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FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome

Disclosure: J. Hayes dorado: None. M. Calla Ayala: None. A. Colque Arias: None. K. Lanuza Gaite: None. M. Rossell Lopez: None. D. Frias Eid: None. Van Wyc-Grumbach syndrome (VWGS) is a rare presentation of long standing prepubertal hypothyroidism characterized by bilateral multicystic enlarged ovari...

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Autores principales: Hayes Dorado, Juan Pablo, Calla Ayala, Marco Antonio, Arias, Andrea Colque, Gaite, Karem Lanuza, Lopez, Marco Rossell, Frias Eid, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555888/
http://dx.doi.org/10.1210/jendso/bvad114.1855
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author Hayes Dorado, Juan Pablo
Calla Ayala, Marco Antonio
Arias, Andrea Colque
Gaite, Karem Lanuza
Lopez, Marco Rossell
Frias Eid, Daniela
author_facet Hayes Dorado, Juan Pablo
Calla Ayala, Marco Antonio
Arias, Andrea Colque
Gaite, Karem Lanuza
Lopez, Marco Rossell
Frias Eid, Daniela
author_sort Hayes Dorado, Juan Pablo
collection PubMed
description Disclosure: J. Hayes dorado: None. M. Calla Ayala: None. A. Colque Arias: None. K. Lanuza Gaite: None. M. Rossell Lopez: None. D. Frias Eid: None. Van Wyc-Grumbach syndrome (VWGS) is a rare presentation of long standing prepubertal hypothyroidism characterized by bilateral multicystic enlarged ovaries, vaginal bleeding and delayed bone age. It appeared that high TSH could produce FSH and LH like activity leading to multiple ovarian cysts. A 7-year-old girl with trisomy 21, presented with vaginal bleeding for 2 days prior to admission. Physical exam revealed bradycardia (68 bbm), apathy, sluggishness, as well as dry skin and eyelid oedema. She had no breast development nor pubic hair.Causes of vaginal bleeding such as trauma, possible abuse, foreign body insertion and urethral prolapse were excluded. There was no purpura or bleeding from other sites.The abdominal sonogram revealed bilateral ovarian cystic masses (V:17.29 cm3 and 16.48 cm3, right and left, respectively). Bone age was delayed almost 3 years behind her chronological age. Laboratory tests revealed TSH 860 μIU/mL, T4 0.71 μg/dL, FSH 8.12 mIU/mL, LH < 0.1 mIU/mL, estradiol 193 pg/mL, thyroid peroxidase Abs 184 IU/mL, thyroglobulin Abs 212 IU/mL, Β-hCG < 0.1mU/mL, confirming severe hypothyroidism. The girl was diagnosed with VWGS due to unrecognized chronic lymphocytic thyroiditis and LT4 treatment (75mug/OD) was initiated. The patient responded with complete remission of symptoms and regression of the ovarian cysts one month after initiation of treatment. It is very important to think of VWGS and investigate for thyroid status during the evaluation of ovarian cysts or isolated premature menarche. Early recognition can eliminate unnecessary surgery to remove ovarian cysts, as appropriate treatment with levothyroxine leads to complete remission of symptoms. Even when the diagnosis of VWGS is confirmed, practitioners must be watchful to consider surgical intervention in the presence of uncontrolled vaginal bleeding, hemodynamic instability, or failure of regression of ovarian cysts with exogenous thyroid hormone replacement. Presentation: Friday, June 16, 2023
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spelling pubmed-105558882023-10-07 FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome Hayes Dorado, Juan Pablo Calla Ayala, Marco Antonio Arias, Andrea Colque Gaite, Karem Lanuza Lopez, Marco Rossell Frias Eid, Daniela J Endocr Soc Thyroid Disclosure: J. Hayes dorado: None. M. Calla Ayala: None. A. Colque Arias: None. K. Lanuza Gaite: None. M. Rossell Lopez: None. D. Frias Eid: None. Van Wyc-Grumbach syndrome (VWGS) is a rare presentation of long standing prepubertal hypothyroidism characterized by bilateral multicystic enlarged ovaries, vaginal bleeding and delayed bone age. It appeared that high TSH could produce FSH and LH like activity leading to multiple ovarian cysts. A 7-year-old girl with trisomy 21, presented with vaginal bleeding for 2 days prior to admission. Physical exam revealed bradycardia (68 bbm), apathy, sluggishness, as well as dry skin and eyelid oedema. She had no breast development nor pubic hair.Causes of vaginal bleeding such as trauma, possible abuse, foreign body insertion and urethral prolapse were excluded. There was no purpura or bleeding from other sites.The abdominal sonogram revealed bilateral ovarian cystic masses (V:17.29 cm3 and 16.48 cm3, right and left, respectively). Bone age was delayed almost 3 years behind her chronological age. Laboratory tests revealed TSH 860 μIU/mL, T4 0.71 μg/dL, FSH 8.12 mIU/mL, LH < 0.1 mIU/mL, estradiol 193 pg/mL, thyroid peroxidase Abs 184 IU/mL, thyroglobulin Abs 212 IU/mL, Β-hCG < 0.1mU/mL, confirming severe hypothyroidism. The girl was diagnosed with VWGS due to unrecognized chronic lymphocytic thyroiditis and LT4 treatment (75mug/OD) was initiated. The patient responded with complete remission of symptoms and regression of the ovarian cysts one month after initiation of treatment. It is very important to think of VWGS and investigate for thyroid status during the evaluation of ovarian cysts or isolated premature menarche. Early recognition can eliminate unnecessary surgery to remove ovarian cysts, as appropriate treatment with levothyroxine leads to complete remission of symptoms. Even when the diagnosis of VWGS is confirmed, practitioners must be watchful to consider surgical intervention in the presence of uncontrolled vaginal bleeding, hemodynamic instability, or failure of regression of ovarian cysts with exogenous thyroid hormone replacement. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10555888/ http://dx.doi.org/10.1210/jendso/bvad114.1855 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Thyroid
Hayes Dorado, Juan Pablo
Calla Ayala, Marco Antonio
Arias, Andrea Colque
Gaite, Karem Lanuza
Lopez, Marco Rossell
Frias Eid, Daniela
FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title_full FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title_fullStr FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title_full_unstemmed FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title_short FRI509 A Girl With Trisomy 21 Presents With Van Wyk-Grumbach Syndrome
title_sort fri509 a girl with trisomy 21 presents with van wyk-grumbach syndrome
topic Thyroid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555888/
http://dx.doi.org/10.1210/jendso/bvad114.1855
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