Antibiotic‐Impregnated Calcium Sulfate Beads for Local Therapy of Severe Skull Base Osteomyelitis
Clinical Case Reports, Volume 14, Issue 6, June 2026.Novel Local Therapy of Severe Skull Base Osteomyelitis. ABSTRACT We report on a patient with severe progressive osteomyelitis of the lateral skull base, despite targeted long‐term antibiotic therapy. Successful treatment and recovery of the facial nerve palsy were achieved through additional surgical debridement and insertion of synthetic calcium ...
Stefan Lyutenski +3 more
wiley +1 more source
Subungual Exostosis Presenting as a Cutaneous Lesion: A Diagnostic Challenge
Clinical Case Reports, Volume 14, Issue 6, June 2026.Beyond skin: Unveiling the bony truth of Subungual Exostosis. ABSTRACT Subungual exostosis is a benign outgrowth arising from the distal phalanx which often presents as a painful, firm mass beneath or adjacent to the nail bed. Subungual exostosis is fundamentally a bone disease that can easily be misinterpreted as a skin or nail abnormality, requiring ...
Sunil Jaiswal +3 more
wiley +1 more source
Hereditary multiple exostoses: are there new plausible treatment strategies?
Expert Opinion on Orphan Drugs, 2018 Introduction: Hereditary multiple exostoses (HME) is a rare congenital pediatric disorder characterized by osteochondromas forming next to the growth plates in young patients.
M. Pacifici
semanticscholar +1 more source
Hereditary multiple exostoses in a15-year-old boy: A case report and review of literature
Nigerian Journal of Paediatrics, 2016 Background: Hereditary Multiple Exostoses (HME) is a rare bone disease, usually associated with deformity and pressure symptoms. It is an autosomal dominant disorder characterized by the development of benign tumours growing outward from the metaphyses ...
Eke GK , Omunakwe HE , Echem RC
doaj
Prosthodontic and Occlusal Management of a Patient With Facial Port‐Wine Stains: A Case Report
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT This study aims to present the prosthetic rehabilitation of a patient affected by Port‐Wine Stain (PWS), a condition involving intraoral tissues that may pose challenges to removable prosthodontic treatment due to altered mucosal resiliency, pronounced hypersensitivity, and vascular fragility.
Ana‐Maria Condor +6 more
wiley +1 more source
Hereditary Multiple Exostoses: a review of clinical appearance and metabolic pattern.
CLINICAL CASES IN MINERAL AND BONE METABOLISM, 2016 Hereditary multiple exostoses (HME) is an inherited genetic condition characterized by the presence of multiple exostoses (osteochondromas). MHE is a relatively rare autosomal dominant disorder, mainly caused by loss of function mutations in two genes ...
G. Beltrami +4 more
semanticscholar +1 more source
Exostosis subungueal y su diagnóstico diferencial: A propósito de un caso clínico
ARS Medica, 2016 Los tumores y pseudotumores ungueales representan un desafío diagnóstico, principalmente dado la compleja anatomía de la uña y la apariencia clínica similar de estas lesiones.
María Teresa Dossi Cataldo +1 more
doaj +1 more source
Do Exostoses Correlate with Contact Disfunctions? A Case Study of a Maxillary Exostosis
Lubricants, 2019 A maxillary exostosis is a benign overgrowth of bone that occurs on the outer or facial surface of the maxilla and is usually located near the premolar or molar teeth.
M. C. Valigi, Silvia Logozzo
semanticscholar +1 more source
Regression of a solitary osteochondroma of the distal humerus in a toddler following trauma
Radiology Case Reports, 2019 Osteochondromas are bone exostoses, with the vast majority extending from the metaphyseal region of long bones and are capped by cartilage. A review of the current literature reveals spontaneous regression of osteochondromas is a rarely documented event,
Paul B. Heyworth, MBBS +1 more
doaj +1 more source
A genotype-phenotype study of hereditary multiple exostoses in forty-six Chinese patients
BMC Medical Genetics, 2017 BackgroundHereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder that can cause a variety of clinical manifestations. We aimed to evaluate the general clinical phenotypic severity of HME by using a scoring system and correlate
Yuchan Li +4 more
semanticscholar +1 more source