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Influence of Covid-19 Pandemic on Safe and Timely Delivery of Systemic Anti-Cancer Therapy, Dubai Hospital Experience 新冠肺炎疫情对安全及时提供全身抗癌治疗的影响:迪拜医院的经验
Pub Date : 2022-12-24 DOI: 10.9734/jcti/2022/v12i4223
M. Latif, Syed Hammad Tirmazi, Dalia M El-Shourbagy
Aims: To analyze the effect of COVID-19 pandemic on timely delivery of systemic anti-cancer treatment including chemotherapy, biological therapy and immunotherapy and assess complication rate. Place and Duration of Study: Department of Oncology, Dubai Hospital, Dubai, UAE from January 2020 to July 2020. Methods: This is a retrospective review of electronic medical records and infusion Centre log of the number of chemotherapy sessions administered in the infusion therapy Centre, Dubai hospital from January 2020 to July 2020. Data on treatment delays, interruptions or discontinuations, and adverse events such as febrile neutropenia were collected and analysed. Results: A total of 1553 systemic treatment sessions were recorded between January 2020 to July 2020 with an average of 222 treatment sessions per month. Physician recorded delays were observed in ninety (5.79%) treatment sessions. The average treatment delay was 7 (2-13) days. Delays were frequently caused by the overall treatment course and disease-related factors (toxicities, disease progression). The highest number of treatment delays (n=23,10.2%) were recorded in April, at the peak of the Covid-19 pandemic, most likely because of the implementation of extreme precautionary measures. There were no interruptions or discontinuations in treatment. Fourteen (<1%) patients developed febrile neutropenia. With treatment, all of them recovered fully. No significant change in systemic treatment related complications were observed during the pandemic. Conclusion: This study found no evidence of an appreciable rise in the number of complications or delays in systemic anticancer treatment during the COVID-19 pandemic. This experience indicates that systemic chemotherapy may be delivered successfully during a pandemic with infection control and safety precautions. However, more research with a larger sample size is needed for more accurate advice in this case.
目的:分析2019冠状病毒病大流行对化疗、生物治疗和免疫治疗等全身抗癌治疗及时交付的影响,并评估并发症发生率。学习地点和时间:2020年1月至2020年7月,阿联酋迪拜迪拜医院肿瘤科。方法:回顾性分析迪拜医院输液治疗中心2020年1月至2020年7月化疗次数的电子病历和输液中心日志。收集和分析了治疗延迟、中断或中断以及发热性中性粒细胞减少等不良事件的数据。结果:2020年1月至2020年7月共记录了1553次全身治疗,平均每月222次。在90次(5.79%)治疗中观察到医生记录的延误。平均治疗延迟7(2 ~ 13)天。延迟通常是由整个治疗过程和疾病相关因素(毒性、疾病进展)引起的。4月是Covid-19大流行的高峰期,治疗延误次数最多(n=23,10.2%),很可能是由于实施了极端预防措施。治疗过程中没有中断或中断。14例(<1%)患者出现发热性中性粒细胞减少症。经过治疗,他们都完全康复了。大流行期间未观察到全身治疗相关并发症的显著变化。结论:本研究未发现证据表明在COVID-19大流行期间并发症或全身抗癌治疗延迟的数量明显增加。这一经验表明,在感染控制和安全预防措施的情况下,全身化疗可以在大流行期间成功实施。然而,在这种情况下,需要更多的研究和更大的样本量来获得更准确的建议。
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引用次数: 0
Histopathological Characteristics of Breast Lesions in a Tertiary Health Institution in Southwest Nigeria: A 9-year Review 尼日利亚西南部一家三级医疗机构乳腺病变的组织病理学特征:9年回顾
Pub Date : 2022-12-20 DOI: 10.9734/jcti/2022/v12i4222
Olabisi Ayo-Aderibigbe, T. Oloyede, A. Adekunle, O. Odujoko, T. Babatunde, S. Ojedokun, A. Salawu
Background: The breast is affected by several diseases, including developmental, inflammatory, and neoplastic. While benign breast neoplasms are usually more common, breast cancer is the most common nonskin cancer and the leading cause of cancer-related deaths in women after lung cancer in the world. Objective: The review aimed to assess the histopathological diagnosis of breast lesions over a period of 9years Methods: This was a retrospective review of eight hundred and fourteen histopathologic cases of breast lesions accessed through laboratory records of all breast lesions cases seen. The demographic data were obtained and the patient’s histology slides were reviewed. The tumors were classified according to the WHO International Classification of breast tumors and Malignant breast tumors were graded according to the Nottingham grading system. Data were analyzed using SPSS version 25. Results: The majority of breast cancer cases were seen in patients below 40 years, malignant cases were predominant in older age groups (40 – 59 years; 57.4%, 60 years and above; 23.3%) and malignancy was significantly associated with age group, p-value < 0.05. The prevailing neoplasm was Benign type (68.3%) while malignant neoplasm accounted for 30.2% and invasive ductal carcinoma (89.1%) was most prevalent. Moreso, the majority were in grade 2; 152 (76.8%) using the Nottigham grading system. However, the commonest benign neoplasm was fibroadenoma (53.7%) followed by fibrocystic change (20.1%). Conclusion:  Breast lesions are common in this environment.  Benign breast neoplasms are more commoner than malignant diseases.  One in three of every sub-Saharan woman diagnosed with malignant breast lesion may not survive five years post-diagnosis. The prognosis of breast malignancies in sub-Saharan is poor due to late Presentation, ignorance, and poverty.
