Symptomatic hypercalcemia and lytic lesions of the skull revealing sarcoidosis: A case report.
Bone sarcoidosis
Imaging
Osteolysis
Skull
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Dec 2024
Dec 2024
Historique:
received:
07
08
2024
accepted:
21
08
2024
medline:
23
9
2024
pubmed:
23
9
2024
entrez:
23
9
2024
Statut:
epublish
Résumé
Sarcoidosis is a systemic granulomatosis of unknown etiology. Mediastinal lymph node and pulmonary involvement are the most characteristic manifestations. However, bone involvement is rare during sarcoidosis. Herein, we describe an atypical case of sarcoidosis revealed by a severe hypercalcemia and lytic lesions of the skull without pulmonary or mediastinal manifestation. A 53-year-old woman was admitted for symptomatic hypercalcemia of 3.8 mmoL/L. The initial good course after hydration combined with a dose of intravenous zoledronate was followed by a relapse of hypercalcemia. Computed tomography (CT) scan showed 2 lytic lesions of the skull and multiple nodules and micronodules in the liver and the spleen which were of normal size. The histological examination showed a non-necrotizing granulomatous hepatitis, with no signs of malignancy. The bone marrow biopsy did not show any abnormality. Assessment for tuberculosis was negative. The diagnosis of sarcoidosis was considered. Oral prednisone therapy allowed total remission.
Identifiants
pubmed: 39308619
doi: 10.1016/j.radcr.2024.08.115
pii: S1930-0433(24)00901-4
pmc: PMC11416470
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
5744-5749Informations de copyright
© 2024 The Authors. Published by Elsevier Inc. on behalf of University of Washington.