Diffuse B-cell lymphoma of the mandible disguised as acute osteomyelitis

Devina Adalja, Ariana Tagliaferri, Abraam Rezkalla, Basil Taha
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Abstract

Background: Primary bone lymphoma (PBL) is a rare form of extra nodal non-Hodgkin’s lymphoma (NHL). Case description: We describe a 39-year-old-male with no medical history who presented with unilateral facial swelling following a tooth extraction. Initial diagnoses after various presentations over the course of three weeks, based on inflammatory and infectious aetiologies. However, the patient was ultimately diagnosed with diffuse large B-cell lymphoma. Discussion: Symptoms of PBL are very similar to inflammatory and infectious diseases of the bone, such as osteomyelitis or osteonecrosis. Clinical features of PBL involving the head and neck include persistent jaw pain, tooth mobility secondary to extensive destruction of bone, and in advanced cases, lip numbness and swelling. On examination it may present as an exposed necrotic bone with surrounding soft tissue oedema. Misdiagnosis of these lesions as an infectious or inflammatory aetiology may lead to an unnecessary delay in lymphoma treatment, and subsequently worsen the prognosis if caught at a later stage. Therefore, any concerning lesion, especially in the oral cavity, must be subjected to early histopathological evaluation to differentiate PBL from osteomyelitis and/or osteonecrosis. Conclusion: This case report highlights the importance of an early histopathological evaluation to prevent delay in the diagnosis of primary bone lymphomas.
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伪装成急性骨髓炎的下颌骨弥漫性B细胞淋巴瘤
背景:原发性骨淋巴瘤(PBL原发性骨淋巴瘤(PBL)是一种罕见的结节外非霍奇金淋巴瘤(NHL)。病例描述我们描述了一名无病史的 39 岁男性患者,拔牙后出现单侧面部肿胀。在三周内出现各种表现后,初步诊断为炎症性和感染性病因。然而,患者最终被诊断为弥漫大 B 细胞淋巴瘤。讨论:PBL的症状与骨髓炎或骨坏死等骨科炎症和感染性疾病非常相似。累及头颈部的PBL临床特征包括持续性下颌疼痛、继发于骨质广泛破坏的牙齿移动,晚期病例还会出现嘴唇麻木和肿胀。检查时可表现为骨头外露坏死,周围软组织水肿。将这些病变误诊为感染性或炎症性病因可能会导致淋巴瘤治疗的不必要延误,如果晚期发现,预后也会恶化。因此,任何相关病变,尤其是口腔内的病变,都必须及早进行组织病理学评估,以区分 PBL 与骨髓炎和/或骨坏死。结论:本病例报告强调了早期组织病理学评估的重要性,以防延误原发性骨淋巴瘤的诊断。
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