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Graft aneurysm as long-term complication of a polyester prosthesis and its adequate management - short review based on a systematic review of literature and a representative case report 涤纶假体长期并发症的移植物动脉瘤及其适当的处理-基于文献系统回顾和代表性病例报告的简短回顾
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.006
Udo Barth * , Klaus Wasseroth , Zuhir Halloul , Frank Meyer

Introduction

A material-associated true aneurysm after previous use of a vascular prosthesis for arterial reconstruction mostly in peripheral arterial occlusion disease (PAOD) is considered a rare but serious complication.

Case description

A 49 year old male patient underwent several sequential steps of arterial recanalization/reconstruction because of PAOD, stage IIb (walking distance, <100m) according to local findings with endovascular measures and vascularsurgical bypass implantation by means of a femoropoliteal P1-prosthetic bypass at the right and left leg (the right distal prosthetic segment was extended with a venous bypass to the P3-segment because of a distal suture aneurysm and arterial thrombosis of the right calf. After 10 years, a true prosthetic aneurysm was diagnosed at the right thigh using Duplex-ultrasonography and complementary MR-angiography. It was successfully treated with a femoro(prosthetico)-infragenual 6-mm-Gore®-Propaten® bypass (W.L. Gore, Putzbrunn, Germany) down to the P3-segment of the right popliteal artery. Nineteen articles were found in the literature search, which had been published since 1995. Most frequently, pseudoaneurysms of knitted polyester prostheses at the femoro-popliteal segment occurred after approximately 12.91 years in average. In one third of cases, 2 ore more aneurysms of dacron prostheses were described. Histological and electromicroscopic investigations revealed mainly breakings of filaments and foreign body reactions. In more than half of the patients, the aneurysm was resected and for reconstruction, an interponate was implanted. Complete removal of the prosthesis and endovascular therapy were only 2nd choice.

Results and Conclusions

Development of true prosthetic aneurysms has not been satisfyingly clarified yet. It belongs to the late complication profile - even it occurs rarely - and should be controlled after a postoperative interval of one decade if the arterial recanalization/reconstruction was performed using prosthetic material after previously - in the sequential approach - endovascular intervention and venous bypass could not be used.

主要是外周动脉闭塞症(PAOD)患者在先前使用血管假体进行动脉重建后出现的材料相关性真动脉瘤被认为是一种罕见但严重的并发症。病例描述:一名49岁男性患者因pad接受了几个连续步骤的动脉再通/重建,IIb期(步行距离,<100)根据局部发现行血管内措施和血管外科旁路植入,分别在右腿和左腿行股动脉p1假体旁路(由于右小腿远端缝合动脉瘤和动脉血栓形成,右远端假体段通过静脉旁路延伸至p3段)。10年后,在右大腿使用双超声和补充磁共振血管造影诊断出一个真正的假动脉瘤。采用股骨(假体)-骨折内6 mm Gore®-Propaten®旁路(W.L. Gore, Putzbrunn, Germany)至右侧腘动脉p3段成功治疗。在文献检索中发现了19篇文章,这些文章自1995年以来一直发表。针织涤纶假体在股腘段的假性动脉瘤最常见,平均发生时间约为12.91年。在三分之一的病例中,描述了2个以上的涤纶假体动脉瘤。组织学和电镜检查主要显示纤维断裂和异物反应。在超过一半的病人中,动脉瘤被切除,为了重建,植入了一个interponate。完全切除假体和血管内治疗是第二选择。结果与结论假性动脉瘤的发展尚未得到令人满意的阐明。它属于晚期并发症,即使很少发生,如果在先前的顺序入路中不能使用血管内介入和静脉旁路后使用假体材料进行动脉再通/重建,则应在术后间隔10年后加以控制。
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引用次数: 0
Time from recognition of sepsis to treatment - A 2-month retrospective study of compliance of IV antibiotics at Queen's Hospital Burton 从确认败血症到治疗的时间-伯顿女王医院静脉注射抗生素依从性的2个月回顾性研究
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.023
Joshua Agilinko *, Anuttara Bhadra

Introduction

Sepsis is the presence (probable or documented) of infection. With its systemic manifestations of severe sepsis and septic shock posing a major healthcare burden in the UK and globally, there is clearly a potential for physician and patient awareness. Current evidence suggests that administration of appropriate antibiotic therapy within 1 hour on recognition of sepsis and its sequelae improves mortality rates among patients. In the UK, the National Institute of Clinical Excellence (NICE) and The Surviving Sepsis Campaign (SSC) recommends the use of intravenous antibiotics within the first hour of recognition of sepsis.

