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International Journal of Case Reports in Surgery最新文献

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Giant mature ovarian teratoma case report 巨大成熟卵巢畸胎瘤1例
Pub Date : 2023-01-01 DOI: 10.22271/27081494.2023.v5.i1a.75
Dema Adwan, Solaiman Al-marrawi, Aya Takla, Ameena Odeh, Wasim Alnjjad, Ayat Ebrahim
Germ cell tumors are malignant (cancerous) or nonmalignant (benign, noncancerous) tumors that are comprised mostly of germ cells, the cells that develop in the embryo and become the cells that make up the reproductive system in male and female. Most ovarian tumors are of germ cell origin. A 18-year-old virginal Syrian female was taken to the emergency Department at Damascus university of obstetrics and gynecology on 31.1.2023 with gradual distension of abdomen which had been noticed by parents for the last 6 months. As bedside ultrasonography (USG) showed mixed echogenic mass in the lower abdomen, CT scan of abdomen was requested for further delineation. CT scan of abdomen done on 1.2.2023 showed a giant (about 13×23×26 cm) mixed density mass with homogenously enhancing well defined borders in the abdomen extending from the pelvic cavity to the epigastric region and crossing the medial line causing significant pressure effect downwards towards urinary bladder and contrast material filled guts outwards and backwards mostly occupying the anterior part of abdominal cavity. The tumor was removed surgically and diagnosed as ovarian teratoma histopathologically.
生殖细胞瘤是恶性(癌)或非恶性(良性,非癌)肿瘤,主要由生殖细胞组成,生殖细胞在胚胎中发育,并成为构成男性和女性生殖系统的细胞。大多数卵巢肿瘤起源于生殖细胞。一名18岁的叙利亚处女于2023年1月31日被送往大马士革妇产科大学急诊科,其腹部渐进式膨胀已被父母发现6个月。床边超声显示下腹部混合回声肿物,要求腹部CT进一步描绘。2023年2月1日腹部CT示:腹部一巨大(约13×23×26 cm)混合密度肿块,边界均匀增强,从盆腔延伸至上腹部,并穿过中线,向下压迫膀胱,向外和向后填充肠子造影剂,主要占据腹腔前部。经手术切除,病理诊断为卵巢畸胎瘤。
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引用次数: 0
Colorectal intussusception caused by a pedunculated lipoma: A rare case report 结直肠肠套叠致带蒂脂肪瘤1例
Pub Date : 2023-01-01 DOI: 10.22271/27081494.2023.v5.i1a.70
Aymane Jbilou, Younes Aggouri, A. Ahallat, S. Aitlaalim
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引用次数: 0
Challenges in diagnosis and management of a giant non-functioning adrenocortical carcinoma: A case report 巨大的无功能肾上腺皮质癌的诊断和治疗的挑战:1例报告
Pub Date : 2023-01-01 DOI: 10.22271/27081494.2023.v5.i1a.77
Dr. Subashini R, D. Ms, D. Ms
Adrenocortical carcinoma (ACC) despite being a rare endocrine malignancy arising from adrenal cortex carries a poor prognosis. It is also challenging to diagnose these tumours preoperatively especially if it is a non-functioning tumour. As the rarity of the disease pose a great challenge in taking up statistically significant studies that would be needed to improve the management strategies and outcomes of ACC, all the recommendations are based on retrospective case series or expert opinions. Hence Multidisciplinary approach is warranted to improve the outcomes in the management of ACC. Despite the enormous progress achieved in the biological knowledge of this tumor, the ACC remains an oncological disease burdened by a high mortality. Surgery is still the first therapeutic option and the only potentially curative treatment.
