CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES
Case Report: Choroid plexus carcinoma (CPC) is a rare and aggressive intracranial neoplasm, constituting 1–4% of all brain tumors and approximately 40% of choroid plexus tumors. Classified as a WHO Grade III malignancy, CPC is characterized by a poor prognosis, with reported 5-year survival rates ar...
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| Language: | English |
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Elsevier
2024-12-01
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| Series: | Hematology, Transfusion and Cell Therapy |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2531137924028980 |
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| author | Şule Çalışkan Kamış Begül Yağcı Barbaros Şahin Karagün |
| author_facet | Şule Çalışkan Kamış Begül Yağcı Barbaros Şahin Karagün |
| author_sort | Şule Çalışkan Kamış |
| collection | DOAJ |
| description | Case Report: Choroid plexus carcinoma (CPC) is a rare and aggressive intracranial neoplasm, constituting 1–4% of all brain tumors and approximately 40% of choroid plexus tumors. Classified as a WHO Grade III malignancy, CPC is characterized by a poor prognosis, with reported 5-year survival rates around 40%. In contrast, choroid plexus papilloma (CPP), classified as a WHO Grade I tumor, is a benign and slow-growing lesion originating from the epithelial cells of the choroid plexus.This report presents four cases of choroid plexus tumors: two diagnosed as choroid plexus carcinoma (WHO Grade III) and two as choroid plexus papillomas (WHO Grade I). The CPP cases were managed with observation and followed up without active treatment. Among the CPC cases, a 3-year-old patient received initial radiotherapy followed by chemotherapy based on the CPT-SIOP-2000 protocol. A 7-month-old patient with CPC was treated with chemotherapy (CPT-SIOP-2000 protocol), while radiotherapy was deferred due to her age of less than 3 years.Multidisciplinary treatment strategies for CPC include maximal surgical resection followed by chemotherapy and radiotherapy. The CPT-SIOP-2000 study has demonstrated that the Carboplatin/Etoposide/Vincristine (CarbEV) chemotherapy protocol is effective in treating CPC. |
| format | Article |
| id | doaj-art-86ce6e9556ed419ca0a12175ed1a08a0 |
| institution | Kabale University |
| issn | 2531-1379 |
| language | English |
| publishDate | 2024-12-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Hematology, Transfusion and Cell Therapy |
| spelling | doaj-art-86ce6e9556ed419ca0a12175ed1a08a02024-12-26T08:57:07ZengElsevierHematology, Transfusion and Cell Therapy2531-13792024-12-0146S62CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASESŞule Çalışkan Kamış0Begül Yağcı1Barbaros Şahin Karagün2Adana City Training and Research Hospital; Corresponding author.Adana City Training and Research HospitalAdana City Training and Research HospitalCase Report: Choroid plexus carcinoma (CPC) is a rare and aggressive intracranial neoplasm, constituting 1–4% of all brain tumors and approximately 40% of choroid plexus tumors. Classified as a WHO Grade III malignancy, CPC is characterized by a poor prognosis, with reported 5-year survival rates around 40%. In contrast, choroid plexus papilloma (CPP), classified as a WHO Grade I tumor, is a benign and slow-growing lesion originating from the epithelial cells of the choroid plexus.This report presents four cases of choroid plexus tumors: two diagnosed as choroid plexus carcinoma (WHO Grade III) and two as choroid plexus papillomas (WHO Grade I). The CPP cases were managed with observation and followed up without active treatment. Among the CPC cases, a 3-year-old patient received initial radiotherapy followed by chemotherapy based on the CPT-SIOP-2000 protocol. A 7-month-old patient with CPC was treated with chemotherapy (CPT-SIOP-2000 protocol), while radiotherapy was deferred due to her age of less than 3 years.Multidisciplinary treatment strategies for CPC include maximal surgical resection followed by chemotherapy and radiotherapy. The CPT-SIOP-2000 study has demonstrated that the Carboplatin/Etoposide/Vincristine (CarbEV) chemotherapy protocol is effective in treating CPC.http://www.sciencedirect.com/science/article/pii/S2531137924028980 |
| spellingShingle | Şule Çalışkan Kamış Begül Yağcı Barbaros Şahin Karagün CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES Hematology, Transfusion and Cell Therapy |
| title | CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES |
| title_full | CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES |
| title_fullStr | CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES |
| title_full_unstemmed | CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES |
| title_short | CHOROID PLEXUS CARCINOMA AND CHOROID PLEXUS PAPILLOMA; RARE CASES |
| title_sort | choroid plexus carcinoma and choroid plexus papilloma rare cases |
| url | http://www.sciencedirect.com/science/article/pii/S2531137924028980 |
| work_keys_str_mv | AT sulecalıskankamıs choroidplexuscarcinomaandchoroidplexuspapillomararecases AT begulyagcı choroidplexuscarcinomaandchoroidplexuspapillomararecases AT barbarossahinkaragun choroidplexuscarcinomaandchoroidplexuspapillomararecases |