Results 11 to 20 of about 16,958 (227)
Advanced Biomedical Research, 2020 Diffuse idiopathic skeletal hyperostosis (DISH) also known as Forestier disease is a noninflammatory, systemic skeletal disease of unknown etiology. DISH is usually asymptomatic but may compress the posterior wall of the aero digestive tract and lead to ...
Mohammad Zarei +3 more
doaj +1 more source
Transient hypercalcemia in a patient with SAPHO syndrome
Journal of General and Family Medicine, 2022 We here report a case of SAPHO (synovitis‐acne‐pustulosis‐hyperostosis‐osteitis) syndrome with hypercalcemia. The patient was diagnosed with SAPHO syndrome at the age of 54, because he exhibited osteitis and hyperostosis around the sternoclavicular ...
Tadashi Yoshida, Mototsugu Oya
doaj +1 more source
Diagnostics, 2022 Background: Diffuse idiopathic skeletal hyperostosis (DISH) is a pathology characterized by enthesis ossification, but there have been few reports on epidemiological surveys.
Hisanori Ikuma +6 more
doaj +1 more source
Clinical Images: Successfully treated mandibular osteomyelitis by tumor necrosis factor inhibitor in SAPHO syndrome. [PDF]
Arthritis RheumatolArthritis &Rheumatology, Volume 78, Issue 4, Page 993-994, April 2026.
Oba S +5 more
europepmc +2 more sources
The Use of Bone Morphogenetic Protein in the Intervertebral Disk Space in Minimally Invasive Transforaminal Lumbar Interbody Fusion [PDF]
, 2019 Study Design: Retrospective Cohort. Objective: The objective of this study was to characterize one surgeon’s experience over a 10-year period using rhBMP-2 in the disk space for minimally invasive transforaminal lumbar interbody fusion (MIS TLIF ...
Anderson +28 more
core +1 more source
Melorheostosis: Two atypical cases
Indian Journal of Radiology and Imaging, 2014 Melorheostosis is an uncommon mesenchymal dysplasia that rarely affects the axial skeleton.We describe two atypical cases of melorheostosis with classical imaging findings - the first one involving the cervico-dorsal spine with encroachment of left ...
Binit Sureka +5 more
doaj +1 more source
Osteomielitis crónica multifocal recurrente: estado del arte
Medicina U.P.B., 2016 La osteomielitis crónica multifocal recurrente es una enfermedad autoinflamatoria que se caracteriza por focos estériles de inflamación ósea que producen dolor recurrente.
Hernán Darío Gallego Eusse +2 more
doaj +1 more source
Craniometaphyseal and craniodiaphyseal dysplasia, head and neck manifestations and management [PDF]
, 2007 Craniometaphyseal and craniodiaphyseal dysplasia are rare genetic disorders of bone due to modelling errors of long bones and skull bones. These syndromes present with multiple ENT symptomatology from an early age.
Bailey, CM +3 more
core +1 more source
Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies [PDF]
, 2018 Hyperphosphatemic familial tumoral calcinosis (HFTC)/hyperostosis-hyperphosphatemia syndrome (HHS) is an autosomal recessive disorder of ectopic calcification due to deficiency of or resistance to intact fibroblast growth factor 23 (iFGF23). Inactivating
Burbelo +14 more
core +1 more source
Headache in a patient with Klinefelter's syndrome and hyperostosis frontalis interna. [PDF]
, 2007 Hyperostosis frontalis interna (HFI) has been reported in older women, but reports in men are rare. We present a novel case of migraine headache in a gentleman with Klinefelter's syndrome and HFI, along with a discussion of possible pathophysiologic ...
Liebeskind, David S +2 more
core +2 more sources