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Volumn 22, Issue 5, 2012, Pages 542-546

Minimally invasive follicular thyroid carcinoma developed in dyshormonogenetic multinodular goiter due to thyroid peroxidase gene mutation

Author keywords

[No Author keywords available]

Indexed keywords

IODIDE; LEVOTHYROXINE; PHENYLALANINE; SERINE; THYROID PEROXIDASE; THYROTROPIN;

EID: 84860458833     PISSN: 10507256     EISSN: 15579077     Source Type: Journal    
DOI: 10.1089/thy.2011.0478     Document Type: Article
Times cited : (30)

References (29)
  • 1
    • 34249338694 scopus 로고    scopus 로고
    • Increase in congenital hypothyroidism in new york state and in the united states
    • Harris KB, Pass KA 2007 Increase in congenital hypothyroidism in New York State and in the United States. Mol Genet Metab 91:268-277.
    • (2007) Mol. Genet. Metab. , vol.91 , pp. 268-277
    • Harris, K.B.1    Pass, K.A.2
  • 2
    • 77951824353 scopus 로고    scopus 로고
    • Trends in incidence rates of congenital hypothyroidism related to select demographic factors: Data from the united states
    • California Massachusetts New York and Texas
    • Hinton CF, Harris KB, Borgfeld L, Drummond-Borg M, Eaton R, Lorey F, Therrell BL, Wallace J, Pass KA 2010 Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas. Pediatrics 125:S37-S47.
    • (2010) Pediatrics , vol.125
    • Hinton, C.F.1    Harris, K.B.2    Borgfeld, L.3    Drummond-Borg, M.4    Eaton, R.5    Lorey, F.6    Therrell, B.L.7    Wallace, J.8    Pass, K.A.9
  • 3
    • 79960842943 scopus 로고    scopus 로고
    • Genetic causes of congenital hypothyroidism due to dyshormonogenesis
    • Grasberger H, Refetoff S 2011 Genetic causes of congenital hypothyroidism due to dyshormonogenesis. Curr Opin Pediatr 23:421-428.
    • (2011) Curr. Opin Pediatr. , vol.23 , pp. 421-428
    • Grasberger, H.1    Refetoff, S.2
  • 4
  • 5
    • 0033756917 scopus 로고    scopus 로고
    • Two decades of screening for congenital hypothyroidism in the netherlands: TPO gene mutations in total iodide organification defects an update
    • Bakker B, Bikker H, Vulsma T, de Randamie JS, Wiedijk BM, De Vijlder JJ 2000 Two decades of screening for congenital hypothyroidism in the Netherlands: TPO gene mutations in total iodide organification defects (an update). J Clin Endocrinol Metab 85:3708-3712.
    • (2000) J. Clin. Endocrinol. Metab. , vol.85 , pp. 3708-3712
    • Bakker, B.1    Bikker, H.2    Vulsma, T.3    De Randamie, J.S.4    Wiedijk, B.M.5    De Vijlder, J.J.6
  • 6
    • 0347993689 scopus 로고    scopus 로고
    • Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect
    • Nascimento AC, Guedes DR, Santos CS, Knobel M, Rubio IG, Medeiros-Neto G 2003 Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect. Thyroid 13:1145-1151.
    • (2003) Thyroid , vol.13 , pp. 1145-1151
    • Nascimento, A.C.1    Guedes, D.R.2    Santos, C.S.3    Knobel, M.4    Rubio, I.G.5    Medeiros-Neto, G.6
  • 8
    • 0037323540 scopus 로고    scopus 로고
    • Management of simple nodular goiter: Current status and future perspectives
    • Hegedus L, Bonnema SJ, Bennedbaek FN 2003 Management of simple nodular goiter: current status and future perspectives. Endocr Rev 24:102-132.
    • (2003) Endocr. Rev. , vol.24 , pp. 102-132
    • Hegedus, L.1    Bonnema, S.J.2    Bennedbaek, F.N.3
  • 9
    • 0019844309 scopus 로고
    • The diagnosis of malignancy in dyshormonogenetic goiter
    • Vickery AL Jr. 1981 The diagnosis of malignancy in dyshormonogenetic goiter. J Clin Endocrinol Metab 10:317-335.
    • (1981) J. Clin. Endocrinol. Metab. , vol.10 , pp. 317-335
    • Vickery Jr., A.L.1
  • 10
    • 77749285723 scopus 로고    scopus 로고
    • Biallelic p R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinoma
    • Raef H, Al-Rijjal R, Al-Shehri S, Zou M, Al-Mana H, Baitei EY, Parhar RS, Al-Mohanna FA, Shi Y 2010 Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinoma. J Clin Endocrinol Metab 95:1000-1006.
    • (2010) J. Clin. Endocrinol. Metab. , vol.95 , pp. 1000-1006
    • Raef, H.1    Al-Rijjal, R.2    Al-Shehri, S.3    Zou, M.4    Al-Mana, H.5    Baitei, E.Y.6    Parhar, R.S.7    Al-Mohanna, F.A.8    Shi, Y.9
  • 11
    • 33644826791 scopus 로고    scopus 로고
    • Metastatic follicular thyroid carcinoma arising from congenital goiter as result of a novel splice donor site mutation in the thyroglobulin gene
    • Alzahrani AS, Baitei EY, Zou M, Shi Y 2006 Metastatic follicular thyroid carcinoma arising from congenital goiter as result of a novel splice donor site mutation in the thyroglobulin gene. J Clin Endocrinol Metab 91:740-746.
