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The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors
AIMS: Resistance to thyroid hormone (RTH) and pituitary tumors are both rare diseases, and the differential diagnosis of these two diseases is difficult in some cases. There are also patients who have both conditions, making diagnosis more difficult. To better understand this aspect, we analyzed the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950495/ https://www.ncbi.nlm.nih.gov/pubmed/36843601 http://dx.doi.org/10.3389/fendo.2023.1131044 |
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author | Zhao, Junyu Xu, Lusi Li, Chunyu Wang, Fei Liao, Lin Dong, Jianjun |
author_facet | Zhao, Junyu Xu, Lusi Li, Chunyu Wang, Fei Liao, Lin Dong, Jianjun |
author_sort | Zhao, Junyu |
collection | PubMed |
description | AIMS: Resistance to thyroid hormone (RTH) and pituitary tumors are both rare diseases, and the differential diagnosis of these two diseases is difficult in some cases. There are also patients who have both conditions, making diagnosis more difficult. To better understand this aspect, we analyzed the clinical characteristics and gene mutations of RTH coexisting with pituitary tumors. METHODS: Database retrieval was conducted in the PubMed, Cochrane Library, and SinoMed databases, and the search contents were case reports or case series of patients with RTH coexisting with pituitary tumors. The demographic, clinical manifestations, and imaging characteristics of pituitary tumors and gene mutations were summarized. RESULTS: Thirteen articles involving 16 patients with RTH coexistent with pituitary tumors, consisting of 13 female patients, one male patient, and two patients with unknown sex, were included. The patients were 10 to 79 years old and most patients were 41-55 years old (43.75%). The 16 patients were from seven different countries and three continents (Asia, the Americas, and Europe). All the patients showed an abnormal secretion of TSH, and five patients underwent transsphenoidal surgery. Finally, four patients were pathologically confirmed to have TSHoma. A total of 11 different mutations occurred at nine amino acid sequence sites (251, 310, 344, 347, 383, 429, 435, 438, and 453). Two different mutations occurred in both the no. 435 and no. 453 amino acid sequences. Fourteen patients provided their treatment histories, and all had undergone different treatment regimens. CONCLUSIONS: Patients with both RTH and pituitary tumors had multiple clinical manifestations and different thyroid functions, imaging characteristics of pituitary tumors, genetic mutations of THRβ, and treatments. However, due to the limited number of cases, the patients were mainly women. Further studies with more cases that focus on the mechanism are still needed. |
format | Online Article Text |
id | pubmed-9950495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99504952023-02-25 The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors Zhao, Junyu Xu, Lusi Li, Chunyu Wang, Fei Liao, Lin Dong, Jianjun Front Endocrinol (Lausanne) Endocrinology AIMS: Resistance to thyroid hormone (RTH) and pituitary tumors are both rare diseases, and the differential diagnosis of these two diseases is difficult in some cases. There are also patients who have both conditions, making diagnosis more difficult. To better understand this aspect, we analyzed the clinical characteristics and gene mutations of RTH coexisting with pituitary tumors. METHODS: Database retrieval was conducted in the PubMed, Cochrane Library, and SinoMed databases, and the search contents were case reports or case series of patients with RTH coexisting with pituitary tumors. The demographic, clinical manifestations, and imaging characteristics of pituitary tumors and gene mutations were summarized. RESULTS: Thirteen articles involving 16 patients with RTH coexistent with pituitary tumors, consisting of 13 female patients, one male patient, and two patients with unknown sex, were included. The patients were 10 to 79 years old and most patients were 41-55 years old (43.75%). The 16 patients were from seven different countries and three continents (Asia, the Americas, and Europe). All the patients showed an abnormal secretion of TSH, and five patients underwent transsphenoidal surgery. Finally, four patients were pathologically confirmed to have TSHoma. A total of 11 different mutations occurred at nine amino acid sequence sites (251, 310, 344, 347, 383, 429, 435, 438, and 453). Two different mutations occurred in both the no. 435 and no. 453 amino acid sequences. Fourteen patients provided their treatment histories, and all had undergone different treatment regimens. CONCLUSIONS: Patients with both RTH and pituitary tumors had multiple clinical manifestations and different thyroid functions, imaging characteristics of pituitary tumors, genetic mutations of THRβ, and treatments. However, due to the limited number of cases, the patients were mainly women. Further studies with more cases that focus on the mechanism are still needed. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950495/ /pubmed/36843601 http://dx.doi.org/10.3389/fendo.2023.1131044 Text en Copyright © 2023 Zhao, Xu, Li, Wang, Liao and Dong https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Zhao, Junyu Xu, Lusi Li, Chunyu Wang, Fei Liao, Lin Dong, Jianjun The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title | The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title_full | The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title_fullStr | The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title_full_unstemmed | The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title_short | The clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
title_sort | clinical characteristics and gene mutations associated with thyroid hormone resistance syndrome coexisting with pituitary tumors |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950495/ https://www.ncbi.nlm.nih.gov/pubmed/36843601 http://dx.doi.org/10.3389/fendo.2023.1131044 |
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