Case description

To determine the number of patients receiving their antibiotics within 1 hour from recognition of sepsis and to assess compliance of Queen’s Hospital Burton Trust (QHBT) with the NICE and Surviving Sepsis Campaign’s recommendation for early antibiotic therapy. A 2-month retrospective chart analysis was conducted to determine the interval from documented onset of sepsis to initial administration of antibiotic for patients at QHBT. Inclusion criteria included patients presenting to Accident and Emergency aged 16 and over scoring 4 or more on their NEWS (National Early Warning Chart Scoring) chart. Patients presenting to a paediatric and gynaecological/obstetric setting were excluded. Patients started on antibiotics at the GP were also excluded.

Results and Conclusions

Charts of 82 patients with documented sepsis were reviewed. 51 patients received their antibiotics within 1 hour representing 62% of all patients presenting to Accident and Emergency at QHBT over the 2 months period. At QHBT, over the 2-month period, very few patients receiving their antibiotics within 1 hour. Therefore, the administration of antibiotics in 38% of all patients exceeded the 1 hour period recommended by NICE and Surviving Sepsis Campaign guidelines. These results have been used as a baseline for future quality assurance and improvement initiatives aimed at minimizing the time to antibiotic administration for this group of patients, who are at high risk of death. Data have been shared with physicians, allied health professionals and patient groups at board meetings. A re-audit is in process with initial results looking promising.

败血症是指存在(可能的或记录的)感染。在英国和全球范围内,严重败血症和感染性休克的系统性表现构成了主要的医疗负担,医生和患者显然有潜在的意识。目前的证据表明,在确认败血症及其后遗症后1小时内给予适当的抗生素治疗可提高患者的死亡率。在英国,国家临床卓越研究所(NICE)和生存败血症运动(SSC)建议在识别败血症的第一个小时内使用静脉注射抗生素。病例描述:确定脓毒症确诊后1小时内接受抗生素治疗的患者人数,并评估女王医院伯顿信托基金会(QHBT)对NICE和存活脓毒症运动推荐的早期抗生素治疗的依从性。进行了为期2个月的回顾性图表分析,以确定从记录的败血症发作到QHBT患者首次使用抗生素的时间间隔。纳入标准包括16岁及以上出现事故和急诊的患者,其NEWS(国家预警表评分)表得分为4分或以上。在儿科和妇科/产科就诊的患者被排除在外。在全科医生处开始使用抗生素的患者也被排除在外。结果与结论回顾性分析82例败血症患者的病历。51名患者在1小时内接受了抗生素治疗,占2个月期间在QHBT急诊科就诊的所有患者的62%。在QHBT,在2个月期间,很少有患者在1小时内接受抗生素治疗。因此,38%的患者使用抗生素的时间超过了NICE和生存败血症运动指南推荐的1小时。这些结果已被用作未来质量保证和改进举措的基线,旨在最大限度地减少这组死亡风险高的患者使用抗生素的时间。数据已在董事会会议上与医生、联合保健专业人员和患者团体共享。重新审核正在进行中,初步结果看起来很有希望。
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引用次数: 0
Splenic pseudo-aneurysm complicating acute pancreatitis: Endovascular trans-catheter embolisation with coils and N-butyl cyanoacrylate 脾假性动脉瘤并发急性胰腺炎:血管内经导管栓塞线圈和氰基丙烯酸酯正丁酯
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.08.002
Joshua Agilinko, Maaz Syed, Imran Parwes, Manan Ahmed

Splenic aneurysms are rare but life-threatening complications of acute pancreatitis. The main risk is aneurysmal rupture and subsequent death from haemorrhage if not treated promptly.

For a long time, surgery has been the mainstay of definite treatment of splenic aneurysms. In this report, we highlight a partially ruptured splenic aneurysm which was successfully treated via endovascular trans-catheter embolisation using N-butyl cyanoacrylate glue and metallic coils.

