首页 > 最新文献

Clinical case reports and reviews最新文献

英文 中文
Recurrent infective endocarditis in a drug addict 吸毒成瘾者复发性感染性心内膜炎
Pub Date : 2018-01-01 DOI: 10.15761/CCRR.1000409
G. Menafra, A. Pingitore, A. Gurgo, D. Magrí, E. Pagannone, M. Testa, M. Volpe
{"title":"Recurrent infective endocarditis in a drug addict","authors":"G. Menafra, A. Pingitore, A. Gurgo, D. Magrí, E. Pagannone, M. Testa, M. Volpe","doi":"10.15761/CCRR.1000409","DOIUrl":"https://doi.org/10.15761/CCRR.1000409","url":null,"abstract":"","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447038","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: 1
Case ReportA case of asynchronous bilateral cancer of the oral commissure 病例报告1例非同步双侧口腔连合癌
Pub Date : 2018-01-01 DOI: 10.15761/ccrr.1000416
T. Imaizumi, M. Ooishi, H. Irie, T. Inoue, Y. Narisawa, Y. Yamaguchi
In Western nations, lip cancer accounts for 15%–30% of all oral cancers; however, lip cancer is far less common in Japan, accounting for only 0.9%–3.6% of oral cancers (references ) [1-3]. Lip cancer usually occurs in the lower lip, and is rarely seen in the oral commissure [35]. Histologically, most cases are squamous cell carcinoma [6]. To our knowledge, only one case of bilateral squamous cell carcinoma of the oral commissure has previously been reported [7].
在西方国家,口腔癌占所有口腔癌的15%-30%;而在日本,唇部癌的发病率相对较低,仅占口腔癌的0.9%-3.6%(文献)[1-3]。唇癌通常发生在下唇,很少见于口腔连合区。组织学上多数为鳞状细胞癌[6]。据我们所知,只有一例双侧口腔连合鳞状细胞癌曾被报道过。
{"title":"Case ReportA case of asynchronous bilateral cancer of the oral commissure","authors":"T. Imaizumi, M. Ooishi, H. Irie, T. Inoue, Y. Narisawa, Y. Yamaguchi","doi":"10.15761/ccrr.1000416","DOIUrl":"https://doi.org/10.15761/ccrr.1000416","url":null,"abstract":"In Western nations, lip cancer accounts for 15%–30% of all oral cancers; however, lip cancer is far less common in Japan, accounting for only 0.9%–3.6% of oral cancers (references ) [1-3]. Lip cancer usually occurs in the lower lip, and is rarely seen in the oral commissure [35]. Histologically, most cases are squamous cell carcinoma [6]. To our knowledge, only one case of bilateral squamous cell carcinoma of the oral commissure has previously been reported [7].","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447527","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
Rectus sheath hematoma presenting as an abdominal mass 腹直肌鞘血肿表现为腹部肿块
Pub Date : 2018-01-01 DOI: 10.15761/CCRR.1000420
K. Sivananthan, Karthigesu Aimanan, S. Kanthasamy, A. Azman, Ramesh R. Thangaratnam, Chew Loon Guan
Rectus sheath hematoma is a rare clinical condition and often misdiagnosed cause of abdominal mass. It is a well-documented complication of abdominal trauma, surgery and excessive strain on abdominal musculature. This is a case report of rectus sheath hematoma in which the clinical features and ultrasound findings favored intraperitoneal mass. However, CT scan well delineates the mass and pointed towards the diagnosis of rectus sheath hematoma.
