Department of Surgery, AIIMS, New Delhi, India.
Department of Pathology, AIIMS, New Delhi, India.
J Med Case Rep. 2024 Nov 1;18(1):535. doi: 10.1186/s13256-024-04835-2.
Coexisting parathyroid adenoma, thyroid carcinoma, and tuberculosis of thyroid is a very rare phenomenon. Primary thyroid tuberculosis is itself very rare despite high global prevalence of tuberculosis in developing countries. Majority of thyroid tuberculosis identified in postoperative histopathology or cytopathology. The coexistence of thyroid cancer with tuberculosis or parathyroid adenoma has been reported in the literature but not a single case of the three pathologies coexisting together has been found in the literature published. We are presenting a rare case of a constellation of synchronous parathyroid adenoma, thyroid carcinoma, and thyroid tuberculosis. This case report will provoke researchers to work on understanding the association of hypercalcemia or chronic inflammation leading to development of malignancy or parathyroid adenoma in the presence of hypothyroidism will give future perspective in managing such patients.
A Islam lady aged 45 years old, diagnosed with hypothyroidism, was evaluated for pregnancy loss and rapid weight gain from 13 years back and started on tablets of levothyroxine 25 µg once daily. She was doing well until the past 2 years; there after she noticed insidious onset of a swelling over anterior aspect of right side of the neck and bone pain in back and lower limbs. Patient underwent routine investigations and was found to have raised serum calcium (11.4 mg/dl) and parathyroid hormone (253 pg/ml). Anti-thyroid peroxidase (TPO) and anti-thyroglobulin (Tg) level were normal. Ultrasounds showed multiple nodules in both lobe of thyroid and left inferior parathyroid adenoma. The patient underwent total thyroidectomy with left inferior parathyroidectomy, and final histopathology showed features of subacute granulomatous thyroiditis along with hurthle cell change in right lobe of thyroid. The left lobe additionally showed necrotizing epitheloid cell granulomas, which on Zeihl-Neelson staining revealed presence of acid-fast bacilli. Sections from the isthmus show a focus of papillary thyroid microcarcinoma. The left inferior parathyroid gland sent as a frozen sample was found to be parathyroid adenoma. On 6-month follow-up, the patient was feeling much relief in bone pain and tolerating antitubercular drugs uneventfully.
Coexistence of parathyroid adenoma, nonmedullary thyroid carcinoma, and thyroid tuberculosis is extremely rare. Surgery is curative for hyper parathyroidism and thyroid carcinoma. Thyroid tuberculosis responds well to current antitubercular drugs. Its etiology needs to be explored more; the probable hypothesis is chronic inflammation due to latent tuberculosis might leads to development of thyroid carcinoma and parathyroid adenoma. Further studies need to be done for better understanding of underlying mechanism and better management options for such patients. To the best of our knowledge, similar cases have not been reported.
甲状旁腺腺瘤、甲状腺癌和甲状腺结核同时存在是一种非常罕见的现象。尽管发展中国家的结核病全球发病率很高,但原发性甲状腺结核本身就非常罕见。大多数甲状腺结核是在术后组织病理学或细胞学检查中发现的。尽管文献中已有甲状腺癌与结核病或甲状旁腺腺瘤同时存在的报道,但尚未发现文献中有这三种病变同时存在的单一病例。我们报告了一例甲状旁腺腺瘤、甲状腺癌和甲状腺结核同时存在的罕见病例。本病例报告将促使研究人员深入研究高钙血症或慢性炎症与甲状腺功能减退症导致恶性肿瘤或甲状旁腺腺瘤发展之间的关系,为管理此类患者提供未来的视角。
一位 45 岁的伊斯兰女性,被诊断为甲状腺功能减退症,因流产和 13 年前开始的体重迅速增加而接受评估,并开始每天服用左旋甲状腺素 25 µg。直到过去 2 年,她的病情一直很好;此后,她注意到右侧颈前出现逐渐出现肿胀,并伴有背部和下肢骨痛。患者接受了常规检查,发现血清钙(11.4mg/dl)和甲状旁腺激素(253pg/ml)升高。抗甲状腺过氧化物酶(TPO)和抗甲状腺球蛋白(Tg)水平正常。超声显示甲状腺两叶多发结节和左侧下甲状旁腺腺瘤。患者接受了全甲状腺切除术和左侧下甲状旁腺切除术,最终组织病理学显示右侧甲状腺亚急性肉芽肿性甲状腺炎伴 Hurthle 细胞改变。左叶另外显示坏死性上皮样细胞肉芽肿,Zeihl-Neelson 染色显示有抗酸杆菌。峡部切片显示一个乳头状甲状腺微癌灶。作为冷冻样本送检的左侧下甲状旁腺腺被发现为甲状旁腺腺瘤。在 6 个月的随访中,患者骨痛明显缓解,能够耐受抗结核药物。
甲状旁腺腺瘤、非髓样甲状腺癌和甲状腺结核同时存在极为罕见。手术是治疗甲状旁腺功能亢进和甲状腺癌的有效方法。甲状腺结核对目前的抗结核药物反应良好。其病因需要进一步探讨;可能的假设是潜伏性结核病引起的慢性炎症可能导致甲状腺癌和甲状旁腺腺瘤的发展。需要进一步研究以更好地了解潜在机制,并为此类患者提供更好的管理选择。据我们所知,尚未有类似病例报告。