The Atypical Presentation of Diffuse Large B-cell Lymphoma in a Lower Limb Soft Tissue Mass: A Case Report

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.

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Publication Details

Journal
Cureus
Published
2025-06-24
DOI
https://doi.org/10.7759/cureus.86676
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
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article

The Atypical Presentation of Diffuse Large B-cell Lymphoma in a Lower Limb Soft Tissue Mass: A Case Report

Clarisse Simões Coelho, Ana Cristina Silva, Ana Sofia Martins, Filipe Leal et al.
Cureus
Lymphoma Diagnosis and Treatment
article

The Atypical Presentation of Diffuse Large B-cell Lymphoma in a Lower Limb Soft Tissue Mass: A Case Report

Clarisse Simões Coelho, Ana Cristina Silva, Ana Sofia Martins, Filipe Leal, Amélia Gaspar
article en

Abstract

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.

CureusVol. 17(6)
University of Coimbra (PT)
Zero hunger
Openalex Percentile: Top 78%
Lymphoma Diagnosis and Treatment
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