[下颌骨管扩大和下唇感觉减退显示下颌骨非霍奇金淋巴瘤]。

F Hakkou, S Chbicheb, W El Wady
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引用次数: 0

摘要

简介:原发性淋巴瘤的下颌骨是罕见的,最常表现为无痛肿胀。它们常与牙源性病变相混淆。因此,他们的诊断被推迟了。作者报告了一个孤立的下颌淋巴瘤的情况下,下唇的感觉减退和扩大的左侧下颌管。病例报告:一名35岁的女性患者因半下颌疼痛和左唇感觉减退而就诊。临床上,我们注意到在牙齿前面有一个前庭肿瘤。全景x线片显示左侧下颌骨管广泛扩大,从下颌孔延伸至颏孔。活检显示为b细胞淋巴瘤。没有找到其他本地化。经过7个疗程的基于R-CHOP的化疗和局部放疗后,患者在治疗18个月后缓解。讨论:原发性下颌骨淋巴瘤是罕见的;约占结外非霍奇金淋巴瘤的0.6%。它发生在任何年龄,主要影响男性。它们通常表现为无痛的肿胀,有时在口腔中溃烂。它们经常被误诊为牙齿问题。治疗方法包括放疗和/或化疗。骨淋巴瘤的预后比其他骨恶性肿瘤好,5年生存率为40-50%。
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[Enlargement of mandibular canal and lower lip hypoesthesia revealing non-Hodgkin’s lymphoma of the mandible].

Introduction: Primary lymphoma of the mandible are rare and most often revealed by painless swelling. They are often confused with odontogenic lesions. Hence, their diagnosis is delayed. The authors report the case of an isolated mandibular lymphoma revealed by hypoesthesia of the lower lip and enlargement of the left mandibular canal.

Case report: A 35-year-old woman patient consulted for hemi-mandibular pain with episodes of left labial hypoesthesia. Clinically, we noted the presence of a vestibular tumor in front of tooth 34. A panoramic radiograph revealed that the left mandibular canal was widely enlarged, extending from the mandibular foramen to the mental foramen. The biopsy revealed a B-cell lymphoma. No other localization was found. After treatment with seven courses of a chemotherapy based on R-CHOP followed by local radiotherapy, the patient was in remission eighteen months after treatment.

Discussion: Primitive lymphoma of the mandible are rare; they represent about 0.6% of extra-nodal non-Hodgkin lymphoma. They occur at any age and mainly affect males. They most often come out as a painless swelling, sometimes ulcerated in the mouth. They are often misdiagnosed as a dental problem. Treatment combines variably radiotherapy and/or chemotherapy. The prognosis of bone lymphoma is more favorable than others malignancies bone, with a survival rate of 40-50% at five years.

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