Rheumatoid arthritis, Klippel-Feil`s syndrome and Pott`s disease in Cardinal Carlo de` Medici (1595-1666)

CER194
2009 Vol.27, N°4
PI 0594, PF 0602
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PMID: 19772790 [PubMed]

Received: 09/02/2009
Accepted : 20/03/2009
In Press: 10/11/2009
Published: 10/11/2009

Abstract

OBJECTIVES:
A paleopathological study was carried out on the skeletal remains of Cardinal Carlo de` Medici (1595-1666), son of the Grand Duke Ferdinando I (1549-1609) and Cristina from Lorraine (1565-1636), to investigate the articular pathology described in the archival sources.
METHODS:
The skeletal remains of Carlo, buried in the Basilica of San Lorenzo in Florence, have been exhumed and submitted to macroscopic and radiological examination.
RESULTS:
The skeleton of Carlo revealed a concentration of different severe pathologies. Ankylosis of the cervical column, associated with other facial and spine anomalies suggests a diagnosis of congenital disease: the Klippel-Feil syndrome. In addition, the cervical segment presents the results of the tuberculosis (Pott`s disease) from which the Cardinal suffered in his infancy. The post-cranial skeleton shows an ankylosing disease, mainly symmetrical and extremely severe, involving the large as well as small articulations, and characterized by massive joint fusion, that totally disabled the Cardinal in his last years of life.
CONCLUSIONS:
The final diagnosis suggests an advanced, ankylosing stage of rheumatoid arthritis.