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Castleman’s Disease Presenting as a Parotid Mass in the Pediatric Population: A Report of 2 Cases

机译:小儿占腮腺肿块的Castleman病:2例报告

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Introduction. Angiofollicular lymph node hyperplasia (Castleman’s disease) is a nonmalignant lymphoproliferative disorder that generally involves the lymph nodes of young adults, most commonly in the mediastinum. Rarely, Castleman’s disease may present in the parotid gland. The disease can be further classified into unicentric or multicentric forms, with considerable differences in presentation, treatment, and prognosis.Case(s). We present cases of two pediatric patients, aged 7 and 11, who both presented with a slow-growing, painless parotid mass. In each case, the mass was excised via a superficial parotidectomy and the diagnosis made postoperatively upon further pathologic examination. At 6 months of follow-up, both had fully intact facial nerve function and no evidence of recurrence.Discussion. Castleman’s disease presents a diagnostic challenge in the head and neck region, as radiographic characteristics and fine needle aspiration results are often inconclusive. Definitive diagnosis requires surgical excision for pathologic examination. The unicentric form generally presents as a painless mass and can be successfully treated with complete excision. The multicentric form is associated with constitutional symptoms and its treatment remains controversial.Conclusion. Although rare, clinicians should be aware of both forms of Castleman’s disease when creating a differential diagnosis for parotid masses.
机译:介绍。血管滤泡性淋巴结增生(卡斯尔曼病)是一种非恶性淋巴增生性疾病,通常涉及年轻人的淋巴结,最常见于纵隔。罕见的是,腮腺炎可出现Castleman病。该疾病可进一步分为单中心型或多中心型,在表现,治疗和预后上有相当大的差异。我们介绍了两名年龄分别为7和11岁的小儿患者,他们均出现了缓慢增长的无痛腮腺肿块。在每种情况下,均通过腮腺浅表切除术切除肿块,并在进一步病理检查后进行诊断。随访6个月,两人的面神经功能均完整无损,无复发迹象。 Castleman病在头部和颈部区域提出了诊断挑战,因为放射线照相特征和细针抽吸结果通常尚无定论。明确的诊断需要手术切除以进行病理检查。单中心形式通常表现为无痛性肿块,可以完全切除成功治疗。多中心型与体质症状有关,其治疗仍存在争议。尽管很少见,但临床医生在对腮腺肿块进行鉴别诊断时应注意两种形式的卡斯曼病。

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