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Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity
BACKGROUND: Congenital goiter is a common thyroid metabolic disorder characterized by low levels of thyroid hormone, subsequent secretion of excess thyroid-stimulating hormone (TSH) from the pituitary gland, and compensatory hyperplasia of the glands. The presence of signet ring cells (SRCs) does no...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603664/ https://www.ncbi.nlm.nih.gov/pubmed/33129336 http://dx.doi.org/10.1186/s12917-020-02637-4 |
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author | Wang, Jinling Ding, Yulin Sulijid, Jirintai Zhao, Li Lu, Shoufeng Wang, Xiaoyu Liu, Yonghong |
author_facet | Wang, Jinling Ding, Yulin Sulijid, Jirintai Zhao, Li Lu, Shoufeng Wang, Xiaoyu Liu, Yonghong |
author_sort | Wang, Jinling |
collection | PubMed |
description | BACKGROUND: Congenital goiter is a common thyroid metabolic disorder characterized by low levels of thyroid hormone, subsequent secretion of excess thyroid-stimulating hormone (TSH) from the pituitary gland, and compensatory hyperplasia of the glands. The presence of signet ring cells (SRCs) does not provide sufficient evidence for the diagnosis of a thyroid tumor, making histopathological diagnosis challenging. In addition, SRCs can also appear in congenital goiter. Therefore, a comprehensive diagnosis of congenital goiter is warranted based on clinical symptoms, autopsy, histopathology, and laboratory examination. CASE PRESENTATION: A juvenile giraffe at the Ordos Zoo in Ordos presented with symptoms of loss of appetite, serious salivation, and slow growth rate since birth. Its height and weight were significantly lower than those of other giraffes of the same age. The animal ultimately died at 17 months of age. Autopsy revelaed that the thyroids were hard, with an uneven surface and with the presence of many small raised follicles, and dense in cross-section. Other organs were visibly atrophic. Histopathologically, diffuse follicles were irregular in size and shape in the hyperplastic goiter. Some follicles were collapsed due to lack of colloids. The follicles were lined by single or multiple layers of hyperplastic follicular cells (HFCs), some of which were exfoliated in the lumen. The HFCs were either cuboidal with eosinophilic cytoplasm and many red small granules or showed SRC differentiation, with nuclei pressed to one edge of the cell and distorted by cytoplasmic mucin that appeared as a single clear vacuole HFCs and as a foamy, multivesicular cytoplasmic material in others. Scattered necrosis of myocardial cells and hepatocytes, cerebral hemorrhage, necrosis of intestinal villi, and obvious atrophy of organs were also observed. Immunohistochemical tests were strongly positive for thyroglobulin and thyroid transcription factor-1 (TTF-1) in the cytoplasm of HFCs. CONCLUSIONS: Here we present a case of congenital goiter with areas of SRC differentiation in the thyroid of a juvenile giraffe. |
format | Online Article Text |
id | pubmed-7603664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76036642020-11-02 Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity Wang, Jinling Ding, Yulin Sulijid, Jirintai Zhao, Li Lu, Shoufeng Wang, Xiaoyu Liu, Yonghong BMC Vet Res Case Report BACKGROUND: Congenital goiter is a common thyroid metabolic disorder characterized by low levels of thyroid hormone, subsequent secretion of excess thyroid-stimulating hormone (TSH) from the pituitary gland, and compensatory hyperplasia of the glands. The presence of signet ring cells (SRCs) does not provide sufficient evidence for the diagnosis of a thyroid tumor, making histopathological diagnosis challenging. In addition, SRCs can also appear in congenital goiter. Therefore, a comprehensive diagnosis of congenital goiter is warranted based on clinical symptoms, autopsy, histopathology, and laboratory examination. CASE PRESENTATION: A juvenile giraffe at the Ordos Zoo in Ordos presented with symptoms of loss of appetite, serious salivation, and slow growth rate since birth. Its height and weight were significantly lower than those of other giraffes of the same age. The animal ultimately died at 17 months of age. Autopsy revelaed that the thyroids were hard, with an uneven surface and with the presence of many small raised follicles, and dense in cross-section. Other organs were visibly atrophic. Histopathologically, diffuse follicles were irregular in size and shape in the hyperplastic goiter. Some follicles were collapsed due to lack of colloids. The follicles were lined by single or multiple layers of hyperplastic follicular cells (HFCs), some of which were exfoliated in the lumen. The HFCs were either cuboidal with eosinophilic cytoplasm and many red small granules or showed SRC differentiation, with nuclei pressed to one edge of the cell and distorted by cytoplasmic mucin that appeared as a single clear vacuole HFCs and as a foamy, multivesicular cytoplasmic material in others. Scattered necrosis of myocardial cells and hepatocytes, cerebral hemorrhage, necrosis of intestinal villi, and obvious atrophy of organs were also observed. Immunohistochemical tests were strongly positive for thyroglobulin and thyroid transcription factor-1 (TTF-1) in the cytoplasm of HFCs. CONCLUSIONS: Here we present a case of congenital goiter with areas of SRC differentiation in the thyroid of a juvenile giraffe. BioMed Central 2020-10-31 /pmc/articles/PMC7603664/ /pubmed/33129336 http://dx.doi.org/10.1186/s12917-020-02637-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Wang, Jinling Ding, Yulin Sulijid, Jirintai Zhao, Li Lu, Shoufeng Wang, Xiaoyu Liu, Yonghong Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title | Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title_full | Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title_fullStr | Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title_full_unstemmed | Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title_short | Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
title_sort | congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603664/ https://www.ncbi.nlm.nih.gov/pubmed/33129336 http://dx.doi.org/10.1186/s12917-020-02637-4 |
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