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Transient femoral nerve palsy in spica cast treatment for developmental dysplasia of the hip. 短暂性股神经麻痹用石膏石膏治疗发育性髋关节发育不良。
Q3 Medicine Pub Date : 2018-09-26 DOI: 10.4081/pmc.2018.200
Luisella Pedrotti, Barbara Bertani, Gabriella Tuvo, Redento Mora, Mario Mosconi, Federica De Rosa

A 4 months and half female child come to our attention for congenital dislocation of the left hip, previously treated in another hospital with abduction bracing, without satisfactory results. After progressive longitudinal bilateral traction, closed reduction under general anesthesia was performed and a spica cast was applied in the so-called human position. The patients remained in the spica cast for 6 weeks and then the plaster cast was renewed in narcosis for another 6 weeks. Once the second cast has been removed left femoral nerve palsy was detected. Orthopaedic treatment was interrupted and in 3 months the nerve completely recovered, while the hip was still stable. We followed the child regularly since then, she is now five years old, she is totally asymptomatic, X-rays shows a residual acetabular dysplasia, with no sign of avascular necrosis.

一例4个半月的女婴先天性左髋关节脱位,曾在另一家医院接受外展支具治疗,但效果不佳。在渐进式纵向双侧牵引后,全麻下进行闭合复位,并在所谓的人位上应用spica石膏。患者先用石膏石膏固定6周,再用石膏石膏继续麻醉6周。第二根石膏取出后,发现左股神经麻痹。骨科治疗中断,3个月后神经完全恢复,髋关节仍然稳定。从那时起,我们定期对孩子进行随访,她现在已经五岁了,她完全没有症状,x光片显示髋臼发育不良,没有血管坏死的迹象。
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引用次数: 2
Clinical side effects after oral administration of palm oil and Alchornea cordifolia decoction in a child. 小儿口服棕榈油加堇叶汤后的临床副反应。
Q3 Medicine Pub Date : 2018-09-26 DOI: 10.4081/pmc.2018.152
Paulo Muntu Bunga, Jephté Bambi Nzita, Gerry Mubungu, Sophie Nyembo Mangaza, Nono Joelle Seudjip, Michel Ntetani Aloni

Alchornea cordifolia is known to be a plant with a variety of medicinal properties and is quoted by many traditional healers to treat a variety of medicinal problems in the Democratic Republic of Congo. However, very little is known about its potential toxicity. We report the case of a 9-year-old boy referred for assessment of suspected bronchial troubles without a history of atopic disease or drug allergy who developed dyspnea, dysphagia, asthenia and lingual ulcers within 30 minutes after nasal and oral administration of decoction of palm oil associated with A. cordifolia leaves in water. In the present report, adverse effects of A. cordifolia therapy may be related to the mixtures of active compounds that they contain and can cause the symptoms observed in our patient. These findings call for caution in the use of A. cordifolia especially in children.

众所周知,Alchornea cordifolia是一种具有多种药用特性的植物,在刚果民主共和国,许多传统治疗师都引用它来治疗各种医学问题。然而,人们对其潜在毒性知之甚少。我们报告一例9岁男童,无特应性疾病或药物过敏史,经鼻和口服棕榈叶相关水煎液30分钟内出现呼吸困难、吞咽困难、虚弱和舌溃疡。在本报告中,堇青花治疗的不良反应可能与它们所含的活性化合物的混合物有关,并可能导致本患者观察到的症状。这些发现呼吁在使用堇青花时要谨慎,尤其是在儿童中。
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引用次数: 1
Robotic removal of Müllerian duct remnants in pediatric patients: our experience and a review of the literature. 机器人切除小儿患者<s:1>勒氏管残余:我们的经验和文献回顾。
Q3 Medicine Pub Date : 2018-05-30 DOI: 10.4081/pmc.2018.182
Mario Lima, Michela Maffi, Niel Di Salvo, Giovanni Ruggeri, Michele Libri, Tommaso Gargano, Hubert Lardy

Persistent Müllerian duct syndrome is a disorder of sexual development, which features a failure of involution of Müllerian structures. An enlarged prostatic utricle is a kind of Müllerian duct remnant (MDR) with a tubular shaped structure communicating with the prostatic urethra. Treatment is aimed at relieving symptoms when present, preserve fertility and prevent neoplastic degeneration. We describe 3 cases of successful robot assisted-removal of symptomatic MDRs. The first case came to our attention for pseudo-incontinence; the other two for recurrent urinary tract infections. The patients have not presented such symptoms anymore on follow-up. We then reviewed existent literature on authors who have recently investigated the main issues concerning MDRs and have attempted a roboticassisted approach on them. Robot-assisted laparoscopy can be considered a valid, safe and effective minimally-invasive technique for the primary treatment of prostatic utricle.

