Myint Zin W, Chow Robert D
Department of Medicine, MedStar Good Samaritan Hospital, Baltimore, MD, USA;
Department of Medicine, University of Maryland Medical Center Midtown Campus, Baltimore, MD, USA.
J Community Hosp Intern Med Perspect. 2015 Feb 3;5(1):26360. doi: 10.3402/jchimp.v5.26360. eCollection 2015.
Sarcoidosis is an inflammatory disease characterized by non-caseating granulomas that can be present in diverse organ systems. Sarcoidosis can be associated with malignancy, presenting either preceding, during, or after chemotherapy. We herewith report a case of sarcoidosis mimicking cancer recurrence that developed after radioactive iodine therapy for papillary thyroid cancer.
A 68-year-old Caucasian woman was found to have an incidental mediastinal lymph node. She underwent biopsy, which revealed sarcoidosis. There was no further treatment or evidence of recurrence over the ensuing 9 years. She was then diagnosed with low-grade papillary thyroid cancer in the right posterior lobe and treated with total thyroidectomy followed by radioactive iodine therapy. Six months later, she was found to have elevated serum thyroglobulin. Post-remnant ablation scan showed increased tracer uptake in the bed of the thyroid. Though two thyroid ultrasound scans were negative, she was treated with I-131 for possible recurrence. She then developed right hip pain, prompting further investigation. Though a skeletal survey was negative, an 18-fluorodeoxyglucose positron emission tomography (PET) scan study revealed multiple hypermetabolic skeletal lesions in both humeri and the proximal left femur. In addition, hypermetabolic hilar and mediastinal nodes were noted. As widespread cancer metastasis was suspected, bone biopsy was performed, which showed non-caseating granulomas, consistent with recurrence of sarcoidosis.
Sarcoid lesions may mimic metastatic disease or recurrence in oncologic patients. Biopsy and histopathology examination should be performed to confirm the diagnosis. Recurrence or reactivation of sarcoidosis has been proposed to result from altered immunologic milieu because of the presence of either active cancer or its therapy. Teodorovic and colleagues postulated that the radioactive I-131 therapy leads to reduced secretion of Th2 cytokines such as interleukin (IL)-4, IL-5, and IL-13. Few case reports of sarcoidosis associated with papillary carcinoma have been published; this is the first report of systemic recurrence of sarcoidosis associated with papillary thyroid carcinoma after treatment with radioactive iodine therapy.
结节病是一种以非干酪样肉芽肿为特征的炎症性疾病,可累及多种器官系统。结节病可与恶性肿瘤相关,可在化疗前、化疗期间或化疗后出现。我们在此报告一例在放射性碘治疗甲状腺乳头状癌后出现类似癌症复发的结节病病例。
一名68岁的白种女性偶然发现纵隔淋巴结肿大。她接受了活检,结果显示为结节病。在随后的9年里,没有进一步的治疗或复发迹象。之后她被诊断出右后叶患有低级别甲状腺乳头状癌,并接受了全甲状腺切除术,随后进行了放射性碘治疗。六个月后,她的血清甲状腺球蛋白升高。残余甲状腺消融扫描显示甲状腺床处放射性示踪剂摄取增加。尽管两次甲状腺超声扫描均为阴性,但她仍接受了I-131治疗以排除可能的复发。随后她出现右髋部疼痛,促使进一步检查。尽管骨骼检查为阴性,但18氟脱氧葡萄糖正电子发射断层扫描(PET)研究显示双侧肱骨和左股骨近端有多个高代谢性骨骼病变。此外,还发现肺门和纵隔淋巴结高代谢。由于怀疑有广泛的癌症转移,进行了骨活检,结果显示为非干酪样肉芽肿,与结节病复发一致。
结节病病变可能模仿肿瘤患者的转移性疾病或复发。应进行活检和组织病理学检查以确诊。有人提出,由于存在活动性癌症或其治疗,免疫环境改变导致结节病复发或再激活。Teodorovic及其同事推测,放射性I-131治疗会导致Th2细胞因子如白细胞介素(IL)-4、IL-5和IL-13的分泌减少。很少有关于结节病与乳头状癌相关的病例报告;这是第一例放射性碘治疗甲状腺乳头状癌后结节病全身复发的报告。