Herediter Non-Medüller Tiroid Kanserleri
Özet
Cowden, Gardner, Carney Kompleksi gibi ailesel kanser sendromları ile ilişkilidir. Bu kanserler genellikle ilgili sendromların belirtileriyle birlikte ortaya çıkar ve belirli kromozomlardaki mutasyonlar gibi genetik kökenlere sahiptir. Yüksek rekürens ve agresif seyirleri dolayısyla yakın izlem ve total tiroidektominin de dahil olduğu radikal tedaviler uygulanmaktadır. Ailesel olgularda genetik danışmanlık önem arz etmektedir.
It is associated with familial cancer syndromes such as Cowden, Gardner, Carney Complex. These cancers often occur along with symptoms of related syndromes and have genetic origins, such as mutations in certain chromosomes. Due to their high recurrence and aggressive course, close monitoring and radical treatments, including total thyroidectomy, are applied. Genetic counseling is important in familial cases.
Referanslar
Nosé V. Thyroid cancer of follicular cell origin in inherited tumor syndromes. Adv Anat Pathol. 2010;17(6):428-436.
2.Harach HR, Williams GT, Williams ED. Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm. Histopathology. 1994;25(6):549-561.
Cameselle-Teijeiro J, Chan JK. Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma? Mod Pathol. 1999;12(4):400-411.
Cetta F, Montalto G, Gori M, Curia MC, Cama A, Olschwang S. Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study. J Clin Endocrinol Metab. 2000;85(1):286-292.
Ishikawa Y, Sugano H, Matsumoto T, Furuichi Y, Miller RW, Goto M. Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype–phenotype relations to cell type and race. Cancer. 1999;85(6):1345-1352.
Reardon W, Coffey R, Phelps PD, Luxon LM, Stephens D, Kendall-Taylor P, et al. Pendred syndrome--100 years of underascertainment?. QJM. 1997;90(7):443-447.
Capezzone M, Marchisotta S, Cantara S, Busonero G, Brilli L, Pazaitou-Panayiotou K, et al. Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity. Endocr Relat Cancer. 2008;15(4):1075-1081.
Bakhsh A, Kirov G, Gregory JW, Williams ED, Ludgate M. A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer. Endocr Relat Cancer. 2006;13(2):475-483.
McKay JD, Lesueur F, Jonard L, Pastore A, Williamson J, Hoffman L, et al. Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. Am J Hum Genet. 2001;69(2):440-446.
Malchoff CD, Sarfarazi M, Tendler B, Forouhar F, Whalen G, Joshi V, et al. Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome. J Clin Endocrinol Metab. 2000;85(5):1758-1764.
Canzian F, Amati P, Harach HR, Kraimps JL, Lesueur F, Barbier J, et al. A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2. Am J Hum Genet. 1998;63(6):1743-1748.
Musholt TJ, Musholt PB, Petrich T, Oetting G, Knapp WH, Klempnauer J. Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatment. World J Surg. 2000;24:1409-1417.
Sippel RS, Caron NR, Clark OH. An evidence-based approach to familial nonmedullary thyroid cancer: screening, clinical management, and follow-up. World J Surg. 2007;31:924-933.
Hemminki K, Eng C, Chen B. Familial risks for nonmedullary thyroid cancer. J Clin Endocrinol Metab. 2005;90(10):5747-5753.
Kebebew E. Hereditary non-medullary thyroid cancer. World J Surg. 2008;32:678-682.
Uchino S, Noguchi S, Kawamoto H, Yamashita H, Watanabe S, Yamashita H, et al. Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population. World J Surg. 2002;26:897-902.
Alsanea O, Wada N, Ain K, Wong M, Taylor K, Ituarte PH, et al. Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series. Surgery. 2000;128(6):1043-1051.
Grossman RF, Tu SH, Duh QY, Siperstein AE, Novosolov F, Clark OH. Familial nonmedullary thyroid cancer: an emerging entity that warrants aggressive treatment. Arch Surg. 1995;130(8):892-899.
Vriens MR, Sabanci Ü, Epstein HD, Ngai S, Duh QY, Siperstein AE, et al. Reliability of fine-needle aspiration in patients with familial nonmedullary thyroid cancer. Thyroid. 1999;9(10):1011-1016.
