Abstract
Follicular carcinoma may typically present as a single, painless thyroid nodule in an older (>55 years of age) male, although it is more common in women by twofold or more. Lymphadenopathy due to involved cervical nodes is uncommon, but distant metastases will be present in lung or bone in 10–20% of patients at the time of initial presentation (15–19). At presentation, all routine blood thyroid function tests will be within normal limits, including the serum TSH (except in the presence of severe iodine deficiency and endemic goiter). Serum thyroglobulin (Tg) may be elevated, but a diagnosis should not be inferred from serum Tg levels. Utility of Tg monitoring is discussed elsewhere in this volume (Chapters 22 and 31), and may be adversely affected by the presence of interfering antithyroglobulin antibodies, which usually falsely lower serum Tg levels. This may be more problematic with immunoluminometric assays than with highly specific radioimmunoassays for thyroglobulin (20). Unfortunately, as many as 25–35% of thyroid cancer patients may have underlying Hashimoto’ s disease with positive thyroid autoantibodies. Future management of such patients may be facilitated by measurement of thyroglobulin mRNA in serum (21). Other techniques may allow distinction between circulating thyroglobulin derived from benign versus malignant thyroid tissue (22). Patients with known metastatic or residual thyroid cancer should be followed up by an endocrinologist/thyroid specialist in addition to their primary care physician. The physician should ensure that serum Tg is being measured only in a laboratory of the highest quality. Ideally, this should be in the same laboratory at each follow-up time interval, and the laboratory should provide companion Tg levels on a remeasurement of stored serum from the prior venapuncture. In the postoperative state, a clearly measurable or rising serum Tg while the patient is TSH-suppressed on levothyroxine may be a definite clue to recurrence, but serum Tg levels are usually most useful when measured while the patient is hypothyroid, for example, during preparation for follow-up scanning. The current availability of recombinant human TSH has facilitated monitoring Tg before and after rhTSH stimulation (see Chapter 14).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Schwartz AE, Clark OH, Ituarte P, LoGerfo P. Thyroid surgery-the choice. J Clin Endocrinol Metab 1998; 83: 1097–1105.
Taylor T, Specker B, Robbins J, Sperling M, Ho M, Ain K. Outcome after treatment of high-risk papillary and non-Hürthle cell follicular thyroid carcinoma. Ann Intern Med 1998; 129: 622–627.
Lin JD, Kao PF, Chao TC. The effects of radioactive iodine in thyroid remnant ablation and treatment of well differentiated thyroid carcinoma. Brit J Radiol 1998; 71: 307–313.
Pelikan DM, Lion HL, Hermans J, Goslings BM. The role of radioactive iodine in the treatment of advanced differentiated thyroid carcinoma. Clin Endocrinol 1997; 47: 713–720.
Lin JD, Chao TC, Huang MJ, Weng HF, Tzen KY. Use of radioactive iodine for thyroid remnant ablation in well-differentiated thyroid carcinoma to replace thyroid reoperation. Amer J Clin Oncol 1998; 21: 77–81.
Sherman SI, Brierley JD, Sperling M, Ain KB, Bigos ST, Cooper DS, et al. Prospective multicenter study of thyroid carcinoma treatment: Initial analysis of staging and outcome. Cancer 1998; 83: 1012–1021.
Hundahl SA, Fleming ID, Fremgen AM, Menck FIR. A national cancer data base report on 53,856 cases of thyroid carcinoma treated in the U.S., 1985–1995. Cancer 1998; 83: 2638 2648.
Grebe SKG, Hay ID. Follicular thyroid cancer. Endocrinol Metab Clin North Am 1995; 24: 761–801.
Goldman ND, Coniglio JU, Falk SA. Thyroid cancers I: Papillary, follicular, and Hürthle cell. Otolaryngol Clin North Am 1996; 29: 593–609.
Dulgeroff AJ, Hershman JM. Medical therapy for differentiated thyroid carcinoma. Endocr Rev 1994; 15: 500–515.
Emerick GT, Duh Q-Y, Siperstein AE, Burrow GN, Clark OH. Diagnosis, treatment, and outcome of follicular thyroid carcinoma. Cancer 1993; 72: 3287–3295.
