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Rare Variant of Meckel’s Diverticulum on the Mesenteric Border Complicated by Perforation: Case Report and Literature Review 罕见的Meckel憩室在肠系膜边界变异并穿孔病例报告及文献复习
Pub Date : 2018-10-11 DOI: 10.4172/2165-7920.10001176
J. Al-Qahtani, Ali Sm, A. Qabbani, M. Yousif, M. Khattabi, Khan Mb, Z. Aftab
Background: Meckle’s Diverticulum (MD) is a remnant of vitello intestinal duct found in approximately 2-4% of normal population and is usually located on the anti-mesenteric border of terminal ileum. Its variant, the mesenteric type is even rarer, with only a few cases reported in literature.Case: We describe a case of inflamed mesenteric MD that presented with clinical findings of acute appendicitis, but, upon exploration, was diagnosed as inflamed mesenteric MD, that was removed, and the patient recovered without any complications and went home in good condition. We also review all the mesenteric MD cases reported in the literature since 1941.Conclusion: MD is a rare operative finding, but knowledge of its rare variant must be kept in mind as the signs and symptoms closely resemble acute appendicitis.
背景:梅克尔憩室(Meckle’s Diverticulum, MD)是一种存在于正常人群2-4%的vitello肠管残余,通常位于回肠末端的反肠系膜边界。它的变体,肠系膜型更罕见,文献中只有少数病例报道。病例:我们描述了一例炎症性肠系膜MD,临床表现为急性阑尾炎,但经检查,诊断为炎症性肠系膜MD,切除手术后,患者康复,无任何并发症,出院情况良好。我们也回顾了自1941年以来所有文献报道的肠系膜MD病例。结论:MD是一种罕见的手术发现,但由于其体征和症状与急性阑尾炎非常相似,因此必须牢记其罕见变体的知识。
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引用次数: 3
Return to previous activities and quality of life in patients with femoral intertrochanteric fracture surgery 股骨粗隆间骨折术后患者恢复活动及生活质量的研究
Pub Date : 2018-09-28 DOI: 10.4172/2165-7920-C1-018
pSiavash Azarbanip
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引用次数: 2
Postnatal outcomes following prenatal diagnosis of placental mosaicism: Case reports from literature 产前诊断胎盘嵌合后的产后结果:文献中的病例报告
Pub Date : 2018-09-28 DOI: 10.4172/2165-7920-C1-017
pCristina Rossip
T he purpose was to study the bone mineral density (BMD), vertebral pain (VP) and physical performance indices (PPI) in women of older age groups with vertebral fractures (VF) depending on their localization. Materials & Methods: 139 women aged 50-89 years old were examined and divided into 2 groups: I – patients without any history of osteoporotic fractures (WF), II – women with VF at the thoracic and/or lumbar spine. Subsequently, patients of the second group were divided into subgroups depending on the localization of VF (at thoracic (TF), lumbar spine (LF) or combined fractures (CF)). The assessment of the severity of VP was performed using a 11-component numerical rating scale, the physical capabilities - using static and dynamic functional tests (Thomayer, Schober tests, chest excursion, lateral trunk lean, 3-, 4-, 15-meter tests, "stand up from the chair" etc.), BMD was detected using DXA. Findings: It was found that BMD indices in women with VF were significantly lower than controls (without any previous fractures) regardless of their localization. Most of the VP indices at thoracic spine in women with TF and CF were significantly higher compared to controls, in contrast to patients with LF. It was shown that for women with TF results of breath holding and 15-meter tests were significantly worse compared with control, whereas in persons with LF results of Schober index, lateral trunk lean, hand grip strength and test "stand up from the chair" were worse. In patients with CF most of PPI
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引用次数: 0
Impressive Response of Advanced Hepatocellular Carcinoma to Cisplatin Combined with Sorafenib, Nivolumab, and PG2 Immunomodulatory Injection: A Case Report 晚期肝癌对顺铂联合索拉非尼、尼沃单抗和PG2免疫调节注射液的令人印象深刻的反应:一例报告
Pub Date : 2018-08-30 DOI: 10.4172/2165-7920.10001161
Chung-Kuan W, Ping-Hsiu W, Hung-Chih L
Hepatocellular carcinoma (HCC) is an aggressive tumor, and sorafenib is the only proven drug for treating advanced HCC with limited survival outcome. We present a case of severe right lower chest pain in a 54-year-old man. A computed tomography (CT) scan revealed liver cirrhosis and multiple HCCs with inferior vena cava invasion, regional nodal and right adrenal metastases, and hemoperitoneum. His hepatitis B virus (HBV) deoxyribonucleic acid (DNA) level and alpha-fetoprotein (AFP) remained high even after transcutaneous arterial catheter embolization for ruptured HCCs. He received combination therapy of entecavir, sorafenib, nivolumab, cisplatin, and PG2 injection. The follow-up positron emission tomography-CT confirmed no tumor in the liver, and alpha-fetoprotein and HBV DNA titers showed a promising decrease. This novel combination had encouraging therapeutic effects for advanced HCCs, which decreased viral replication without side effects.