脾动脉瘤是罕见但危及生命的急性胰腺炎并发症。如果不及时治疗,主要风险是动脉瘤破裂和随后因出血死亡。长期以来,手术一直是脾动脉瘤明确治疗的主要方法。在这个报告中,我们强调了一个部分破裂的脾动脉瘤,成功地通过血管内经导管栓塞使用氰基丙烯酸丁酯胶和金属线圈。
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引用次数: 1
Giant cell tumor of the tendon sheath arising from anterior cruciate ligament 起源于前交叉韧带的腱鞘巨细胞瘤
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.09.001
J.K. Wong , W.H. Chan
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引用次数: 4
Inflammatory fibroid polyp - a cause of small bowel obstruction 炎性肌瘤息肉——引起小肠梗阻
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.025
Hiam Al-Droubi *, Neeraj Lal, Hussain Najam, Shahzad Khan, Himaz Marzook, Naseem Waraich, Sam McBride

Introduction

Inflammatory fibroid polyps (IFPs) are rare, benign tumours originating from the submucosa of stomach or small bowel. They account for only 0.1-3.0% of all gastric polyps. Histogenesis remains unknown. In adults, benign tumours such as IFPs are an uncommon cause of small bowel obstruction.

Case description

A 54 year old male patient with known hypertension presented to the emergency department with a 24 hour history of sudden onset and severe right iliac fossa pain, which progressively worsened. He was pyrexial on admission, had decreased appetite and had significant weight loss over the previous few months. There were no other gastrointestinal symptoms. The clinical examination and laboratory findings were consistent with a diagnosis of appendicitis. However, a CT scan of the abdomen and pelvis was suggestive of small bowel obstruction. This scan was reported by two radiologists due to the inconclusive aetiology of the small bowel obstruction. Though the first impression was acute-on-chronic crohn’s disease, on further analysis of the images a well defined oval shaped homogenous mass was noted in the distal ileum. An MRI scan confirmed terminal ileal inflammatory changes with intraluminal cystic changes. The patient underwent a laparoscopic right hemicolectomy. Intraoperatively, a cystic mass in the terminal ileum was found to be causing small bowel obstruction. Histology revealed that the mass was composed of fusiform and stellate shaped stromal cells with marked oedema and eosinophilia consistent with the diagnosis of IFP. The patient had an uneventful postoperative recovery.

Results and Conclusions

Despite the fact that inflammatory fibroid polyps are very rare lesions, they should be taken into consideration as a differential diagnosis in patients presenting with small bowel obstruction, as prompt surgical resection is the only known effective treatment.

炎性肌瘤息肉(IFPs)是一种罕见的良性肿瘤,起源于胃或小肠粘膜下层。它们仅占所有胃息肉的0.1-3.0%。组织发生尚不清楚。在成人中,良性肿瘤如IFPs是小肠梗阻的罕见原因。病例描述一名已知高血压的54岁男性患者,因24小时突然发作和严重的右髂窝疼痛进行性恶化而就诊于急诊科。入院时发热,食欲下降,前几个月体重明显减轻。没有其他胃肠道症状。临床检查和实验室检查结果符合阑尾炎的诊断。然而,腹部和骨盆的CT扫描提示小肠梗阻。由于小肠梗阻的病因不明,两名放射科医生报告了这一扫描结果。虽然第一印象是急性慢性克罗恩病,但在进一步分析图像时,在回肠远端发现了一个清晰的椭圆形均匀肿块。MRI扫描证实终末期回肠炎性改变伴腔内囊性改变。病人接受了腹腔镜右半结肠切除术。术中,发现回肠末端的囊性肿块引起小肠梗阻。组织学显示肿块由梭状和星状基质细胞组成,伴有明显的水肿和嗜酸性粒细胞增多,符合IFP的诊断。病人术后恢复顺利。结果与结论尽管炎性肌瘤息肉是非常罕见的病变,但在出现小肠梗阻的患者中,应将其作为鉴别诊断,因为及时手术切除是已知唯一有效的治疗方法。
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引用次数: 0
Transposition of a pancreas transplant from the bladder to the terminal ileum twenty years after combined allogenic kidney-pancreas-transplantation 同种异体肾胰联合移植后二十年胰腺移植从膀胱转位至回肠末端
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.011
Astrid Stula * , Tanja Maier , Anna Heverhagen , Josef Geks

Introduction

During the first years of combined allogenic kidney-pancreas-transplantation bladder diversion of the exocrine pancreas secretion was used. After reporting urological and systemic complications it was switched to an enteric diversion with excellent results of pancreas function. Today enteric diversion of the pancreatic ductal secretion is the standard procedure. Nevertheless there are still patients alive with bladder diversion from the early years of transplantation with a good pancreatic function but loss of kidney function. This case describes such a patient and how we dealt with the problem.