持续性腰勒氏管综合征是一种性发育障碍,其特征是腰勒氏管结构退化失败。肥大的前列腺小囊是一种与前列腺尿道相通的管状结构的勒氏管残余(MDR)。治疗的目的是缓解症状,保持生育能力,防止肿瘤变性。我们描述了3例成功的机器人辅助去除症状性mdr的病例。第一例引起我们注意的是假性尿失禁;另外两例为复发性尿路感染。随访时患者均未出现上述症状。然后,我们回顾了现有的文献,作者最近调查了有关mdr的主要问题,并尝试了机器人辅助方法。机器人辅助腹腔镜是一种有效、安全、有效的微创前列腺小囊初级治疗技术。
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引用次数: 18
Kearns-Sayre syndrome is genetically and phenotypically heterogeneous. 卡恩斯-塞尔综合征具有遗传和表型异质性。
Q3 Medicine Pub Date : 2018-05-29 DOI: 10.4081/pmc.2018.193
Josef Finsterer, Sinda Zarrouk-Mahjoub

Not available.

不可用。
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引用次数: 5
Torsion of huge epididymal cyst in a 16-year-old boy: case report and review of the literature. 16岁男孩巨大附睾囊肿扭转:病例报告及文献复习。
Q3 Medicine Pub Date : 2018-05-29 DOI: 10.4081/pmc.2018.162
Cosimo Bleve, Maria Luisa Conighi, Valeria Bucci, Lorenzo Costa, Salvatore Fabio Chiarenza

Epididymal cysts (ECs) are relatively common in adults, rare in children. Normally their treatment is conservative. They may be situated anywhere in the organ, frequently in the region of the head. Torsion of these cysts is extremely rare in both children and adults, causing acute scrotal swelling. The diagnosis is intraoperative. A 16-year-old boy was referred to our Divisional Clinic by the treating physician for scrotal swelling appeared 4 months earlier. Absence of a history of minor scrotal trauma. Ultrasonography showed a 40×50 mm fluid-filled right para-testicular mass. We performed surgery finding a large black cyst connected to the head of the epididymis with 720°-degrees rotation. Histology revealed an acquired EC. The particularity of our case is due to the absence of symptoms in association with a big EC twisted of 720° degrees. This is the only case reported in literature. All patients with EC torsion reported presented symptoms related to acute scrotum.

附睾囊肿(ECs)在成人中比较常见,在儿童中比较少见。通常他们的治疗是保守的。它们可能位于器官的任何地方,通常在头部区域。这些囊肿的扭转在儿童和成人中极为罕见,引起急性阴囊肿胀。诊断是术中诊断。一位16岁的男孩,因4个月前出现阴囊肿胀而被主治医生转介到我们的分科诊所。没有轻微阴囊外伤史。超声显示右侧睾丸旁有一40×50毫米充满液体的肿块。我们在手术中发现一个大的黑色囊肿连接到附睾头部,旋转720°。组织学显示后天性EC。我们病例的特殊性是由于没有与大EC扭曲720°相关的症状。这是文献报道的唯一病例。所有EC扭转患者均报告出现与急性阴囊相关的症状。
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引用次数: 7
Robot-assisted thoracoscopic repair of a late-onset Bochdalek hernia: a case report. 机器人辅助胸腔镜治疗迟发性Bochdalek疝1例报告。
Q3 Medicine Pub Date : 2018-05-25 DOI: 10.4081/pmc.2018.173
Mario Lima, Niel Di Salvo, Sara Ugolini, Michele Libri, Giovanni Ruggeri

Bochdalek hernia (BH) is a major malformation that consists of a postero-lateral diaphragmatic defect through which abdominal contents can migrate into the thorax. It is most commonly a neonatal pathology associated with significant morbidity and mortality. Rarely, this type of congenital diaphragmatic hernia (CDH) presents later in life, some even in adulthood. Indications for surgery are not clear even though the majority of authors, being aware of the possible severe complications, recommend surgical correction in all cases. Many surgical approaches have been tried for this pathology, both open (laparotomic or thoracotomic) and minimally invasive (laparoscopic or thoracoscopic). We report a case of a late-onset BH corrected with a robot-assisted thoracoscopic procedure. The use of robotic technology for CDH has never been described to date.