背景:乳腺受多种疾病的影响,包括发育性、炎症性和肿瘤性疾病。虽然乳腺良性肿瘤通常更常见,但乳腺癌是最常见的非皮肤癌,也是世界上仅次于肺癌的女性癌症相关死亡的主要原因。目的:本综述旨在评估9年来乳腺病变的组织病理学诊断方法:回顾性分析814例乳腺病变的组织病理学病例,通过对所有乳腺病变病例的实验室记录进行分析。我们获得了患者的人口统计数据,并回顾了患者的组织学切片。肿瘤按照WHO乳腺肿瘤国际分类进行分类,恶性乳腺肿瘤按照Nottingham分级系统进行分级。数据分析采用SPSS version 25。结果:乳腺癌以40岁以下的患者居多,恶性肿瘤以40 ~ 59岁的老年患者居多;57.4%, 60岁及以上;23.3%)、恶性肿瘤与年龄组有显著相关性,p值< 0.05。肿瘤以良性为主(68.3%),恶性占30.2%,以浸润性导管癌为主(89.1%)。此外,大多数是二年级学生;152所(76.8%)采用诺丁汉评分系统。然而,最常见的良性肿瘤是纤维腺瘤(53.7%),其次是纤维囊性变(20.1%)。结论:乳腺病变在这种环境下较为常见。乳腺良性肿瘤比恶性肿瘤更常见。每三名被诊断患有乳房恶性病变的撒哈拉以南妇女中,就有一人可能在诊断后五年内无法存活。在撒哈拉以南地区,由于出现较晚、无知和贫穷,乳腺恶性肿瘤的预后较差。
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引用次数: 0
Hormone Positive HER2 Negative Breast Cancer Metastatic to the Rectum: A Case Report 激素阳性HER2阴性乳腺癌转移至直肠1例报告
Pub Date : 2022-11-25 DOI: 10.9734/jcti/2022/v12i4221
A. Chehal, Ashraf Alakkad, A. Uttamchandani, Rawia M. Mohamed, R. Church, Sonia Otsmane
Background: The rectum is an uncommon site for metastases from Invasive Ductal Carcinoma (IDC) of the breast, and it poses risks such as perforation and obstruction. Case Report: A 50-year-old non-diabetic, non-alcoholic, and nonsmoker premenopausal female patient diagnosed with rectal metastasis primarily originating from breast cancer. In 2009, the patient was diagnosed with stage IV hormone positive, Her-2 (+2) negative, FISH positive right breast cancer with cervical (C6) vertebrae metastasis seen on PET scan. As she had oligo metastasis with a single bony focus, she was treated with intent to cure. For this purpose, she received radiation therapy to the cervical vertebrae, resulting in a complete response. This was followed by pseudo-neoadjuvant chemotherapy with six cycles of Docetaxel and trastuzumab. The patient then underwent a right-modified radical mastectomy. The pathology showed no complete response with residual 2.5 cm invasive carcinoma (PT2), and 4 out of 25 Axillary lymph nodes were positive for metastases (PN2). She was given (pseudo) adjuvant radiotherapy to the chest wall and lymphatics and was started on (pseudo) adjuvant tamoxifen. Trastuzumab was completed for one year as a (pseudo) adjuvant setting. Her disease seemed to be cleared up as no new cancer signs were reported by follow-up full body scans (CT/PET). After seven years, in May 2016, her PET-CT scan showed multiple new hypermetabolic osseous lesions, in keeping with metastasis involving the right shoulder, mid-thoracic spine, left aspect of L5, right sacrum, and the greater trochanteric region of the left femur and left ischium. She also presented a new hypermetabolic retroperitoneal paracaval lymph node, in keeping with metastasis. The new ill-defined hypodensity in the left hepatic lobe was associated with increased FDG uptake, which is suspicious for early metastasis. She also presented a tiny right lung peri-fissural nodularity that was too small to be characterized by PET. She was treated with Zoladex 