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Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis
Hemochromatosis is an inherited genetic disorder of iron metabolism which can also occur as a secondary result of iron-overload. It leads to organ damage such as cardiomyopathy, liver cirrhosis, hypogonadism, and diabetes. This paper discusses a case of secondary hemochromatosis associated with repe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Endocrine Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970271/ https://www.ncbi.nlm.nih.gov/pubmed/24741460 http://dx.doi.org/10.3803/EnM.2014.29.1.91 |
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author | Jeong, Hyung Ki An, Joon Hwan Kim, Hyoung Sang Cho, Eun Ae Han, Min Gui Moon, Jung Sik Kim, Hee Kyung Kang, Ho-Cheol |
author_facet | Jeong, Hyung Ki An, Joon Hwan Kim, Hyoung Sang Cho, Eun Ae Han, Min Gui Moon, Jung Sik Kim, Hee Kyung Kang, Ho-Cheol |
author_sort | Jeong, Hyung Ki |
collection | PubMed |
description | Hemochromatosis is an inherited genetic disorder of iron metabolism which can also occur as a secondary result of iron-overload. It leads to organ damage such as cardiomyopathy, liver cirrhosis, hypogonadism, and diabetes. This paper discusses a case of secondary hemochromatosis associated with repeated transfusions, presenting as asymptomatic hypoparathyroidism and subclinical hypothyroidism with multiple organ involvement. The 29-year-old female, who had severe aplastic anemia, received multiple transfusions totaling approximately 1,400 units of red blood cells over 15 years. During her routine laboratory examination, hypocalcemia was detected with decreased intact parathyroid hormone and increased thyroid stimulating hormone. Serum ferritin, iron, and total iron binding capacity had increased to 27,583.03 ng/mL, 291 µg/dL, and 389 µg/dL, respectively. She had unusually bronze skin and computed tomography revealed iron deposition in the thyroid, liver, and heart. Multiorgan involvement as seen in this case is rare in hemochromatosis associated with secondary transfusions. To the best of the author's knowledge, this is the first case report in Korea of hypoparathyroidism and subclinical hypothyroidism due to iron deposition in the parathyroid and thyroid gland. |
format | Online Article Text |
id | pubmed-3970271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39702712014-04-16 Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis Jeong, Hyung Ki An, Joon Hwan Kim, Hyoung Sang Cho, Eun Ae Han, Min Gui Moon, Jung Sik Kim, Hee Kyung Kang, Ho-Cheol Endocrinol Metab (Seoul) Case Report Hemochromatosis is an inherited genetic disorder of iron metabolism which can also occur as a secondary result of iron-overload. It leads to organ damage such as cardiomyopathy, liver cirrhosis, hypogonadism, and diabetes. This paper discusses a case of secondary hemochromatosis associated with repeated transfusions, presenting as asymptomatic hypoparathyroidism and subclinical hypothyroidism with multiple organ involvement. The 29-year-old female, who had severe aplastic anemia, received multiple transfusions totaling approximately 1,400 units of red blood cells over 15 years. During her routine laboratory examination, hypocalcemia was detected with decreased intact parathyroid hormone and increased thyroid stimulating hormone. Serum ferritin, iron, and total iron binding capacity had increased to 27,583.03 ng/mL, 291 µg/dL, and 389 µg/dL, respectively. She had unusually bronze skin and computed tomography revealed iron deposition in the thyroid, liver, and heart. Multiorgan involvement as seen in this case is rare in hemochromatosis associated with secondary transfusions. To the best of the author's knowledge, this is the first case report in Korea of hypoparathyroidism and subclinical hypothyroidism due to iron deposition in the parathyroid and thyroid gland. Korean Endocrine Society 2014-03 2014-03-14 /pmc/articles/PMC3970271/ /pubmed/24741460 http://dx.doi.org/10.3803/EnM.2014.29.1.91 Text en Copyright © 2014 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jeong, Hyung Ki An, Joon Hwan Kim, Hyoung Sang Cho, Eun Ae Han, Min Gui Moon, Jung Sik Kim, Hee Kyung Kang, Ho-Cheol Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title | Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title_full | Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title_fullStr | Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title_full_unstemmed | Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title_short | Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis |
title_sort | hypoparathyroidism and subclinical hypothyroidism with secondary hemochromatosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970271/ https://www.ncbi.nlm.nih.gov/pubmed/24741460 http://dx.doi.org/10.3803/EnM.2014.29.1.91 |
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