口腔毛状白斑:真性红细胞增多症患者的罕见病变。

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
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引用次数: 0

摘要

虽然已经有一些关于血液肿瘤患者口腔毛状白斑(OHL)的报道,但据我们所知,这项研究是第一次报道这种病变影响真性红细胞增多症患者。一例54岁男性真性红细胞增多症患者,双侧舌缘出现不可去除的白色斑块,表面粗糙。根据临床、组织病理学和原位杂交的特点,建立OHL。确诊后两个月,患者出现脾肿大,开始使用鲁索利替尼。骨髓活检显示真性红细胞增多症后骨髓纤维化。患者接受了同种异体单倍体造血干细胞移植,口腔病变完全缓解。OHL是免疫抑制的重要标志。在本病例中,OHL是在真性红细胞增多症发展为骨髓纤维化的过程中被诊断出来的,其早期诊断可能有助于更好的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Oral Hairy Leukoplakia: A Rare Involvement in a Patient with Polycythemia Vera.

Oral Hairy Leukoplakia: A Rare Involvement in a Patient with Polycythemia Vera.

Oral Hairy Leukoplakia: A Rare Involvement in a Patient with Polycythemia Vera.

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.

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