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Diffuse Large B-cell Lymphoma Presenting as an Oops Lesion in the Nasolabial Fold: A Case Report

Authors
Heo, Young JinBaek, Hye JinLee, Yoon JungKoh, Hyun Min
Issue Date
Dec-2022
Publisher
NLM (Medline)
Keywords
Cysts; diffuse large B-cell lymphoma; face; nasolabial fold; non-Hodgkin lymphoma; ultrasonography
Citation
Current medical imaging, v.19, no.7, pp 784 - 787
Pages
4
Indexed
SCIE
SCOPUS
Journal Title
Current medical imaging
Volume
19
Number
7
Start Page
784
End Page
787
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/59545
DOI
10.2174/1573405619666221125143942
ISSN
1573-4056
1875-6603
Abstract
BACKGROUND: Diffuse large B-cell lymphomas are the most common type of non-Hodgkin lymphoma. Because cutaneous lymphomas predominantly originate from the T cells, primary cutaneous diffuse large B-cell lymphomas are considered a rare subtype of extranodal diffuse large B-cell lymphomas that commonly involve the subcutaneous tissues of the trunk and extremities. To date, only a single case of facial primary cutaneous diffuse large B-cell lymphoma has been reported in the literature. CASE REPORT: We present a case of primary cutaneous diffuse large B-cell lymphoma presented with a small painless nodule in the right nasolabial fold that had persisted for 10 days in a 67-year-old man. Ultrasonographic findings of this lesion mimicked the features of a complicated epidermal inclusion cyst. Primary cutaneous diffuse large B-cell lymphoma was confirmed by an excisional biopsy of the mass. CONCLUSION: The diagnosis of primary cutaneous diffuse large B-cell lymphomas presenting as oops lesions in daily clinical practice can be challenging due to their rarity and nonspecific clinical and radiological findings. Therefore, clinical suspicion and awareness are critical for the accurate diagnosis and management of patients with palpable soft tissue masses in the head and neck region. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.
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