3.6 mg injection monthly, Femara 2.5 mg daily, Palbociclib 125 mg PO daily for 21 days over a 28-day cycle, and Denosumab 120 mg monthly. The treatment was initiated in Singapore. As previously stated, Her-2 testing was reported as negative. The patient went into complete remission for more than six years, as documented by the PET scan conducted on January 19, 2022. Later, in June 2022, the patient developed signs and symptoms of intestinal obstruction (abdominal pain, nausea, and vomiting) and was diagnosed with rectal cancer metastases of breast origin. Conclusion:  As the patient first developed breast cancer with oligo-bony metastasis, which was successfully treated with chemotherapy and radiotherapy, but later relapsed in the lung, liver, lymph nodes, and multiple bony sites. She was treated successfully via hormonal and targeted therapy. Finally, she relapsed in the form of rectal metastasis.
背景:直肠是乳腺浸润性导管癌(Invasive Ductal Carcinoma, IDC)转移的罕见部位,存在穿孔、梗阻等风险。病例报告:一名50岁非糖尿病、非酒精、非吸烟的绝经前女性患者,诊断为直肠转移,主要源于乳腺癌。2009年诊断为IV期激素阳性,Her-2(+2)阴性,FISH阳性右乳腺癌,PET扫描显示颈(C6)椎骨转移。由于她有一个单一的骨转移灶,她的治疗意图治愈。为此,她接受了颈椎放射治疗,完全缓解。随后是伪新辅助化疗,6个周期的多西他赛和曲妥珠单抗。患者随后接受了右侧改良根治性乳房切除术。病理显示未完全缓解,残余2.5 cm浸润性癌(PT2), 25个腋窝淋巴结中有4个转移阳性(PN2)。她给予胸壁和淋巴管(伪)辅助放疗,并开始服用(伪)辅助他莫昔芬。曲妥珠单抗作为(伪)辅助设置完成了一年。随后的全身扫描(CT/PET)没有发现新的癌症迹象,她的疾病似乎已经消失了。7年后,2016年5月,她的PET-CT扫描显示多发新的高代谢骨性病变,与转移相一致,累及右肩、胸椎中棘、L5左侧、右骶骨、左股骨大转子区和左坐骨。她还提出了一个新的高代谢腹膜后腔旁淋巴结,与转移保持一致。左肝叶新出现的不明确的低密度与FDG摄取增加有关,这可能与早期转移有关。她还表现出一个微小的右肺裂周结节,太小而无法通过PET表征。患者每月注射Zoladex 3.6 mg, Femara每天2.5 mg, Palbociclib每天125 mg PO,共21天,28天周期,Denosumab每月120 mg。这种治疗是在新加坡开始的。如前所述,Her-2检测报告为阴性。根据2022年1月19日进行的PET扫描记录,患者完全缓解了六年多。随后,于2022年6月,患者出现肠梗阻的体征和症状(腹痛、恶心、呕吐),并被诊断为乳腺癌转移。结论:由于该患者首先发生乳腺癌伴少骨转移,经化疗和放疗治疗成功,但随后在肺、肝、淋巴结及多骨部位复发。她通过激素和靶向治疗成功治疗。最后,她以直肠转移的形式复发。
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引用次数: 0
Effects of Thymoquinone and Cisplatin on C-MYC, KRAS, p53 and EGFR Gene Expression in Lung Cancer Cell Lines 百里醌和顺铂对肺癌细胞系C-MYC、KRAS、p53和EGFR基因表达的影响
Pub Date : 2022-11-14 DOI: 10.9734/jcti/2022/v12i4220
Bayrakçi Onur, Karaman Taşdemir Demet, Ilhan Sedat, Işik Ahmet Ferudun
Lung cancer is one of the most common causes of death.It is known that  genetic reasons in its etiology.Lung cancer has been shown to be associated with the EGFR,P53,KRAS and c-MYC genes.Thymoquinone is an antitumoral and antineoplastic bioactive substance procured from Nigella sativa plant.Cisplatin is a frequently used chemotherapeutic agent in the treatment of lung cancer.Our study has been conducted to examine the effects of Tq and Cis on gene expressions on lung cancer cell lines.Potential effects of Tq and Cis on A549,HTB54, CRL5820 and BEAS2B cell lines and cell viability using MTT has been evaluated.Cell culture has been effectuated with RPMI supplemented with 10% FBS,1% antibiotic and DMEM(37°C, %5 CO2).Cells were cultured for 24 h in 96 well plates(2500/ml cells) 10% FBS RPMI