肾上腺皮质癌(ACC)是一种罕见的内分泌恶性肿瘤,起源于肾上腺皮质,预后较差。术前诊断这些肿瘤也具有挑战性,特别是如果它是一个无功能的肿瘤。由于该病的罕见性对开展具有统计学意义的研究提出了巨大挑战,这些研究将需要改善ACC的管理策略和结果,因此所有建议都是基于回顾性病例系列或专家意见。因此,多学科的方法是必要的,以改善预后的管理ACC。尽管在这种肿瘤的生物学知识方面取得了巨大进展,但ACC仍然是一种高死亡率的肿瘤疾病。手术仍然是第一种治疗选择,也是唯一可能治愈的治疗方法。
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引用次数: 0
Mandibular brown tumor revealing an ectopic parathyroid adenoma 下颌骨棕色肿瘤显示异位甲状旁腺瘤
Pub Date : 2023-01-01 DOI: 10.22271/27081494.2023.v5.i1a.69
Dr. Lefqih Imane, Dr. Hachem Taleb Elemine, Dr. Labiba Sbiki, Pr. Mohamed Bouchikh, Pr. Abdellah Achir
{"title":"Mandibular brown tumor revealing an ectopic parathyroid adenoma","authors":"Dr. Lefqih Imane, Dr. Hachem Taleb Elemine, Dr. Labiba Sbiki, Pr. Mohamed Bouchikh, Pr. Abdellah Achir","doi":"10.22271/27081494.2023.v5.i1a.69","DOIUrl":"https://doi.org/10.22271/27081494.2023.v5.i1a.69","url":null,"abstract":"","PeriodicalId":169045,"journal":{"name":"International Journal of Case Reports in Surgery","volume":"9 44 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124682189","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
Verrucous hemangioma: A potential differential diagnosis for malignant melanoma: A case report and review 疣状血管瘤:恶性黑色素瘤的潜在鉴别诊断:一个病例报告和回顾
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2c.66
Dr. Roshan Nayak
{"title":"Verrucous hemangioma: A potential differential diagnosis for malignant melanoma: A case report and review","authors":"Dr. Roshan Nayak","doi":"10.22271/27081494.2022.v4.i2c.66","DOIUrl":"https://doi.org/10.22271/27081494.2022.v4.i2c.66","url":null,"abstract":"","PeriodicalId":169045,"journal":{"name":"International Journal of Case Reports in Surgery","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124892465","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
Retiform hemangioendothelioma: A rare case of slow growing vascular tumor with review of literature 网状血管内皮瘤:一例罕见的生长缓慢的血管肿瘤并复习文献
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2a.45
D. Shah, D. S. Chaudhary, H. Contractor, Milauni Dave
Retiform hemangioendotheliomas are extremely rare tumors of vascular origin. Overall incidence of hemangioendothelioma being <1/1000000. They are low grade angiosarcomas with little risk of metastasis. It usually occurs as a single skin or subcutaneous lesion on the trunk or extremities commonly seen in middle aged adults [1] . Due to its rarity no well-defined guidelines are there for its management, follow up and dealing with local recurrence [2] . Therefore we would like to discuss the case of Retiform Hemangioendothelioma over scapular region in an adult lady which presented with its classical features and how it was managed.
