Leal Filipe, Gaspar Amélia, Silva Cristina, Coelho Clarisse, Martins Ana Sofia
Family Health Unit, USF Mondego, Coimbra Local Health Unit, Coimbra, PRT.
Cureus. 2025 Jun 24;17(6):e86676. doi: 10.7759/cureus.86676. eCollection 2025 Jun.
We report a case of an 80-year-old male with a progressively enlarging, painful mass in the left lower limb, initially misdiagnosed as cellulitis. The patient did not respond to antibiotic therapy, prompting further investigation. Imaging revealed two large soft tissue masses, and biopsy confirmed diffuse large B-cell lymphoma (DLBCL) of germinal center origin. Despite treatment with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) chemotherapy and palliative radiotherapy, the disease progressed, and the patient died approximately one year after diagnosis. This report illustrates the diagnostic challenge posed by extranodal DLBCL when it mimics common soft tissue infections. Delayed diagnosis in our case was caused by the benign clinical presentation and limited access to imaging in the primary care setting. Clinicians should maintain a high index of suspicion for malignancy in atypical or unresponsive soft tissue lesions. Early referral, multidisciplinary evaluation, and appropriate imaging are critical to improving outcomes in such rare presentations.
我们报告一例80岁男性患者,其左下肢有一个逐渐增大的疼痛性肿块,最初被误诊为蜂窝织炎。患者对抗生素治疗无反应,促使进一步检查。影像学检查发现两个大的软组织肿块,活检证实为生发中心来源的弥漫性大B细胞淋巴瘤(DLBCL)。尽管接受了R-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱和泼尼松)化疗及姑息性放疗,但疾病仍进展,患者在诊断后约一年死亡。本报告说明了结外DLBCL在模仿常见软组织感染时所带来的诊断挑战。我们病例中的诊断延迟是由于临床表现良性以及基层医疗环境中影像学检查受限所致。临床医生对非典型或无反应的软组织病变应保持高度的恶性肿瘤怀疑指数。早期转诊、多学科评估及适当的影像学检查对于改善此类罕见病例的治疗结果至关重要。