Yuri de Lima Medeiros, Dandara Menezes de Araujo Oliveira, Agnaldo Rocha Prata Júnior, Laura Luiza Trindade de Souza, Clóvis Antonio Lopes Pinto, Graziella Chagas Jaguar, Fabio Abreu Alves
{"title":"口腔毛状白斑:真性红细胞增多症患者的罕见病变。","authors":"Yuri de Lima Medeiros, Dandara Menezes de Araujo Oliveira, Agnaldo Rocha Prata Júnior, Laura Luiza Trindade de Souza, Clóvis Antonio Lopes Pinto, Graziella Chagas Jaguar, Fabio Abreu Alves","doi":"10.18502/ijhoscr.v19i2.18556","DOIUrl":null,"url":null,"abstract":"<p><p>Although there have been some reports of oral hairy leukoplakia (OHL) in patients with hematologic neoplasms, to the best of our knowledge, this study is the first to report this lesion affecting a patient with polycythemia vera. A 54-year-old male patient diagnosed with polycythemia vera presented with non-removable white patches with a rough surface on the bilateral border of the tongue. According to clinical, histopathological and in situ hybridization features, OHL was established. Two months after diagnosis, the patient developed splenomegaly and initiated ruxolitinib. Bone marrow biopsy showed post-polycythemia vera myelofibrosis. The patient underwent allogeneic haploidentical hematopoietic stem-cell transplant, achieving complete remission of the oral lesion. OHL is an important marker of immunosuppression. In the present case, OHL was diagnosed during the progression of polycythemia vera to myelofibrosis and its early diagnosis may have contributed to a better clinical outcome.</p>","PeriodicalId":94048,"journal":{"name":"International journal of hematology-oncology and stem cell research","volume":"19 2","pages":"191-194"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12368715/pdf/","citationCount":"0","resultStr":"{\"title\":\"Oral Hairy Leukoplakia: A Rare Involvement in a Patient with Polycythemia Vera.\",\"authors\":\"Yuri de Lima Medeiros, Dandara Menezes de Araujo Oliveira, Agnaldo Rocha Prata Júnior, Laura Luiza Trindade de Souza, Clóvis Antonio Lopes Pinto, Graziella Chagas Jaguar, Fabio Abreu Alves\",\"doi\":\"10.18502/ijhoscr.v19i2.18556\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Although there have been some reports of oral hairy leukoplakia (OHL) in patients with hematologic neoplasms, to the best of our knowledge, this study is the first to report this lesion affecting a patient with polycythemia vera. A 54-year-old male patient diagnosed with polycythemia vera presented with non-removable white patches with a rough surface on the bilateral border of the tongue. According to clinical, histopathological and in situ hybridization features, OHL was established. Two months after diagnosis, the patient developed splenomegaly and initiated ruxolitinib. Bone marrow biopsy showed post-polycythemia vera myelofibrosis. The patient underwent allogeneic haploidentical hematopoietic stem-cell transplant, achieving complete remission of the oral lesion. OHL is an important marker of immunosuppression. In the present case, OHL was diagnosed during the progression of polycythemia vera to myelofibrosis and its early diagnosis may have contributed to a better clinical outcome.</p>\",\"PeriodicalId\":94048,\"journal\":{\"name\":\"International journal of hematology-oncology and stem cell research\",\"volume\":\"19 2\",\"pages\":\"191-194\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12368715/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of hematology-oncology and stem cell research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18502/ijhoscr.v19i2.18556\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of hematology-oncology and stem cell research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/ijhoscr.v19i2.18556","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Oral Hairy Leukoplakia: A Rare Involvement in a Patient with Polycythemia Vera.
Although there have been some reports of oral hairy leukoplakia (OHL) in patients with hematologic neoplasms, to the best of our knowledge, this study is the first to report this lesion affecting a patient with polycythemia vera. A 54-year-old male patient diagnosed with polycythemia vera presented with non-removable white patches with a rough surface on the bilateral border of the tongue. According to clinical, histopathological and in situ hybridization features, OHL was established. Two months after diagnosis, the patient developed splenomegaly and initiated ruxolitinib. Bone marrow biopsy showed post-polycythemia vera myelofibrosis. The patient underwent allogeneic haploidentical hematopoietic stem-cell transplant, achieving complete remission of the oral lesion. OHL is an important marker of immunosuppression. In the present case, OHL was diagnosed during the progression of polycythemia vera to myelofibrosis and its early diagnosis may have contributed to a better clinical outcome.