appropriate medium.The cells have been exposured 100 μM Tq and 200 μM Cis for 4h under incubation conditions.DMSO has been used for negative control.RT PCR has been conducted using SYBR Green qPCR Master Mix(reference gene GAPDH).As a result, p53 gene suppression has been shown in lung adenocarcinoma with Tq and Cis and epidermoid carcinoma with Cis only.EGFR gene suppression has been shown in lung adenocarsinoma with Tq only and epidermoid carcinoma with Cis only.C-MYC gene suppression has been shown in lung adenocarsinoma with both substances(more at Tq).It has been shown that KRAS gene suppression does not occur in any cell line.In addition, it has been shown that no gene expression is suppressed after Tq and cis exposure in the mesothelioma cell line.
肺癌是最常见的死亡原因之一。已知其病因有遗传原因。肺癌已被证明与EGFR、P53、KRAS和c-MYC基因有关。百里醌是一种从黑草植物中提取的抗肿瘤、抗肿瘤活性物质。顺铂是肺癌治疗中常用的化疗药物。我们研究了Tq和Cis对肺癌细胞系基因表达的影响。利用MTT技术评估了Tq和Cis对A549、HTB54、CRL5820和BEAS2B细胞株的潜在影响及细胞活力。在RPMI中添加10%胎牛血清、1%抗生素和DMEM(37°C, %5 CO2)进行细胞培养。细胞在96孔板(2500/ml细胞)10% FBS RPMI合适培养基中培养24 h。细胞在100 μM Tq和200 μM Cis条件下孵育4h。采用DMSO作为阴性对照。RT PCR采用SYBR Green qPCR Master Mix(参比基因GAPDH)。因此,p53基因抑制已在Tq和Cis的肺腺癌和仅Cis的表皮样癌中被证实。仅Tq型肺腺癌和仅Cis型表皮样癌均有EGFR基因抑制,两种物质的肺腺癌均有c - myc基因抑制(Tq型较多)。已有研究表明,KRAS基因抑制并不发生在任何细胞系中。此外,已有研究表明,在间皮瘤细胞系中,Tq和cis暴露后没有基因表达受到抑制。
{"title":"Effects of Thymoquinone and Cisplatin on C-MYC, KRAS, p53 and EGFR Gene Expression in Lung Cancer Cell Lines","authors":"Bayrakçi Onur, Karaman Taşdemir Demet, Ilhan Sedat, Işik Ahmet Ferudun","doi":"10.9734/jcti/2022/v12i4220","DOIUrl":"https://doi.org/10.9734/jcti/2022/v12i4220","url":null,"abstract":"Lung cancer is one of the most common causes of death.It is known that  genetic reasons in its etiology.Lung cancer has been shown to be associated with the EGFR,P53,KRAS and c-MYC genes.Thymoquinone is an antitumoral and antineoplastic bioactive substance procured from Nigella sativa plant.Cisplatin is a frequently used chemotherapeutic agent in the treatment of lung cancer.Our study has been conducted to examine the effects of Tq and Cis on gene expressions on lung cancer cell lines.Potential effects of Tq and Cis on A549,HTB54, CRL5820 and BEAS2B cell lines and cell viability using MTT has been evaluated.Cell culture has been effectuated with RPMI supplemented with 10% FBS,1% antibiotic and DMEM(37°C, %5 CO2).Cells were cultured for 24 h in 96 well plates(2500/ml cells) 10% FBS RPMI appropriate medium.The cells have been exposured 100 μM Tq and 200 μM Cis for 4h under incubation conditions.DMSO has been used for negative control.RT PCR has been conducted using SYBR Green qPCR Master Mix(reference gene GAPDH).As a result, p53 gene suppression has been shown in lung adenocarcinoma with Tq and Cis and epidermoid carcinoma with Cis only.EGFR gene suppression has been shown in lung adenocarsinoma with Tq only and epidermoid carcinoma with Cis only.C-MYC gene suppression