甲状腺乳头状癌和霍奇金淋巴瘤的同步原发性恶性肿瘤:干预措施和结果。

IF 0.6 4区 医学 Q4 PATHOLOGY
Malaysian Journal of Pathology Pub Date : 2023-08-01
A Abd Rahim, R Muhammad, F Ismail, Y P Wong, R Che Abdul Aziz, G Y Chong, W F Wan Jamaludin
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引用次数: 0

摘要

甲状腺癌并不常见。乳头状甲状腺癌(PTC)代表了分化甲状腺癌的大多数,是先前暴露于电离辐射的公认并发症。更罕见的是PTC与霍奇金淋巴瘤(HL)作为多发性原发恶性肿瘤同时发生。我们报告一个33岁的三个孩子的母亲谁发展无症状甲状腺结节四年,颈部肿胀最近十个月。她否认有体质症状或B型症状,甲状腺检查正常。最初,基于超声扫描发现左侧甲状腺肿大和锁骨上淋巴结(LN)肿大,怀疑甲状腺转移癌。然而,甲状腺结节的细针穿刺检查尚无定论,锁骨上淋巴结怀疑为HL。计算机断层扫描发现甲状腺有一个大肿块,纵隔、肺门、隆突下和腋窝有淋巴结病变,尺寸可达6厘米。左侧半甲状腺切除术合并左侧锁骨上淋巴结活检显示左侧甲状腺叶PTC大小为38 x 25 x 18 mm,左侧锁骨上淋巴结不确定为HL。右侧完成甲状腺切除术,双侧中央颈部清扫及右侧锁骨上淋巴结切除术活检显示右侧锁骨上淋巴结存在HL,右侧中央淋巴结存在HL和转移性PTC。经过多学科的讨论,患者在术后四周接受化疗并完全缓解。鉴于罕见病例,本报告强调了在缺乏既定指南的情况下以患者为中心的方法和多学科共识的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synchronous primary malignancies of papillary thyroid carcinoma and Hodgkin lymphoma: Interventions and outcome.

Thyroid carcinoma is uncommon. Papillary thyroid carcinoma (PTC) represents the majority of differentiated thyroid carcinoma and is a recognised complication of prior exposure to ionizing radiation. Even more uncommon is the synchronous occurrence of PTC with Hodgkin lymphoma (HL) as multiple primary malignancies. We report a 33-year-old mother of three who developed asymptomatic thyroid nodule for four years, and neck swelling for the recent ten months. She denied constitutional symptoms or B symptoms, and thyroid profiles were normal. Initially, metastatic thyroid cancer was suspected based on ultrasound scan findings of enlarged left thyroid gland and enlarged supraclavicular lymph nodes (LN). However, fine needle aspiration examinations of the thyroid nodule were inconclusive, and the supraclavicular LN was suspicious of HL. Computerised tomography scan detected a large mass at the thyroid glands and lymphadenopathies in the mediastinal, hilar, subcarinal and axilla with dimensions up to 6 cm. Left hemi-thyroidectomy with left supraclavicular LN biopsy revealed PTC in the left thyroid lobe measuring 38 x 25 x 18 mm, and the left supraclavicular LN was not definitive of HL. Completion thyroidectomy on the right side, bilateral central neck dissection and excision biopsy of the right supraclavicular LN revealed the presence of HL in the right supraclavicular LN, and both HL and metastatic PTC in right central LN. After multidisciplinary discussions, the patient received chemotherapy at four weeks postoperatively and achieved complete remission. This report highlights the importance of patient-centered approach and multidisciplinary consensus within lack of established guidelines, given rarity of the case.

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来源期刊
CiteScore
3.60
自引率
5.60%
发文量
34
期刊介绍: The Malaysian Journal of Pathology is the official journal of the College of Pathologists, Academy of Medicine Malaysia. The primary purpose of The Journal is to publish the results of study and research in Pathology, especially those that have particular relevance to human disease occurring in Malaysia and other countries in this region. The term PATHOLOGY will be interpreted in its broadest sense to include Chemical Pathology, Cytology, Experimental Pathology, Forensic Pathology, Haematology, Histopathology, Immunology, Medical Microbiology and Parasitology. The Journal aims to bring under one cover publications of regional interest embracing the various sub-specialities of Pathology. It is expected that the articles published would be of value not only to pathologists, but also to medical practitioners in search of a scientific basis for the problems encountered in their practice, and to those with an interest in diseases which occur in the tropics.
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