Case description

A 53-year old male patient presented with a progressive renal failure twenty years after combined allogenic kidney-pancreas-transplantation with bladder diversion of the exocrine pancreas secretions. Urine excretion was declining with a pre-dialysis renal failure. Still the pancreas transplant was working properly without the need of insulin therapy. We therefore carried out a separation of the graft duodeno-cystostomy and re-established diversion by a side-to-side graft duodenal-recipient ileal anastomosis. This was done by a 2-layer hand sewn technique. Bladder catheter, drainage near the bladder and drainage near the anastomosis were removed after 5, 8 and 10 days respectively. The pancreas showed proper function without the need of insulin therapy. The patient was released from hospital 14 days after the operation.

Results and Conclusions

Transposition of a pancreas transplant from the bladder to the terminal ileum twenty years after primary transplantation is technically possible. In this case it was also reasonable in order to protect the bladder from the aggressive pancreatic ductal secretion. Because of the declining urine excretion due to progressive failure of the kidney transplant the exocrine secretion was not properly diluted anymore with the risk of hematuria, lower urinary tract infections, reflux-associated pancreatitis and transitional cell dysplasia. These conditions could limit the opportunity for the patient for a second kidney donation.

Take home message

Transposition of a pancreas transplant from the bladder to the terminal ileum twenty years after primary transplantation is technically possible and reasonable to offer the patient a chance for a second kidney donation.

前言:在异体肾胰联合移植的头几年,采用膀胱转移外分泌胰腺的方法。在报告泌尿系统和全身并发症后,它被切换到肠转移,胰腺功能的良好结果。今天肠内转移胰管分泌物是标准的手术程序。尽管如此,仍有早期膀胱转移患者存活,胰腺功能良好,但肾功能丧失。这个案例描述了这样一个病人以及我们是如何处理这个问题的。病例描述:一名53岁男性患者,在异体肾胰联合移植20年后出现进行性肾衰竭,并伴有胰腺外分泌膀胱转移。尿排泄量随着透析前肾功能衰竭而下降。尽管如此,胰腺移植手术仍然正常工作,不需要胰岛素治疗。因此,我们对移植十二指肠-膀胱吻合术进行分离,并通过侧对侧移植十二指肠-受体回肠吻合术重新建立分流。这是通过两层手工缝制技术完成的。术后5、8、10 d分别拔除膀胱导管、膀胱附近引流、吻合口附近引流。胰腺功能正常,无需胰岛素治疗。病人在手术后14天出院。结果与结论首次胰腺移植后20年将胰腺从膀胱移植到回肠末端在技术上是可行的。在这种情况下,为了保护膀胱免受侵略性胰腺导管分泌物的侵害也是合理的。由于肾脏移植的进行性衰竭导致尿液排泄减少,外分泌不再适当稀释,有血尿、下尿路感染、反流相关性胰腺炎和移行细胞发育不良的风险。这些情况可能会限制患者进行第二次肾脏捐赠的机会。在初次移植后二十年将胰腺从膀胱移植到回肠末端,这在技术上是可行的,也是合理的,可以为患者提供第二次肾脏捐赠的机会。
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引用次数: 0
Pancreatic malignancy presenting as duodenal ulcer (D1) 胰腺恶性肿瘤表现为十二指肠溃疡(D1)
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.012
Azzam Al-Amin * , Tim Stephenson , Muhammad Shiwani

Introduction

Malignant ulcer at the duodenal bulb is extremely rare. The commonest cause of ulcers here is peptic ulcer disease. Therefore the routine biopsy of ulcer at D1 is not routinely recommended, to avoid complications.

Case description

An 83-year-old lady presented to the surgical outpatient clinic with upper abdominal pain radiating to left side of her chest. She had recent history of significant weight loss, approximately 22kg. Abdominal examination was unremarkable.