Robbins J, Merino MJ, Boice JD, Ron E, Ain KB, Alexander HR, et al. Thyroid cancer: a lethal endocrine neoplasm. Ann Intern Med 1991; 115: 133–147.
Schlumberger MJ. Papillary and follicular thyroid carcinoma. N Engl J Med 1998; 338: 297–306.
Cooper DS, Schneyer CR. Follicular and Hürthle cell carcinoma of the thyroid. Endocr Metab Clin North Am 1990; 19: 577–591.
Jensen MH, Davis RK, Derrick L. Thyroid cancer: a computer-assisted review of 5287 cases. Otolaryngol Head Neck Surg 1990; 102: 51–65.
Ruegemer JJ, Hay ID, Bergstralh EJ, Ryan JJ, Offord KP, Gorman CA. Distant metastases in differentiated thyroid carcinoma: a multivariate analysis of prognostic variables. J Clin Endocrinol Metab 1988; 67: 501–508.
Schlumberger M, Tubiana M, de Vathaire F, Hill C, Gardet P, Travagli JP, et al. Longterm results of treatment of 283 patients with lung and bone metastases from differentiated thyroid carcinoma. J Clin Endocrinol Metab 1986; 960–966.
Young RL, Mazzaferri EL, Rahe AJ, Dorfman SG. Pure follicular carcinoma: impact of therapy in 214 patients. J Nucl Med 1980; 21: 733–737.
Simpson WJ, McKinney SE, Carruthers JS, Gospodarowicz MK, Sutliffe SB, Panzanella T. Papillary and follicular thyroid cancer: prognostic factors in 1578 patients. Am J Med 1987; 83: 479–488.
Spencer CA, Takeuchi M, Kazaroxyan M, Wang CC, Guttler RB, Singer PA, et al. Serum thyroglobulin autoantibodies: prevalence, influence on serum thyroglobulin measurement, and prognostic significance in patients with differentiated thyroid carcinoma. J Clin Endocrinol Metab 1998; 83: 1121–1127.
Ringel MD, Ladenson PW, Levine MA. Molecular diagnosis of residual and recurrent thyroid cancer by amplification of thyroglobulin messenger ribonucleic acid in peripheral blood. J Clin Endocrinol Metab 1998; 83:4435–4442. Editorial comment by Haber RS, The diagnosis of recurrent thyroid cancer-a new approach. J Clin Endocrinol Metab 83: 4189–4190.
Maruyama M, Kato R, Kobayashi S, Kasuga Y. A method to differentiate between thyroglobulin derived from normal thyroid tissue and from thyroid carcinoma based on anlysis of reactivity to lectins. Arch Path Lab Med 1998; 122: 715–720.
Arturi F, Russo D, Giuffrida D, Ippolito A, Perrotti N, Vigneri R, Filetti S. Early diagnosis by genetic analysis of differentiated thyroid cancer metastases in small lymph nodes. J Clin Endocrinol Metab 1997; 82: 1638–1641.
Winzer R, Schmutzler C, Jakobs TC, Ebert R, Rendl J, Reiners C, et al. Reverse transcriptasepolymerase chain reaction analysis of thyrocyte-relevant genes in fine-needle aspiration biopsies of the human thyroid. Thyroid 1998; 8: 981–987.
Umbricht CB, Saji M, Westra WH, Udelsman R, Zeiger MA, Sukumar S. Telomerase activity: a marker to distinguish follicular thyroid adenoma from carcinoma. Cancer Res 1997; 57: 2144–2147.
Franceschi S. Iodine intake and thyroid carcinoma-a potential risk factor. Exper Clin Endocrinol Diab 1998; 106 (Suppl 3): S38 - S44.
Galanti MR, Hansson L, Bergstrom R, Wolk A, Hjartaker A, Lund E, et al. Diet and the risk of papillary and follicular thyroid carcinoma: a population-based case-control study in Sweden and Norway. Cancer Causes Control 1997; 8: 205–214.
Moosa M, Mazzaferri EL. Outcome of differentiated thyroid cancer diagnosed in pregnant women. J Clin Endocrinol Metab 1997; 82: 2862–2866.