肝细胞癌(HCC)是一种侵袭性肿瘤,索拉非尼是唯一一种已被证明治疗生存率有限的晚期HCC的药物。我们报告一例54岁男性的严重右下胸痛。计算机断层扫描显示肝硬化和多发性HCC伴下腔静脉侵犯、区域淋巴结和右肾上腺转移以及腹腔积血。他的乙型肝炎病毒(HBV)脱氧核糖核酸(DNA)水平和甲胎蛋白(AFP)水平即使在经皮动脉导管栓塞破裂的HCC后仍然很高。他接受了恩替卡韦、索拉非尼、尼沃单抗、顺铂和PG2注射液的联合治疗。随后的正电子发射断层扫描CT证实肝脏中没有肿瘤,甲胎蛋白和HBV DNA滴度显示出有希望的下降。这种新的组合对晚期HCC具有令人鼓舞的治疗效果,减少了病毒复制,没有副作用。
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引用次数: 1
The Loose Cannon! - Cutaneous Manifestation of Langerhans Cell Histiocytosis 逍遥大炮!朗格汉斯细胞组织细胞增多症的皮肤表现
Pub Date : 2018-08-30 DOI: 10.4172/2165-7920.10001160
B. Ramly
A 6-year-old girl presented with symptoms of diabetes insipidus with no neurological abnormalities. Presence of erythematous, dried, plaque like lesions on her scalp had guided the clinicians/paediatricians to liase with different sub-specialities which included dermatologists, pathologists, haematologists, endocrinologists, oncologists, and radiologists. The diagnosis of Langerhans cell histiocytosis (LCH) was rendered and confirmed by positive immunostaining for anti CD1a and/or anti S-100 protein antibodies. Other work up were done for the patient to detect any organs involved and either LCH infiltrates the liver, lungs, spleen or hematopoietic system. The patient was then treated with chemotherapy as according to LCH-IV protocol group 1 initial treatment for multisystem Langerhans Cell Histiocytosis. She responded very well to the therapy and is still under follow up. In this case, we will also be discussing about the importance of genetics of Langerhans Cell Histiocytosis.
一名6岁女孩出现尿崩症症状,无神经系统异常。她的头皮上出现红斑、干燥、斑块状病变,这引导临床医生/儿科医生与不同的亚专业联系,包括皮肤科医生、病理科医生、血液科医生、内分泌科医生、肿瘤学家和放射科医生。Langerhans细胞组织细胞增多症(LCH)的诊断是通过抗CD1a和/或抗S-100蛋白抗体的阳性免疫染色来进行和证实的。对患者进行了其他检查,以检测任何涉及的器官,以及LCH浸润肝、肺、脾或造血系统。根据LCH-IV方案第1组多系统郎格汉斯细胞组织细胞增多症的初始治疗,对患者进行化疗。她对治疗反应良好,目前仍在随访中。在这种情况下,我们还将讨论朗格汉斯细胞组织细胞增多症遗传学的重要性。
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引用次数: 0
A Case of Nicotine vs. Psychosis 尼古丁与精神病的一个案例
Pub Date : 2018-08-24 DOI: 10.26420/austinjclincaserep.2018.1134
Kabuye A
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引用次数: 0
Paget’s Disease of the Bone Mimicking Metastasis: Two Case Reports 佩吉特骨转移病2例报告
Pub Date : 2018-08-24 DOI: 10.4172/2165-7920.10001159
S. Paolino, M. Pendolino, E. Alessandri, M. Cutolo, C. Pizzorni
Paget’s disease of the bone (PDB) is a focal metabolic bone disorder generally asymptomatic which is characterized by excessive bone resorption followed by increased bone formation. The diagnosis of PDB requires a high index of suspicion, any condition characterized by sclerosis of bone, like metastasis from solid tumors, need to be excluded. We reported two cases of incidental diagnosis of this PDB in oncologic patients. The bone disorder, in these circumstances, is a challenge for timely radiographic diagnosis and histopathologic confirmation.
骨佩吉特病(PDB)是一种通常无症状的局灶性代谢性骨疾病,其特征是骨吸收过度,随后骨形成增加。PDB的诊断需要高度的怀疑指数,任何以骨骼硬化为特征的疾病,如实体瘤转移,都需要排除。我们报告了两例肿瘤患者偶然诊断为PDB的病例。骨病,在这些情况下,是一个挑战,及时放射诊断和组织病理学确认。
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引用次数: 0
Recurrent Haemarthrosis after Total Knee Arthroplasty: Investigation and Management 全膝关节置换术后复发性血关节病的调查与处理
Pub Date : 2018-08-21 DOI: 10.4172/2165-7920.10001158
X. He, Y. Li, K. Zhang, T. Hua
Recurrent haemarthrosis is a relatively rare complication of total knee arthroplasty, and only a few cases have been reported; hence, it is hard to determine comprehensive diagnosis and treatment guidelines. We report a case of haemarthrosis in 50-year-old male patient 14 months postoperatively. Investigations (ultrasound, aspiration, and arthroscopy) and managements (non-surgical, arthroscopy and open exploration) were performed, and the clinical effects of these interventions were analyzed separately. Clinical evidence indicates that the cause of this case was rupture of a pseudoaneurysm of the medial superior genicular artery. A brief review is involved in discussion part.
复发性关节血肿是全膝关节置换术中相对罕见的并发症,只有少数病例被报道;因此,很难制定全面的诊断和治疗指南。我们报告一例50岁男性患者术后14个月的血关节病。进行调查(超声、抽吸和关节镜检查)和处理(非手术、关节镜检查和开放探查),并分别分析这些干预措施的临床效果。临床证据表明,本病例的原因是假动脉瘤破裂的内侧膝上动脉。讨论部分是一个简短的回顾。
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引用次数: 0
Laparoscopic Removal of Left Non-Communicated Horn and Left Salpingectomy 腹腔镜左非连通角切除及左输卵管切除术
Pub Date : 2018-06-30 DOI: 10.26420/austinjclincaserep.2019.1133
Felemban A
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引用次数: 1
Outflow Obstruction in Takotsubo Cardiomyopathy Takotsubo型心肌病的流出道阻塞
Pub Date : 2018-06-21 DOI: 10.26420/austinjclincaserep.2018.1131
S. C
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引用次数: 0
期刊
Journal of clinical case reports
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