原发性卵巢淋巴瘤1例,表现为直肠粘膜下肿瘤。

Il Soon Jung, Seul Young Kim, Kyu Seup Kim, Kwang Hun Ko, Jae Kyu Sung, Hyun Young Jeong, Ji Yeoun Kim, Hee Seok Moon
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引用次数: 2

摘要

原发性卵巢淋巴瘤是一种罕见的恶性肿瘤,其症状或体征通常是非特异性的。在这篇文章中,我们报告一个非常罕见的病例,最初表现为直肠粘膜下肿瘤样病变,并伴有排便障碍,由原发性卵巢淋巴瘤引起,累及双侧。一名42岁妇女到忠南大学医院就诊,主诉持续排便障碍6个月。结肠镜检查显示直肠被一个模拟直肠粘膜下肿瘤的外源性肿块压迫。磁共振检查发现双侧卵巢肿瘤,直径分别为9.3 cm和5.4 cm,压迫直肠,未见淋巴结肿大。诊断是建立在双侧附件切除术和切除组织的组织学研究之后。肿瘤分类为弥漫性大b细胞淋巴瘤。患者接受了6个周期的标准CHOP(环磷酰胺、羟基柔红霉素、长春新碱、强的松龙)治疗,目前正在接受治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A case of primary ovarian lymphoma presenting as a rectal submucosal tumor.

A case of primary ovarian lymphoma presenting as a rectal submucosal tumor.

A case of primary ovarian lymphoma presenting as a rectal submucosal tumor.

A case of primary ovarian lymphoma presenting as a rectal submucosal tumor.

Primary ovarian lymphoma is a rare malignancy whose symptoms or signs are usually nonspecific. In this article, we report a very rare case initially presenting as a rectal submucosal-tumor-like lesion with a defecation disturbance caused by primary ovarian lymphoma with bilateral involvement. A 42-year-old woman visited chungnam national university hospital complaining of persistent defecation disturbance for 6 months. Colonoscopy demonstrated compression of the rectum by an extrinsic mass mimicking a rectal submucosal tumor. Magnetic resonance imaging detected bilateral ovarian tumors, 9.3 cm and 5.4 cm each in diameter, compressing the rectum without enlarged lymph nodes. The diagnosis was established following a bilateral adnexectomy and histological studies of the excised tissue. The tumor was classified as a diffuse large B-cell lymphoma. The patient was prescribed six cycles of standard CHOP (cyclophosphamide, hydroxydaunorubicin, vincristine, prednisolone) regimen and is presently on treatment.

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