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hyperostosis/edema
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Postoperative obstructing laryngeal edema in patients with diffuse idiopathic skeletal hyperostosis of cervical spine -A report of two cases-.
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Two cases were reported in which severe postoperative laryngeal edema were developed after the operation of diffuse idiopathic skeletal hyperostosis (DISH) of cervical spine. In the first case, sudden airway obstruction was developed in the general ward 6 hour after uneventful decompression surgery
Wiskott-Aldrich syndrome presenting with early onset recurrent acute hemorrhagic edema and hyperostosis.
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We report two unusual presenting manifestations of Wiskott-Aldrich syndrome (WAS), recurrent acute hemorrhagic edema of infancy (AHEI); a form of cutaneous vasculitis and hyperostosis of the tibia. Though cutaneous vasculitis is known to occur in WAS, presentation in early infancy and as AHEI is
Antenatal-onset infantile cortical hyperostosis and nonimmune hydrops.
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Infantile cortical hyperostosis antenatal onset is an uncommon disease characterized by polyhydramnios, anasarca or hydrops, pulmonary hypoplasia, hepatomegaly, bowed hyperostotic long bones, and a poor prognosis. Sonographically the intrauterine manifestations may be similar to those of
Diffuse idiopathic skeletal hyperostosis causing obstructing laryngeal edema.
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Diffuse idiopathic skeletal hyperostosis (DISH), or ankylosing hyperostosis ("Forestier's disease"), is an ossifying diathesis of unknown etiology. Diagnosis is primarily radiologic: osseous bridging of at least four contiguous vertebral bodies, a radiolucent line between the deposited bone and the
Tonsillectomy Leads to Remission of Bone Marrow Edema and Palmoplantar Pustulosis in Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome
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Response to: "Diffuse Idiopathic Skeletal Hyperostosis and Ankylosing Spondylitis. Comment on the article by Latourte et al" by Olmedo-Garzón and Ruiz-Ollero.
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We would like to thank F.J. Olmedo-Garzón and A. Ruiz-Ollero for their interest in our article examining the presence of imaging features suggestive of axial spondyloarthritis (axSpA) in patients with diffuse idiopathic skeletal hyperostosis (DISH) (1). We have read with great interest their
Hyperostosis in Newborn Pigs.
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Hyperostosis "thick legs" is reported in a case involving 7 of a litter of 11 purebred Landrace piglets. The 12 limbs involved showed variable degrees of thickening and immobility; tension and fixation of the skin. Necropsy revealed extensive fibrous connective tissue, enlargement and edema of
Diffuse idiopathic skeletal hyperostosis: a case of dysphagia.
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OBJECTIVE
To present and discuss the clinical manifestations, radiographic features, and treatment of a patient with diffuse idiopathic skeletal hyperostosis complicated by dysphagia. This case serves as an educational tool by bringing attention to an uncommon complication of a common disorder. An
Diffuse Idiopathic Skeletal Hyperostosis and Ankylosing Spondylitis. Comment on the article by Latourte et al.
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We read with great interest the article by Latourte et al about axial spondyloarthritis (SpA) like imaging in Diffuse Idiopathic Skeletal Hyperostosis (DISH) (1). On the spine magnetic resonance imaging, 76.9% of their cohort of patients with symptomatic DISH had at least 1 inflammatory lesion, as
Magnetic resonance imaging in diffuse idiopathic skeletal hyperostosis: similarities to axial spondyloarthritis.
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Diffuse idiopathic skeletal hyperostosis (DISH) is a non-inflammatory condition that involves calcification and ossification of the spinal ligaments and entheses. While, characteristic magnetic resonance imaging (MRI) lesions of the spine in patients with axial spondyloarthritis, another
A Rare Case of Lethal Prenatal-Onset Infantile Cortical Hyperostosis.
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Infantile cortical hyperostosis, or Caffey's disease, usually presents with typical radiological features of soft tissue swelling and cortical thickening of the underlying bone. The disease can be fatal when it presents antenatally, especially before a gestational age of 35 weeks. This fatal,
Prenatal infantile cortical hyperostosis (Caffey's disease): a 'hepatic myeloid hyperplasia-pulmonary hypoplasia sequence' can explain the lethality of early onset cases.
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BACKGROUND
Infantile cortical hyperostosis (ICH) is benign and self-limiting when it presents near or after birth but is usually lethal when it presents earlier.
METHODS
We present the clinical, ultrasonic, radiographic and pathologic findings in an instructive case of early onset prenatal
Whole Body Magnetic Resonance Imaging Features in Diffuse Idiopathic Skeletal Hyperostosis in Conjunction with Clinical Variables to Whole Body MRI and Clinical Variables in Ankylosing Spondylitis.
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OBJECTIVE
Discrimination of diffuse idiopathic skeletal hyperostosis (DISH) and ankylosing spondylitis (AS) can be challenging. Usefulness of whole-body magnetic resonance imaging (WB-MRI) in diagnosing spondyloarthritis has been recently proved. We assessed the value of clinical variables alone and
Cervical ankylosing hyperostosis and airway obstruction.
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Forestier's disease, or ankylosing hyperostosis of the cervical spine, has been described to cause dysphagia, foreign body sensation, and aspiration. We report two patients with ankylosing hyperostosis producing ulceration of the posterior plate of the cricoid cartilage, inflammatory edema, and
[Infantile cortical hyperostosis (Caffey-Silverman syndrome). Histologic, histochemical and electron microscopic studies].
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Infantile cortical hyperostosis, also known as Caffey's disease or Caffey-Silverman syndrome, is an uncommon clinico-pathological lesion of unknown etiology and uncertain histogenesis. One of the most striking features is the early age of patients at the onset of the disease, showing swelling of the
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