Thewjitcharoen Yotsapon, Krittiyawong Sirinate, Butadej Siriwan, Nakasatien Soontaree, Polchart Somsong, Junyangdikul Pairoj, Kanchanapituk Auchai, Himathongkam Thep
Diabetes and Thyroid Center, Theptarin Hospital.
Division of Anatomical and Clinical Pathology, Samitivej Srinakarin Hospital, Bangkok, Thailand.
Medicine (Baltimore). 2020 Apr;99(16):e19892. doi: 10.1097/MD.0000000000019892.
The unpredictability of thyroid cancer can be striking, as the disease may rapidly progress to death in some individuals. Herein, we reported a rare case of aggressive papillary thyroid cell carcinoma (PTC) in an elderly patient de-differentiated into squamous cell carcinoma (SCC).
We describe a case of a 79-year-old Thai woman presented with hoarseness and neck mass for 2 months and she had been diagnosed with a 3-cm papillary thyroid carcinoma (PTC) in the right side of the thyroid gland. Later on PTC de-differentiated into SCC within 3 years after initial presentation.
De-differentiation from papillary thyroid carcinoma to squamous cell carcinoma.
The patient underwent a total thyroidectomy at the initial hospital and received high dose radioactive iodine (RAI) treatment at our hospital 1 month following the surgery and then was lost to follow-up. Two years later she came back with new development of right solid-cystic neck mass which was found to be recurrent PTC. A radical neck dissection was done and another high dose RAI treatment was given. However, she developed recurrent mass with tenderness at the site above previous solid cystic mass 6 months later. Re-exploration of the neck mass revealed an inflamed midline mass 2 cm with enlarged right lateral cervical lymph nodes.
A histopathological examination of the midline neck mass showed poorly differentiated SCC with lymphatic invasion. The intermingling of two morphologically distinct tumors, a typical PTC and a poorly differentiated SCC, had been identified in 1 out of 14 excised cervical lymph nodes. The patient underwent external beam radiation without chemotherapy. She is still in stable condition at 18 months post-treatment.
This case clearly demonstrated that SCC transformed from a pre-existing PTC. The clinician should consider a possible transformation of papillary thyroid cancer into more aggressive histological types in elderly patients who present with rapidly progressive clinical behavior. However, some patients could have long-term survival if the tumor did not transform into anaplastic thyroid cancer.
甲状腺癌的不可预测性可能非常显著,因为该疾病在某些个体中可能迅速发展至死亡。在此,我们报告了一例罕见的侵袭性甲状腺乳头状细胞癌(PTC),发生在一名老年患者身上,该肿瘤已去分化为鳞状细胞癌(SCC)。
我们描述了一例79岁的泰国女性,出现声音嘶哑和颈部肿块2个月,她被诊断为甲状腺右侧叶有一个3厘米的甲状腺乳头状癌(PTC)。初次就诊后3年内,PTC去分化为SCC。
从甲状腺乳头状癌去分化为鳞状细胞癌。
患者在最初的医院接受了全甲状腺切除术,并在术后1个月在我院接受了高剂量放射性碘(RAI)治疗,随后失访。两年后,她因右侧实性囊性颈部肿块再次出现而回来就诊,发现是复发性PTC。进行了根治性颈清扫术,并再次给予高剂量RAI治疗。然而,6个月后她在先前实性囊性肿块上方的部位出现了有压痛的复发性肿块。对颈部肿块进行再次探查发现一个2厘米的中线炎性肿块,右侧颈外侧淋巴结肿大。
对中线颈部肿块的组织病理学检查显示为低分化SCC伴淋巴浸润。在14个切除的颈部淋巴结中,有1个发现了两种形态学上不同的肿瘤混合存在,一种是典型的PTC,另一种是低分化SCC。患者接受了外照射放疗,未进行化疗。治疗后18个月她仍处于稳定状态。
该病例清楚地表明SCC是由先前存在的PTC转化而来。对于临床表现迅速进展的老年患者,临床医生应考虑甲状腺乳头状癌可能转化为更具侵袭性的组织学类型。然而,如果肿瘤没有转化为未分化甲状腺癌,一些患者可能会长期存活。