Case Reports in Oncological Medicine最新文献

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Malignant Gastrointestinal Neuroectodermal Tumor (GNET) with Prolonged Disease-Free Survival after Platinum-Based Chemotherapy. 恶性胃肠道神经外胚层肿瘤(GNET)在铂基化疗后延长无病生存期。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-30 eCollection Date: 2020-01-01 DOI: 10.1155/2020/8880202
Daulath Singh, Mohammed K Atieh, Mark A Russell, Muaiad Kittaneh
{"title":"Malignant Gastrointestinal Neuroectodermal Tumor (GNET) with Prolonged Disease-Free Survival after Platinum-Based Chemotherapy.","authors":"Daulath Singh,&nbsp;Mohammed K Atieh,&nbsp;Mark A Russell,&nbsp;Muaiad Kittaneh","doi":"10.1155/2020/8880202","DOIUrl":"https://doi.org/10.1155/2020/8880202","url":null,"abstract":"<p><p>Malignant gastrointestinal neuroectodermal tumor (GNET) is a rare disease with a handful of cases described in literature. GNET has only become a well-known/widely accepted entity in the recent years, but it is still not listed in the database of rare diseases. Due to the rarity of disease, there are no guidelines on standard therapeutic approaches in the adjuvant or metastatic setting. Here, we describe a unique case of GNET with a 7-year disease-free survival following adjuvant cisplatin and etoposide chemotherapy. This is the longest disease-free survival that has ever been described in literature and may support using this combination in a larger cohort of patients in the context of a global clinical trial. We will also review the histopathologic features of GNET and potential therapeutic options in the metastatic setting.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"8880202"},"PeriodicalIF":0.9,"publicationDate":"2020-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8880202","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38155474","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: 6
Peripheral Medulloepithelioma: A Rare Entity to Know. 外周髓样上皮瘤:一种罕见的肿瘤。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-26 eCollection Date: 2020-01-01 DOI: 10.1155/2020/6817407
W Matrane, S Cherkaoui, M Regragui, N Bennani Guebessi, M Karkouri, S Salam, A Madani, A Quessar, N Khoubila
{"title":"Peripheral Medulloepithelioma: A Rare Entity to Know.","authors":"W Matrane,&nbsp;S Cherkaoui,&nbsp;M Regragui,&nbsp;N Bennani Guebessi,&nbsp;M Karkouri,&nbsp;S Salam,&nbsp;A Madani,&nbsp;A Quessar,&nbsp;N Khoubila","doi":"10.1155/2020/6817407","DOIUrl":"https://doi.org/10.1155/2020/6817407","url":null,"abstract":"<p><p>According to the World Health Organization, medulloepithelioma belongs to the embryonal neoplasm entity. It is a very rare, highly malignant tumor typically affecting infants and young children. Usually, the tumor arises in the eye or in the central nervous system; a peripheral location has been rarely reported without an established treatment. The recognition and separation of this neoplasm from other differential tumors are mandatory for better understanding of its biology and determination of optimal treatment. This paper reports a case of an ectopic intrapelvic medulloepithelioma with liver metastasis in a 3-year-old girl.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"6817407"},"PeriodicalIF":0.9,"publicationDate":"2020-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/6817407","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38169386","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: 1
Clinical Significance of Pain in Differential Diagnosis between Spinal Meningioma and Schwannoma. 疼痛在脊髓脑膜瘤和神经鞘瘤鉴别诊断中的临床意义。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-26 eCollection Date: 2020-01-01 DOI: 10.1155/2020/7947242
Dorota Olex-Zarychta
{"title":"Clinical Significance of Pain in Differential Diagnosis between Spinal Meningioma and Schwannoma.","authors":"Dorota Olex-Zarychta","doi":"10.1155/2020/7947242","DOIUrl":"10.1155/2020/7947242","url":null,"abstract":"<p><p>While common MRI characteristics for schwannomas exist, diagnosis by imaging alone remains challenging. Detailed analysis of symptoms reported by the patient is very important in the differential diagnosis between meningioma and schwannoma in cases where MRI images are not sufficient for determining the tumor type. The pain, its classification of the character, and the timing seem to be an important predictive symptom in the differential diagnosis of spinal schwannoma.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"7947242"},"PeriodicalIF":0.9,"publicationDate":"2020-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/7947242","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38156900","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: 2
Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy. 曾接受 BRAF 靶向疗法和免疫疗法治疗的晚期转移性黑色素瘤患者对伊匹单抗/尼伐单抗再挑战和 BRAF 抑制剂/MEK 抑制剂再挑战的反应。
IF 0.6
Case Reports in Oncological Medicine Pub Date : 2020-06-25 eCollection Date: 2020-01-01 DOI: 10.1155/2020/4392562
Caitlyn N Myrdal, Srinath Sundararajan
{"title":"Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy.","authors":"Caitlyn N Myrdal, Srinath Sundararajan","doi":"10.1155/2020/4392562","DOIUrl":"10.1155/2020/4392562","url":null,"abstract":"<p><p>Little is known about the optimal sequencing of targeted therapy and immunotherapy in the treatment of patients with BRAF<sup>V600</sup>-mutated metastatic melanoma. BRAF/MEK inhibition often has the benefit of rapid disease regression; however, resistance is frequently seen with long-term use. Treatment with immune checkpoint inhibitors offers the potential for long-term response but displays a lower rate of objective response. The benefit of synergy between therapies is apparent; however, there is limited data regarding optimal sequencing in the treatment of advanced melanoma. We present the case of a 62-year-old gentleman with advanced BRAF<sup>V600</sup>-mutated melanoma who followed an unconventional treatment path. After progressing on single-agent vemurafenib, he had response to multiple modalities of immunotherapy before progression. After, he had a substantial response to multiple BRAF/MEK inhibitor rechallenges before developing resistance. The patient is now stable after a retrial of combination immunotherapy. Our case illustrates that with the right sequencing of therapy, meaningful clinical responses can be elicited with rechallenging of targeted therapy and immunotherapy in metastatic melanoma.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"4392562"},"PeriodicalIF":0.6,"publicationDate":"2020-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334770/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38156899","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
Oxaliplatin-Induced Lhermitte's Sign in Gastric Cancer. 奥沙利铂诱导的胃癌Lhermitte征象
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-24 eCollection Date: 2020-01-01 DOI: 10.1155/2020/8826657
Takeshi Okamoto, Koichi Takagi, Katsuyuki Fukuda
{"title":"Oxaliplatin-Induced Lhermitte's Sign in Gastric Cancer.","authors":"Takeshi Okamoto,&nbsp;Koichi Takagi,&nbsp;Katsuyuki Fukuda","doi":"10.1155/2020/8826657","DOIUrl":"https://doi.org/10.1155/2020/8826657","url":null,"abstract":"<p><p>A 64-year-old Japanese man with no significant medical history presented with epigastric discomfort of 2-weeks' duration. He was diagnosed with metastatic HER2-positive gastric cancer. Chemotherapy with capecitabine, oxaliplatin, and trastuzumab was initiated. During the eighth cycle, he suddenly complained of electric shock-like pain in both legs upon neck flexion, consistent with Lhermitte's sign. Oxaliplatin was discontinued, and Lhermitte's sign resolved after 3 months. Neurotoxicity is commonly observed in platinum-based chemotherapy, but Lhermitte's sign is rare. This is the first report of oxaliplatin-induced Lhermitte's sign in a gastric cancer patient.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"8826657"},"PeriodicalIF":0.9,"publicationDate":"2020-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8826657","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38156901","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: 3
Readministration of Cancer Drugs in a Patient with Chemorefractory Metastatic Colorectal Cancer. 一名化疗难治性转移性结直肠癌患者的抗癌药再用药。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-23 eCollection Date: 2020-01-01 DOI: 10.1155/2020/2351810
Tetsuro Kawagoe, Go Ikeda, Yu Oshiro, Yuta Maruki, Keiko Kaneko, Katsuhiko Iwakiri
{"title":"Readministration of Cancer Drugs in a Patient with Chemorefractory Metastatic Colorectal Cancer.","authors":"Tetsuro Kawagoe,&nbsp;Go Ikeda,&nbsp;Yu Oshiro,&nbsp;Yuta Maruki,&nbsp;Keiko Kaneko,&nbsp;Katsuhiko Iwakiri","doi":"10.1155/2020/2351810","DOIUrl":"https://doi.org/10.1155/2020/2351810","url":null,"abstract":"<p><p>A 63-year-old woman was admitted to our institution for severe pain in her right lower abdomen caused by the perforation of cecal cancer. She underwent emergency surgery, from which she was diagnosed with cecal carcinoma with liver, lung, and lymph node metastases. As she was taking aspirin to prevent cerebral infarction, anti-vascular endothelial growth factor (receptor) antibody and regorafenib therapy were not used. Thus, we started a modified FOLFOX 6+cetuximab regimen. This first-line treatment initially achieved a partial response (PR), but she then developed progressive disease (PD) after 14 months. We changed the regimen to