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Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease
CASE REPORT: A 29-year-old wheelchair-bound woman was presented to us by the gastroenterologist with suspected osteomalacia. She had lived in the Netherlands all her life and was born of Moroccan parents. Her medical history revealed iron deficiency, growth retardation, and celiac disease, for which...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235277/ https://www.ncbi.nlm.nih.gov/pubmed/22207878 http://dx.doi.org/10.1007/s11657-011-0059-7 |
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author | Rabelink, Noortje M. Westgeest, Hans M. Bravenboer, Nathalie Jacobs, Maarten A. J. M. Lips, Paul |
author_facet | Rabelink, Noortje M. Westgeest, Hans M. Bravenboer, Nathalie Jacobs, Maarten A. J. M. Lips, Paul |
author_sort | Rabelink, Noortje M. |
collection | PubMed |
description | CASE REPORT: A 29-year-old wheelchair-bound woman was presented to us by the gastroenterologist with suspected osteomalacia. She had lived in the Netherlands all her life and was born of Moroccan parents. Her medical history revealed iron deficiency, growth retardation, and celiac disease, for which she was put on a gluten-free diet. She had progressive bone pain since 2 years, difficulty with walking, and about 15 kg weight loss. She had a short stature, scoliosis, and pronounced kyphosis of the spine and poor condition of her teeth. Laboratory results showed hypocalcemia, an immeasurable serum 25-hydroxyvitamin D level, and elevated parathyroid hormone and alkaline phosphatase levels. Spinal radiographs showed unsharp, low contrast vertebrae. Bone mineral density measurement at the lumbar spine and hip showed a T-score of −6.0 and −6.5, respectively. A bone scintigraphy showed multiple hotspots in ribs, sternum, mandible, and long bones. A duodenal biopsy revealed villous atrophy (Marsh 3C) and positive antibodies against endomysium, transglutaminase, and gliadin, compatible with active celiac disease. A bone biopsy showed severe osteomalacia but normal bone volume. She was treated with calcium intravenously and later orally. Furthermore, she was treated with high oral doses of vitamin D and a gluten-free diet. After a few weeks of treatment, her bone pain decreased, and her muscle strength improved. DISCUSSION: In this article, the pathophysiology and occurrence of osteomalacia as a complication of celiac disease are discussed. Low bone mineral density can point to osteomalacia as well as osteoporosis. |
format | Online Article Text |
id | pubmed-3235277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-32352772011-12-27 Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease Rabelink, Noortje M. Westgeest, Hans M. Bravenboer, Nathalie Jacobs, Maarten A. J. M. Lips, Paul Arch Osteoporos Case Report CASE REPORT: A 29-year-old wheelchair-bound woman was presented to us by the gastroenterologist with suspected osteomalacia. She had lived in the Netherlands all her life and was born of Moroccan parents. Her medical history revealed iron deficiency, growth retardation, and celiac disease, for which she was put on a gluten-free diet. She had progressive bone pain since 2 years, difficulty with walking, and about 15 kg weight loss. She had a short stature, scoliosis, and pronounced kyphosis of the spine and poor condition of her teeth. Laboratory results showed hypocalcemia, an immeasurable serum 25-hydroxyvitamin D level, and elevated parathyroid hormone and alkaline phosphatase levels. Spinal radiographs showed unsharp, low contrast vertebrae. Bone mineral density measurement at the lumbar spine and hip showed a T-score of −6.0 and −6.5, respectively. A bone scintigraphy showed multiple hotspots in ribs, sternum, mandible, and long bones. A duodenal biopsy revealed villous atrophy (Marsh 3C) and positive antibodies against endomysium, transglutaminase, and gliadin, compatible with active celiac disease. A bone biopsy showed severe osteomalacia but normal bone volume. She was treated with calcium intravenously and later orally. Furthermore, she was treated with high oral doses of vitamin D and a gluten-free diet. After a few weeks of treatment, her bone pain decreased, and her muscle strength improved. DISCUSSION: In this article, the pathophysiology and occurrence of osteomalacia as a complication of celiac disease are discussed. Low bone mineral density can point to osteomalacia as well as osteoporosis. Springer-Verlag 2011-06-15 2011 /pmc/articles/PMC3235277/ /pubmed/22207878 http://dx.doi.org/10.1007/s11657-011-0059-7 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Case Report Rabelink, Noortje M. Westgeest, Hans M. Bravenboer, Nathalie Jacobs, Maarten A. J. M. Lips, Paul Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title | Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title_full | Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title_fullStr | Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title_full_unstemmed | Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title_short | Bone pain and extremely low bone mineral density due to severe vitamin D deficiency in celiac disease |
title_sort | bone pain and extremely low bone mineral density due to severe vitamin d deficiency in celiac disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235277/ https://www.ncbi.nlm.nih.gov/pubmed/22207878 http://dx.doi.org/10.1007/s11657-011-0059-7 |
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