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首发为疼痛性牙龈肿胀和牙齿松动的散发性伯基特淋巴瘤:一次挽救生命的转诊

Sporadic Burkitt Lymphoma First Presenting as Painful Gingival Swellings and Tooth Hypermobility: A Life-Saving Referral.

作者信息

Papadopoulou Erofili, Kouri Maria, Velonis Dimitrios, Andreou Anastasia, Georgaki Maria, Damaskos Spyridon, Piperi Evangelia, Delli Konstantina, Karoussis Ioannis K, Vlachou Antonia, Avgerinou Georgia, Kattamis Antonis, Nikitakis Nikolaos G

机构信息

Department of Oral Medicine & Pathology and Hospital Dentistry, School of Dentistry, National and Kapodistrian University of Athens (NKUA), Greece 2 Thivon Street, 11527 Athens, Greece.

Department of Oral Diagnosis and Radiology, School of Dentistry, National and Kapodistrian University of Athens (NKUA), 11527 Athens, Greece.

出版信息

Dent J (Basel). 2024 Dec 25;13(1):6. doi: 10.3390/dj13010006.

Abstract

Burkitt lymphoma (BL) is an aggressive non-Hodgkin lymphoma (NHL), subdivided into endemic, sporadic, and immunodeficiency-associated forms. While jaw lesions are common in endemic BL, they are infrequent in sporadic cases, only rarely constituting the first manifestation of the disease. The aim of this study is to present a rare pediatric case of sporadic BL first manifesting as gingival swellings and tooth hypermobility and provide a review of all the published sporadic BL case reports as the first sign of disease. An 11-year-old Caucasian female was referred for the evaluation of hypermobility of posterior lower teeth, associated with painful gingival swellings of 20 days duration. Clinical examination revealed right facial asymmetry and bilateral prominent swellings of the posterior lower gingiva. A panoramic radiograph revealed ill-defined radiolucent lesions in the posterior mandible bilaterally. On computed tomography, soft-tissue masses were identified along the mandibular ramus extending into the maxillary sinus bilaterally. The histopathologic and immunohistochemical analyses of the lesions led to a diagnosis of Burkitt lymphoma (BL). The patient underwent a full staging work-up, revealing bone marrow involvement and widespread disease. A multi-chemotherapy regimen was initiated with the regression of oral lesions and symptoms within a few weeks and complete disease remission after nine chemotherapy cycles. The patient remains free of disease 11 years later. This case underscores the critical importance of the timely diagnosis and life-saving referral of rapidly growing jaw lesions, which may represent the first sign of an underlying lymphoreticular malignancy with aggressive course, such as BL.

摘要

伯基特淋巴瘤(BL)是一种侵袭性非霍奇金淋巴瘤(NHL),分为地方性、散发性和免疫缺陷相关型。虽然颌部病变在地方性BL中很常见,但在散发性病例中并不常见,很少作为疾病的首发表现。本研究的目的是报告一例罕见的儿童散发性BL,首发表现为牙龈肿胀和牙齿松动,并对所有已发表的以疾病首发症状为表现的散发性BL病例报告进行综述。一名11岁的白种女性因下颌后牙松动伴持续20天的疼痛性牙龈肿胀而前来评估。临床检查发现右侧面部不对称,双侧下颌后牙龈明显肿胀。全景X线片显示双侧下颌后缘有边界不清的透射性病变。计算机断层扫描显示沿下颌支双侧有软组织肿块延伸至上颌窦。病变的组织病理学和免疫组化分析诊断为伯基特淋巴瘤(BL)。患者接受了全面的分期检查,发现骨髓受累及广泛病变。开始采用多药化疗方案,几周内口腔病变和症状消退,九个化疗周期后疾病完全缓解。11年后患者仍无疾病复发。该病例强调了及时诊断和将快速生长的颌部病变转诊以挽救生命的至关重要性,这些病变可能是侵袭性病程的潜在淋巴网状恶性肿瘤(如BL)的首发症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2217/11764000/172703174a0a/dentistry-13-00006-g001.jpg

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