has been shown in lung adenocarsinoma with both substances(more at Tq).It has been shown that KRAS gene suppression does not occur in any cell line.In addition, it has been shown that no gene expression is suppressed after Tq and cis exposure in the mesothelioma cell line.","PeriodicalId":161223,"journal":{"name":"Journal of Cancer and Tumor International","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130304185","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
Management Outcome of Multi-sites Keloids of Multiple Aetiologies in a Young Female Nigerian: A Case Report 尼日利亚一位年轻女性多部位多病因瘢痕疙瘩的治疗结果:1例报告
Pub Date : 2022-10-01 DOI: 10.9734/jcti/2022/v12i3219
R. S. Ajani, A. Adenipekun
Background: Keloids are exaggerated cutaneous scars with a preponderance of fibrous tissue that may complicate wound healing in people that are predisposed to its development. Its management could be challenging with very high probability of recurrence following surgical excision alone. A case of multiple keloids involving both breasts and anterior chest wall of different aetiologies in a young adult female Nigerian without family history of keloid is being reported. She had extralesional excisions of the keloids with immediate external beam radiotherapy followed by serial triamcinolone acetonide injections of the surgical sites. Conclusion: The triple therapy of surgical excision, post-excision radiation and corticosteroid injection offers an excellent outcome in terms of recurrence.
背景:瘢痕疙瘩是一种以纤维组织为主的夸张的皮肤疤痕,可能使易患瘢痕疙瘩的人的伤口愈合复杂化。单纯手术切除后复发的可能性非常高,其治疗可能具有挑战性。一例多发性瘢痕疙瘩累及乳房和前胸壁的不同病因的年轻成年女性尼日利亚无瘢痕疙瘩家族史报告。患者行瘢痕瘤外切术,立即行外束放射治疗,并在手术部位连续注射曲安奈德。结论:手术切除、术后放疗和皮质类固醇注射三联疗法治疗复发效果良好。
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引用次数: 0
A Rare Case Report of Radionecrosis Mandible after Irradiation for Breast Cancer 乳腺癌放射治疗后下颌骨放射性坏死1例
Pub Date : 2022-08-31 DOI: 10.9734/jcti/2022/v12i430188
A. Prathap, George Varghese, R. S. Nidhin, Geethu Philo Varghese, R. B. Aiswarya
Management of irradiated patients with cancer in the head and neck region is a challenging scenario. Radiotherapy promotes cellular and vascular insufficiency that results in a low response rate in the healing. Consequently, surgical procedures in irradiated tissues present high rates of complication. Osteoradionecrosis (ORN) is the most severe sequelae caused by radiotherapy. ORN can occur due to multiple reasons, of which periodontal disease, traumatic injury induced by ill-fitting dentures and trauma after surgery or tooth extraction are the most common. The management of this side effect is difficult and can result in bone or soft tissue loss, affecting the quality of life since majority of patients with ORN have various comorbidities associated. In this article we present a case report of osteoradionecrosis secondary to irradiation for breast cancer which is not frequently reported in literature.