Bochdalek疝(BH)是一种主要的畸形,由后外侧膈缺损组成,腹部内容物可通过该缺损迁移到胸腔。它是最常见的新生儿病理与显著的发病率和死亡率相关。这种类型的先天性膈疝(CDH)很少出现在以后的生活中,有些甚至出现在成年期。手术指征尚不清楚,尽管大多数作者意识到可能出现的严重并发症,建议在所有病例中进行手术矫正。许多手术方法已被尝试用于这种病理,包括开放(剖腹或开胸)和微创(腹腔镜或胸腔镜)。我们报告一例迟发性BH纠正与机器人辅助胸腔镜手术。迄今为止,机器人技术在CDH中的应用从未被描述过。
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引用次数: 3
Laparoscopic treatment of symptomatic simple renal cysts in children: single-center experience. 儿童单纯性肾囊肿的腹腔镜治疗:单中心经验。
Q3 Medicine Pub Date : 2018-05-24 DOI: 10.4081/pmc.2018.168
Antonio Marte, Lucia Pintozzi

Simple renal cysts, although common in adults, are rare in children. They are usually discovered incidentally in the course of the study of other urinary tract symptoms, although they are not always asymptomatic. Renal cysts can be classified as being either simple or complex. The purpose of this review is to present our case series of simple symptomatic renal cysts treated with laparoscopy. Nineteen patients with symptomatic renal cysts (6 to 13.5 cm) were referred to our institution between January 2006 and January 2017. They comprised 12 (40.5%) females and seven (59.5%) males, aged 8 to 15, with a mean age of 12.2 years. Of these patients, nine had previously been treated unsuccessfully by ultrasound-guided aspiration/alcoholization with 95%-ethanol, between 9 and 13 months prior to the laparoscopy. Five patients had undergone one treatment and four had undergone two treatments. All of the patients were treated by laparoscopic threetrocar deroofing. The cysts were opened and the wall excised using scissors and a monopolar hook. In most cases, to better handle the edges of the cyst and obtain a better grip, a needle was used to aspirate a small amount of fluid (used for cytological examination). The wall of the cyst was excised, the cyst edges were sealed, and the perirenal fat was placed on the bottom of the cyst (wadding technique). The mean operating time was 95 minutes (range 50- 150). The postoperative course was uneventful for all of the patients. The hospital stay ranged from one to three days. All of the patients were asymptomatic following the treatment. At a mean follow-up time of 3.6 years, none of the patients had experienced a recurrence. Renal function, as assessed by a MAG3 renal scintigraphy scan, was well-preserved in all of the patients, and all of them undergo an annual ultrasound scan.

单纯性肾囊肿虽然在成人中很常见,但在儿童中很少见。它们通常在研究其他尿路症状的过程中偶然发现,尽管它们并不总是无症状的。肾囊肿可分为简单型和复杂型。本综述的目的是介绍我们的病例系列单纯性症状性肾囊肿腹腔镜治疗。在2006年1月至2017年1月期间,有19例症状性肾囊肿(6至13.5 cm)患者转介到我们的机构。其中女性12例(40.5%),男性7例(59.5%),年龄8 ~ 15岁,平均年龄12.2岁。在这些患者中,有9例在腹腔镜检查前9至13个月,曾通过超声引导下吸入/ 95%乙醇酒精化治疗失败。5名患者接受了一次治疗,4名患者接受了两次治疗。所有患者均行腹腔镜三针穿刺治疗。将囊肿切开,并用剪刀和单极钩切除囊肿壁。在大多数情况下,为了更好地处理囊肿边缘并获得更好的抓地力,使用针抽吸少量液体(用于细胞学检查)。切除囊肿壁,封闭囊肿边缘,将肾周脂肪置于囊肿底部(填塞技术)。平均手术时间为95分钟(范围50- 150分钟)。所有患者的术后过程均平安无事。住院时间从一到三天不等。所有患者经治疗后均无症状。在平均3.6年的随访时间里,没有患者复发。通过MAG3肾显像扫描评估,所有患者的肾功能都保存良好,并且所有患者每年都接受一次超声扫描。
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引用次数: 6
Nutritional management of surgical newborns and infants in the acute phase and during follow up. 外科新生儿和婴儿急性期及随访期间的营养管理。
Q3 Medicine Pub Date : 2018-05-23 DOI: 10.4081/pmc.2018.197
Fabio Mosca

The neonatal period represents a crucial stage of life since it is characterized by the development of organ structure and function. Early life is particularly susceptible to environmental factors through a programming effect. As a result, inadequate nutrition in early life leads to long-term mental and physical developmental alterations and increased mortality and morbidity. In this review, we will summarize available evidence with a particular focus on metabolic responses to surgical trauma, nutritional strategies that can be implemented in surgical infants and specific barriers to nutritional support after surgery.

