in adolescents who practiced sports and who had undergone Achilles tenotomy for congenital clubfoot in childhood. Authors report two cases of atraumatic Achilles tendon injury (subcutaneous rupture and intratendinous ossification) in adult patients who had been treated for congenital clubfoot in childhood. In both cases, no causes determining the injury were identified; in the medical history there was a Z-plasty lengthening of the Achilles tendon, performed within the first year of life, which could be considered a predisposing factor. The usefulness of long-term monitoring of patients treated for CCF with surgical procedures on the Achilles tendon is therefore hypothesized, in order to promptly identify by symptoms, clinical pictures and ultrasound criteria, tendon suffering that may predispose subcutaneous rupture.
先天性内翻足(CCF)的治疗在大多数情况下需要对跟腱进行外科手术,即肌腱切开术或在特定情况下采用z形成形术延长。许多作者研究了跟腱切断术的结果,描述了手术后3-6周完全的临床和超声肌腱纤维完整性恢复。然而,对手术肌腱的力学特性知之甚少。最近,在青少年进行体育运动和在儿童时期因先天性内翻足而接受跟腱切断术的情况下,发生了跟腱皮下断裂的病例。作者报告两例非外伤性跟腱损伤(皮下断裂和腱内骨化)的成人患者曾治疗先天性畸形足在儿童时期。在这两起案件中,都没有确定造成伤害的原因;在病史中,在出生后一年内进行了跟腱z形成形术,这可能是一个易感因素。因此,假设对接受跟腱手术治疗的CCF患者进行长期监测的有用性,以便通过症状、临床图片和超声标准及时识别可能诱发皮下断裂的肌腱疼痛。
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引用次数: 0
Rectovestibular fistula: Which surgical approach is suitable? A randomized controlled trial. 直肠前庭瘘:哪种手术入路合适?一项随机对照试验。
Q3 Medicine Pub Date : 2022-04-08 DOI: 10.4081/pmc.2022.278
S. Abdelmohsen, M. Osman, H. Mostafa, M. Fathy, I. Ibrahim, M. Mostafa, A. Eltayeb, Osama Abdullah Abdul Raheem
The management of a vestibular fistula is a challenge for pediatric surgeons. We compared four different operative techniques in terms of postoperative complications, continence, and cosmetic appearance. This prospective, randomized, comparative study included female children with rectovestibular fistulae who were selected from patients with Anorectal Malformations (ARMs) treated between January 2016 and July 2020. The patients were randomly divided into four groups based on the operative technique: Trans-Sphincter Anorectoplasty (TSARP), Posterior Sagittal Anorectoplasty (PSARP), Classic Anterior Sagittal Anorectoplasty (ASARP), and modified ASARP. The incidence of vestibular fistulae among all patients with ARMs was 13.4%. The total number of patients with vestibular fistula was 112, including eighty-four (75%) with rectovestibular fistulae and twenty-eight (25%) with anovestibular fistulae. Associated congenital anomalies were found in nineteen (22.6%) patients. The percentage of parents satisfied with the cosmetic appearance and continence of their children was the highest after TSARP. PSARP had the lowest incidence regarding vaginal wall injuries. TSARP is the best operative technique for handling rectovestibular fistulae and is suitable for infants and children. In the TSARP technique, the external sphincter muscle can be preserved following complete dissection of the rectum without the need for a midline skin incision. A midline skin incision is required in the modified ASARP technique.