FOLFIRI, followed by trifluridine/tipiracil, but her progression-free survival periods were 2.7 months and 1 month, respectively. Although we cycled through the available array of standard cancer drugs, the patient showed a good performance status, and some benefit from treatment still seemed plausible. We readministered the 5-fluorouracil oral preparation S-1, which maintained stable disease (SD) for 7 months. After PD emerged, we readministered the anti-epidermal growth factor receptor (EGFR) antibody panitumumab for 7.5 months of SD. Finally, 39 months after her diagnosis, she died from rapidly progressing disease. However, her relatively long survival implies that readministering drugs similar to those used in previous regimens might benefit patients with metastatic colorectal cancer.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"2351810"},"PeriodicalIF":0.9,"publicationDate":"2020-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/2351810","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38144448","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
Primary Leiomyosarcoma of the Gallbladder. 原发性胆囊平滑肌肉瘤。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-22 eCollection Date: 2020-01-01 DOI: 10.1155/2020/3603689
Anwar Chammout, Mike Ghabally, Christina Masri, Nour Tantak, Fadi Ward, Ghefar Omar
{"title":"Primary Leiomyosarcoma of the Gallbladder.","authors":"Anwar Chammout,&nbsp;Mike Ghabally,&nbsp;Christina Masri,&nbsp;Nour Tantak,&nbsp;Fadi Ward,&nbsp;Ghefar Omar","doi":"10.1155/2020/3603689","DOIUrl":"https://doi.org/10.1155/2020/3603689","url":null,"abstract":"<p><p>Leiomyosarcoma (LMS) of the gallbladder is an extremely rare entity. Most reported cases were mistakenly diagnosed preoperatively as cholecystitis with or without cholelithiasis. We believe that our article demonstrates the 5<sup>th</sup> case of gallbladder LMS that was suspected preoperatively to be malignant rather than cholecystitis, which fortunately led to radical resection of the tumor instead of simple cholecystectomy. However, the definitive diagnosis relies exclusively on histological and immunohistochemical techniques. We present a case of a 62-year-old Caucasian female complaining of signs and symptoms suggestive for cholecystitis. On ultrasonography, the gallbladder appeared enlarged and filled with a necrotic mass; thus, the presence of adenocarcinoma was suspected. Multislice Computerized Tomography (MSCT) demonstrated no distant metastasis. An extensive radical cholecystectomy was performed, and histological techniques confirmed a leiomyosarcoma diagnosis. In addition, adjuvant chemotherapy of doxorubicin and ifosfamide was administrated. The patient was on follow-up for 2 years and is doing well till date. The discrimination of gallbladder sarcoma preoperatively remains a clinical and radiological challenge. Although radical resection of the tumor remains the mainstay of the treatment, we believe that adjuvant chemotherapy should be administrated in such cases. However, further studies are required in this field.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"3603689"},"PeriodicalIF":0.9,"publicationDate":"2020-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/3603689","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38156898","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
Intestinal Perforation due to Neutropenic Enterocolitis in a Patient Treated with Bevacizumab for Ovarian Cancer. 贝伐单抗治疗卵巢癌患者中性粒细胞减少性小肠结肠炎引起的肠道穿孔。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-16 eCollection Date: 2020-01-01 DOI: 10.1155/2020/7231358
Akinori Sasaki, Kenichi Harano, Takahiro Kogawa, Nobuaki Matsubara, Yoichi Naito, Ako Hosono, Hirofumi Mukai, Takayuki Yoshino, Toru Mukohara
{"title":"Intestinal Perforation due to Neutropenic Enterocolitis in a Patient Treated with Bevacizumab for Ovarian Cancer.","authors":"Akinori Sasaki,&nbsp;Kenichi Harano,&nbsp;Takahiro Kogawa,&nbsp;Nobuaki Matsubara,&nbsp;Yoichi Naito,&nbsp;Ako Hosono,&nbsp;Hirofumi Mukai,&nbsp;Takayuki Yoshino,&nbsp;Toru Mukohara","doi":"10.1155/2020/7231358","DOIUrl":"https://doi.org/10.1155/2020/7231358","url":null,"abstract":"<p><p>Intestinal perforation is a rare adverse event of antineoplastic therapy. However, once it occurs, it is potentially fatal. This report describes a case of intestinal perforation caused by bevacizumab in a patient with ovarian cancer who concurrently developed neutropenic enterocolitis. A 66-year-old woman diagnosed with metastatic ovarian cancer received combination chemotherapy with carboplatin, gemcitabine, and bevacizumab. On day 14, she developed grade 4 pancytopenia and febrile neutropenia, which resulted in neutropenic enterocolitis and intestinal perforation. Emergency surgery was performed, and an intestinal perforation found in the ascending colon was closed. Postoperatively, she developed an intra-abdominal abscess requiring peritoneal drainage. She was discharged from the hospital on recovery.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"7231358"},"PeriodicalIF":0.9,"publicationDate":"2020-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/7231358","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38114952","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: 1
