Adalja Devina, Tagliaferri Ariana, Rezkalla Abraam, Taha Basil
Department of Internal Medicine, St Joseph's University Medical Center, Paterson, USA.
Department of Gastroenterology and Transplant Hepatology, Creighton University, Phoenix, USA.
Eur J Case Rep Intern Med. 2024 Jan 22;11(2):004243. doi: 10.12890/2024_004243. eCollection 2024.
Primary bone lymphoma (PBL) is a rare form of extra nodal non-Hodgkin's lymphoma (NHL).
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.
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.
This case report highlights the importance of an early histopathological evaluation to prevent delay in the diagnosis of primary bone lymphomas.
Resemblance in symptoms: Primary bone lymphoma (PBL) symptoms overlap with bone infections, necessitating careful consideration and differential diagnosis to prevent misjudgment.Head and neck manifestations: recognising PBL's signs in the head and neck region, such as jaw pain and bone destruction, aids in timely identification and treatment.Timely biopsy significance: swift histopathological assessment for suspicious lesions is critical to avoid delays in diagnosing primary bone lymphomas.
原发性骨淋巴瘤(PBL)是结外非霍奇金淋巴瘤(NHL)的一种罕见形式。
我们报告一名39岁男性,无病史,在拔牙后出现单侧面部肿胀。在三周的病程中,基于炎症和感染病因进行了各种诊断。然而,该患者最终被诊断为弥漫性大B细胞淋巴瘤。
PBL的症状与骨的炎症和感染性疾病非常相似,如骨髓炎或骨坏死。累及头颈部的PBL的临床特征包括持续性颌骨疼痛、由于广泛骨质破坏导致的牙齿松动,以及在晚期出现唇部麻木和肿胀。检查时可能表现为暴露的坏死骨伴有周围软组织水肿。将这些病变误诊为感染性或炎症性病因可能导致淋巴瘤治疗的不必要延迟,如果在晚期才发现,随后会使预后恶化。因此,任何可疑病变,尤其是口腔内的病变,必须尽早进行组织病理学评估,以将PBL与骨髓炎和/或骨坏死区分开来。
本病例报告强调了早期组织病理学评估对于预防原发性骨淋巴瘤诊断延迟的重要性。
症状相似性:原发性骨淋巴瘤(PBL)的症状与骨感染重叠,需要仔细考虑和鉴别诊断以防止误诊。头颈部表现:认识到PBL在头颈部区域的体征,如颌骨疼痛和骨质破坏,有助于及时识别和治疗。及时活检的意义:对可疑病变进行快速组织病理学评估对于避免原发性骨淋巴瘤诊断延迟至关重要。