Results and Conclusions

Haemoglobin and Liver Function Tests were normal. Gastroscopy showed one large 3cm ulcer with a shaggy base and rolled over margin in the first part of the duodenum (D1) which appeared malignant. Initial histology confirmed adenocarcinoma of uncertain origin. CT scan showed a 2.9x3.7cm partially cystic mass lesion in the head of the pancreas that was locally invading into the first part of the duodenum, with no evidence of metastases. Immunohistochemistry showed strong Ca19.9 positive, favouring primary pancreatic origin.

Take home message

Pancreatic cancer presenting as an ulcer in D1 is very rare. If a suspicious looking ulcer is found endoscopically at D1, it should be biopsied. A CT scan of the abdomen is also important in the work-up of such cases.

十二指肠球部恶性溃疡极为罕见。溃疡最常见的病因是消化性溃疡。因此,为避免并发症,不推荐对D1处的溃疡进行常规活检。病例描述一名83岁的女士因上腹部疼痛放射到左胸就诊于外科门诊。她最近体重明显减轻,大约22公斤。腹部检查无明显异常。结果与结论血红蛋白、肝功能检查正常。胃镜检查显示十二指肠前段一3cm大溃疡,基底粗糙,边缘翻滚(D1),呈恶性。初步组织学证实为腺癌,来源不明。CT示胰腺头部2.9x3.7cm部分囊性肿块,局部侵犯十二指肠前段,未见转移。免疫组化显示强烈的Ca19.9阳性,支持原发性胰腺起源。带回家的信息胰腺癌表现为D1的溃疡是非常罕见的。如果内窥镜在D1处发现可疑溃疡,应进行活检。腹部CT扫描在此类病例的检查中也很重要。
{"title":"Pancreatic malignancy presenting as duodenal ulcer (D1)","authors":"Azzam Al-Amin * ,&nbsp;Tim Stephenson ,&nbsp;Muhammad Shiwani","doi":"10.1016/j.nhccr.2017.10.012","DOIUrl":"10.1016/j.nhccr.2017.10.012","url":null,"abstract":"<div><h3>Introduction</h3><p>Malignant ulcer at the duodenal bulb is extremely rare. The commonest cause of ulcers here is peptic ulcer disease. Therefore the routine biopsy of ulcer at D1 is not routinely recommended, to avoid complications.</p></div><div><h3>Case description</h3><p>An 83-year-old lady presented to the surgical outpatient clinic with upper abdominal pain radiating to left side of her chest. She had recent history of significant weight loss, approximately 22kg. Abdominal examination was unremarkable.</p></div><div><h3>Results and Conclusions</h3><p>Haemoglobin and Liver Function Tests were normal. Gastroscopy showed one large 3cm ulcer with a shaggy base and rolled over margin in the first part of the duodenum (D1) which appeared malignant. Initial histology confirmed adenocarcinoma of uncertain origin. CT scan showed a 2.9x3.7cm partially cystic mass lesion in the head of the pancreas that was locally invading into the first part of the duodenum, with no evidence of metastases. Immunohistochemistry showed strong Ca19.9 positive, favouring primary pancreatic origin.</p></div><div><h3>Take home message</h3><p>Pancreatic cancer presenting as an ulcer in D1 is very rare. If a suspicious looking ulcer is found endoscopically at D1, it should be biopsied. A CT scan of the abdomen is also important in the work-up of such cases.</p></div>","PeriodicalId":100954,"journal":{"name":"New Horizons in Clinical Case Reports","volume":"2 ","pages":"Pages 24-25"},"PeriodicalIF":0.0,"publicationDate":"2017-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.nhccr.2017.10.012","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87720924","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
Symptomatic steroid induce multifocal diaphyseal bone infarcts treated with intra-medullary nailing 髓内钉治疗症状性类固醇诱导的多局灶骨干骨梗死
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.010
Taimoor Sehgol *, Richard Boyle

Introduction

Non traumatic osteonecrosis is the ischaemic death of cellular elements within bone. Etiological factors implicated include long term corticiosteroid use, alcoholism, sickle cell disease, systemic lupus erythematosus, amongst others. Common sites of involvement include the proximal femur, knee, shoulder, ankle. Metaphyseal-diaphyseal lesions have been well described radiolographically, however are commonly considered asymptomatic. There is thus a paucity of literature describing techniques used for symptomatic diaphyseal or metaphyseal lesions not involving the epiphyseal region.

