Cherubism as a systemic skeletal disease: evidence from an aggressive case.


Journal

BMC musculoskeletal disorders
ISSN: 1471-2474
Titre abrégé: BMC Musculoskelet Disord
Pays: England
ID NLM: 100968565

Informations de publication

Date de publication:
21 Aug 2020
Historique:
received: 04 05 2020
accepted: 10 08 2020
entrez: 23 8 2020
pubmed: 23 8 2020
medline: 15 5 2021
Statut: epublish

Résumé

Cherubism is a rare autosomal dominant genetic condition caused by mutations in the SH3BP2 gene. This disease is characterized by osteolysis of the jaws, with the bone replaced by soft tissue rich in fibroblasts and multinuclear giant cells. SH3BP2 is a ubiquitous adaptor protein yet the consequences of SH3BP2 mutation have so far been described as impacting only face. Cherubism mouse models have been generated and unlike human patients, the knock-in mice exhibit systemic bone loss together with a systemic inflammation. In light of these observations, we decided to search for a systemic cherubism phenotype in a 6-year-old girl with an aggressive cherubism. We report here the first case of cherubism with systemic manifestations. Bone densitometry showed low overall bone density (total body Z-score = - 4.6 SD). Several markers of bone remodelling (CTx, BALP, P1NP) as well as inflammation (TNFα and IL-1) were elevated. A causative second-site mutation in other genes known to influence bone density was ruled out by sequencing a panel of such genes. If this systemic skeletal cherubism phenotype should be confirmed, it would simplify the treatment of severe cherubism patients and allay reservations about applying a systemic treatment such as those recently published (tacrolimus or imatinib) to a disease heretofore believed to be localised to the jaws.

Sections du résumé

BACKGROUND BACKGROUND
Cherubism is a rare autosomal dominant genetic condition caused by mutations in the SH3BP2 gene. This disease is characterized by osteolysis of the jaws, with the bone replaced by soft tissue rich in fibroblasts and multinuclear giant cells. SH3BP2 is a ubiquitous adaptor protein yet the consequences of SH3BP2 mutation have so far been described as impacting only face. Cherubism mouse models have been generated and unlike human patients, the knock-in mice exhibit systemic bone loss together with a systemic inflammation.
CASE PRESENTATION METHODS
In light of these observations, we decided to search for a systemic cherubism phenotype in a 6-year-old girl with an aggressive cherubism. We report here the first case of cherubism with systemic manifestations. Bone densitometry showed low overall bone density (total body Z-score = - 4.6 SD). Several markers of bone remodelling (CTx, BALP, P1NP) as well as inflammation (TNFα and IL-1) were elevated. A causative second-site mutation in other genes known to influence bone density was ruled out by sequencing a panel of such genes.
CONCLUSIONS CONCLUSIONS
If this systemic skeletal cherubism phenotype should be confirmed, it would simplify the treatment of severe cherubism patients and allay reservations about applying a systemic treatment such as those recently published (tacrolimus or imatinib) to a disease heretofore believed to be localised to the jaws.

Identifiants

pubmed: 32825821
doi: 10.1186/s12891-020-03580-z
pii: 10.1186/s12891-020-03580-z
pmc: PMC7441549
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
SH3BP2 protein, human 0
Sh3bp2 protein, mouse 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

564

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Auteurs

Anne Morice (A)

Laboratoire de Physiopathologie Orale Moléculaire, INSERM UMRS 1138, Equipe 5, Centre de Recherche de Cordeliers, 75006, Paris, France. annemoriceaertgeerts@gmail.com.
Université Paris Descartes, 75006, Paris, France. annemoriceaertgeerts@gmail.com.
APHP, Necker Enfants Malades, Service de Chirurgie Maxillo-faciale et Plastique, 75015, Paris, France. annemoriceaertgeerts@gmail.com.
APHP, CRMR des Malformations Rares de la Face et de la Cavité Buccale, 75015, Paris, France. annemoriceaertgeerts@gmail.com.

