Diffuse large B-cell lymphoma misdiagnosed as cellulitis

Dear Editors, A 77-year-old woman with type 2 diabetes mellitus and hypertension presented to our hospital with swelling in the right leg. The patient had been treated with antibiotics for cellulitis three 10 years before admission and experienced recurrent hospitalization for right leg cellulitis (Figure 1A). Despite antibiotic and diuretic therapies, the swelling did not resolve completely. She did not report fever, night sweats, and weight loss.Clinical examination revealed diffuse swelling and redness extending from the right thigh to the calf. Numerous infiltrative plaques and nodules with irregular borders, 1-2 cm in size, were present within the erythematous lesions. No pain or tenderness was observed. Laboratory workup revealed anemia, hypoalbuminemia, elevated C-reactive protein, and a soluble interleukin-2 receptor (sIL-2R) level of 25,700 IU/mL. Computed tomography scan revealed nodules in the left breast and lungs. Core needle biopsy of the lesion on the left breast confirmed 5 an invasive ductal carcinoma. Punch biopsy of the skin lesion on the right leg revealed dense and diffuse infiltration of atypical cells with large nuclei under the subcutis.Immunohistochemical staining was negative for CD3, CD10, and CD138 and positive for CD20, CD-79a, MUM-1, BCL-6, BCL-2, and PD-L1 (Figure 1B, 1C, 1D, and 1E). Hence, PCDLBCL-LT (primary cutaneous diffuse large B-cell lymphomas-leg type) was diagnosed. After diagnosis, 10 she was started on R-CHOP chemotherapy (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone). The skin lesion gradually epithelialized (Figure 1F) and sIL-2R level decreased. Despite treatment, the patient died of multiple organ failure two months after admission.PCDLBCL-LT presenting as cellulitis-like is rare, with only a few reported cases [1, 2, 3].Previous reports initially misdiagnosed cases as bacterial infections. DLBCL is a non-Hodgkin lymphoma that occurs with extranodal or nodal involvement. The primary sites of the extranodal type include the gastrointestinal tract, head and neck, skin, and soft tissues.PCDLBCL was diagnosed if a patient presented with no extracutaneous involvement upon diagnosis. The patient presented with left breast cancer and lung nodules. This patient showed a three-year history of repeated cellulitis in the right leg, which we initially assumed to be DLBCL. Although we have no definite evidence because of the lack of a chest radiography three years before her first visit, we speculated that this patient had which may 5 have spread to the lungs as multiple nodules. PCDLBCL-LT typically present as nodules, and rarely mimic diffuse cellulitis-like clinical findings. The diagnosis of PCDLBCL presenting with cellulitis-like is challenging because of its rarity and clinical features. Provided its aggressive pathology [4], this disease should be considered if patients do not respond to antibiotic therapies. 10