Unicentric Castleman disease in intraparotid lymph node: a case report.

IF 3.5 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Young Heon Jeong, Jin Seok Kim, Heonwoo Lee, Kang-Min Ahn
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引用次数: 0

Abstract

Background: Castleman disease (CD) is a rare lymphoproliferative disorder characterized by non-neoplastic lymph node hyperplasia. Unicentric Castleman disease (UCD), the most common clinical form, typically presents as a solitary, asymptomatic mass. Involvement of intraparotid lymph nodes is rare and often mimics salivary gland neoplasms, complicating preoperative diagnosis.

Case presentation: A 35-year-old female presented with a painless, enlarging mass in the left parotid region. Contrast-enhanced CT revealed a well-demarcated, homogeneously enhancing mass with additional smaller lesions in adjacent lymph node regions. A conservative excisional approach was performed with preservation of the facial nerve. Histopathological evaluation confirmed the hyaline-vascular variant of UCD. Postoperative follow-up showed spontaneous regression of adjacent lymphadenopathy and resolution of transient facial nerve palsy.

Conclusion: CD should be considered in the differential diagnosis of encapsulated parotid masses with associated lymphadenopathy. Recognizing its clinical and radiologic features may facilitate accurate diagnosis and prevent overtreatment. Complete surgical excision is curative in most UCD cases.

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腮腺内淋巴结单中心Castleman病1例报告。
背景:Castleman病(CD)是一种罕见的以非肿瘤性淋巴结增生为特征的淋巴增生性疾病。单中心型Castleman病(UCD)是最常见的临床形式,通常表现为孤立的无症状肿块。腮腺内淋巴结的累及是罕见的,通常与唾液腺肿瘤相似,使术前诊断复杂化。病例介绍:35岁女性,左侧腮腺区无痛性肿物。增强CT显示一个界限清晰,均匀增强的肿块,并在邻近淋巴结区域有其他较小的病变。在保留面神经的情况下,采用保守切除方法。组织病理学检查证实为透明血管型UCD。术后随访显示邻近淋巴结病变自发消退,短暂性面神经麻痹消退。结论:腮腺包膜性肿物合并淋巴结病的鉴别诊断应考虑CD。认识其临床和放射学特征有助于准确诊断和防止过度治疗。在大多数UCD病例中,完全手术切除是可以治愈的。
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来源期刊
Maxillofacial Plastic and Reconstructive Surgery
Maxillofacial Plastic and Reconstructive Surgery DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.30
自引率
13.00%
发文量
37
审稿时长
13 weeks
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