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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
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.
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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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