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基础之外:揭示霍奇金淋巴瘤中的上腔静脉压迫

Beyond The Basics: Unveiling Superior Vena Cava Compression in Hodgkin's Lymphoma.

作者信息

Tangutoori Shivendra, Gullapalli Dedeepya, Kommineni Sai S, Vangara Avinash, Sajnani Kamlesh, Ganti Subramanya Shyam

机构信息

Internal Medicine, Appalachian Regional Healthcare, Harlan, USA.

Hematology and Oncology, Appalachian Regional Healthcare, Harlan, USA.

出版信息

Cureus. 2024 Nov 25;16(11):e74434. doi: 10.7759/cureus.74434. eCollection 2024 Nov.

DOI:10.7759/cureus.74434
PMID:39723308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11669435/
Abstract

Hodgkin's lymphoma (HL) is a malignancy of the lymphocytes in the lymph nodes and presents with non-specific systemic symptoms like fever, night sweats, and weight loss. While HL often involves the mediastinum, it rarely causes superior vena cava (SVC) syndrome, and eosinophilia is noted in approximately 15% of cases. Here, we report a unique presentation of HL in a 52-year-old male with a history of chronic pruritus, chronic kidney disease, and inactive hepatitis B. The patient presented with progressive cough and dyspnea over an eight-month period and developed right-sided ptosis, neck swelling, and engorged veins in the chest, suggesting Horner's syndrome and SVC syndrome. Imaging revealed an enlarged mediastinal mass and a pleural effusion, with subsequent biopsy confirming classical HL. Notably, the patient exhibited severe eosinophilia and a pruritic rash, which are uncommon features seen with HL. Following a multidisciplinary discussion, he was diagnosed with stage IV B x (bulky) HL and was started on a chemotherapy regimen with brentuximab vedotin plus AVD, which led to significant symptom resolution and reduction in tumor size. This case highlights the importance of considering HL in patients presenting with chronic pruritus, eosinophilia, and mediastinal masses. It emphasizes the need for comprehensive diagnostic evaluation in challenging cases and underscores the effectiveness of modern chemotherapy regimens in managing advanced stages of HL.

摘要

霍奇金淋巴瘤(HL)是一种淋巴结中淋巴细胞的恶性肿瘤,表现为发热、盗汗和体重减轻等非特异性全身症状。虽然HL常累及纵隔,但很少引起上腔静脉(SVC)综合征,约15%的病例会出现嗜酸性粒细胞增多。在此,我们报告一例52岁男性HL的独特表现,该患者有慢性瘙痒、慢性肾病和非活动性乙型肝炎病史。患者在八个月内出现进行性咳嗽和呼吸困难,并出现右侧上睑下垂、颈部肿胀和胸部静脉怒张,提示霍纳综合征和SVC综合征。影像学检查显示纵隔肿块增大和胸腔积液,随后活检确诊为经典型HL。值得注意的是,该患者表现出严重的嗜酸性粒细胞增多和瘙痒性皮疹,这是HL中少见的特征。经过多学科讨论,他被诊断为IV B x(大包块)期HL,并开始接受苯达莫司汀联合阿霉素(AVD)的化疗方案,该方案使症状明显缓解,肿瘤大小缩小。本病例强调了在出现慢性瘙痒、嗜酸性粒细胞增多和纵隔肿块的患者中考虑HL的重要性。它强调了在具有挑战性的病例中进行全面诊断评估的必要性,并强调了现代化疗方案在治疗晚期HL中的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/b562cc4c1a47/cureus-0016-00000074434-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/556fc2cf7be0/cureus-0016-00000074434-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/daf41a5d9995/cureus-0016-00000074434-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/827ad457be96/cureus-0016-00000074434-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/b562cc4c1a47/cureus-0016-00000074434-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/556fc2cf7be0/cureus-0016-00000074434-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/daf41a5d9995/cureus-0016-00000074434-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/827ad457be96/cureus-0016-00000074434-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11669435/b562cc4c1a47/cureus-0016-00000074434-i06.jpg

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本文引用的文献

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