Pub Date : 2022-08-21DOI: 10.51626/ijor.2022.03.00017
The concept of field cancerization was proposed by Slaughter et al. in 1953. Field cancerization of the mucosa of aerodigestive tract frequently develops on account of tobacco and alcohol usage. The oral cavity is one of the predominant and prevalent sites of development of potential malignancies, therefore, it comes into direct contact with many carcinogens. All of the epithelium beyond the boundaries of tumour can undergo histological changes and may have more than one independent area of malignancy. The mucosa undergoes a change, perhaps due to carcinogen exposure and is therefore more susceptible to the development of many foci of malignant transformation. This explains the high incidence of recurrence of oral cancer, the rate being 32.7%, despite excision of tumour or other therapies. So, diagnosis and treatment of oral cancer should not only be focused on the lesion, but also on the field from which it developed. In this article, we emphasize on the concept of field cancerization, highlight the carcinogenic influence of tobacco and alcohol in the development of multiple primary tumours in the oral cavity by presenting clinical cases. Keywords: Field cancerization; Squamous cell carcinoma; Metastasis; Second primary tumours; Synchronous/ Metachronous tumours3.
{"title":"Oral Field Cancerization: A Review with Case Reports","authors":"","doi":"10.51626/ijor.2022.03.00017","DOIUrl":"https://doi.org/10.51626/ijor.2022.03.00017","url":null,"abstract":"The concept of field cancerization was proposed by Slaughter et al. in 1953. Field cancerization of the mucosa of aerodigestive tract frequently develops on account of tobacco and alcohol usage. The oral cavity is one of the predominant and prevalent sites of development of potential malignancies, therefore, it comes into direct contact with many carcinogens. All of the epithelium beyond the boundaries of tumour can undergo histological changes and may have more than one independent area of malignancy. The mucosa undergoes a change, perhaps due to carcinogen exposure and is therefore more susceptible to the development of many foci of malignant transformation. This explains the high incidence of recurrence of oral cancer, the rate being 32.7%, despite excision of tumour or other therapies. So, diagnosis and treatment of oral cancer should not only be focused on the lesion, but also on the field from which it developed. In this article, we emphasize on the concept of field cancerization,\u0000highlight the carcinogenic influence of tobacco and alcohol in the development of multiple primary tumours in the oral cavity by presenting clinical cases.\u0000Keywords: Field cancerization; Squamous cell carcinoma; Metastasis; Second primary tumours; Synchronous/ Metachronous tumours3.","PeriodicalId":247564,"journal":{"name":"International Journal on Oncology and Radiotherapy","volume":"127 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130258851","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}
Pub Date : 2022-08-01DOI: 10.51626/ijor.2022.03.00016
Gastrointestinal Stromal Tumor (GIST) is an uncommon stromal malignancy of Gastrointestinal (GI) tract. GISTs have been increasingly reported in sites other than GI tract. Currently, GISTs are considered metastatic when they occur outside GI tract; however, there is a possibility of a primary stromal tumor of omentum and/or gynecologic tract with similar mutation profile and histopathology but different prognosis and clinical behavior. Here, we report a case of 52-year-old female with widespread lesions in her abdomen and pelvis, which turned out to be a GIST; however, no lesions were identified in the GI tract which raises the possibility of omental or ovarian primary stromal tumor. Since GISTs are mutation derived tumors, it is highly likely that the stroma of other locations can undergo similar tumorigenesis due to mutations in c-KIT and/or PDGFRA genes and present similarly to primary GI tract GISTs. More studies are required to look for other possible primary sites and difference in clinical behavior and prognosis to appropriately stage the patient before treatment, as GISTs that occur outside GI tract tends to behave aggressively and are usually resistant to imatinib therapy. Keywords: Gastrointestinal stromal tumor; Omentum; Endometrium; Metastasis; Epithelioid; Carcinomatosis