Case description

Our patient is a 40-year-old woman diagnosed with Arnold-Chiari malformation in 2005 who was then surgically treated with foramen magnum decompression. In 2010 she was treated with 4 months of Dexamethasone 2mg for chemical meningitis. She presented to the Orthopaedic outpatient clinic in 2012, 16 months after ceasing steroid medication, with a 6 month history of difficulty walking due to pain in bilateral groins and bilaterally along her shins, left worse than right. MRI of both hips demonstrated anterior serpiginous lesions within the femoral heads consisted with AVN (Ficat II). MRI of lower legs showed isolated bone infarct in the metaphyseal-dyaphyseal region of her tibias bilaterally. She had bilateral total hip arthroplasties with immediate relief of hip symptoms. Our patient underwent bilateral tibial intramedullary nailing using a Stryker T2 nail with a medial parapatellar approach. At both the 6 week and 5 month follow-up she had no further pain, was non tender to palpation and was very satisfied with result.

Results and Conclusions

We are unaware of any reports of the development of symptomatic diaphyseal osteonecrosis in patients receiving corticosteroids for the treatment of meningitis. Much of the literature regarding management of osteonecrosis is focused on the treatment of epiphyseal lesions in the femoral head and around the knee. Diaphyseal lesions have been well described radiologically but are often defined as asymptomatic and clinically insignificant. Our use of intramedullary nailing thus illustrates an effective surgical option for the treatment of symptomatic diaphyseal osteonecrosis.

Take home message

Osteonecrosis must be considered in all patients receiving high dose or long term steroids for any indication. Intramedullary nailing can be a successful method of treating symptomatic diaphyseal osteonecrosis of long bones.

非外伤性骨坏死是骨内细胞成分的缺血性死亡。涉及的病因因素包括长期使用皮质类固醇、酗酒、镰状细胞病、系统性红斑狼疮等。常见受累部位包括股骨近端、膝关节、肩部、踝关节。干骺端-干骺端病变已被很好地描述,但通常被认为是无症状的。因此,缺乏文献描述不累及骨骺区的症状性干骺端或干骺端病变的技术。病例描述:我们的患者是一名40岁的女性,于2005年被诊断为Arnold-Chiari畸形,随后接受了枕骨大孔减压手术治疗。2010年,她因化学性脑膜炎接受了4个月的2mg地塞米松治疗。2012年,在停止类固醇药物治疗16个月后,患者到骨科门诊就诊,有6个月的行走困难病史,原因是双侧腹股沟和双侧胫骨疼痛,左侧比右侧更严重。双髋MRI显示股骨头内的前蛇形病变与AVN一致(Ficat II)。下肢MRI显示双侧胫骨干骺端-干骺端孤立性骨梗死。她接受了双侧全髋关节置换术,髋关节症状立即得到缓解。我们的患者采用内侧髌旁入路的Stryker T2髓内钉行双侧胫骨髓内钉。在6周和5个月的随访中,她没有进一步的疼痛,触诊无痛,结果非常满意。结果和结论:我们未发现任何接受皮质类固醇治疗的脑膜炎患者出现症状性骨干性骨坏死的报告。许多关于骨坏死处理的文献都集中在股骨头和膝关节周围骨骺病变的治疗上。骨干病变已经有很好的影像学描述,但通常被定义为无症状和临床无关。因此,髓内钉是治疗症状性骨干骨坏死的一种有效的手术选择。带回家的信息:在所有接受大剂量或长期类固醇治疗的患者中,任何适应症都必须考虑骨质坏死。髓内钉是治疗长骨症状性骨干骨坏死的一种成功方法。
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引用次数: 0
Bouveret’s Syndrome: The rarest obstructing gallstone 布韦莱特综合征:最罕见的梗阻性胆结石
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.08.004
Joshua Bramson , Arthur Topilow , Ronald Matteotti