网状血管内皮瘤是一种极为罕见的血管源性肿瘤。血管内皮瘤总体发病率<百万分之一。它们是低级别血管肉瘤,几乎没有转移的风险。它通常发生在躯干或四肢的单个皮肤或皮下病变,常见于中年人。由于其罕见,没有明确的指导方针来管理,随访和处理局部复发[2]。因此,我们想讨论的情况下,网状血管内皮瘤的肩胛骨区域在一个成年女性,提出了其典型特征和如何处理。
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引用次数: 0
Rare case of colonic angiodysplasia with massive bleeding 结肠血管发育不良伴大出血1例
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2c.81
Dr. Aniket Zarkar, Dr. Sushil Deshmukh
Colonic diverticular bleeding is the most common cause of overt, acute lower gastrointestinal bleeding in adults. Patients with diverticular bleeding usually experience large volume hematochezia and require hospitalization for management. Colonoscopy is the test of choice for most patients, although patients with massive bleeding may require computed tomography (CT) angiography followed by angiography. Surgical intervention for diverticular bleeding is reserved for patients who have failed all other modalities. Colonic diverticular bleeding is the most common cause of hematochezia (maroon or bright red blood) in hospitalized patients, although the proportion of cases attributed to diverticular bleeding varies across series. For example, 13 percent of cases were attributed to diverticular bleeding in a multicenter study in the United Kingdom versus 63 percent in a multicenter study in Japan. We present the case of 60 yrs old male patient who presented with the complaint of pain in abdomen and blood clots per rectum (Approx. 500 - 600 ml)
结肠憩室出血是成人明显急性下消化道出血最常见的原因。憩室出血患者通常有大量便血,需要住院治疗。结肠镜检查是大多数患者的首选检查,尽管大量出血的患者可能需要计算机断层扫描(CT)血管造影,然后再进行血管造影。憩室出血的手术干预是为所有其他方式失败的患者保留的。结肠憩室出血是住院患者中最常见的便血(栗色或鲜红色血液)的原因,尽管憩室出血的病例比例在不同系列中有所不同。例如,在英国的一项多中心研究中,13%的病例归因于憩室出血,而在日本的一项多中心研究中,这一比例为63%。我们报告一例60岁男性患者,主诉腹部疼痛,直肠有血块(约500 - 600毫升)。
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引用次数: 0
Reoperation for chest wall deformity after repair of cardiac rupture caused by Nuss procedure: Wung procedure Nuss手术致心脏破裂修补术后胸壁畸形再手术
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2b.57
Dr. Wenlin Wang, Dr. Weiguang Long, Dr. Yang Liu, Dr. Bin Cai, Dr. Juan Luo
{"title":"Reoperation for chest wall deformity after repair of cardiac rupture caused by Nuss procedure: Wung procedure","authors":"Dr. Wenlin Wang, Dr. Weiguang Long, Dr. Yang Liu, Dr. Bin Cai, Dr. Juan Luo","doi":"10.22271/27081494.2022.v4.i2b.57","DOIUrl":"https://doi.org/10.22271/27081494.2022.v4.i2b.57","url":null,"abstract":"","PeriodicalId":169045,"journal":{"name":"International Journal of Case Reports in Surgery","volume":"229 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122218636","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 retrospective study of traumatic brain injury within emergency department at government medical college, Jammu 查谟政府医学院急诊科外伤性脑损伤回顾性研究
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2c.67
Shahnawaz Ahmed Chowdhary, Aaqib Pervaiz Butt, Mohd Akber Lone, Kulbir Singh Jat
{"title":"A retrospective study of traumatic brain injury within emergency department at government medical college, Jammu","authors":"Shahnawaz Ahmed Chowdhary, Aaqib Pervaiz Butt, Mohd Akber Lone, Kulbir Singh Jat","doi":"10.22271/27081494.2022.v4.i2c.67","DOIUrl":"https://doi.org/10.22271/27081494.2022.v4.i2c.67","url":null,"abstract":"","PeriodicalId":169045,"journal":{"name":"International Journal of Case Reports in Surgery","volume":"17 Suppl 2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124547320","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
Meckel’s diverticulum with heterotophic pancreatic epithelium presenting with intestinal obstruction in a 22 year old male 一例22岁男性梅克尔憩室伴胰腺上皮异养性表现为肠梗阻
Pub Date : 2022-07-01 DOI: 10.22271/27081494.2022.v4.i2c.65
Dr.Nida Khan, D. M. Kumar
{"title":"Meckel’s diverticulum with heterotophic pancreatic epithelium presenting with intestinal obstruction in a 22 year old male","authors":"Dr.Nida Khan, D. M. Kumar","doi":"10.22271/27081494.2022.v4.i2c.65","DOIUrl":"https://doi.org/10.22271/27081494.2022.v4.i2c.65","url":null,"abstract":"","PeriodicalId":169045,"journal":{"name":"International Journal of Case Reports in Surgery","volume":"19 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127764294","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
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International Journal of Case Reports in Surgery
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