霍奇金淋巴瘤的多发性原发性口腔软组织表现——病例报告及文献复习。

Oral and maxillofacial surgery Pub Date : 2013-03-01 Epub Date: 2012-04-18 DOI:10.1007/s10006-012-0321-1
P W Kämmerer, E Schiegnitz, T Hansen, G F Draenert, H D Kuffner, M O Klein
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引用次数: 11

摘要

背景:霍奇金淋巴瘤(HL)是一种淋巴增生性肿瘤,组织学上由单核和多核霍奇金细胞和里德斯滕伯格细胞(HRS)组成。大约4%的头颈部淋巴恶性肿瘤是HL。典型的疾病表现为结节性病变。淋巴瘤累及结外、口腔软组织是非常罕见的。病例报告:一名73岁男性下颌骨左磨牙后区可疑溃疡病变被分配到我们医院。先前的抗炎治疗没有成功。随后,进行了三次活组织检查,结果显示只有炎症。最后,左侧臼齿后区和左侧内颊的两次活检显示HRS细胞CD15和CD30阳性表达,与霍奇金淋巴瘤相对应。未发现淋巴结或骨受累。患者被指定接受放化疗,但在诊断为多器官衰竭后3周死亡。在文献回顾中,连同本报告,发现9例原发性口腔黏膜HL。因此,这是第一例未累及淋巴结的口腔黏膜多发结外HL。讨论:表现为原发性口腔病变的HL的临床特征和影像学表现都不是典型的。特别是当只有少量活检标本可用时,组织学诊断仍然具有挑战性,可能导致治疗延误,并可能导致预后明显恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple primary enoral soft tissue manifestations of a Hodgkin lymphoma--case report and literature review.

Background: Hodgkin lymphoma (HL) are lymphoproliferative neoplasms, histologically comprising of mononuclear and multinucleated Hodgkin and Reed Sternberg cells (HRS). About 4 % of all lymphatic malignancies of the head and neck are HL. The typical disease presents itself as a nodal lesion. Extranodal, enoral soft tissue involvement by HL is very rare.

Case report: A 73-year-old man with a suspect, ulcerating lesion in the left retromolar region of the mandible was assigned to our hospital. Prior anti-inflammatory therapy has been without success. Subsequently, three biopsies were taken which could only show inflammation. Finally, two biopsies from the left retromolar region and the left inner cheek showed HRS cells with positive expressions of CD15 and CD30 corresponding to a Hodgkin lymphoma. No lymphatic node or bone involvement could be detected. The patient was designated to receive radio-chemotherapy, but died 3 weeks after diagnosis of multiple organ failure. In a literature review, together with this report, nine cases were found concerning primary HL of the oral mucosa. Accordingly, this is the first case of primary multiple extranodal HL in the oral mucosa in absence of lymphatic node involvement.

Discussion: Neither clinical features nor radiological appearances of HL presenting as primary enoral lesions are pathognomonic. Especially when only small biopsy specimens are available, histological diagnosis remains challenging, may lead to a delay in therapy and may result in a significant worse prognosis.

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