Autopsy Revealed an Extremely Rare Case of Hodgkin Lymphoma With Intranodal Extramedullary Hematopoiesis and Hemophagocytosis in a Patient With Severe Thrombocytopenia.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2025-02-19 eCollection Date: 2025-02-01 DOI:10.7759/cureus.79298
Aoi Utsunomiya, Yotaro Asano, Shiori Meguro, Yasuyuki Nagata, Kotaro Nakano, Hideya Kawasaki, Isao Kosugi, Yasunori Enomoto, Satoshi Baba, Toshihide Iwashita
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Abstract

In this report, we present an extremely rare case of Hodgkin lymphoma with severe thrombocytopenia, where extramedullary hematopoiesis (EMH) and hemophagocytosis were simultaneously observed within the lymph nodes. Approximately 40 days before the patient's death, computed tomography performed at another hospital revealed enlargement of deep lymph nodes, including hilar, mediastinal, and mesenteric lymph nodes. Thirteen days before death, the patient was admitted to the hospital with marked hematuria, systemic purpura, mild renal dysfunction, and severe thrombocytopenia; two days later, he was transferred to our institution. On admission, almost all lymph nodes were enlarged, which led us to suspect malignant lymphoma. Blood examination findings suggested that immune thrombocytopenia was a possible cause of severe thrombocytopenia. However, due to severe thrombocytopenia, we could not perform a pathological diagnosis via excisional biopsy of the lymph nodes. Despite treatment with dexamethasone (DEX) pulse therapy, immunoglobulin therapy, and platelet transfusion, the platelet count did not increase. Ultimately, the patient died due to multi-organ hemorrhage. Postmortem pathological examination revealed classic Hodgkin lymphoma in the enlarged lymph nodes, along with EMH and hemophagocytosis within the same lymph nodes. We conducted a literature review and found no prior reports of cases where malignant lymphoma coexisted with EMH and hemophagocytosis within the same lymph node, making this the first reported case.

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尸检发现一例极其罕见的霍奇金淋巴瘤伴结内髓外造血和噬血细胞症的严重血小板减少症患者。
在本报告中,我们报告了一例极其罕见的霍奇金淋巴瘤伴严重血小板减少症,在淋巴结内同时观察到髓外造血(EMH)和噬血细胞现象。大约在患者死亡前40天,在另一家医院进行的计算机断层扫描显示深部淋巴结肿大,包括肺门淋巴结、纵隔淋巴结和肠系膜淋巴结。死亡前13天,患者因明显血尿、全身性紫癜、轻度肾功能障碍和严重的血小板减少症入院;两天后,他被转到我们的机构。入院时,几乎所有淋巴结肿大,我们怀疑为恶性淋巴瘤。血液检查结果提示,免疫性血小板减少症是严重血小板减少症的可能原因。然而,由于严重的血小板减少症,我们无法通过淋巴结切除活检进行病理诊断。尽管进行了地塞米松(DEX)脉冲治疗、免疫球蛋白治疗和血小板输注,血小板计数并未增加。最终,患者因多器官出血而死亡。死后病理检查显示肿大淋巴结内典型霍奇金淋巴瘤,同时在同一淋巴结内伴有EMH和噬血细胞症。我们进行了文献回顾,没有发现在同一淋巴结内恶性淋巴瘤与EMH和噬血共存的病例报道,因此这是第一例报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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