{"title":"Metastatic Gastrointestinal Stromal Tumor to the Omentum and Endometrium: A Case Report","authors":"","doi":"10.51626/ijor.2022.03.00016","DOIUrl":"https://doi.org/10.51626/ijor.2022.03.00016","url":null,"abstract":"Gastrointestinal Stromal Tumor (GIST) is an uncommon stromal malignancy of Gastrointestinal (GI) tract. GISTs have been increasingly reported in sites other than GI tract. Currently, GISTs are considered metastatic when they occur outside GI tract; however, there is a possibility of a primary stromal tumor of omentum and/or gynecologic tract with similar mutation profile and histopathology but different prognosis and clinical behavior. Here, we report a case of 52-year-old female with widespread lesions in her abdomen and pelvis, which turned out to be a GIST; however, no lesions were identified in the GI tract which raises the possibility of omental or ovarian primary stromal tumor. Since GISTs are mutation derived tumors, it is highly likely that the stroma of other locations can undergo similar tumorigenesis due to mutations in c-KIT and/or PDGFRA genes and present similarly to primary GI tract GISTs. More studies are required to look for other possible primary sites and difference in clinical behavior and prognosis to appropriately stage the patient before treatment, as GISTs that occur outside GI tract tends to behave aggressively and are usually resistant to imatinib therapy.\u0000Keywords: Gastrointestinal stromal tumor; Omentum; Endometrium; Metastasis; Epithelioid; Carcinomatosis","PeriodicalId":247564,"journal":{"name":"International Journal on Oncology and Radiotherapy","volume":"80 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":"126209897","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}
Pub Date : 2022-07-23DOI: 10.51626/ijor.2022.03.00015
This short communication highlights lack of resources in Pathology in developing countries which ultimately affects pathology residency training as well as routine practice of lab medicine. There are a few recommendations to help alleviate pathology manpower in resource limited countries including digitization of teaching resources, integration of pathology education into systems-based curriculum, concept of virtual electives, specialization within pathology practices beyond the academic centers and competency-based certification. Opportunities like digital pathology, virtual trainings and online courses can play an important role in pathology education and for covering all kind of curricula. These changes will also implement a standardized education system of international quality. The digital world has a lot to offer in terms of training and there are extensive learning options if we learn to utilize them properly. More and more remote platforms are becoming available in the form of elective opportunities and online teaching sessions. It is important to promote these platforms as they do not have border restrictions and they are a perfect example of how education should be free and accessible to everyone around the world. Keywords: Digital pathology; Virtual training; Electives; Pathology education; Manpower; Competen
{"title":"Digital Pathology Implementation can Help Alleviate Limited Pathology Services in Developing Countries","authors":"","doi":"10.51626/ijor.2022.03.00015","DOIUrl":"https://doi.org/10.51626/ijor.2022.03.00015","url":null,"abstract":"This short communication highlights lack of resources in Pathology in developing countries which ultimately affects pathology residency training as well as routine practice of lab medicine. There are a few recommendations to help alleviate pathology manpower in resource limited countries including digitization of teaching resources, integration of pathology education into systems-based curriculum, concept of virtual\u0000electives, specialization within pathology practices beyond the academic centers and competency-based certification. Opportunities like digital pathology, virtual trainings and online courses can play an important role in pathology education and for covering all kind of curricula. These changes will also implement a standardized education system of international quality. The digital world has a lot to offer in terms of training and there are extensive learning options if we learn to utilize them properly. More and more remote platforms are becoming available in the form of elective opportunities and online teaching sessions. It is important to promote these platforms as they do not have border restrictions and they are a perfect example of how education should be free and accessible to everyone around the world.\u0000Keywords: Digital pathology; Virtual training; Electives; Pathology education; Manpower; Competen","PeriodicalId":247564,"journal":{"name":"International Journal on Oncology and Radiotherapy","volume":"96 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128584385","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}
Pub Date : 2022-07-23DOI: 10.51626/ijor.2022.03.00014
Sinonasal papillomas, also called Schneiderian papillomas, are uncommon benign epithelial tumors arising from the pseudostratified ciliated sinonasal mucosa. Three subtypes of sinonasal papillomas have been described, namely exophytic papilloma, inverted papilloma, and oncocytic papilloma. These papillomas usually have a favorable prognosis, however, frequent recurrences and local aggressiveness has been observed. These may undergo malignant transformation in rare instances. We report a case of a 70-year-old male with multiple co-morbidities presenting with nasal obstruction and bleeding for 3 months. CT and MRI sinuses demonstrated a polypoid mass within the right nasal cavity extending into the nasopharynx, likely arising from the right maxillary sinus. Histopathology revealed a diagnosis of carcinoma (poorly differentiated, NOS) ex combined inverted and oncocytic types sinonasal papilloma (Schneiderian papilloma) with multifocal severe dysplasia (carcinoma in situ). Importance of correct diagnosis lies in the fact that these tumors show recurrence and malignant transformation, thus, requiring long-term follow-up. Keywords: Schneiderian papilloma; Sinonasal papilloma; Malignant transformation; Radiotherapy; Oncocytic
