SAPHO Syndrome Presenting With Atlo-Epistrophic Synovitis and Left Vocal Cord Paresis: A Challenging Diagnosis

Author:

Maranini Beatrice1,Ciancio Giovanni1,Rinaldi Rosa2,Borrelli Massimo3,Pugliatti Maura4,Govoni Marcello1

Affiliation:

1. Rheumatology Unit, Department of Medical Sciences, University of Ferrara, Ferrara, Italy

2. Pathology Unit, ASST Mantova, Ospedale Carlo Poma, Mantova, Italy

3. Neurororadiology Unit, Department of Radiology, Azienda Ospedaliero-Universitaria Sant’Anna, Ferrara, Italy

4. Department of Neuroscience and Rehabilitation, University of Ferrara, Ferrara, Italy

Abstract

SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) is a rare syndrome mainly characterized by cutaneous and osteoarticular manifestations. The most typical osteoarticular manifestations are localized to the anterior chest wall and include a usually noninfectious osteitis, hyperostosis, and synovitis of the sternoclavicular joints. However, clinical presentation of SAPHO syndrome can be quite heterogeneous. Several clinical and radiological features are shared with other well-defined pathological entities, and clinical signs and symptoms often occur at different timepoints. Mainly due to this complexity and its rarity, there are currently no validated diagnostic criteria for SAPHO syndrome. Inflammation of the soft tissues around the bones and possible nerve compression could contribute to dysphagia, hypophonia, or obstruction of the airways. Neurologic manifestations could therefore be part of this multiorgan involvement. Here, we present a case of SAPHO syndrome with atypical onset symptoms, characterized by left vocal cord paralysis, acute neck pain due to osteolytic atlantoepistrophic lesion, and an unusual cutaneous manifestation, diagnosed as mid-dermal elastolysis. The latest two, to the best of our knowledge, have been here first described in a case of SAPHO syndrome.

Funder

università degli studi di ferrara

Publisher

SAGE Publications

Subject

Rheumatology,Immunology and Allergy

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