    • (2006) J. Clin. Endocrinol. Metab. , vol.91 , pp. 740-746
    • Alzahrani, A.S.1    Baitei, E.Y.2    Zou, M.3    Shi, Y.4
  • 12
    • 26944500520 scopus 로고    scopus 로고
    • High incidence of thyroid cancer in long standing goiter with thyroglobulin mutations
    • Hishinuma A, Fukata S, Kakudo K, Murato Y, Ieiri T 2005 High incidence of thyroid cancer in long standing goiter with thyroglobulin mutations. Thyroid 15:1079-1084.
    • (2005) Thyroid , vol.15 , pp. 1079-1084
    • Hishinuma, A.1    Fukata, S.2    Kakudo, K.3    Murato, Y.4    Ieiri, T.5
  • 15
    • 0029892866 scopus 로고    scopus 로고
    • Long-term sequelae of hearing impairment in congenital hypothyroidism
    • Rovert J, Wynsome W, Bliss B, Buchanan L, Ehrlich R 1996 Long-term sequelae of hearing impairment in congenital hypothyroidism. J Pediatr 128:776-783.
    • (1996) J. Pediatr , vol.128 , pp. 776-783
    • Rovert, J.1    Wynsome, W.2    Bliss, B.3    Buchanan, L.4    Ehrlich, R.5
  • 16
    • 0019380270 scopus 로고
    • Congenital goiter and development of metastatic follicular carcinoma with evidence for a leak of nonhormonal iodide: Clinical pathological kinetic and biochemical studies and review of literature
    • Cooper DS, Axelrod L, De Groot LJ, Vickery AL, Maloof F 1981 Congenital goiter and development of metastatic follicular carcinoma with evidence for a leak of nonhormonal iodide: clinical, pathological, kinetic, and biochemical studies and review of literature. J Clin Endocrinol Metab 52:294-305.
    • (1981) J. Clin. Endocrinol. Metab. , vol.52 , pp. 294-305
    • Cooper, D.S.1    Axelrod, L.2    De Groot, L.J.3    Vickery, A.L.4    Maloof, F.5
  • 17
    • 0000443462 scopus 로고
    • A report of the occurrence of deaf-mutism and goiter in four of six siblings of a north american family
    • Thieme ET 1957 A report of the occurrence of deaf-mutism and goiter in four of six siblings of a North American family. Ann Surg 146:941-948.
    • (1957) Ann. Surg. , vol.146 , pp. 941-948
    • Thieme, E.T.1
  • 18
    • 0000724726 scopus 로고
    • Familial association of nerve deafness with nodular goiter and thyroid carcinoma
    • Elman DS 1958 Familial association of nerve deafness with nodular goiter and thyroid carcinoma.NEngl JMed 31:219-223.
    • (1958) N. Engl. J. Med. , vol.31 , pp. 219-223
    • Elman, D.S.1
  • 20
    • 70349328252 scopus 로고    scopus 로고
    • Papillary carcinoma of the thyroid developed in congenital dyshormonogenetic hypothyroidism without goiter: Diagnosis by FNAB
    • Drut R, Moreno A 2009 Papillary carcinoma of the thyroid developed in congenital dyshormonogenetic hypothyroidism without goiter: diagnosis by FNAB. Diagn Cytopathol 37:707-709.
    • (2009) Diagn. Cytopathol. , vol.37 , pp. 707-709
    • Drut, R.1    Moreno, A.2
  • 21
    • 33745115856 scopus 로고    scopus 로고
    • Pathogenesis diagnosis and management of thyroid nodules in children
    • Niedziela M 2006 Pathogenesis, diagnosis and management of thyroid nodules in children. Endocr Relat Cancer 13:427-453.
    • (2006) Endocr. Relat. Cancer , vol.13 , pp. 427-453
    • Niedziela, M.1
  • 22
    • 72549096515 scopus 로고    scopus 로고
    • The association between serum TSH concentration and thyroid cancer
    • Boelaert K 2009 The association between serum TSH concentration and thyroid cancer. Endocr Relat Cancer 16:1065-1072.
    • (2009) Endocr. Relat. Cancer , vol.16 , pp. 1065-1072
    • Boelaert, K.1
  • 24
    • 23844467711 scopus 로고    scopus 로고
    • TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5
    • Karges B, Krause G, Homoki J, Debatin KM, de Roux N, Karges W 2005 TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5. J Endocrinol 186:377-385.
    • (2005) J. Endocrinol. , vol.186 , pp. 377-385
    • Karges, B.1    Krause, G.2    Homoki, J.3    Debatin, K.M.4    De Roux, N.5    Karges, W.6
  • 25
    • 25444455858 scopus 로고    scopus 로고
    • Cytological features of dyshormonogenetic goiter: Case report and review of literature
    • Deshpande AH, Bobhate SK 2005 Cytological features of dyshormonogenetic goiter: case report and review of literature. Diagn Cytopathol 33:252-254.
    • (2005) Diagn. Cytopathol. , vol.33 , pp. 252-254
    • Deshpande, A.H.1    Bobhate, S.K.2
  • 29
    • 80052782508 scopus 로고    scopus 로고
    • Molecular analysis of thyroid tumors
    • Bhaijee F, Nikiforov YE 2011 Molecular analysis of thyroid tumors. Endocr Pathol 22:126-133.
    • (2011) Endocr. Pathol. , vol.22 , pp. 126-133
    • Bhaijee, F.1    Nikiforov, Y.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.