Triponez, F., Wong, M., Sturgeon, C., Caron, N., Ginzinger, D. G., Segal, M. R., ... & Clark, O. H. (2006). Does familial non-medullary thyroid cancer adversely affect survival?. World journal of surgery, 30, 787-793.
Ito, Y., Kakudo, K., Hirokawa, M., Fukushima, M., Yabuta, T., Tomoda, C., ... & Miyauchi, A. (2009). Biological behavior and prognosis of familial papillary thyroid carcinoma. Surgery, 145(1), 100-105.
Referanslar
Nosé V. Thyroid cancer of follicular cell origin in inherited tumor syndromes. Adv Anat Pathol. 2010;17(6):428-436.
2.Harach HR, Williams GT, Williams ED. Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm. Histopathology. 1994;25(6):549-561.
Cameselle-Teijeiro J, Chan JK. Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma? Mod Pathol. 1999;12(4):400-411.
Cetta F, Montalto G, Gori M, Curia MC, Cama A, Olschwang S. Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study. J Clin Endocrinol Metab. 2000;85(1):286-292.
Ishikawa Y, Sugano H, Matsumoto T, Furuichi Y, Miller RW, Goto M. Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype–phenotype relations to cell type and race. Cancer. 1999;85(6):1345-1352.
Reardon W, Coffey R, Phelps PD, Luxon LM, Stephens D, Kendall-Taylor P, et al. Pendred syndrome--100 years of underascertainment?. QJM. 1997;90(7):443-447.
Capezzone M, Marchisotta S, Cantara S, Busonero G, Brilli L, Pazaitou-Panayiotou K, et al. Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity. Endocr Relat Cancer. 2008;15(4):1075-1081.
Bakhsh A, Kirov G, Gregory JW, Williams ED, Ludgate M. A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer. Endocr Relat Cancer. 2006;13(2):475-483.
McKay JD, Lesueur F, Jonard L, Pastore A, Williamson J, Hoffman L, et al. Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. Am J Hum Genet. 2001;69(2):440-446.
Malchoff CD, Sarfarazi M, Tendler B, Forouhar F, Whalen G, Joshi V, et al. Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome. J Clin Endocrinol Metab. 2000;85(5):1758-1764.
Canzian F, Amati P, Harach HR, Kraimps JL, Lesueur F, Barbier J, et al. A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2. Am J Hum Genet. 1998;63(6):1743-1748.
Musholt TJ, Musholt PB, Petrich T, Oetting G, Knapp WH, Klempnauer J. Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatment. World J Surg. 2000;24:1409-1417.
Sippel RS, Caron NR, Clark OH. An evidence-based approach to familial nonmedullary thyroid cancer: screening, clinical management, and follow-up. World J Surg. 2007;31:924-933.
Hemminki K, Eng C, Chen B. Familial risks for nonmedullary thyroid cancer. J Clin Endocrinol Metab. 2005;90(10):5747-5753.
Kebebew E. Hereditary non-medullary thyroid cancer. World J Surg. 2008;32:678-682.
Uchino S, Noguchi S, Kawamoto H, Yamashita H, Watanabe S, Yamashita H, et al. Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population. World J Surg. 2002;26:897-902.
Alsanea O, Wada N, Ain K, Wong M, Taylor K, Ituarte PH, et al. Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series. Surgery. 2000;128(6):1043-1051.
Grossman RF, Tu SH, Duh QY, Siperstein AE, Novosolov F, Clark OH. Familial nonmedullary thyroid cancer: an emerging entity that warrants aggressive treatment. Arch Surg. 1995;130(8):892-899.
Vriens MR, Sabanci Ü, Epstein HD, Ngai S, Duh QY, Siperstein AE, et al. Reliability of fine-needle aspiration in patients with familial nonmedullary thyroid cancer. Thyroid. 1999;9(10):1011-1016.
Triponez, F., Wong, M., Sturgeon, C., Caron, N., Ginzinger, D. G., Segal, M. R., ... & Clark, O. H. (2006). Does familial non-medullary thyroid cancer adversely affect survival?. World journal of surgery, 30, 787-793.
Ito, Y., Kakudo, K., Hirokawa, M., Fukushima, M., Yabuta, T., Tomoda, C., ... & Miyauchi, A. (2009). Biological behavior and prognosis of familial papillary thyroid carcinoma. Surgery, 145(1), 100-105.