Bouveret’s Syndrome is the rarest form of gallstone ileus. It is characterized by the passage of a large gallstone through a cholecystoduodenal fistula resulting in obstruction of the proximal bowel. The rarity, and non-specific presentation of Bouveret’s Syndrome, make it a frequently overlooked diagnosis, with a significant associated mortality. We report the case of an 86 year old male presenting to the Emergency Department with nausea, vomiting, and constipation. Diagnosis of Bouveret’s Syndrome was made by CT scan of the abdomen demonstrating a large stone in the proximal duodenum. After failed attempts at endoscopic removal of the gallstone, the patient was taken for surgical enterotomy and foreign body retrieval. Bouveret’s syndrome is a rare entity with limited evidence to favor one approach to management over another. In this case, we review the diagnostic and therapeutic options for this rare form of small bowel obstruction.

布韦莱特综合征是胆石性肠梗阻中最罕见的一种。它的特征是一个大的胆结石通过胆囊十二指肠瘘管导致近端肠阻塞。布韦莱特综合征的罕见性和非特异性表现使其成为一种经常被忽视的诊断,并伴有显著的相关死亡率。我们报告的情况下,86岁的男性提出到急诊科恶心,呕吐,便秘。腹部CT扫描显示十二指肠近端有一大块结石,诊断为布韦莱特综合征。在内镜下取出胆结石失败后,患者被送往手术肠切开和异物取出。布韦莱特综合征是一种罕见的疾病,证据有限,支持一种治疗方法优于另一种。在这种情况下,我们回顾诊断和治疗的选择,这种罕见的形式的小肠梗阻。
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引用次数: 3
Giant incisional hernia containing a large renal cyst 巨大切口疝,含大肾囊肿
Pub Date : 2017-11-01 DOI: 10.1016/j.nhccr.2017.10.030
Anna Wöstemeier * , Daniel Perez , Roland Dahlem , Jakob R Izbicki , Nathaniel Melling

Introduction

Hernias are common surgical diseases. Incidence of incisional hernia depends upon the size and location of the former incision and ranges from 3 to 20 percent. In clinical practice the variability of surgical techniques for hernia repair is great and a wide range of publications are available. Surgery for renal cysts depends on whether they are classified simple or complex. Simple cysts are more common and the majority requires no treatment. Complex renal cysts are associated with an increased risk of malignancy. This is the first report on a giant incisional hernia containing bowl combined with a voluminous renal cyst.

Case description

An 80-year-old female diagnosed with a giant incisional hernia combined with a large left renal cyst was referred to our surgical department from a peripheral hospital for hernia repair. Physical examination showed a ventral incisional hernia (50x50cm) extending to the upper thigh with multiple skin lesions and clinical signs of obstipation. CT scan revealed two hernial orifices measuring 13cm and 4.5cm in diameter. The giant hernial sac contained not only incarcerated small and large bowl but also a large left renal cyst containing 3 litres of fluid.

Results and Conclusions

We performed a second median laparotomy with complete release of all abdominal adhesions. The renal cyst was resected and its base marsupialized. Hernia repair was achieved by both sided compartment separation as described by Ramirez combined with an intraperitoneal onlay mesh sized 40cmx60cm. Intraoperative measurement of creatinine in the cyst fluid revealed no connection to the urinary tract making further renal surgery unnecessary. By resecting the renal cyst, intraabdominal volume was markedly reduced allowing tension free abdominal wall reconstruction. Histological examination of the cyst, the hernial sacs and the resected skin revealed no surprising findings. Postoperative recovery was uneventful and drains were removed before discharge. Bowel movement started on the third postoperative day. Wound dehiscence was treated by negative pressure wound therapy and no recurrence has yet been detected two months postoperatively.

Take home message

Surgical repair of giant incisional hernias is challenging and is associated with significant morbidity and mortality. Individual planning of abdominal wall reconstruction is key for successful treatment and is even the more important in complex hernias with loss of domain or accompanying intraabdominal pathologies.

