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子宫内弥漫性大 B 细胞淋巴瘤的意外表现:病例报告。

Diffuse large B-cell lymphoma in the uterus with unexpected manifestations: a case report.

机构信息

Hama University, Faculty of Medicine, Hama, Syria.

Al Asad Hospital, Hama, Syria.

出版信息

J Med Case Rep. 2024 Jul 16;18(1):325. doi: 10.1186/s13256-024-04657-2.

Abstract

BACKGROUND

Lymphoid neoplasm is a common disease, arising from lymphoid cells. It is divided into Hodgkin lymphoma and non-Hodgkin lymphoma. Non-Hodgkin lymphoma can be intranodular or extranodular, which happens in 25% of primary cases. The most common locations of extranodular non-Hodgkin lymphoma are the skin and gastrointestinal tract. The genital tract is a rare location; most lymphomas arise from the cervix and vagina, while the uterine corpus is an extremely rare location. In our case, the patient was diagnosed with primary extranodular non-Hodgkin lymphoma in different locations of her genital tract.

CASE PRESENTATION

A 48-year-old nonparous Syrian woman complained of diffuse abdominal pain, fatigue, debility, high fever, vomiting, and urinary retention for a week. The last menstrual period of the patient was 5 years previously. The physical examination showed periodic abdominal pain with severe fatigue and increased abdominal size. The laboratory investigations were within normal limits except for a low level of hemoglobin and a high level of cancer antigen 125. The radiological investigations showed a uterine sizable lobulated mass with irregular borders and high and heterogeneous density, extending to the right and left ovaries, enlargement lymph nodes around the abdominal aortic and right iliac vessels, and severe right pleural effusion with right inferior lobe atelectasis. A total hysterectomy and oophorectomy were done. The histopathological examination showed that the patient had non-Hodgkin lymphoma (primary tumor).

CONCLUSION

Primary non-Hodgkin lymphoma in the female genital tract is an extremely rare disease. Fast diagnosis and treatment can improve the outcomes, so this differential diagnosis should be in our minds even in the absence of systematic manifestations of lymphoma. More studies are needed to explain the pathology of this disease and to put guidelines that determine the perfect methods for diagnosis and treatment.

摘要

背景

淋巴肿瘤是一种常见疾病,起源于淋巴细胞。它分为霍奇金淋巴瘤和非霍奇金淋巴瘤。非霍奇金淋巴瘤可以是结节内或结节外的,在原发性病例中占 25%。结节外非霍奇金淋巴瘤最常见的部位是皮肤和胃肠道。生殖道是一个罕见的部位;大多数淋巴瘤发生在宫颈和阴道,而子宫体是一个极其罕见的部位。在我们的病例中,患者被诊断为生殖道不同部位的原发性结节外非霍奇金淋巴瘤。

病例介绍

一位 48 岁的未育叙利亚妇女因弥漫性腹痛、疲劳、虚弱、高热、呕吐和尿潴留一周来就诊。患者的末次月经是 5 年前。体格检查显示周期性腹痛,伴有严重疲劳和腹部增大。实验室检查除了血红蛋白水平低和癌抗原 125 水平高外,均在正常范围内。影像学检查显示子宫大小呈分叶状肿块,边界不规则,密度高且不均匀,向左右卵巢延伸,腹主动脉和右髂血管周围淋巴结肿大,右侧胸腔大量积液伴右下叶肺不张。行全子宫切除术和卵巢切除术。组织病理学检查显示患者患有非霍奇金淋巴瘤(原发性肿瘤)。

结论

女性生殖道原发性非霍奇金淋巴瘤是一种极为罕见的疾病。快速诊断和治疗可以改善预后,因此即使没有淋巴瘤的系统表现,我们也应该考虑到这种鉴别诊断。需要更多的研究来解释这种疾病的病理学,并制定出确定诊断和治疗的完美方法的指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42a1/11251107/bb861550ad3a/13256_2024_4657_Fig1_HTML.jpg

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