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一位八旬老人的胆囊滤泡性淋巴瘤:病例报告及文献综述

Follicular Lymphoma of the Gallbladder in an Octogenarian: A Case Report and Literature Review.

作者信息

Myers Mikayla, Dakkak Bassel, Sirigireddy Swapna, Shanti Ibrahim, Ferguson Drew, Elghezewi Abdelwahap, Ben Khayal Mustafa, Alagha Zakaria, Sherif Ahmed, Tackett Eva-Pattont

机构信息

Joan Edwards School of Medicine, Huntington, WV, USA.

出版信息

J Investig Med High Impact Case Rep. 2025 Jan-Dec;13:23247096251342035. doi: 10.1177/23247096251342035. Epub 2025 May 27.

Abstract

Primary follicular lymphoma (PFL) is an indolent subtype of non-Hodgkin lymphoma that typically involves lymphoid tissues. Gallbladder involvement is exceedingly rare and poses significant diagnostic challenges. Few cases in the literature describe gallbladder follicular lymphoma, particularly in elderly male patients, leaving notable gaps in clinical understanding and management. Herein, we present the case of an 82-year-old male who presented with acute abdominal pain and unintentional weight loss. Initial imaging, including contrast-enhanced computed tomography, ultrasound, and magnetic resonance imaging, revealed a suspicious gallbladder mass with wall thickening and regional lymphadenopathy, raising concern for malignancy. Endoscopic ultrasound-guided fine needle aspiration and subsequent immunophenotyping confirmed a diagnosis of PFL. The patient underwent radical cholecystectomy with lymphadenectomy, and histopathological examination corroborated the diagnosis of gallbladder follicular lymphoma. During follow-up, the patient developed complications, yet no evidence of lymphoma recurrence was observed. A literature review identified 8 similar cases, further emphasizing the rarity of this presentation. Future research should focus on optimizing diagnostic techniques, refining therapeutic strategies, and conducting longer-term follow-up studies to better assess patient outcomes in such a rare disease. This case highlights the need for heightened clinical suspicion and comprehensive evaluation in atypical presentations of extranodal lymphoma.

摘要

原发性滤泡性淋巴瘤(PFL)是一种惰性非霍奇金淋巴瘤亚型,通常累及淋巴组织。胆囊受累极为罕见,带来了重大的诊断挑战。文献中很少有病例描述胆囊滤泡性淋巴瘤,尤其是老年男性患者,这在临床认识和管理方面留下了显著空白。在此,我们报告一例82岁男性患者,其表现为急性腹痛和非故意体重减轻。包括增强计算机断层扫描、超声和磁共振成像在内的初始影像学检查显示胆囊有可疑肿块,伴有壁增厚和区域淋巴结病,引发了对恶性肿瘤的担忧。内镜超声引导下细针穿刺及随后的免疫表型分析确诊为PFL。患者接受了根治性胆囊切除术及淋巴结清扫术,组织病理学检查证实为胆囊滤泡性淋巴瘤。在随访期间,患者出现了并发症,但未观察到淋巴瘤复发的证据。文献回顾发现了8例类似病例,进一步凸显了这种表现的罕见性。未来的研究应侧重于优化诊断技术、完善治疗策略以及开展长期随访研究,以便更好地评估这种罕见疾病患者的预后。该病例强调了在结外淋巴瘤非典型表现中提高临床怀疑和进行全面评估的必要性。

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