疝是常见的外科疾病。切口疝的发生率取决于前切口的大小和位置,范围从3%到20%。在临床实践中,疝修补手术技术的可变性很大,并且有广泛的出版物。肾囊肿的手术取决于它们是简单的还是复杂的。单纯性囊肿更为常见,大多数不需要治疗。复杂肾囊肿与恶性肿瘤的风险增加有关。这是一个巨大的切口疝包含碗合并大体积肾囊肿的第一个报告。病例描述一名80岁女性,诊断为巨大切口疝合并左肾大囊肿,从周边医院转到我们的外科进行疝气修复。体格检查显示腹侧切口疝(50x50cm),延伸至大腿上部,多发皮肤病变,临床表现为梗阻。CT扫描显示两个疝口,直径分别为13cm和4.5cm。巨大的疝囊不仅包含嵌顿的小碗和大碗,还包含一个含有3升液体的大左肾囊肿。结果和结论我们进行了第二次剖腹切开术,腹部粘连完全解除。切除肾囊肿并将其底部有袋化。疝气修复是通过Ramirez所描述的双侧腔室分离以及40cmx60cm的腹膜内嵌片网来实现的。术中测量囊肿液中的肌酐显示与尿路无关,因此无需进一步的肾脏手术。通过切除肾囊肿,腹腔内容量明显减少,从而使无张力腹壁重建成为可能。对囊肿、疝囊和切除的皮肤进行组织学检查,无意外发现。术后恢复顺利,出院前清除引流管。术后第三天开始排便。采用负压创面治疗创面裂开,术后2个月无复发。手术修复巨大切口疝是具有挑战性的,具有显著的发病率和死亡率。腹壁重建的个体化规划是成功治疗的关键,对于腹壁区域丧失或伴随腹内病变的复杂疝更为重要。
{"title":"Giant incisional hernia containing a large renal cyst","authors":"Anna Wöstemeier * ,&nbsp;Daniel Perez ,&nbsp;Roland Dahlem ,&nbsp;Jakob R Izbicki ,&nbsp;Nathaniel Melling","doi":"10.1016/j.nhccr.2017.10.030","DOIUrl":"10.1016/j.nhccr.2017.10.030","url":null,"abstract":"<div><h3>Introduction</h3><p>Hernias are common surgical diseases. Incidence of incisional hernia depends upon the size and location of the former incision and ranges from 3 to 20 percent. In clinical practice the variability of surgical techniques for hernia repair is great and a wide range of publications are available. Surgery for renal cysts depends on whether they are classified simple or complex. Simple cysts are more common and the majority requires no treatment. Complex renal cysts are associated with an increased risk of malignancy. This is the first report on a giant incisional hernia containing bowl combined with a voluminous renal cyst.</p></div><div><h3>Case description</h3><p>An 80-year-old female diagnosed with a giant incisional hernia combined with a large left renal cyst was referred to our surgical department from a peripheral hospital for hernia repair. Physical examination showed a ventral incisional hernia (50x50cm) extending to the upper thigh with multiple skin lesions and clinical signs of obstipation. CT scan revealed two hernial orifices measuring 13cm and 4.5cm in diameter. The giant hernial sac contained not only incarcerated small and large bowl but also a large left renal cyst containing 3 litres of fluid.</p></div><div><h3>Results and Conclusions</h3><p>We performed a second median laparotomy with complete release of all abdominal adhesions. The renal cyst was resected and its base marsupialized. Hernia repair was achieved by both sided compartment separation as described by Ramirez combined with an intraperitoneal onlay mesh sized 40cmx60cm. Intraoperative measurement of creatinine in the cyst fluid revealed no connection to the urinary tract making further renal surgery unnecessary. By resecting the renal cyst, intraabdominal volume was markedly reduced allowing tension free abdominal wall reconstruction. Histological examination of the cyst, the hernial sacs and the resected skin revealed no surprising findings. Postoperative recovery was uneventful and drains were removed before discharge. Bowel movement started on the third postoperative day. Wound dehiscence was treated by negative pressure wound therapy and no recurrence has yet been detected two months postoperatively.</p></div><div><h3>Take home message</h3><p>Surgical repair of giant incisional hernias is challenging and is associated with significant morbidity and mortality. Individual planning of abdominal wall reconstruction is key for successful treatment and is even the more important in complex hernias with loss of domain or accompanying intraabdominal pathologies.</p></div>","PeriodicalId":100954,"journal":{"name":"New Horizons in Clinical Case Reports","volume":"2 ","pages":"Page 32"},"PeriodicalIF":0.0,"publicationDate":"2017-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.nhccr.2017.10.030","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90455105","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}
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New Horizons in Clinical Case Reports
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