LiVolsi VA, Asa SL. The demise of follicular carcinoma of the thyroid gland. Thyroid 1994; 4: 233–236.
Fad NR, Shi Y, Zou M. Molecular basis of thyroid cancer. Endocr Rev 1994; 15: 202–232.
Challeton C, Bounacer A, DuVillard JA, Caillou B, DeVathaire F, Monier R, et al. Pattern of ras and gsp oncogene mutations in radiation-associated human thyroid tumors. Oncogene 1995; 11: 601–603.
Roque L, Clode A, Belge G, Pinto A, Bartnitzke S, Santos JR, et al. Follicular thyroid carcinoma: chromosome analysis of 19 cases. Genes, Chromosomes & Cancer 1998; 21: 250–255.
Russo D, Aruri F, Schlumberger M, Caillou B, Monier R, Filetti S, Suarez HG. Activating mutations of the TSH receptor in differentiated thyroid carcinoma. Oncogene 1995; 11: 1907 1911.
Russo D, Tumino S, Arturi F, Vigneri P, Grasso G, Pontecorvi A, et al. Detection of an activating mutation of the thyrotropin receptor in a case of an autonomously hyperfunctioning thyroid insular carcinoma. J Clin Endocrinol Metab 1997; 82: 735–738.
Tielens ET, Sherman SI, Hruban RH, Ladenson PW. Follicular variant of papillary thyroid carcinoma: a clinical pathologic study. Cancer 1994; 73: 424–431.
Baloch ZW, Gupta PK, Yu GH, Sack MJ, LiVolsi VA. Follicular variant of papillary carcinoma. Cytologic and histologic correlation. Amer J Clin Path 1999; 111: 216–222.
Collins SL. Thyroid cancer: controversies and etiopathogenesis of thyroid cancer. In Falk S, editor. Thyroid disease: endocrinology, surgery, nuclear medicine, and radiotherapy, 2nd ed. New York: Raven Press, 1997: 495–564.
Paphavasit A, Thompson GB, Hay ID, Grant CS, van Heerden JA, Ilstrup DM, et al. Follicular and Hürthle cell thyroid neoplasms: is frozen section evaluation worthwhile? Arch Surg 1997; 132: 674–678.
Vassilopoulou-Sellin R, Klein MJ, Smith TH, Samaan HA, Frankenthaler RA, Goepfert H, et al. Pulmonary metastases in children and young adults with differentiated thyroid cancer. Cancer 1993; 71: 1348–1352.
Samuel AM, Rajashekharrao B, Shah DH. Pulmonary metastases in children and adolescents with well-differentiated thyroid cancer. J Nucl Med 1998; 39: 1531–1536.
Feinmesser R, Lubin E, Segal K, Noyek A. Carcinoma of the thyroid in children-a review. J Ped Endocrinol Metab 1997; 10: 561–568.
Cady B. Staging in thyroid carcinoma. Cancer 1998; 83: 844–847.
Sherman SI. Editorial: Staging in thyroid carcinoma-a reply. Cancer 1998; 83: 848–850.
Brierley JD, Panzarella T, Tsng RW, Gospodarowicz MK, O’Sullivan B. A comparison of different staging systems predictability of patient outcome: thyroid carcinoma as an example. Cancer 1997; 79: 2414–2423.
Loh K-C, Greenspan FS, Gee L, Miller TR, Yeo PPB. Pathological tumor-node-metastasis (pTNM) staging for papillary and follicular thyroid carcinomas: a retrospective analysis of 700 patients. J Clin Endocrinol Metab 1997; 82: 3553–3562.
Hay ID, Bergstralh EJ, Goellner JR, Ebersold JR, Grant CS. Predicting outcome in papillary thyroid carcinoma: Development of a reliable prognostic scoring system in a cohort of 1779 patients treated surgically at one institution during 1940 through 1989. Surgery 1993; 114: 1050–1058.
DeGroot LJ, Kaplan EL, Straus FH, Shukla MS. Does the method of management of papillary thyroid carcinoma make a difference in outcome? World J Surg 1994; 18: 123–130.