摘要直肌鞘血肿是一种罕见的临床疾病,常被误诊为腹部肿块的原因。这是一种有充分证据的腹部创伤、手术和腹部肌肉过度紧张的并发症。这是一例报告的直肌鞘血肿,其临床特征和超声结果倾向于腹膜内肿块。然而,CT扫描很好地描绘了肿块,并指出了直肌鞘血肿的诊断。
{"title":"Rectus sheath hematoma presenting as an abdominal mass","authors":"K. Sivananthan, Karthigesu Aimanan, S. Kanthasamy, A. Azman, Ramesh R. Thangaratnam, Chew Loon Guan","doi":"10.15761/CCRR.1000420","DOIUrl":"https://doi.org/10.15761/CCRR.1000420","url":null,"abstract":"Rectus sheath hematoma is a rare clinical condition and often misdiagnosed cause of abdominal mass. It is a well-documented complication of abdominal trauma, surgery and excessive strain on abdominal musculature. This is a case report of rectus sheath hematoma in which the clinical features and ultrasound findings favored intraperitoneal mass. However, CT scan well delineates the mass and pointed towards the diagnosis of rectus sheath hematoma.","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447583","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
The use of the superior gluteal artery perforator flap to cover sacral defects 应用臀上动脉穿支皮瓣修复骶骨缺损
Pub Date : 2018-01-01 DOI: 10.15761/ccrr.1000406
M. Fazlurrahman, A. Haider, Muhammad Asif Ahsan
{"title":"The use of the superior gluteal artery perforator flap to cover sacral defects","authors":"M. Fazlurrahman, A. Haider, Muhammad Asif Ahsan","doi":"10.15761/ccrr.1000406","DOIUrl":"https://doi.org/10.15761/ccrr.1000406","url":null,"abstract":"","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67446869","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: 1
Leishmaniasis of the ear treated successfully by photodynamic therapy 光动力疗法成功治疗耳利什曼病
Pub Date : 2018-01-01 DOI: 10.15761/ccrr.1000410
H. Bay, S. Elloudi, S. Benkirane, Z. Douhi, S. Gallouj, F. Mernissi
Cutaneous Leishmaniasis (CL) are zoonoses caused by parasites of the genus Leishmania, transmission occurs by bite of a gnat called sandfly. It is a worldwide health problem. In fact, The World Health Organization (WHO) considers leishmaniasis to be one of the most serious parasitic diseases including Morocco because of the global warming [1,2]. In Morocco, major leshmaniasis, tropica and infantum are prevalent and are very common [2]. Among the problems reported in the treatment of cutaneous leishmaniosis are difficulty in determining clinical diagnosis due to lack of access tomicroscopy onmany basic health services [3]; the serious side effects of pentavalent antimonial drugs and the variability of the efficacy against the different forms of Leishmania [3], making drugs and medical attention an expensive treatment because of the side effects [3]; besides, there have also been reports of patients not responding to drugs due to drug resistance or increased immunosuppression [3]. Photodynamic Therapy (PDT) is non-invasive therapy and can be repeated when necessary without damage to the patient’s health and without causing resistance in the parasite [4-7]. We report a case illustrate this difficulty to diagnosis and treat leshmaniasis in the immunocompromised who was treated successfully by (PDT).