Aline Joly (A)

APHP, Necker Enfants Malades, Service de Chirurgie Maxillo-faciale et Plastique, 75015, Paris, France.
APHP, CRMR des Malformations Rares de la Face et de la Cavité Buccale, 75015, Paris, France.

Manon Ricquebourg (M)

BIOSCAR, INSERM U1132, Université de Paris, Hôpital Lariboisière, 75010, Paris, France.
Service de Biochimie et Biologie Moléculaire, CHU-Paris-GH Saint Louis Lariboisière Widal, Paris, France.

Gérard Maruani (G)

Université Paris Descartes, 75006, Paris, France.
Institut Necker Enfants-Malades, INSERM U1151 - CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, 75014, Paris, France.
Service de Physiologie, Hôpital Necker - Enfants Malades and Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, 75015, Paris, France.

Emmanuel Durand (E)

IR4M - Université Paris-Sud, CNRS, Université Paris-Saclay, F91401, Orsay, France.

Louise Galmiche (L)

Université Paris Descartes, 75006, Paris, France.
APHP, Necker Enfants Malades, Service d'Anatomopathologie et cytologie, 75015, Paris, France.

Jeanne Amiel (J)

Université Paris Descartes, 75006, Paris, France.
APHP, Necker Enfants Malades, Département de Génétique Médicale, 75015, Paris, France.

Yoann Vial (Y)

APHP, Hôpital Robert Debré, Département de Génétique, 75019, Paris, France.
INSERM UMR 1131, Institut de Recherche Saint-Louis, Université de Paris, Paris, France.

Hélène Cavé (H)

APHP, Hôpital Robert Debré, Département de Génétique, 75019, Paris, France.
INSERM UMR 1131, Institut de Recherche Saint-Louis, Université de Paris, Paris, France.

Kahina Belhous (K)

APHP, Necker Enfants Malades, Service d'imagerie médicale pédiatrique, 75015, Paris, France.

Marie Piketty (M)

APHP, Necker Enfants Malades, Service des Explorations Fonctionnelles, 75015, Paris, France.

Martine Cohen-Solal (M)

Service de Biochimie et Biologie Moléculaire, CHU-Paris-GH Saint Louis Lariboisière Widal, Paris, France.

Ariane Berdal (A)

Laboratoire de Physiopathologie Orale Moléculaire, INSERM UMRS 1138, Equipe 5, Centre de Recherche de Cordeliers, 75006, Paris, France.
UFR Odontologie, Garancière, Université Paris Diderot, 75006, Paris, France.

Corinne Collet (C)

BIOSCAR, INSERM U1132, Université de Paris, Hôpital Lariboisière, 75010, Paris, France.
Service de Biochimie et Biologie Moléculaire, CHU-Paris-GH Saint Louis Lariboisière Widal, Paris, France.

Arnaud Picard (A)

Laboratoire de Physiopathologie Orale Moléculaire, INSERM UMRS 1138, Equipe 5, Centre de Recherche de Cordeliers, 75006, Paris, France.
Université Paris Descartes, 75006, Paris, France.
APHP, Necker Enfants Malades, Service de Chirurgie Maxillo-faciale et Plastique, 75015, Paris, France.
APHP, CRMR des Malformations Rares de la Face et de la Cavité Buccale, 75015, Paris, France.

Amelie E Coudert (AE)

Laboratoire de Physiopathologie Orale Moléculaire, INSERM UMRS 1138, Equipe 5, Centre de Recherche de Cordeliers, 75006, Paris, France.
Service de Biochimie et Biologie Moléculaire, CHU-Paris-GH Saint Louis Lariboisière Widal, Paris, France.
UFR Odontologie, Garancière, Université Paris Diderot, 75006, Paris, France.

Natacha Kadlub (N)

Laboratoire de Physiopathologie Orale Moléculaire, INSERM UMRS 1138, Equipe 5, Centre de Recherche de Cordeliers, 75006, Paris, France.
Université Paris Descartes, 75006, Paris, France.
APHP, Necker Enfants Malades, Service de Chirurgie Maxillo-faciale et Plastique, 75015, Paris, France.
APHP, CRMR des Malformations Rares de la Face et de la Cavité Buccale, 75015, Paris, France.

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