Results 71 to 80 of about 11,244 (223)

6 - Diffuse idiopathic skeletal hyperostosis (DISH)

open access: yes, 2020
Homme adulte présentant une maladie de Forestier. Sépulture 300 du site de Bobigny, Hôpital Avicenne (fouille 2003). E. Jacquot, CD93. La maladie de Forestier ou maladie hyperostosique ou Diffuse Idiopathic Skeletal Hyperostosis (DISH) ((https://www ...
Valérie Delattre
core  

Bilateral Avascular Necrosis of the Femoral Heads in Ankylosing Spondylitis Requiring Staged Total Hip Arthroplasty: A Case Report of Diagnostic and Therapeutic Challenges

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Ankylosing spondylitis (AS) is a chronic immune‐mediated inflammatory arthropathy primarily affecting the axial skeleton but may involve peripheral joints, particularly the hips. Avascular necrosis (AVN) of the femoral head represents a severe, underrecognized complication whose pathogenesis in AS is multifactorial—encompassing disease ...
Syeda Simrah Shah   +5 more
wiley   +1 more source

A Deceiving Massive Opacification of the Maxillary Sinus: Odontogenic Cyst Mimicking Odontogenic Sinusitis

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Considered the second most common type of odontogenic cysts, dentigerous cysts (DCs) are developmental lesions most often detected incidentally on radiographic imaging. The pathogenesis of DCs is not fully understood, but they are widely regarded as developmental cysts originating from the dental follicle.
Anastasia Urbanelli   +4 more
wiley   +1 more source

Psoriasis-associated Petrous Hyperostosis Causing Trigeminal Neuralgia: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Trigeminal Neuralgia (TN) is most commonly caused by Neurovascular Conflict (NVC); bony aetiologies are rare. We report a 31-year-old woman with a 10-year history of psoriasis who presented with a 3-month history of intermittent, severe, paroxysmal right
Rohini Chaudhari, Sourabh Zambre
doaj   +1 more source

[Sternocostoclavicular hyperostosis. Association with pustular psoriasis and systemic vasculitis]

open access: yes, 1988
A female patient with sternocostoclavicular hyperostosis has been followed for 14 years. The case merits special attention because of its association with psoriasis and with an episode of systemic vasculitis.
Sauvain, M J, Wieland, T, Pirovino, M
core  

Hyperostosis in meningioma: a retrospective exploration of histological correlates.

open access: yes
PURPOSE: Meningiomas are the most common type of primary brain tumour. Hyperostosis is commonly associated but remains incompletely understood. This study aimed to evaluate the relationship between meningioma-associated hyperostosis and other tumour ...

core   +1 more source

Hyperostosis Frontalis Interna in a Child With Severe Traumatic Brain Injury

open access: yes, 2017
Hyperostosis frontalis interna is an unexplained irregular thickening of the inner table of the frontal bone. Hyperostosis frontalis interna was first identified in 1719 by Morgagni as a symptom of a more generalized syndrome characterized by virilism ...
Xin Wang, Yaxiong Li, Yan Li
core   +1 more source

Historical Records of Tumours in New Zealand Marine Fishes

open access: yesNew Zealand Journal of Marine and Freshwater Research, Volume 60, Issue 2, June 2026.
Tumours were first described in New Zealand marine fishes in 1982 but those early records have been difficult to access and subsequently few tumours have been collected and little has been published. This review updates records of identified tumours from teleosts in the New Zealand marine environment and may encourage more work to identify background ...
John Brian Jones
wiley   +1 more source

A case study of symptomatic severe diffuse cranial hyperostosis

open access: yesInterdisciplinary Neurosurgery, 2020
This case report discusses an incident of cranial hyperostosis that was discovered after an episode of syncope on imaging. A CT and MRI work-up revealed intracranial volume loss and cerebral herniation into the posterior fossa.
Kayla Byrne   +2 more
doaj   +1 more source

Fetal MRI and postnatal findings of severe infantile cortical hyperostosis: A case report of prenatal Caffey disease with literature review

open access: yesRadiology Case Reports
Caffey disease, also known as infantile cortical hyperostosis, is a rare skeletal disorder characterized by self-limited cortical bone hyperostosis and soft tissue swelling, typically presenting within the first 6 months of life. We report a rare case of
Rutger S. Gunther, MD   +2 more
doaj   +1 more source

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