皮肤利什曼病是由利什曼属寄生虫引起的人畜共患疾病,通过白蛉叮咬传播。这是一个世界性的健康问题。事实上,由于全球变暖,世界卫生组织(WHO)认为利什曼病是包括摩洛哥在内的最严重的寄生虫病之一[1,2]。在摩洛哥,主要的利什曼病、热带病和婴儿病很流行,而且很常见。皮肤利什曼病治疗中报告的问题包括:由于许多基本卫生服务机构缺乏显微镜检查,难以确定临床诊断[b];五价锑药物的严重副作用以及对不同形式利什曼原虫[3]的疗效差异,由于副作用[3],使药物和医疗护理成为昂贵的治疗;此外,也有患者因耐药或免疫抑制bbb增加而对药物无反应的报道。光动力疗法(PDT)是一种非侵入性疗法,可以在必要时重复进行,不会损害患者的健康,也不会引起寄生虫的耐药性[4-7]。我们报告了一个病例,说明这种困难的诊断和治疗利什曼病在免疫功能低下谁是成功的治疗(PDT)。
{"title":"Leishmaniasis of the ear treated successfully by photodynamic therapy","authors":"H. Bay, S. Elloudi, S. Benkirane, Z. Douhi, S. Gallouj, F. Mernissi","doi":"10.15761/ccrr.1000410","DOIUrl":"https://doi.org/10.15761/ccrr.1000410","url":null,"abstract":"Cutaneous Leishmaniasis (CL) are zoonoses caused by parasites of the genus Leishmania, transmission occurs by bite of a gnat called sandfly. It is a worldwide health problem. In fact, The World Health Organization (WHO) considers leishmaniasis to be one of the most serious parasitic diseases including Morocco because of the global warming [1,2]. In Morocco, major leshmaniasis, tropica and infantum are prevalent and are very common [2]. Among the problems reported in the treatment of cutaneous leishmaniosis are difficulty in determining clinical diagnosis due to lack of access tomicroscopy onmany basic health services [3]; the serious side effects of pentavalent antimonial drugs and the variability of the efficacy against the different forms of Leishmania [3], making drugs and medical attention an expensive treatment because of the side effects [3]; besides, there have also been reports of patients not responding to drugs due to drug resistance or increased immunosuppression [3]. Photodynamic Therapy (PDT) is non-invasive therapy and can be repeated when necessary without damage to the patient’s health and without causing resistance in the parasite [4-7]. We report a case illustrate this difficulty to diagnosis and treat leshmaniasis in the immunocompromised who was treated successfully by (PDT).","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447212","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
A 59-year-old Female Post Bariatric Surgery with Severe Vitamin D Deficiency and Severe Hypocalcemia Induced by Denosumab Injection for Osteoporosis 1例59岁女性减肥手术后,Denosumab注射治疗骨质疏松导致严重维生素D缺乏和严重低钙血症
Pub Date : 2018-01-01 DOI: 10.15761/ccrr.1000419
J. Beal, Soemiwati W Holland, Krishna Chalasani, M. A. Hossain
Denosumab is a human monoclonal antibody that binds receptor activator of nuclear factor kappa-B ligand (RANKL) and inhibits interaction between RANKL and RANK on the surface of osteoclasts, which prevents osteoclast formation and causes decreased bone resorption and increased bone mass [1]. Osteoporosis is characterized by low bone mass, microarchitectural disruption, and increased skeletal fragility. It is common in those who have undergone Rouxen-Y gastric bypass surgery, which causes reduced gastric acid levels necessary for adequate calcium absorption and decreased vitamin D due to relative bypass of its primary absorption points in the duodenum and proximal jejunum [2,3]. Denosumab is a reasonable option for osteoporosis treatment in patients with gastric bypass surgery due to intestinal malabsorption and risk of anastomotic ulceration with oral bisphosphonates [4]. A rare yet potentially fatal adverse effect of denosumab is severe hypocalcemia and Vitamin D deficiency, which is often prolonged secondary to its long half-life and therefore difficult to treat in many cases [5]. We present a case of denosumab-induced severe hypocalcemia in a patient with history of gastric bypass who also was found to have acute severe hypovitaminosis D despite post-treatment vitamin D supplementation. Thus we hypothesize a potentially causal relationship between denosumab and acute severe vitamin D deficiency in high-risk patients, specifically with intestinal malabsorption and resultant predisposition to becoming vitamin D deficient.