Watson RG, Brennan MD, Goellner JR, van Heerden JA, McConahey WM, Taylor WF. Invasive Hürthle cell carcinoma of the thyroid: natural history and management. Mayo Clin Proc 1984; 59: 851–855.
Sanders LE, Silverman M. Follicular and Hürthle cell carcinoma: predicting outcome and directing therapy. Surgery 1998; 124: 967–974.
Bronner MP, LiVolsi VA. Oxyphilic (Askenasy/Hürthle cell) tumors of the thyroid: microscopic features predict biologic behavior. Surg Pathol 1988; 1: 137–150.
Chen H, Nicol TL, Zeiger MA, Dooley WC, Ladenson PW, Cooper DS, et al. Hürthle cell neoplasms of the thyroid: are there factors predictive of malignancy? Ann Surg 1998; 227: 542–546.
Samaan NA, Schultz PN, Haynie TP, Ordonez NG. Pulmonary metastasis of differentiated thyroid carcinoma: treatment results in 101 patients. J Clin Endocrinol Metab 1985; 60: 376–380.
Samaan NA, Schultz PN, Hickey RC, Goepfert H, Haynie TP, Johnston DA, et al. The results of various modalities of treatment of well differentiated thyroid carcinoma: a retrospective review of 1599 patients. J Clin Endocrinol Metab 1992; 75: 714–720.
Har-El G, Hadar T, Segal K, Levy R, Sidi J. Hürthle cell carcinoma of the thyroid gland: a tumor of moderate malignancy. Cancer 1986; 57: 1613–1617.
Thoresen SO, Akslen LA, Glattre E, Haldorsen T, Lund EV, Schoultz M. Survival and prognostic factors in differentiated thyroid carcinoma: a multivariate analysis of 1055 cases. Br J Surg 1989; 59: 231–235.
Arturi F, Russo D, Schlumberger M, duVillard JA, Caillou B, Vigneri P, et al. Iodide symporter gene expression in human thyroid tumors. J Clin Endocrinol Metab 1998; 83: 2493–2496.
Grunwald F, Pakos R, Bender H, Menzel C, Otte R, Palmedo H, et al. Redifferentiation therapy with retinoic acid in follicular thyroid cancer. J Nucl Med 1998; 39: 1555–1558.
Grunwald F, Menzel C, Bender H, Palmedo H, Otte R, Fimmers R, et al. Redifferentiation therapy-induced radioiodine uptake in thyroid cancer. J Nucl Med 1998; 39: 1903–1906.
Schmutzler C, Wnzer R, Meissner-Weigl J, Kohrle J. Retinoic acid increases sodium/iodide symporter mRNA levels in human thyroid cancer cell lines and suppresses expression of functional symporter in nontransformed FRTL-5 rat thyroid cells. Biochem Biophys Res Comm 1997; 240: 832–838.
Lazzi S, Spina d, Als C, Tosi P, Mazzucchelli L, Kraft Rainer, et al. Oncocytic (Hürthle cell) tumors of the thyroid: Distinct growth patterns compared with clinicopathological features. Thyroid 1999; 9: 97–103.
Simpson WJ, Panzarella T, Carruthers JS, Gospodarowicz MK, Sutcliffe SB. Papillary and follicular thyroid cancer: impact of treatment in 1578 patients. Int J Radiat Oncol Biol Physiol 1988; 14: 1063–1075.
Tubiana M, Haddad E, Schlumberger M, Hill C, Rougier P, Sarrazin D. External radiotherapy in thyroid cancer. Cancer 1985; 55 (Suppl): 2062–2071.
Lin JD, Tsang NM, Huang MJ, Weng HF. Results of external beam radiotherapy in patients with well differentiated thyroid carcinoma. Jpn J Clin Oncol 1997; 27: 244–247.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2000 Springer Science+Business Media New York
About this chapter
Cite this chapter
Wartofsky, L. (2000). Follicular Thyroid Carcinoma. In: Wartofsky, L. (eds) Thyroid Cancer. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-199-2_27
Download citation
DOI: https://doi.org/10.1007/978-1-59259-199-2_27
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-1-4757-6845-9
Online ISBN: 978-1-59259-199-2
eBook Packages: Springer Book Archive