脾切除术在导致B细胞原发性脾淋巴瘤的不明原因发热中的关键作用。

E. Muço, R. Osmenaj, R. Bode, Amarildo Blloshmi, Jona Prendi, L. Berdica
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引用次数: 0

摘要

背景:Petersdorf和Beeson于1961年首次提出“不明原因发热”(FUO)一词,其定义为复发性发热>38.3°C,持续时间>3周,在住院评估1周后仍未确诊。经典FUO的病因主要包括感染、恶性肿瘤、非感染性炎症性疾病和各种原因,而一些病例仍未确诊。原发性脾脏淋巴瘤(PSL)是一种罕见的恶性淋巴瘤。在许多情况下,脾切除术是治疗巨大脾肿大的首选方法。病例介绍:一名54岁的女性,有39°C以下的高烧、出汗、疲劳和体重减轻一个月的病史。她的家庭医生用抗生素(头孢菌素)治疗了她10天,但没有好转。入院时,患者有明显的脾肿大,但没有明显的淋巴结肿大。患者的炎症标志物增多。自身免疫性疾病的各项指标均为阴性。对特定传染病的筛查和血液培养结果均为阴性。腹部电脑断层扫描显示脾脏肿大。进行了脾切除术,并将脾脏送去进行组织学分析。与此同时,患者接受了复杂的治疗。组织学和免疫组织化学分析证实了弥漫性大B细胞非霍奇金淋巴瘤伴弥漫性红髓浸润的诊断。之后,患者接受了全身化疗。结论:我们强烈建议临床医生对FUO患者的恶性肿瘤有较高的怀疑指数。有时脾切除术可能是解决问题的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Key Role of Splenectomy in Fever of unknown Origin which Resulted to be B-cell primary Splenic Lymphoma.
Background: The term ‘fever of unknown origin’ (FUO) was first introduced by Petersdorf and Beeson in 1961, and it is defined as recurrent fever >38.3°C, lasting for >3 weeks, remaining undiagnosed after 1 week of in-hospital evaluation. The etiologies of classic FUO include mainly infections, malignancies, non-infectious inflammatory diseases, and miscellaneous causes, while some cases remain undiagnosed. Primary splenic lymphoma (PSL) is a rare malignant lymphoma. In many cases, splenectomy is the treatment of choice for massive splenomegaly. Case presentation: A 54-year-old woman presented with a history of high fever up to 39°C, sweating, fatigue, and weight loss for one month. She had been treated by her family physician with antibiotics (cephalosporin) for 10 days but without improvement. On admission, the patient had palpable splenomegaly but no palpable lymphadenopathy. The patient had increased markers of inflammation. The indicators of autoimmune disease were all negative. Screening for specific infectious diseases and the blood cultures all came out negative. Abdominal computerized tomography (CT) revealed an enlarged spleen. The splenectomy was performed and the spleen was sent for histological analysis. Meanwhile, the patient was subject to a complex treatment. Histological and immunohistochemical analysis confirmed the diagnosis of diffuse large B-cell non-Hodgkin lymphoma with diffuse red pulp infiltration. Afterward, the patient underwent systemic chemotherapy. Conclusion: We strongly suggest that clinicians should have a high index of suspicion for malignancies in cases with FUO. Sometimes splenectomy can be the key to solving the problem.
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