弥漫性大b细胞非霍奇金淋巴瘤并发自发性肠穿孔1例报告

F. C. Makhandule, M. M. Z. U. Bhuiyan, K. N. Mongwe
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摘要

背景:肠道非霍奇金淋巴瘤是引起急性腹痛的罕见原因。本病例报告的主要目的是分享我们在HIV感染下自发性肠穿孔的弥漫性大B细胞非霍奇金淋巴瘤的治疗经验。方法:报告一例弥漫性大b细胞非霍奇金淋巴瘤合并自发性肠穿孔:39岁女性患者,有1天急腹症病史。她是已知的逆转录病毒疾病,CD4计数534,病毒载量131,抗逆转录病毒治疗固定剂量方案持续时间超过5年,正在接受消化性溃疡疾病治疗。胸片:显示气腹伴穿孔。开腹手术发现空肠穿孔,小肠内容物漏出。手术切除,一期吻合,冲洗。术后情况顺利,术后4天出院。切除的部分被送去做组织学检查,结果显示空肠穿孔继发于弥漫性大B细胞非霍奇金淋巴瘤。结论:肠道淋巴瘤的诊断对发达国家和发展中国家都是一个挑战;然而,将危险因素与体征和症状结合起来可以帮助人们做出诊断。因此,重要的是始终保持高度的怀疑指数,特别是对患有淋巴结病的艾滋病毒患者。Doi: 10.28991/SciMedJ-2023-05-01-05全文:PDF
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Case Report on Diffuse Large B-Cell Non-Hodgkin Lymphoma with a Spontaneous Bowel Perforation
Background: Intestinal Non-Hodgkin lymphoma is an uncommon cause of acute abdominal pain. The main objective of the present case report is to share our experience with Diffuse Large B Cell Non-Hodgkin Lymphoma with spontaneous bowel perforation in a setting of HIV. Method: Description of a Case Report Diffuse Large B-Cell Non-Hodgkin Lymphoma with a spontaneous bowel perforation: A 39-year-old female patient presented with a one-day history of acute abdomen. She is known retroviral disease reactive with CD4 count 534, Viral Load 131 on Antiretroviral Treatment-Fixed Dose Regimen duration of more than 5 years and was being treated for Peptic Ulcer Disease. Chest X-ray: showed pneumoperitoneum consistent with a perforation. A Laparotomy was performed and found a perforated Jejunum leaking small bowel contents. Resection and primary anastomosis were performed, and washout was done. Post-Operative condition was uneventful, and she was discharged four days after the operation. The resected portion was sent for histology, which showed perforation of the Jejunum secondary to a Diffuse Large B Cell Non-Hodgkin Lymphoma. Conclusion: The diagnosis of Intestinal Lymphoma poses a diagnostic challenge for both developed and developing countries; however, coupling the risk factors with signs and symptoms can assist one in making a diagnosis. It is therefore important to always have a high index of suspicion, particularly for HIV patients with lymphadenopathy. Doi: 10.28991/SciMedJ-2023-05-01-05 Full Text: PDF
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