头颈部肿瘤放疗患者的管理是一个具有挑战性的场景。放疗促进细胞和血管功能不全,导致愈合反应率低。因此,辐照组织的外科手术并发症的发生率很高。放射性骨坏死(osteradionecrosis, ORN)是放射治疗最严重的后遗症。ORN的发生有多种原因,其中最常见的是牙周病、假牙不合适引起的创伤性损伤和手术或拔牙后的创伤。这种副作用的管理是困难的,并且可能导致骨或软组织丢失,影响生活质量,因为大多数ORN患者有各种相关的合并症。在这篇文章中,我们提出一个病例报告继发骨放射性坏死的辐照乳腺癌,这是不常见的文献报道。
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引用次数: 0
Diagnostic Challenges in Osteoradionecrosis of the Jaw 颌骨放射性骨坏死的诊断挑战
Pub Date : 2022-08-23 DOI: 10.9734/jcti/2022/v12i430187
Büşra Yilmaz, E. Somay, A. Kucuk, E. Topkan
Osteoradionecrosis of the jaws (ORNJ) is a severe radiotherapy (RT) complication that occurs in 2% to 22% of individuals with head and neck cancers (HNC) who are treated with RT or concurrent chemo-RT. The accurate diagnosis of ORNJ is crucial for appropriate and prompt management. On the other hand, various ORNJ stages can resemble osteomyelitis, medication-related osteonecrosis of the jaw (MRONJ), and tumor recurrences. This challenging situation is primarily due to the clinical and radiologic similarities between ORNJ and these non-RT-related conditions. Image analysis techniques such as panoramic imaging (PI), computed tomography (CT), magnetic resonance imaging (MRI), bone scintigraphy, positron emission tomography (PET), and single photon emission CT (SPECT) might help to avoid diagnostic obstacles. Despite the fact that the general characteristics of ORNJ have been reported in the literature, there is no clear consensus on its definitive diagnosis. Therefore, the current review aims to address ORNJ and its clinical and radiological aspects, as well as provide evidence to inform on the approaches to be used in removing the complexity in diagnosis, with a specific focus on radiological and nuclear medicine techniques.
颌骨放射性骨坏死(ORNJ)是一种严重的放疗(RT)并发症,在接受RT或同期化疗-RT治疗的头颈癌(HNC)患者中发生率为2%至22%。ORNJ的准确诊断对于适当和及时的治疗至关重要。另一方面,不同的ORNJ分期可能类似于骨髓炎、药物相关性颌骨骨坏死(MRONJ)和肿瘤复发。这种具有挑战性的情况主要是由于ORNJ与这些非rt相关疾病之间的临床和放射学相似性。图像分析技术,如全景成像(PI)、计算机断层扫描(CT)、磁共振成像(MRI)、骨闪烁成像、正电子发射断层扫描(PET)和单光子发射CT (SPECT)可能有助于避免诊断障碍。尽管ORNJ的一般特征已在文献中报道,但对其最终诊断尚无明确的共识。因此,本综述旨在解决ORNJ及其临床和放射学方面的问题,并为消除诊断复杂性所使用的方法提供证据,特别关注放射和核医学技术。
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引用次数: 0
A Rare Breast Carcinosarcoma in a Young Female 一例罕见的年轻女性乳腺癌肉瘤
Pub Date : 2022-08-03 DOI: 10.9734/jcti/2022/v12i430185
M. Al-Share, Michleen Al-Awabdeh, Maysaa Al-Khalaileh, Mohammad Abu-Jeyyab, Hanan Al-Asbahi
Metaplastic breast cancer (MBC) is a rare aggressive type of breast cancer, as this form of cancer makes up only 1% of overall breast cancers. It mainly presents with a rapid-growing mass.  Establishing the diagnosis is based on histopathology, as imaging studies show the same features as other types of breast cancer. The treatment protocol for MBC is similar to those for invasive ductal carcinomas owing to the lack of standardized management modality for metaplastic breast cancer per se.   