{"title":"Carcinoma Ex Combined Inverted and Oncocytic Types Sinonasal Papilloma with Multifocal Severe Dysplasia: A Case Report","authors":"","doi":"10.51626/ijor.2022.03.00014","DOIUrl":"https://doi.org/10.51626/ijor.2022.03.00014","url":null,"abstract":"Sinonasal papillomas, also called Schneiderian papillomas, are uncommon benign epithelial tumors arising from the pseudostratified ciliated sinonasal mucosa. Three subtypes of sinonasal papillomas have been described, namely exophytic papilloma, inverted papilloma, and oncocytic papilloma. These papillomas usually have a favorable prognosis, however, frequent recurrences and local aggressiveness has been observed.\u0000These may undergo malignant transformation in rare instances. We report a case of a 70-year-old male with multiple co-morbidities presenting with nasal obstruction and bleeding for 3 months. CT and MRI sinuses demonstrated a polypoid mass within the right nasal cavity extending into the nasopharynx, likely arising from the right maxillary sinus. Histopathology revealed a diagnosis of carcinoma (poorly differentiated,\u0000NOS) ex combined inverted and oncocytic types sinonasal papilloma (Schneiderian papilloma) with multifocal severe dysplasia (carcinoma in situ). Importance of correct diagnosis lies in the fact that these tumors show recurrence and malignant transformation, thus, requiring long-term follow-up.\u0000Keywords: Schneiderian papilloma; Sinonasal papilloma; Malignant transformation; Radiotherapy; Oncocytic","PeriodicalId":247564,"journal":{"name":"International Journal on Oncology and Radiotherapy","volume":"60 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130648933","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}
Pub Date : 2022-07-20DOI: 10.51626/ijor.2022.03.00013
Diffuse midline glioma, H3K27M-mutant, WHO grade IV (DMGM), is a newly established entity in the 2016 WHO classification. It is uncommon and the median age of diagnosis is 5-11 years. Due to their rarity in adults, their recognition can be challenging even though the histopathology and phenotypes of adult and pediatric cases are similar. We report a case of a middle-aged female who presented with seizures and persistent headache, where imaging revealed an enhancing suprasellar mass involving the hypothalamus and fornix and she was diagnosed with H3K27M-mutant diffuse midline glioma. DMGM is extremely rare in adults and therefore, more cases need to be reported to enable their recognize among neuropathologists. Also, this report suggests a needed emphasis on obtaining molecular studies whenever possible if there is a suspicion of H3K27M-mutant DMGM, given that they are extremely aggressive and have poor clinical outcomes in most cases. The case was presented at College of American Pathologists (CAP) annual conference in Chicago (October 2018) and the abstract was published in Archives as an online supplement only. Keywords: Glioma; Suprasellar; Hypothalamus; Fornix; Midbrain; Thalamus
{"title":"Diffuse Midline Glioma H3 K27-Mutant in an Adult: A Rare\u0000Case","authors":"","doi":"10.51626/ijor.2022.03.00013","DOIUrl":"https://doi.org/10.51626/ijor.2022.03.00013","url":null,"abstract":"Diffuse midline glioma, H3K27M-mutant, WHO grade IV (DMGM), is a newly established entity in the 2016 WHO classification. It is uncommon and the median age of diagnosis is 5-11 years. Due to their rarity in adults, their recognition can be challenging even though the histopathology and phenotypes of adult and pediatric cases are similar. We report a case of a middle-aged female who presented with seizures and persistent headache, where imaging revealed an enhancing suprasellar mass involving the hypothalamus and fornix and she was diagnosed with H3K27M-mutant diffuse midline glioma. DMGM is extremely rare in adults and therefore, more cases need to be reported to enable their recognize among neuropathologists. Also, this report suggests a needed emphasis on obtaining molecular studies whenever possible if there is a suspicion of H3K27M-mutant DMGM, given that they are extremely aggressive and have poor clinical outcomes in most cases. The case was presented at College of American Pathologists (CAP) annual conference in Chicago (October 2018) and the abstract was published in Archives as an online supplement only.\u0000Keywords: Glioma; Suprasellar; Hypothalamus; Fornix; Midbrain; Thalamus","PeriodicalId":247564,"journal":{"name":"International Journal on Oncology and Radiotherapy","volume":"76 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133197216","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}