Multi-analytic study of a probable case of fibrous dysplasia (FD) from certosa monumental cemetery (Bologna, Italy).
Adult
Amino Acid Substitution
Cemeteries
/ history
Craniofacial Fibrous Dysplasia
/ diagnostic imaging
Fibrous Dysplasia, Polyostotic
/ diagnostic imaging
History, 19th Century
History, 20th Century
Humans
Italy
Male
Mutation
Osteitis Deformans
/ diagnostic imaging
Osteosarcoma
/ diagnostic imaging
Tomography, X-Ray Computed
/ history
Ancient DNA
Developmental anomaly
Para-functional facets
Pseudo-tumor
Journal
International journal of paleopathology
ISSN: 1879-9825
Titre abrégé: Int J Paleopathol
Pays: Netherlands
ID NLM: 101562474
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
13
06
2018
revised:
08
03
2019
accepted:
08
03
2019
pubmed:
27
3
2019
medline:
11
2
2020
entrez:
27
3
2019
Statut:
ppublish
Résumé
To evaluate, via a multidisciplinary approach, a distinctive paleopathological condition believed to be fibrous dysplasia, found on a 19th/20th century skeleton from Certosa Monumental Cemetery, Bologna, Italy. A skeletonized cranium and mandible recovered from an ossuary in 2014. Pathological alterations were analysed by radiological examination, dental macrowear, histopathological and genetic analyses. The skeleton is believed to be an adult male. Differential diagnoses include Paget's disease, McCune-Albright syndrome, osteochondroma and osteosarcoma. The radiographic findings, along with the solitary nature of the lesions, are strong evidence for the diagnosis of fibrous dysplasia (FD). Genetic analysis further revealed a frequency of ˜1% of mutant alleles with the R201C substitution, one of the post-zygotic activating mutation frequently associated with FD. The multi-analytical method employed suggests a diagnosis of monostotic form of FD. The diagnostic design incorporates multiple lines of evidence, including macroscopic, histopathological, and genetic analyses. Through the use of a multi-analytic approach, robust diagnoses can be offered. This case serves as one of the oldest examples of FD from an historical context. The genetic mutation detected, associated with FD, has not been previously reported in historical/ancient samples.
Identifiants
pubmed: 30913508
pii: S1879-9817(18)30110-4
doi: 10.1016/j.ijpp.2019.03.003
pii:
doi:
Types de publication
Historical Article
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-8Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.