Early Detection and Central Nervous System Prophylaxis in Patients With High-Risk Features of Primary Lymphoma of the Female Genital Tract: The Key to Improved Prognosis

IF 3.9 4区 医学 Q2 HEMATOLOGY Hematological Oncology Pub Date : 2025-02-06 DOI:10.1002/hon.70035
Bingyi Wang, Yaxiao Lu, Jing Zhao, Lanfang Li, Lihua Qiu, Zhengzi Qian, Shiyong Zhou, Xianhuo Wang, Huilai Zhang
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Abstract

Primary lymphoma of the female genital tract (PLFGT) is a rare disease. The incidence is gradually increasing each year. There have been few reports about PLFGT, and most of them have involved individual cases and small-sample retrospective analyses. The pathogenesis of PLFGT is still under exploration and may be associated with hormones, inflammation/infection, and immunodeficiency. Diffuse large B-cell lymphoma (DLBCL) is the most common pathological type. The majority of the patients presented with vaginal bleeding, abdominal pain, an abdominal mass, and other nonspecific symptoms. Lymphoma-associated B symptoms are quite rare. These patients initially visited gynecological departments, possibly leading to misdiagnosis due to nonspecific features. The treatment strategies for and prognosis of PLFGT differ substantially from those of other gynecologic malignancies. Thus, interdisciplinary cooperation among gynecologists, pathologists, and hematologists is essential.

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女性生殖道原发性淋巴瘤高危患者的早期发现和中枢神经系统预防:改善预后的关键
原发性女性生殖道淋巴瘤(PLFGT)是一种罕见的疾病。发病率每年都在逐渐增加。目前关于PLFGT的报道较少,且多为个例和小样本回顾性分析。PLFGT的发病机制仍在探索中,可能与激素、炎症/感染和免疫缺陷有关。弥漫性大b细胞淋巴瘤(DLBCL)是最常见的病理类型。大多数患者表现为阴道出血、腹痛、腹部肿块和其他非特异性症状。淋巴瘤相关的B型症状相当罕见。这些患者最初去妇科就诊,可能由于非特异性特征导致误诊。PLFGT的治疗策略和预后与其他妇科恶性肿瘤有很大不同。因此,妇科医生、病理学家和血液学家之间的跨学科合作是必不可少的。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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