前庭瘘管的处理是儿科外科医生面临的一个挑战。我们比较了四种不同的手术技术的术后并发症,尿失禁,和美容外观。这项前瞻性、随机、比较研究纳入了2016年1月至2020年7月期间治疗的肛门直肠畸形(ARMs)患者中患有直肠前庭瘘的女童。根据手术技术将患者随机分为四组:经括约肌肛肠成形术(TSARP)、后矢状肛肠成形术(PSARP)、经典前矢状肛肠成形术(ASARP)和改良ASARP。所有ARMs患者前庭瘘的发生率为13.4%。前庭瘘112例,其中直肠前庭瘘84例(75%),肛门前庭瘘28例(25%)。19例(22.6%)患者发现先天性异常。TSARP后,家长对孩子的外观和尿失禁满意的比例最高。PSARP对阴道壁损伤的发生率最低。TSARP是治疗直肠前庭瘘的最佳手术技术,适用于婴幼儿。在TSARP技术中,在完全切除直肠后可以保留外括约肌,而不需要在中线切开皮肤。在改良的ASARP技术中,需要一个中线皮肤切口。
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引用次数: 0
Surgical management of large scalp infantile hemangioma in 30-month-old infant. 30月龄婴幼儿大头皮血管瘤的外科治疗。
Q3 Medicine Pub Date : 2022-03-21 DOI: 10.4081/pmc.2022.279
Cosimo Bleve, Maria Luisa Conighi, Enrico Valerio, Mario Cutrone, Giuseppe Iannucci, Alessandro Segna, Salvatore Fabio Chiarenza

Infantile Hemangiomas (IH) are the most common benign tumor of infancy, occurring in over 10% of newborns. The head and neck is the most frequently affected area (60%), and the scalp is a typical site for such large lesions. Scalp-IHs are usually focal lesions that can be both disfiguring and may lead to complications such as ulceration and bleeding. We describe a case of a 30-months old female who presented a large scalp-IH at birth that rapidly grew in the first year of life. Topical and systemic treatments (with timolol ointment and oral propranolol, respectively) were not effective in reducing dimensions of the hemangioma. After vascular imaging study, the patient underwent surgical resection of the IH and primary closure with excellent cosmetic outcome. When medical therapy is ineffective or cosmetic and functional integrity is threatened, early surgery allows to completely removing large scalp-IHs, with good cosmetic results.

婴儿血管瘤(IH)是婴儿时期最常见的良性肿瘤,发生在10%以上的新生儿中。头颈部是最常受影响的区域(60%),而头皮是这种大病变的典型部位。头皮- ihs通常是局灶性病变,可毁容,并可能导致并发症,如溃疡和出血。我们描述了一个30个月大的女性谁提出了一个大的头皮ih在出生后的第一年迅速增长。局部和全身治疗(分别使用噻洛尔软膏和口服心得安)对减小血管瘤尺寸无效。在血管影像学检查后,患者接受了手术切除IH并进行了初步闭合,取得了良好的美容效果。当药物治疗无效或美容和功能完整性受到威胁时,早期手术可以完全切除大的头皮,具有良好的美容效果。
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引用次数: 2
Minimally invasive pilonidal sinus disease (PSD) treatment in pediatric patients: A narrative review. 儿科患者微创毛毛窦疾病(PSD)治疗:叙述性回顾。
Q3 Medicine Pub Date : 2022-03-15 DOI: 10.4081/pmc.2022.281
M. Cerulo, Assunta Turco, C. Esposito
Pilonidal sinus is a common disease of the natal cleft, which can lead to complications including infection and abscess formation. Various operative techniques are available options for the treatment of this pathology, but the ideal technique is still debatable. Analyzing the literature we found out that more recently minimally invasive approaches have been described. In particular, the mechanism of an endoscopic approach relies on the use of the endoscope without cutaneous tissue damage. Advantages include shorter operative time and time to discharge, which impact resource management in both primary and secondary care: patients undergoing endoscopic technique have a high satisfaction rate, probably due to the low level of postoperative pain and early return to daily activities. Published results of studies of newer approaches have demonstrated a lower short and long-term complication rate compared to open surgery. However, very poor reports are available in literature about pediatric population.
