Mohan Suresh, DeNardo Bradley, Stachurski Dariusz, Greene Welch Jennifer, Groblewski Jan C
The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA; Division of Pediatric Hematology/Oncology, Hasbro Children's Hospital, Providence, RI 02903, USA.
Case Rep Otolaryngol. 2016;2016:6469073. doi: 10.1155/2016/6469073. Epub 2016 Mar 16.
Objectives. To describe the presentation and management of a child with Progressive Transformation of Germinal Centers (PTGC), an uncommon condition characterized by significant persistent lymphadenopathy, who developed papillary thyroid carcinoma and to explore and review potential links between PTGC and neoplastic processes in the head and neck. Methods. Case presentation and literature review are used. Results. A 10-year-old female presented with a right parotid mass and cervical lymphadenopathy. Multiple biopsies revealed PTGC without malignancy. Two years later, she developed fatigue and weight gain, and a thyroid nodule was found. Fine needle aspiration was strongly suggestive of papillary thyroid carcinoma. The patient underwent total thyroidectomy and central neck dissection without surgical management of the longstanding right lateral neck lymphadenopathy. Final pathology confirmed papillary thyroid carcinoma. She was treated with radioactive iodine therapy postoperatively and remains free of disease at three years of follow-up. Conclusions. PTGC is considered a benign condition but has previously been associated with Nodular Lymphocyte Predominant Hodgkin Lymphoma (NLPHL). This is the first reported case of papillary thyroid cancer in a child with preexisting cervical PTGC and no defined risk factors for thyroid malignancy. No link has been established with thyroid carcinoma, but patients with PTGC may have a defect in immune surveillance that predisposes them to malignancy.
目的。描述一名患有生发中心进行性转化(PTGC)的儿童的临床表现及治疗情况,PTGC是一种罕见疾病,其特征为显著的持续性淋巴结肿大,该患儿后来发生了甲状腺乳头状癌,并探讨和回顾PTGC与头颈部肿瘤性病变之间的潜在联系。方法。采用病例报告及文献回顾。结果。一名10岁女性患儿出现右侧腮腺肿块及颈部淋巴结肿大。多次活检显示为无恶性病变的PTGC。两年后,她出现疲劳和体重增加,发现甲状腺结节。细针穿刺高度提示为甲状腺乳头状癌。该患者接受了全甲状腺切除术及中央区颈部淋巴结清扫术,但未对长期存在的右侧颈部淋巴结肿大进行手术处理。最终病理确诊为甲状腺乳头状癌。术后她接受了放射性碘治疗,随访三年时仍无疾病复发。结论。PTGC被认为是一种良性疾病,但此前曾与结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)相关。这是首例报道的患有颈部PTGC且无明确甲状腺恶性风险因素的儿童发生甲状腺乳头状癌的病例。虽然尚未确定与甲状腺癌存在关联,但PTGC患者可能存在免疫监视缺陷,使其易患恶性肿瘤。