Gezer Emre, Selek Alev, Tarkun İlhan, Cantürk Zeynep, Çetinarslan Berrin
Department of Endocrinology and Metabolism, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey.
J Med Case Rep. 2019 Apr 20;13(1):95. doi: 10.1186/s13256-019-2025-8.
Papillary thyroid carcinoma is the most common endocrine malignancy. Distant metastasis from differentiated thyroid carcinoma is infrequent and the metastasis rate of papillary thyroid carcinoma is lower than that of follicular thyroid carcinoma. Distant metastases from differentiated thyroid carcinoma are usually seen in the lungs and bones; however, renal metastasis is very rare.
Here we describe an 85-year-old Caucasian woman who presented with right flank pain 10 years ago. We describe a case of papillary thyroid carcinoma presenting as a primary renal tumor with extensive pulmonary and bone metastases. Abdominal screening with computed tomography revealed a mass on her right kidney, which was considered a primary renal cell carcinoma and she underwent a right nephrectomy. Unexpectedly, papillary thyroid carcinoma metastasis was diagnosed from demonstrative histopathological findings, such as positive immunoperoxidase staining for thyroglobulin. A total thyroidectomy was performed. Unenhanced thoracic computed tomography and skeletal scintigraphy revealed bilateral multiple nodules in her lungs and bone metastasis on T10 vertebra and right sacroiliac joint. Initially, 30 Gy radiotherapy was implemented to her T9-10 vertebrae and then she was treated with a total of 800 mCi radioactive iodine for ablation. A radioactive iodine whole body scan was performed after each 200 mCi and continuous progression was shown in each scan. After she was lost to follow-up for 3 years, she referred to our clinic again with a draining mass on her neck and we planned radiotherapy to this giant mass.
Our patient was surprisingly still alive after metastatic disease was diagnosed 10 years ago and she had no major complaint other than a draining mass on her neck. Our primary aim by sharing this case is to underline potential renal metastasis from papillary thyroid carcinoma. In other words, when approaching primary renal tumors, possible distant metastases of other organs need to be kept in mind for differential diagnosis. In addition, it should be noted that if managed appropriately, the long-term survival in patients with papillary thyroid carcinoma with multiple organ metastases could be encouraging.
甲状腺乳头状癌是最常见的内分泌恶性肿瘤。分化型甲状腺癌的远处转移并不常见,且甲状腺乳头状癌的转移率低于滤泡状甲状腺癌。分化型甲状腺癌的远处转移通常见于肺和骨;然而,肾转移非常罕见。
在此,我们描述一位85岁的白种女性,她10年前出现右侧胁腹疼痛。我们报告一例甲状腺乳头状癌表现为原发性肾肿瘤并伴有广泛肺和骨转移的病例。腹部计算机断层扫描筛查发现其右肾有一肿块,当时被认为是原发性肾细胞癌,她接受了右肾切除术。出乎意料的是,通过免疫过氧化物酶染色甲状腺球蛋白呈阳性等典型组织病理学发现确诊为甲状腺乳头状癌转移。随后进行了甲状腺全切术。胸部非增强计算机断层扫描和骨闪烁显像显示双肺多发结节以及T10椎体和右骶髂关节骨转移。最初,对其T9 - 10椎体实施了30 Gy的放疗,然后总共给予800 mCi放射性碘进行消融治疗。每次给予200 mCi放射性碘后均进行放射性碘全身扫描,每次扫描均显示病情持续进展。在失访3年后,她因颈部有一引流性肿块再次就诊于我们的诊所,我们计划对这个巨大肿块进行放疗。
我们的患者在10年前被诊断为转移性疾病后仍令人惊讶地存活,除颈部有一引流性肿块外无其他主要不适。我们分享这个病例的主要目的是强调甲状腺乳头状癌潜在的肾转移。换句话说,在处理原发性肾肿瘤时,需要考虑其他器官可能的远处转移以进行鉴别诊断。此外,应该注意的是,如果处理得当,甲状腺乳头状癌多器官转移患者的长期生存情况可能令人鼓舞。