Localized Chronic Form of Langerhans Cell Histiocytosis in the Femur of a 16-Year-Old Male Successfully Treated with Radiofrequency Ablation. 16岁男性股骨局部慢性朗格汉斯细胞组织细胞增多症经射频消融术成功治疗。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-16 eCollection Date: 2020-01-01 DOI: 10.1155/2020/4052034
Kyriakos Papavasiliou, Antonia Bintoudi, Apostolos Vlahodimos, Eleftherios Tsiridis, Prodromos Hytiroglou, Ioannis Tsitouridis, Fares Sayegh
{"title":"Localized Chronic Form of Langerhans Cell Histiocytosis in the Femur of a 16-Year-Old Male Successfully Treated with Radiofrequency Ablation.","authors":"Kyriakos Papavasiliou,&nbsp;Antonia Bintoudi,&nbsp;Apostolos Vlahodimos,&nbsp;Eleftherios Tsiridis,&nbsp;Prodromos Hytiroglou,&nbsp;Ioannis Tsitouridis,&nbsp;Fares Sayegh","doi":"10.1155/2020/4052034","DOIUrl":"https://doi.org/10.1155/2020/4052034","url":null,"abstract":"<p><p>Only three cases of patients suffering from a localized chronic form of Langerhans cell histiocytosis (LCH) successfully treated with radiofrequency ablation (RFA) have been published so far. This is the first case report of a patient with a localized chronic form of LCH of the femur, which was successfully treated with percutaneous image-guided RFA, and who was evaluated pre-RFA and followed up post-RFA for a period of 48 months, in order to validate the safety and efficacy of this method and to obtain imaging studies depicting the actual in situ changes taking place post-RFA. RFA was proved to be a safe and efficient method when treating patients with a localized chronic form of LCH.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"4052034"},"PeriodicalIF":0.9,"publicationDate":"2020-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/4052034","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38114951","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: 1
Peripheral Cytotoxic T Cell Lymphoma of the Appendix Presenting as Acute Appendicitis. 阑尾周围细胞毒性T细胞淋巴瘤表现为急性阑尾炎。
IF 0.9
Case Reports in Oncological Medicine Pub Date : 2020-06-16 eCollection Date: 2020-01-01 DOI: 10.1155/2020/8569426
Negin Rahmani, Yahya Daneshbod, Hadi Mirfazaelian, Elnaz Vahidi, Sadegh Shirian
{"title":"Peripheral Cytotoxic T Cell Lymphoma of the Appendix Presenting as Acute Appendicitis.","authors":"Negin Rahmani,&nbsp;Yahya Daneshbod,&nbsp;Hadi Mirfazaelian,&nbsp;Elnaz Vahidi,&nbsp;Sadegh Shirian","doi":"10.1155/2020/8569426","DOIUrl":"https://doi.org/10.1155/2020/8569426","url":null,"abstract":"<p><strong>Introduction: </strong>Lymphoma of the appendix is a rare cause of acute appendicitis; however, acute appendicitis is a common first manifestation of appendiceal lymphomas. Cytotoxic peripheral T cell lymphoma (PTCL) is a type of aggressive non-Hodgkin lymphoma that portends a generally poor outcome. Cytotoxic PTCL of the appendix is extremely rare with few cases reported in the literature. <i>Case Presentation</i>. This is the report of a 23-year-old man who had experienced lower abdominal pain for three months before presenting to the emergency department with severe right lower abdominal pain, nausea, vomiting, and anorexia since the day prior to admission. The patient was diagnosed with acute appendicitis, and the pathology report confirmed cytotoxic PTCL of the appendix.</p><p><strong>Conclusion: </strong>Patients with appendiceal PTCL commonly present with signs and symptoms of acute appendicitis due to luminal obstruction by the tumor. Therefore, appendiceal tumors such as PTCL should be considered in the differential diagnosis of patients presenting as acute appendicitis. In addition, since there is no standard chemotherapy regimen for cytotoxic PTCL, this and other case reports hopefully help in providing the clinical evidence needed for establishing appropriate treatment guidelines.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2020 ","pages":"8569426"},"PeriodicalIF":0.9,"publicationDate":"2020-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8569426","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38114953","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
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