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Case Reports
. 2023 Sep 12;15(3):524-531.
doi: 10.3390/hematolrep15030055.

Diffuse Large B-Cell Lymphoma of the Frontal Sinus: A Case Report

Affiliations
Case Reports

Diffuse Large B-Cell Lymphoma of the Frontal Sinus: A Case Report

Anastasia Urbanelli et al. Hematol Rep. .

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common type of Non-Hodgkin Lymphoma (NHL). It often involves the gastrointestinal tract, head and neck, and skin, but virtually any tissue or organ can be affected. The primary NHL of the nasal cavity and paranasal sinuses are extremely rare, causing diagnostic and therapeutic difficulties. We present the case of a 49-year-old woman with a 4-week history of diplopia and right superior eyelid swelling. Clinical, radiological, and histological examination led to the diagnosis of DLBCL of the right frontal sinus with anterior invasion of subcutaneous soft tissues and posterior intracranial involvement of the frontal region. She underwent three cycles of MATRIX chemotherapy, three cycles of R-DA-EPOCH, and CAR-T therapy. Unfortunately, treatments were unsuccessful and the patient died 11 months after diagnosis. In conclusion, an early diagnosis of DLBCL of the frontal sinus is difficult as it is often confused with other nasal pathologies. This causes a delay in treatment.

Keywords: diffuse large B-cell lymphoma; frontal sinus; lymphoma; paranasal sinus tumor; sinonasal neoplasm.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Patient presentation: 5 cm hard fixed bulging in the frontal region determining right proptosis.
Figure 2
Figure 2
Magnetic resonance imaging (MRI): uniformly enhanced mass in the right frontal sinus with anterior invasion of subcutaneous soft tissues, posterior intracranial involvement, and erosion of the anterior ethmoidal roof and lamina papyracea.
Figure 3
Figure 3
Magnetic resonance imaging (MRI) showing a partial response after chemotherapy with R-DA-EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab).

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