High Risk HPV, HSIL and Primary Diffuse Large B Cell Lymphoma of Cervix: An Unsual Case

S. Sreehari
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引用次数: 2

Abstract

Primary malignant non-Hodgkin’s lymphomas in the female genital tract are rare, accounting for less than 1% of all extranodal non-Hodgkin’s lymphomas. HPV infection has well been documented as the causative factor for Carcinoma cervix; not malignant lymphoma of cervix. Here we report an interesting case of primary non-Hodgkin’s lymphomas of uterine cervix with proven HPV 16 infection and High grade squamous intraepithelial lesion with co-existing diffuse large B-cell lymphomas (DLBCL) on histopathological examination and immunohistochemical study. The patient was successfully treated with chemotherapy after Cervical Conisation for HSIL and is now in complete remission with follow up period of 11 months. Gynecological lymphomas can be a diagnostic challenge due to nonspecific symptoms. However, when diagnosed and treated they have a good prognosis. Clinicians should therefore include lymphoma in their differential diagnosis when investigating gynecological symptoms.
高危型HPV、HSIL和宫颈原发性弥漫性大B细胞淋巴瘤:一例未知病例
女性生殖道原发性恶性非霍奇金淋巴瘤很少见,占所有结外非霍奇金淋巴瘤的不到1%。HPV感染已被充分证明是宫颈癌的致病因素;不是宫颈恶性淋巴瘤。在此,我们报告了一例有趣的子宫颈原发性非霍奇金淋巴瘤,经组织病理学检查和免疫组织化学研究证实其感染了HPV16,并伴有高度鳞状上皮内病变,同时伴有弥漫性大B细胞淋巴瘤(DLBCL)。该患者在HSIL宫颈锥切术后成功接受了化疗,目前病情完全缓解,随访期为11个月。由于非特异性症状,妇科淋巴瘤可能是一个诊断挑战。然而,当诊断和治疗时,它们有良好的预后。因此,临床医生在调查妇科症状时,应将淋巴瘤纳入鉴别诊断。
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