Acute liver failure and severe lactic acidosis as initial manifestations of primary intestinal diffuse large B-cell lymphoma: Case report

IF 0.8 Q4 HEMATOLOGY
Leukemia Research Reports Pub Date : 2026-01-01 Epub Date: 2026-02-19 DOI:10.1016/j.lrr.2026.100574
Hideki Mori , Shiro Miura , Momoko Soeda , Yoshitaka Imaizumi
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引用次数: 0

Abstract

Diffuse large B-cell lymphoma (DLBCL) typically presents with lymphadenopathy or extranodal masses, but rarely, predominantly as scattered case reports, as acute liver failure (ALF) with severe lactic acidosis. We report a 79-year-old man who presented with fulminant ALF, leukemoid reaction, and extreme lactic acidosis. Despite intensive care, he rapidly progressed to multiorgan failure and died. Autopsy revealed primary intestinal DLBCL with diffuse hepatic infiltration. This case illustrates the diagnostic challenge in emergency settings and highlights the concept of a “metabolic catastrophe” characterized by ALF, leukemoid reaction, and lactic acidosis. Early recognition of these features should prompt consideration of invasive diagnostic procedures and suspicion for aggressive lymphoma.
急性肝衰竭和严重乳酸性酸中毒为原发性肠弥漫性大b细胞淋巴瘤的初始表现:1例报告。
弥漫性大b细胞淋巴瘤(DLBCL)通常表现为淋巴结病变或结外肿块,但罕见,主要是分散的病例报告,表现为急性肝衰竭(ALF)伴严重乳酸酸中毒。我们报告一个79岁的男性谁提出暴发性ALF,白血病样反应,和极端乳酸酸中毒。尽管进行了重症监护,他还是迅速发展为多器官衰竭而死亡。尸检显示原发性肠内DLBCL伴弥漫性肝脏浸润。本病例说明了在紧急情况下的诊断挑战,并强调了以ALF、类白血病反应和乳酸性酸中毒为特征的“代谢灾难”的概念。早期识别这些特征应提示考虑侵入性诊断程序和对侵袭性淋巴瘤的怀疑。
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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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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