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改良除皱术治疗腮腺区巨大木村病:1例报告及手术治疗策略综述

Giant Kimura Disease of the Parotid Region Managed by Modified Rhytidectomy: A Case Report and Review of Surgical Treatment Strategies.

作者信息

Ishii Tatsuya, Matsuura Naoki, Ntege Edward H, Sunakawa Tomoe, Shimizu Yusuke

机构信息

Plastic and Reconstructive Surgery, University of the Ryukyus Hospital, Ginowan, JPN.

Pathology, University of the Ryukyus Hospital, Ginowan, JPN.

出版信息

Cureus. 2025 Jul 8;17(7):e87498. doi: 10.7759/cureus.87498. eCollection 2025 Jul.

Abstract

Kimura disease (KD) is a rare, chronic inflammatory disorder that typically presents as a painless mass in the head and neck region. It is histologically characterized by lymphoid follicular hyperplasia, eosinophilic infiltration, and vascular proliferation. We report the case of a 66-year-old Japanese man with an 18-year history of recurrent, treatment-resistant KD involving the right parotid region. He presented with a large (9×6.5 cm), well-defined, firm, immobile mass that caused significant facial asymmetry and earlobe ptosis. Surgical excision was performed using a modified rhytidectomy incision, which provided wide exposure and allowed for complete removal with minimal visible scarring. A superficial parotidectomy was performed without elevating the superficial musculoaponeurotic system layer, thus preserving postoperative facial symmetry. Histopathologic examination confirmed KD, revealing follicular hyperplasia with dense eosinophilic infiltration, consistent with the hallmark features of the disease. Diffusion-weighted imaging demonstrated a hyperintense lesion with no evidence of necrosis or invasive characteristics. The patient had an uneventful postoperative course and retained House-Brackmann Grade I facial nerve function. At his six-month follow-up, he exhibited restored facial symmetry, inconspicuous scarring, and no clinical or radiologic evidence of recurrence. This case highlights the importance of integrating aesthetic surgical principles into the management of benign inflammatory lesions in the parotid region, achieving excellent functional and cosmetic outcomes. Long-term surveillance remains ongoing to monitor for potential recurrence.

摘要

木村病(KD)是一种罕见的慢性炎症性疾病,通常表现为头颈部无痛性肿块。其组织学特征为淋巴滤泡增生、嗜酸性粒细胞浸润和血管增生。我们报告一例66岁日本男性病例,其右侧腮腺区复发性、难治性KD病史长达18年。他表现为一个大的(9×6.5厘米)、边界清晰、质地坚硬、固定不动的肿块,导致明显的面部不对称和耳垂下垂。手术切除采用改良除皱切口,该切口提供了广泛的暴露,并允许在最小可见瘢痕的情况下完全切除。在不掀起表浅肌肉腱膜系统层的情况下进行了浅叶腮腺切除术,从而保留了术后面部对称性。组织病理学检查确诊为KD,显示滤泡增生伴密集嗜酸性粒细胞浸润,与该疾病的标志性特征一致。扩散加权成像显示一个高信号病变,无坏死或侵袭性特征的证据。患者术后病程顺利,保留了House-Brackmann I级面神经功能。在他六个月的随访中,他表现出面部对称性恢复、瘢痕不明显,且无临床或影像学复发证据。该病例强调了将美容手术原则纳入腮腺区良性炎性病变管理的重要性,从而实现了良好的功能和美容效果。长期监测仍在进行中,以监测潜在的复发情况。

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