Denosumab是一种人单克隆抗体,结合核因子κ b配体受体激活因子(RANKL),抑制RANKL与RANK在破骨细胞表面的相互作用,阻止破骨细胞形成,导致骨吸收减少,骨量增加[1]。骨质疏松症的特点是骨量低、微结构破坏和骨骼脆弱性增加。在Rouxen-Y胃旁路手术的患者中很常见,由于其主要吸收点在十二指肠和近空肠的相对旁路,导致足够钙吸收所需的胃酸水平降低,维生素D减少[2,3]。Denosumab是胃旁路手术患者治疗骨质疏松症的合理选择,因为口服双膦酸盐[4]存在肠道吸收不良和吻合口溃疡风险。denosumab的一种罕见但可能致命的不良反应是严重的低钙血症和维生素D缺乏症,由于其半衰期长,通常会延长,因此在许多情况下难以治疗。我们提出了一个病例地单抗诱导严重低钙血症患者的胃旁路史,也被发现有急性严重维生素缺乏症D,尽管治疗后补充维生素D。因此,我们假设denosumab与高风险患者急性严重维生素D缺乏症之间存在潜在的因果关系,特别是肠道吸收不良和由此导致的维生素D缺乏症。
{"title":"A 59-year-old Female Post Bariatric Surgery with Severe Vitamin D Deficiency and Severe Hypocalcemia Induced by Denosumab Injection for Osteoporosis","authors":"J. Beal, Soemiwati W Holland, Krishna Chalasani, M. A. Hossain","doi":"10.15761/ccrr.1000419","DOIUrl":"https://doi.org/10.15761/ccrr.1000419","url":null,"abstract":"Denosumab is a human monoclonal antibody that binds receptor activator of nuclear factor kappa-B ligand (RANKL) and inhibits interaction between RANKL and RANK on the surface of osteoclasts, which prevents osteoclast formation and causes decreased bone resorption and increased bone mass [1]. Osteoporosis is characterized by low bone mass, microarchitectural disruption, and increased skeletal fragility. It is common in those who have undergone Rouxen-Y gastric bypass surgery, which causes reduced gastric acid levels necessary for adequate calcium absorption and decreased vitamin D due to relative bypass of its primary absorption points in the duodenum and proximal jejunum [2,3]. Denosumab is a reasonable option for osteoporosis treatment in patients with gastric bypass surgery due to intestinal malabsorption and risk of anastomotic ulceration with oral bisphosphonates [4]. A rare yet potentially fatal adverse effect of denosumab is severe hypocalcemia and Vitamin D deficiency, which is often prolonged secondary to its long half-life and therefore difficult to treat in many cases [5]. We present a case of denosumab-induced severe hypocalcemia in a patient with history of gastric bypass who also was found to have acute severe hypovitaminosis D despite post-treatment vitamin D supplementation. Thus we hypothesize a potentially causal relationship between denosumab and acute severe vitamin D deficiency in high-risk patients, specifically with intestinal malabsorption and resultant predisposition to becoming vitamin D deficient.","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447574","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
The peroneocalcaneus internus tendon: case report of a rare cause of posterior ankle impingement treated by arthroscopy 腓骨跟肌内肌腱:用关节镜治疗一例罕见的后踝关节撞击
Pub Date : 2018-01-01 DOI: 10.15761/CCRR.1000400
Liselore Maeckelbergh, G. Matricali, Sander Wuite
A 20-year-old man, a semiprofessional hurdler, presented on the outpatient clinic with a six months history of pain posterior in the left ankle during sport activities. On physical examination there was pain palpating the posterior ankle joint and around the flexor hallucis longus (FHL) region posteromedial in the ankle during active flexion of the hallux. There was deep pain on the posterior process of the talus with a positive forced plantarflexion posterior impingement test. Magnetic resonance imaging (MRI) showed signs of posterior impingement with limited fluid distension of FHL sheath and a prominent posterior process. SPECT CT showed an increased