Said Anajar, Abire Allaoui, Soukaina Laidi, Hind Alatawna, Loubna Taali, Ilias Tahiri, Amal Hajjij, Mustapha Saadi, Mohammed Zalakh, Fouad Benariba
ENT Department, Face and Neck Surgery, Hospital Cheikh Khalifa, Mohammed VI University of Health Sciences, Casablanca, Morocco.
internal Medecin Department, Hospital Cheikh Khalifa, Mohammed VI University of Health Sciences, Casablanca, Morocco.
Ann Med Surg (Lond). 2022 Jun 15;79:103994. doi: 10.1016/j.amsu.2022.103994. eCollection 2022 Jul.
Parathyroid carcinoma (PC) is considered a rare and uncommon malignancy. Its prevalence is about 0.005% of all cancers. Intrathyroidal location is rare, rendering preoperative diagnosis tedious. Until now, around 700 cases of PC have been documented, reportedly, among them, less than 21 cases of intrathyroidal parathyroid carcinoma have been described in the literature. We report a case of intrathyroidal PC that was taken for a suspicious thyroid nodule, with a literature review.PRESENTATION OF THE CASE: Our case is an asymptomatic intrathyroidal PC imitating a suspicious thyroid nodule, in a 54-year-old woman. A literature review was performed about clinical, radiological features, histopathological findings, and therapeutic options.
The diagnosis of asymptomatic intrathyroidal parathyroid carcinoma, similar to our case report, is even more difficult, our patient had no symptoms of hypercalcemia. Surgery is the cornerstone of the treatment. A better chance to cure this disease is conditioned by complete surgical resection with negative margins microscopically, that was the case of our patient with a very good clinical course after 12 months of follow-up.
甲状旁腺癌(PC)被认为是一种罕见的恶性肿瘤。其患病率约占所有癌症的0.005%。甲状腺内定位罕见,使得术前诊断繁琐。到目前为止,据记载约有700例甲状旁腺癌病例,据报道,其中文献中描述的甲状腺内甲状旁腺癌病例不到21例。我们报告一例甲状腺内甲状旁腺癌病例,该病例最初被误诊为可疑甲状腺结节,并进行文献复习。
我们的病例是一名54岁女性,患有模仿可疑甲状腺结节的无症状甲状腺内甲状旁腺癌。对临床、放射学特征、组织病理学发现和治疗选择进行了文献复习。
与我们的病例报告相似,无症状甲状腺内甲状旁腺癌的诊断更加困难,我们的患者没有高钙血症症状。手术是治疗的基石。治愈这种疾病的更好机会取决于显微镜下切缘阴性的完全手术切除,我们的患者就是如此,随访12个月后临床过程良好。