毛毛窦是先天性唇裂的常见疾病,可导致感染和脓肿形成等并发症。各种手术技术可用于治疗这种病理,但理想的技术仍有争议。通过对文献的分析,我们发现最近有更多的微创方法被描述。特别是,内窥镜入路的机制依赖于内窥镜的使用而没有皮肤组织损伤。优点包括手术时间和出院时间较短,这对初级和二级护理的资源管理都有影响:接受内镜技术的患者满意率高,可能是由于术后疼痛程度低和早期恢复日常活动。已发表的研究结果表明,与开放手术相比,新入路的短期和长期并发症发生率较低。然而,文献中关于儿科人群的报道非常少。
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引用次数: 2
Lichen sclerosus in pediatric age: A new disease or unknown pathology? Experience of single centre and state of art in literature. 儿童期硬化苔藓:一种新疾病还是未知病理?单一中心的经验与文学艺术的境界。
Q3 Medicine Pub Date : 2022-03-01 DOI: 10.4081/pmc.2022.275
R. Angotti, G. Fusi, Elena Coradello, C. Miracco, F. Ferrara, M. Sica, A. Taddei, G. Vasta, M. Messina, F. Molinaro
Lichen Sclerosus (LS) is a chronic inflammatory skin disease with unknown etiology. In pediatric age the main disease "lichenlinked" is the phimosis in male. This is a retrospective study that reports the experience of our clinic and review of the literature. We included all patients affected by pathological phimosis, treated by circumcision between January 2015 and May 2020, older than 6 years old and with an histopathological diagnosis of lichen sclerosus. The aim was to identify prognostic factors based on histological report to plan the clinical management of patients. Statistical analysis was done. We included 207 patients. The mean age of children was 9,78 years (5-18 years, DS±3.29). Based on the histological features we divided patients in 2 groups: early lesions (70/207, 34%) and advanced (137/207, 66%). In term of complications lichen linked we considered meatal stenosis that needed of urethral dilatations. We included 7 patients (7/207, 3,4%). We report P value Statistical Significance in many aspects. An early diagnosis of LS and surgical treatment of foreskin are essential to prevent early and late complications in children. The size of sample is a limit of the study but results encourage our management.
地衣硬化(LS)是一种病因不明的慢性炎症性皮肤病。在小儿年龄段,以男性包茎病为主要疾病。这是一项回顾性研究,报告了我们诊所的经验和文献综述。我们纳入了2015年1月至2020年5月期间接受包皮环切术治疗的所有病理性包茎患者,年龄大于6岁,组织病理学诊断为硬化地衣。目的是根据组织学报告确定影响预后的因素,以制定患者的临床治疗计划。进行统计分析。我们纳入了207名患者。患儿平均年龄9.78岁(5 ~ 18岁,DS±3.29)。根据组织学特征将患者分为早期病变组(70/ 207,34 %)和晚期病变组(137/ 207,66 %)。在并发症方面,我们考虑了需要扩张尿道的金属狭窄。我们纳入了7例患者(7/ 207,3,4%)。我们在许多方面报告P值的统计显著性。早期诊断和手术治疗包皮是必不可少的,以防止早期和晚期并发症的儿童。样本的大小是研究的一个限制,但结果鼓励我们的管理。
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引用次数: 2
Staghorn stone in megapolycalicosis in a child: Still the case for open surgery? Case report. 儿童多钙血症合并鹿角石:仍需开腹手术吗?病例报告。
Q3 Medicine Pub Date : 2022-02-02 DOI: 10.4081/pmc.2022.229
A. Marte
We here report a rare case of congenital megapolycalicosis in a 14-year-old girl complicated by a 24-mm staghorn stone and numerous calculi at the level of all caliceal groups that had become symptomatic in recent weeks with malaise, hematuria, and urinary tract infection. Among the various therapeutic options, we opted for open surgery. The staghorn stone was removed by pyelotomy, and washout of the caliceal cavities released numerous microcalculi of 1.5-9 mm in size that were then removed. To our knowledge, this is the first case of pediatric megacapolycalicosis complicated by staghorn stone, which presents complex problems for the diagnosis and therapy.
我们在此报告一例罕见的先天性多钙血症病例,患者为14岁的女孩,并发24毫米鹿角石和大量结石,近几周出现不适、血尿和尿路感染的症状。在各种治疗方案中,我们选择了开放手术。通过肾盂切开术取出鹿角石,冲洗肾盏腔释放出大量1.5-9毫米大小的微结石,然后将其取出。据我们所知,这是第一例小儿大钙多中毒合并鹿角石的病例,其诊断和治疗存在复杂的问题。
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引用次数: 0
期刊
Pediatria Medica e Chirurgica
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