uptake in the posterior process of the talus. Because of his complaints and high demanding level of sport activities an arthroscopic partial resection of the posterior process was suggested with a release of the FHL. The posterior arthroscopy was performed with the two posterior portals technique described by van Dijk [1]. The presumed FHL was located and the prominence of posterior process of the talus revealed. After resection of the prominence we noticed that the presumed FHL was not moving by flexion and extension of the hallux, but moved just with the mobilisation of the calcaneus. After careful inspection of the tendon, a second tendon anterior to the forementioned tendon was revealed. This tendon prooved to be the FHL, when the hallux was flexed and extended. The anatomically more posterior tendon appeared to be an accessory tendon (Figures 1 and 2). With mobilization of the hallux, there was no movement of this tendon, it only moved when the calcaneum was mobilised. We presumed that it was the peroneocalcaneus internus (PCI) tendon. An accessory posteromedial portal was made to perform a resection with the punch, scissor and shaver, because of the interference with the FHL in his tunnel (Figure 3). After this procedure the FHL could run freely in the tunnel without a sign of impingement. Postoperatively the pain was resolved. The Foot Abstract
一名20岁男子,半职业跨栏运动员,因运动时左脚踝后部疼痛6个月就诊于门诊。体格检查发现,在拇关节主动屈曲时,可触诊踝关节后侧和拇长屈肌(FHL)区周围。距骨后突有深度疼痛,强制跖屈后撞击试验阳性。磁共振成像(MRI)显示后撞击的迹象,FHL鞘有限的液体膨胀和突出的后突。SPECT CT显示距骨后突摄取增高。由于他的抱怨和高要求的运动活动,建议在关节镜下部分切除后突并释放FHL。采用van Dijk[1]描述的两个后门静脉技术进行后关节镜检查。假定的FHL被定位,并显示距骨后突的突出。切除突出后,我们注意到假定的FHL不是通过拇趾的屈伸来移动的,而是通过跟骨的活动来移动的。仔细检查肌腱后,发现前面提到的肌腱前面的第二肌腱。当拇趾屈曲和伸展时,该肌腱被证明是FHL。解剖上更后方的肌腱似乎是副肌腱(图1和2)。当拇趾活动时,该肌腱没有运动,只有当跟骨活动时才运动。我们推测是腓骨跟内肌(PCI)肌腱。由于FHL在隧道中受到干扰,我们使用冲床、剪刀和剃须刀切除了副后内侧门静脉(图3)。手术后,FHL可以在隧道中自由运动,没有碰撞迹象。术后疼痛消失。脚文摘
{"title":"The peroneocalcaneus internus tendon: case report of a rare cause of posterior ankle impingement treated by arthroscopy","authors":"Liselore Maeckelbergh, G. Matricali, Sander Wuite","doi":"10.15761/CCRR.1000400","DOIUrl":"https://doi.org/10.15761/CCRR.1000400","url":null,"abstract":"A 20-year-old man, a semiprofessional hurdler, presented on the outpatient clinic with a six months history of pain posterior in the left ankle during sport activities. On physical examination there was pain palpating the posterior ankle joint and around the flexor hallucis longus (FHL) region posteromedial in the ankle during active flexion of the hallux. There was deep pain on the posterior process of the talus with a positive forced plantarflexion posterior impingement test. Magnetic resonance imaging (MRI) showed signs of posterior impingement with limited fluid distension of FHL sheath and a prominent posterior process. SPECT CT showed an increased uptake in the posterior process of the talus. Because of his complaints and high demanding level of sport activities an arthroscopic partial resection of the posterior process was suggested with a release of the FHL. The posterior arthroscopy was performed with the two posterior portals technique described by van Dijk [1]. The presumed FHL was located and the prominence of posterior process of the talus revealed. After resection of the prominence we noticed that the presumed FHL was not moving by flexion and extension of the hallux, but