新生儿期是生命的关键阶段,因为它的特点是器官结构和功能的发展。通过编程效应,生命早期特别容易受到环境因素的影响。因此,生命早期营养不足会导致长期的精神和身体发育改变,并增加死亡率和发病率。在这篇综述中,我们将总结现有的证据,特别关注手术创伤的代谢反应,可以在手术婴儿中实施的营养策略以及手术后营养支持的具体障碍。
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引用次数: 2
Functional gastrointestinal disorders in newborns: nutritional perspectives. 新生儿功能性胃肠疾病:营养学观点。
Q3 Medicine Pub Date : 2018-05-23 DOI: 10.4081/pmc.2018.198
Roberto Bellù, Manuela Condò

Functional gastrointestinal disorders (FGIDs) definition in children has changed over the years trying to facilitate clinicians, because the diagnostic process is complicated by the interpretation variability of symptoms described by children or by their caregivers for newborns and toddlers. This review refers to the Rome IV classification system, drafted in 2016. FGIDs pathophysiology is multifactorial and still poor understood, with limitations for the therapeutic process, which results often in unnecessary and alternative treatments trying to reduce the relevant caregiver distress, but with increased costs for families and for the National Health Service. This study reports the most recent evidence-based treatments for FGIDs in newborns: though in most cases the first action is an educational and behavioral intervention, reassuring caregivers about the transient and self-limiting natural history of FGIDs, there is now more evidence to recommend probiotics in some infant FGIDs.

多年来,为了方便临床医生,儿童功能性胃肠道疾病(fgid)的定义已经发生了变化,因为儿童或其照顾者对新生儿和幼儿所描述的症状的解释差异使诊断过程变得复杂。本次审查参考了2016年起草的Rome IV分类系统。FGIDs的病理生理是多因素的,但仍然知之甚少,治疗过程也有局限性,这往往导致不必要的替代治疗,试图减少相关护理者的痛苦,但增加了家庭和国家卫生服务的成本。本研究报告了针对新生儿FGIDs的最新循证治疗方法:尽管在大多数情况下,第一个行动是教育和行为干预,让护理人员放心FGIDs的短暂性和自限性自然史,但现在有更多证据建议在一些婴儿FGIDs中使用益生菌。
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引用次数: 2
Feeding dysfunctions and failure to thrive in neonates with congenital heart diseases. 先天性心脏病新生儿的喂养功能障碍和发育不良。
Q3 Medicine Pub Date : 2018-05-23 DOI: 10.4081/pmc.2018.196
Giovanna Mangili, Elena Garzoli, Youcef Sadou

Congenital heart disease (CHD) is the most common neonatal congenital malformation. The variety and severity of clinical presentation depend on the cardiac structures involved and their functional impact. The management of newborns with CHD requires a multidisciplinary approach, in which the nutritional aspect plays an important role. An adequate caloric intake during either preand post-surgical period, in fact, improves the outcome of these patients. In addition, the failure to thrive of these children in childhood has been related to long-term cognitive delay (attention deficit disorders, aggressive behaviour and poor social and emotional development). To date, there is a lack of standardized feeding protocols and caloric goals about how to feed neonates with CHD, and current practice varies widely between centres. The latest American Society for Parenteral and Enteral Nutrition guidelines reiterate the importance of proteins, and recommend early start of enteral nutrition, also in the most severe heart diseases, such as univentricular forms. Necrotizing enterocolitis (NEC), the most frequent and feared complication of early feeding of these newborns, often represents an obstacle in spreading this practice. Furthermore, as demonstrated in premature infants, breastfeeding seems to reduce the incidence of NEC. That is why breastfeeding must be encouraged, even if it can be difficult for these mothers due to delivery complications, associated with infant disease. In addition, eating difficulties may persist even after discharge, because these patients require nutritional support through nasogastric tubes or percutaneous endoscopic gastrostomies.

先天性心脏病(CHD)是最常见的新生儿先天性畸形。临床表现的多样性和严重程度取决于所涉及的心脏结构及其功能影响。新生儿冠心病的管理需要多学科的方法,其中营养方面起着重要的作用。事实上,术前和术后摄入足够的热量可以改善这些患者的预后。此外,这些儿童在童年时期未能茁壮成长与长期认知迟缓(注意力缺陷障碍、攻击行为以及社交和情感发展不良)有关。迄今为止,缺乏关于如何喂养冠心病新生儿的标准化喂养方案和热量目标,目前各中心的做法差异很大。最新的美国肠外和肠内营养协会指南重申了蛋白质的重要性,并建议尽早开始肠内营养,也适用于最严重的心脏病,如单心室形式。坏死性小肠结肠炎(NEC)是这些新生儿早期喂养最常见和最可怕的并发症,往往是传播这种做法的障碍。此外,正如在早产儿中所证明的那样,母乳喂养似乎可以降低NEC的发病率。这就是为什么必须鼓励母乳喂养,即使由于与婴儿疾病相关的分娩并发症,母乳喂养对这些母亲来说可能很困难。此外,即使在出院后,进食困难也可能持续存在,因为这些患者需要通过鼻胃管或经皮内镜胃造口术提供营养支持。
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引用次数: 26
期刊
Pediatria Medica e Chirurgica
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