Lingual thyroid and hyperthyroidism: A new case and review of the literature

被引:30
作者
Abdallah-Matta, MP
Dubarry, PH
Pessey, JJ
Caron, P
机构
[1] CHU Rangueil, Dept Endocrinol & Metab Dis, F-31054 Toulouse, France
[2] Dept Internal Med, Castres, France
[3] CHU Rangueil, Dept ORL, F-31054 Toulouse, France
关键词
lingual thyroid; toxic adenoma; thyrotoxicosis; ectopic thyroid; hyperthyroidism;
D O I
10.1007/BF03344002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lingual thyroid is the result of a defective migration of the thyroid anlage occurring between the 3(rd) and 7(th) week of gestation. Whereas mutations in the transcription factor-2 (TTF-2) and PAX8 and in the TSH receptor genes (TSH-R) have been reported in a minority of patients with thyroid dysgenesis, the etiopathogeny of the majority of cases, and in particular of thyroid ectopy, remains unclear. The majority of patients with thyroid ectopy are asymptomatic, but obstructive symptoms as well as hypothyroidism have been observed. Hyperthyroidism is an exceptionally rare finding. To our knowledge, only 2 cases have been reported in the literature to date. Herein, we describe an unusual case of thyrotoxicosis related to a nodular lesion in a lingual thyroid. Treatment consisted in restoration of a euthyroid state with thionamide followed by surgical removal of the ectopic gland. The underlying molecular cause of the ectopic lingual thyroid and the toxic adenoma in this case could not be identified. We speculate that abnormally early differentiation of the thyroid gland could interfere with the migration process, a hypothesis yet to be confirmed.
引用
收藏
页码:264 / 267
页数:4
相关论文
共 40 条
  • [1] Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland
    Abramowicz, MJ
    Duprez, L
    Parma, J
    Vassart, G
    Heinrichs, C
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) : 3018 - 3024
  • [2] Lingual thyroid: Report of three cases
    Arancibia, P
    Veliz, J
    Barria, M
    Pineda, G
    [J]. THYROID, 1998, 8 (11) : 1055 - 1057
  • [3] AZZAM A, 1988, PRESSE MED, V17, P383
  • [4] Graves' disease and recurrent ectopic thyroid tissue
    Basaria, S
    Cooper, DS
    [J]. THYROID, 1999, 9 (12) : 1261 - 1264
  • [5] Severe congenital hypothyroidism due to a homozygous mutation of the βTSH gene
    Biebermann, H
    Liesenkötter, KP
    Emeis, M
    Obladen, M
    Grüters, A
    [J]. PEDIATRIC RESEARCH, 1999, 46 (02) : 170 - 173
  • [6] CHANIN LR, 1988, LARYNGOSCOPE, V98, P422
  • [7] Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
    Clifton-Bligh, RJ
    Wentworth, JM
    Heinz, P
    Crisp, MS
    John, R
    Lazarus, JH
    Ludgate, M
    Chatterjee, VK
    [J]. NATURE GENETICS, 1998, 19 (04) : 399 - 401
  • [8] A mouse model for hereditary thyroid dysgenesis and cleft palate
    De Felice, M
    Ovitt, C
    Biffali, E
    Rodriguez-Mallon, A
    Arra, C
    Anastassiadis, K
    Macchia, PE
    Mattei, MG
    Mariano, A
    Schöler, H
    Macchia, V
    Di Lauro, R
    [J]. NATURE GENETICS, 1998, 19 (04) : 395 - 398
  • [9] A search for the possible molecular mechanisms of thyroid dysgenesis:: Sex ratios and associated malformations
    Devos, H
    Rodd, C
    Gagné, N
    Laframboise, R
    Van Vliet, G
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (07) : 2502 - 2506
  • [10] Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin β-subunit gene follows an autosomal recessive inheritance
    Doeker, BM
    Pfäffle, RW
    Pohlenz, J
    Andler, W
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05) : 1762 - 1765