moved just with the mobilisation of the calcaneus. After careful inspection of the tendon, a second tendon anterior to the forementioned tendon was revealed. This tendon prooved to be the FHL, when the hallux was flexed and extended. The anatomically more posterior tendon appeared to be an accessory tendon (Figures 1 and 2). With mobilization of the hallux, there was no movement of this tendon, it only moved when the calcaneum was mobilised. We presumed that it was the peroneocalcaneus internus (PCI) tendon. An accessory posteromedial portal was made to perform a resection with the punch, scissor and shaver, because of the interference with the FHL in his tunnel (Figure 3). After this procedure the FHL could run freely in the tunnel without a sign of impingement. Postoperatively the pain was resolved. The Foot Abstract","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67446568","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: 1
Surgical management of gastrointestinal perforation by ingested chicken bone: A case report 鸡骨误食致胃肠道穿孔的外科治疗1例
Pub Date : 2018-01-01 DOI: 10.15761/CCRR.1000407
H. Dong, Xuhui Chen, Yan-Fang Jiang, YHao Chen, Mingyi Wu, Hai-jun Li
Gastrointestinal perforation is a common surgical emergency, but accidental and unnoticed foreign body ingestion is not very uncommon. Most of ingested foreign bodies pass uneventfully through the gastrointestinal tract. Perforation of the gastrointestinal occurs in less than 1% of ingestion of a foreign body [1]. Case of the gastrointestinal perforation caused by eating is rare. It is very difficult for diagnosis sometimes. Here we report a rare case of gastrointestinal perforation caused by eating.
胃肠道穿孔是一种常见的外科急诊,但意外和未被注意的异物摄入并不罕见。大多数被摄入的异物都顺利地通过胃肠道。在摄入异物的情况下,不到1%的人会出现胃肠道穿孔。进食引起胃肠道穿孔的病例很少。有时很难诊断。我们在此报告一例因进食引起的肠胃穿孔。
{"title":"Surgical management of gastrointestinal perforation by ingested chicken bone: A case report","authors":"H. Dong, Xuhui Chen, Yan-Fang Jiang, YHao Chen, Mingyi Wu, Hai-jun Li","doi":"10.15761/CCRR.1000407","DOIUrl":"https://doi.org/10.15761/CCRR.1000407","url":null,"abstract":"Gastrointestinal perforation is a common surgical emergency, but accidental and unnoticed foreign body ingestion is not very uncommon. Most of ingested foreign bodies pass uneventfully through the gastrointestinal tract. Perforation of the gastrointestinal occurs in less than 1% of ingestion of a foreign body [1]. Case of the gastrointestinal perforation caused by eating is rare. It is very difficult for diagnosis sometimes. Here we report a rare case of gastrointestinal perforation caused by eating.","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67447112","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
Wide complex tachycardia in ischemic heart disease patient: What is the rhythm? 缺血性心脏病患者宽复合心动过速:心律是什么?
Pub Date : 2018-01-01 DOI: 10.15761/ccrr.1000388
G. A. Mohani
Received: January 02, 2018; Accepted: February 15, 2018; Published: February 19, 2018 An 84 year-old man presented to Emergency department complaining of cough and fever. He was known to be ischemic heart disease with coronary angiogram done in 2011 showed total occlusion of LAD and 50% Circumflex artery. Recent Echocardiography showed LV EF 35%. No chest pain. He is known to suffer from Parkinsonism non complaint to medications due to hallucination as side effect.
