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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.
Afiliación
  • Freire EBL; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará, Fortaleza, Brazil.
  • Madeira MP; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, Brazil.
  • Lima GEDCP; Health Sciences Center, Christus University Center (UNICHRISTUS), Fortaleza, Brazil.
  • Fernandes VO; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará, Fortaleza, Brazil.
  • Aguiar LB; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, Brazil.
  • Fontenele JPU; Health Sciences Center, Christus University Center (UNICHRISTUS), Fortaleza, Brazil.
  • Montenegro APDR; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará, Fortaleza, Brazil.
  • Marques TF; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, Brazil.
  • Ozório RG; Health Sciences Center, University of Fortaleza, (UNIFOR) Fortaleza, Brazil.
  • d'Alva CB; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará, Fortaleza, Brazil.
  • Montenegro RM; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, Brazil.
Front Endocrinol (Lausanne) ; 12: 683697, 2021.
Article en En | MEDLINE | ID: mdl-34262529
ABSTRACT
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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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Osteítis Deformante / Lipodistrofia Generalizada Congénita Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Osteítis Deformante / Lipodistrofia Generalizada Congénita Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2021 Tipo del documento: Article