化生性乳腺癌(MBC)是一种罕见的侵袭性乳腺癌,因为这种类型的癌症仅占乳腺癌总数的1%。主要表现为快速增长的肿块。诊断是基于组织病理学,因为影像学研究显示了与其他类型乳腺癌相同的特征。由于对转移性乳腺癌本身缺乏标准化的管理模式,MBC的治疗方案与浸润性导管癌的治疗方案相似。
{"title":"A Rare Breast Carcinosarcoma in a Young Female","authors":"M. Al-Share, Michleen Al-Awabdeh, Maysaa Al-Khalaileh, Mohammad Abu-Jeyyab, Hanan Al-Asbahi","doi":"10.9734/jcti/2022/v12i430185","DOIUrl":"https://doi.org/10.9734/jcti/2022/v12i430185","url":null,"abstract":"Metaplastic breast cancer (MBC) is a rare aggressive type of breast cancer, as this form of cancer makes up only 1% of overall breast cancers. It mainly presents with a rapid-growing mass.  Establishing the diagnosis is based on histopathology, as imaging studies show the same features as other types of breast cancer. The treatment protocol for MBC is similar to those for invasive ductal carcinomas owing to the lack of standardized management modality for metaplastic breast cancer per se.   ","PeriodicalId":161223,"journal":{"name":"Journal of Cancer and Tumor International","volume":"19 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123004055","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
Detection of Androgen Receptor Gene Polymorphism in Sudanese Patients of Prostate Cancer in Khartoum State 喀土穆苏丹地区前列腺癌患者雄激素受体基因多态性检测
Pub Date : 2022-08-01 DOI: 10.9734/jcti/2022/v12i430184
Jumaa Abuajila Salem Salama, Dawelbiet Abdelaal Yahia, M. Ali, A. Elsadig, Tarig A. M. Hamid
Background: Prostate cancer (PCa) is the most commonly diagnosed solid tumor among men. Genetic susceptibility had been proposed among the risk factors for the development of this cancer. Aim: To investigate the effect of androgen receptor gene polymorphism in the susceptibility of prostate cancer among Sudanese patients. Methods: This study was conducted in Khartoum State during the period from December 2021 to May 2022. The study population that was selected consisted of one hundred patients, who had prostate cancer, who attended for routine follow-up assessment following their chemotherapy treatment. A total of 5 ml EDTA anti-coagulated venous blood samples were obtained from all participants. Prostate specific antigen (PSA) was measured by competitive chemiluminescence immunoassay. DNA extraction was performed for all samples by chemical method and genotyping was performed by PCR-RFLP method using Eco147I enzyme. Results: The Androgen receptor genotype showed that wild (G/G) type was more frequent (89%) than heterozygous (G/A) type (11%), and allele G was more frequent (94.5%)  than allele A (5.5%). The mean serum PSA level among prostate cancer patients was 18.71+31.68 ng/ml. Comparison of the mean serum PSA levels between different AR genotypes revealed no significant association between the genotype and the hormonal level (p. values > 0.05). Conclusion: Androgen receptor gene polymorphism was detected in this study population as heterozygous type. Moreover; there was no significant association between AR genotype and serum PSA level.
背景:前列腺癌(PCa)是男性最常见的实体肿瘤。遗传易感性被认为是导致这种癌症的危险因素之一。目的:探讨雄激素受体基因多态性对苏丹前列腺癌易感性的影响。方法:本研究于2021年12月至2022年5月在喀土穆州进行。选择的研究人群包括100名前列腺癌患者,他们在化疗后接受了常规的随访评估。所有受试者共采集EDTA抗凝静脉血5 ml。采用竞争化学发光免疫法测定前列腺特异性抗原(PSA)。所有样品采用化学法提取DNA,采用Eco147I酶PCR-RFLP法进行基因分型。结果:雄激素受体基因型显示野生型(G/G)比杂合型(G/A)多出现89%(11%),等位基因G比等位基因A多出现94.5%(5.5%)。前列腺癌患者血清PSA平均值为18.71±31.68 ng/ml。不同AR基因型患者血清PSA均值与激素水平无显著相关性(p值> 0.05)。结论:本研究人群雄激素受体基因多态性为杂合型。此外;AR基因型与血清PSA水平无显著相关性。
{"title":"Detection of Androgen Receptor Gene Polymorphism in Sudanese Patients of Prostate Cancer in Khartoum State","authors":"Jumaa Abuajila Salem Salama, Dawelbiet Abdelaal Yahia, M. Ali, A. Elsadig, Tarig A. M. Hamid","doi":"10.9734/jcti/2022/v12i430184","DOIUrl":"https://doi.org/10.9734/jcti/2022/v12i430184","url":null,"abstract":"Background: Prostate cancer (PCa) is the most commonly diagnosed solid tumor among men. Genetic susceptibility had been proposed among the risk factors for the development of this cancer. \u0000Aim: To investigate the effect of androgen receptor gene polymorphism in the susceptibility