收稿日期:2018年1月02日;录用日期:2018年2月15日;一名84岁男性因咳嗽和发烧到急诊室就诊。已知为缺血性心脏病,2011年冠状动脉造影显示LAD完全闭塞,50%旋动脉闭塞。近期超声心动图显示左室EF 35%。没有胸痛。据悉,他患有帕金森氏症,对药物治疗无怨言,因为副作用是产生幻觉。
{"title":"Wide complex tachycardia in ischemic heart disease patient: What is the rhythm?","authors":"G. A. Mohani","doi":"10.15761/ccrr.1000388","DOIUrl":"https://doi.org/10.15761/ccrr.1000388","url":null,"abstract":"Received: January 02, 2018; Accepted: February 15, 2018; Published: February 19, 2018 An 84 year-old man presented to Emergency department complaining of cough and fever. He was known to be ischemic heart disease with coronary angiogram done in 2011 showed total occlusion of LAD and 50% Circumflex artery. Recent Echocardiography showed LV EF 35%. No chest pain. He is known to suffer from Parkinsonism non complaint to medications due to hallucination as side effect.","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67445078","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
A rare cause of infertility: Uterine isthmocele 一种罕见的不孕原因:子宫峡部膨出
Pub Date : 2018-01-01 DOI: 10.15761/CCRR.1000389
M. Koplay, N. Seher, E. Uysal, H. Cebeci
A 35-year-old female patient with a history of cesarean section 2 times applied to our hospital with the complaints of post-menstrual bleeding for the last 1 year and infertility. In pelvic MRI, in cesarean section scar localization in the anterior uterine corpus, 15x10 mm in size, well-circumscribed hypointense cystic lesions were observed on T1-weighted images, and hyperintense cystic lesions were observed on T2-weighted images (Figure 1). A thinning was observed in the uterine parenchyma in the anterior neighborhood of this area. In patients who have the story of cesarean section in uterine cystic lesions, the uterine isthmocele should be considered in definitive diagnosis. A 35-year-old female patient with a history of cesarean section 2 times applied to our hospital with the complaints of post-menstrual bleeding for the last 1 year. In the transvaginal ultrasonography (TVUSG), anechoic cystic formation was observed in the anterior of the uterine corpus, and pelvic MRI examination was performed on the patient. At MRI, in cesarean section scar localization in the anterior uterine corpus, 15x10 mm in size, well-circumscribed hypointense cystic lesions were observed on T1-weighted images, and well-circumscribed
患者女,35岁,剖宫产2次,主诉1年经后出血,不孕症来我院就诊。盆腔MRI剖宫产术中瘢痕定位于子宫前体,大小为15x10mm, t1加权像上可见边界清晰的低信号囊性病变,t2加权像上可见高信号囊性病变(图1)。该区域前邻区子宫实质变薄。有剖宫产史的子宫囊性病变患者,应考虑子宫峡部膨出作为明确诊断。患者女,35岁,有剖宫产史2次,主诉经后出血1年来我院就诊。经阴道超声(TVUSG)示子宫体前部无回声囊性形成,行盆腔MRI检查。MRI剖宫产术中瘢痕定位于子宫前体,大小15x10mm, t1加权像上可见边界清晰的低信号囊性病变,且边界清晰
{"title":"A rare cause of infertility: Uterine isthmocele","authors":"M. Koplay, N. Seher, E. Uysal, H. Cebeci","doi":"10.15761/CCRR.1000389","DOIUrl":"https://doi.org/10.15761/CCRR.1000389","url":null,"abstract":"A 35-year-old female patient with a history of cesarean section 2 times applied to our hospital with the complaints of post-menstrual bleeding for the last 1 year and infertility. In pelvic MRI, in cesarean section scar localization in the anterior uterine corpus, 15x10 mm in size, well-circumscribed hypointense cystic lesions were observed on T1-weighted images, and hyperintense cystic lesions were observed on T2-weighted images (Figure 1). A thinning was observed in the uterine parenchyma in the anterior neighborhood of this area. In patients who have the story of cesarean section in uterine cystic lesions, the uterine isthmocele should be considered in definitive diagnosis. A 35-year-old female patient with a history of cesarean section 2 times applied to our hospital with the complaints of post-menstrual bleeding for the last 1 year. In the transvaginal ultrasonography (TVUSG), anechoic cystic formation was observed in the anterior of the uterine corpus, and pelvic MRI examination was performed on the patient. At MRI, in cesarean section scar localization in the anterior uterine corpus, 15x10 mm in size, well-circumscribed hypointense cystic lesions were observed on T1-weighted images, and well-circumscribed","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"142 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67445152","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
期刊
Clinical case reports and reviews
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1