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Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report
Paget’s disease of bone (PDB) is a common skeleton disorder in which the diagnosis is suggested by radiological analyses. Congenital generalized lipodystrophy (CGL) is a rare, but a radiologic differential diagnosis of Paget’s disease. Patients present total or almost total lack of subcutaneous adip...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273302/ https://www.ncbi.nlm.nih.gov/pubmed/34262529 http://dx.doi.org/10.3389/fendo.2021.683697 |
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author | Freire, Erika Bastos Lima Madeira, Mayara Ponte Lima, Grayce Ellen da Cruz Paiva Fernandes, Virginia Oliveira Aguiar, Lindenberg Barbosa Fontenele, João Paulo Uchoa Montenegro, Ana Paula Dias Rangel Marques, Thyciara Fontenele Ozório, Renan Galvão d’Alva, Catarina Brasil Montenegro, Renan Magalhães |
author_facet | Freire, Erika Bastos Lima Madeira, Mayara Ponte Lima, Grayce Ellen da Cruz Paiva Fernandes, Virginia Oliveira Aguiar, Lindenberg Barbosa Fontenele, João Paulo Uchoa Montenegro, Ana Paula Dias Rangel Marques, Thyciara Fontenele Ozório, Renan Galvão d’Alva, Catarina Brasil Montenegro, Renan Magalhães |
author_sort | Freire, Erika Bastos Lima |
collection | PubMed |
description | Paget’s disease of bone (PDB) is a common skeleton disorder in which the diagnosis is suggested by radiological analyses. Congenital generalized lipodystrophy (CGL) is a rare, but a radiologic differential diagnosis of Paget’s disease. Patients present total or almost total lack of subcutaneous adipose tissue, leptin deficiency, and precocious ectopic lipid accumulation, which lead to intense insulin resistance, poorly controlled diabetes mellitus, and hypertriglyceridemia. CGL subtypes 1 and 2 present sclerosis and osteolytic lesions that can resemble “pagetic” lesions. The clinical correlation is, therefore, essential. We report a CGL patient with bone lesions in which the radiographic findings led to a misdiagnosis of PDB. This case report brings awareness to CGL, a life-threating condition. Its early recognition is essential to avoid clinical complications and premature death. Therefore, it is important to consider CGL as PDB’s differential diagnosis, especially in countries with high prevalence of this rare disease, such as Brazil. |
format | Online Article Text |
id | pubmed-8273302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82733022021-07-13 Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report Freire, Erika Bastos Lima Madeira, Mayara Ponte Lima, Grayce Ellen da Cruz Paiva Fernandes, Virginia Oliveira Aguiar, Lindenberg Barbosa Fontenele, João Paulo Uchoa Montenegro, Ana Paula Dias Rangel Marques, Thyciara Fontenele Ozório, Renan Galvão d’Alva, Catarina Brasil Montenegro, Renan Magalhães Front Endocrinol (Lausanne) Endocrinology Paget’s disease of bone (PDB) is a common skeleton disorder in which the diagnosis is suggested by radiological analyses. Congenital generalized lipodystrophy (CGL) is a rare, but a radiologic differential diagnosis of Paget’s disease. Patients present total or almost total lack of subcutaneous adipose tissue, leptin deficiency, and precocious ectopic lipid accumulation, which lead to intense insulin resistance, poorly controlled diabetes mellitus, and hypertriglyceridemia. CGL subtypes 1 and 2 present sclerosis and osteolytic lesions that can resemble “pagetic” lesions. The clinical correlation is, therefore, essential. We report a CGL patient with bone lesions in which the radiographic findings led to a misdiagnosis of PDB. This case report brings awareness to CGL, a life-threating condition. Its early recognition is essential to avoid clinical complications and premature death. Therefore, it is important to consider CGL as PDB’s differential diagnosis, especially in countries with high prevalence of this rare disease, such as Brazil. Frontiers Media S.A. 2021-06-28 /pmc/articles/PMC8273302/ /pubmed/34262529 http://dx.doi.org/10.3389/fendo.2021.683697 Text en Copyright © 2021 Freire, Madeira, Lima, Fernandes, Aguiar, Fontenele, Montenegro, Marques, Ozório, d’Alva and Montenegro 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 Freire, Erika Bastos Lima Madeira, Mayara Ponte Lima, Grayce Ellen da Cruz Paiva Fernandes, Virginia Oliveira Aguiar, Lindenberg Barbosa Fontenele, João Paulo Uchoa Montenegro, Ana Paula Dias Rangel Marques, Thyciara Fontenele Ozório, Renan Galvão d’Alva, Catarina Brasil Montenegro, Renan Magalhães Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title | Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title_full | Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title_fullStr | Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title_full_unstemmed | Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title_short | Misdiagnosis of Paget’s Disease of Bone in a Congenital Generalized Lipodystrophy Patient: Case Report |
title_sort | misdiagnosis of paget’s disease of bone in a congenital generalized lipodystrophy patient: case report |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273302/ https://www.ncbi.nlm.nih.gov/pubmed/34262529 http://dx.doi.org/10.3389/fendo.2021.683697 |
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