of prostate cancer among Sudanese patients. \u0000Methods: This study was conducted in Khartoum State during the period from December 2021 to May 2022. The study population that was selected consisted of one hundred patients, who had prostate cancer, who attended for routine follow-up assessment following their chemotherapy treatment. A total of 5 ml EDTA anti-coagulated venous blood samples were obtained from all participants. Prostate specific antigen (PSA) was measured by competitive chemiluminescence immunoassay. DNA extraction was performed for all samples by chemical method and genotyping was performed by PCR-RFLP method using Eco147I enzyme. \u0000Results: The Androgen receptor genotype showed that wild (G/G) type was more frequent (89%) than heterozygous (G/A) type (11%), and allele G was more frequent (94.5%)  than allele A (5.5%). The mean serum PSA level among prostate cancer patients was 18.71+31.68 ng/ml. Comparison of the mean serum PSA levels between different AR genotypes revealed no significant association between the genotype and the hormonal level (p. values > 0.05). \u0000Conclusion: Androgen receptor gene polymorphism was detected in this study population as heterozygous type. Moreover; there was no significant association between AR genotype and serum PSA level.","PeriodicalId":161223,"journal":{"name":"Journal of Cancer and Tumor International","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115995602","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
Endoscopic Assisted Supraorbital Approach for Tumors of Anterior and Middle Skull Base 内镜辅助眶上入路治疗前、中颅底肿瘤
Pub Date : 2022-08-01 DOI: 10.9734/jcti/2022/v12i430183
Mohamed E. Shamia, Ahmed M. Abdelmonem, T. Awad, Nader E. Negm, M. M Kamal
Background Data: The supraorbital eyebrow approach is a minimally invasive keyhole technique that offers wide access to the anterior skull base and parasellar region using the subfrontal corridor, with assistances of neuroendoscopy The approach through the eyebrow permits access to a number of lesions in the subfrontal corridor with minimal brain retraction and a much smaller area of potential injury of main structures. Study Design: This study is a follow up study. Objective: To evaluate the role of supraorbital endoscopic approach for tumors of anterior and middle skull base. Patients and Methods: All the operations were performed at Suez Canal University hospitals, in about 24 months, the first 30 patients having tumors of anterior and middle skull base fulfilling the inclusion criteria were included in this prospective study. Results: Endoscopy can play an important role in improving visualization through the keyhole corridor. With the use of neuroendoscopy, the reach of this approach may be extended even further to include the pituitary fossa, the top third of the clivus, the interpeduncular cistern, the anterior third ventricle, and the medial and anterior temporal lobe and middle fossa.The major advantage of the supraorbital over the endonasal route is a simplified skull base closure and reduced risk of postoperative CSF leak. It is a valuable approach for selected patients. Neuromonitoring may further increase surgical safety. Conclusion: The approach through the eyebrow permits access to a number of lesions in the subfrontal corridor With the use of the assisstence of neuroendoscopy, with minimal brain retraction and a much smaller area of potential injury of anatomical structures.
背景资料:眉眶上入路是一种微创锁眼技术,可在神经内窥镜的辅助下,通过额下通道广泛进入前颅底和鞍旁区域。通过眉入路可进入额下通道的许多病变,脑内缩回最小,主要结构的潜在损伤面积更小。研究设计:本研究为随访研究。目的:探讨眶上入路在颅底前、中部肿瘤治疗中的作用。患者和方法:所有手术均在苏伊士运河大学附属医院进行,在约24个月内,本前瞻性研究纳入了首批30例符合纳入标准的前、中颅底肿瘤患者。结果:内窥镜对提高锁眼通道的可视性具有重要作用。使用神经内窥镜,该入路的范围可以进一步扩大,包括垂体窝、斜坡的前三分之一、脚间池、前第三脑室、内侧和前部颞叶和中窝。眶上径路相对于鼻内径路的主要优点是简化了颅底闭合,降低了术后脑脊液泄漏的风险。对于选定的患者来说,这是一种有价值的方法。神经监测可进一步提高手术安全性。结论:在神经内窥镜的辅助下,经眉入路可以进入额下走廊的许多病变,大脑缩回最小,解剖结构的潜在损伤面积小得多。
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Journal of Cancer and Tumor International
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