Results 1 to 10 of about 1,452 (104)

Dyke-Davidoff-Masson-like syndrome in an adult cat [PDF]

Journal of Feline Medicine and Surgery Open Reports
Case summary A 4-year-old cat was presented with acute onset of lateralised neurological central nervous system (CNS) signs and seizures. Haematological and serum biochemical parameters were within normal limits.
Andrea Thon, Elisa Gamperl-Mikula, Florian Willmitzer, Michael Leschnik, Kristina Anna Lederer   +4 more
doaj   +2 more sources

Melorheostosis: Clinical, radiological, and histopathological features with a literature review. [PDF]

Physiol Rep
Abstract Melorheostosis is a rare sclerosing bone dysplasia that can clinically and radiologically mimic common bone disorders, particularly in atypical presentations. Its heterogeneous manifestations and limited awareness among clinicians frequently contribute to diagnostic delays or misdiagnosis. We report the case of a 34‐year‐old woman with chronic
Koca E, Kavak Ş, Demir B, Comunoglu N, Kantarci F, Koca O.   +5 more
europepmc   +2 more sources

Characteristics of SAPHO Syndrome: Clinical Analysis of 19 Cases [PDF]

Zhongguo quanke yixue, 2022
Background SAPHO syndrome is a rare chronic inflammatory disease of unknown causes with various clinical manifestations, which involves bone joint and skin tissue, and has no specific diagnostic indicators and uniform treatment strategy.
Wenting SUN, Qiuai KOU
doaj   +1 more source

SAPHO—a diagnosis to consider in patients with refractory costochondritis

Egyptian Rheumatology and Rehabilitation, 2022
Background SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, and osteitis) is a rare, heterogeneous, self-limited disease of unknown etiology. It involves progressive bone and joint damage, and skin and bone lesions may occur at different times ...
Viviana Parra-Izquierdo, Hector Cubides, Viviana Rivillas, Juan Sebastián Frías-Ordoñez, Sergio Mora, Joerg Ermann   +5 more
doaj   +1 more source

Clinical Presentation of Schnitzler’s Syndrome: A Rare Autoimmune Disease

Journal of Investigative Medicine High Impact Case Reports, 2023
Schnitzler’s Syndrome (SS) is a rare late-onset acquired autoinflammatory disorder which consists of chronic urticaria associated with a monoclonal IgM-kappa gammopathy, arthralgias, skeletal hyperostosis, lymphadenopathy, and recurrent constitutional ...
Vishal Patel MD, Darshana Balasubramaniam MD, Vanessa Cavero-Chavez MD, Lyda Cuervo-Pardo MD, Catalina Sanchez-Alvarez MD   +4 more
doaj   +1 more source

Skin symptoms as diagnostic clue for autoinflammatory diseases [PDF]

Anais Brasileiros de Dermatologia, 2017
Autoinflammatory disorders are immune-mediated diseases with increased production of inflammatory cytokines and absence of detectable autoantibodies.
Alvaro Moreira, Barbara Torres, Juliano Peruzzo, Alberto Mota, Kilian Eyerich, Johannes Ring   +5 more
doaj   +2 more sources

Do you know this syndrome? Você conhece esta síndrome?

Anais Brasileiros de Dermatologia, 2012
The SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis and osteitis) includes a group of findings characterized by bone lesions usually located on the anterior chest wall, often associated with skin lesions.
Gerson Dellatorre, Caio César Silva de Castro   +1 more
doaj   +1 more source

Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome: A Case of Spine, Pelvis, and Anterior Chest Wall Involvement, with Overlooked Plantar Pustulosis

대한영상의학회지, 2017
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an inflammatory clinical condition with aseptic bone lesions and characteristic skin manifestations.
Hyun Soo Kim, Soh Yong Jeong, Sujin Lee, In-Woon Baek, Jeongmi Park   +4 more
doaj   +1 more source

Computed tomography in terms of thoracic outlet syndrome diagnosis

Исследования и практика в медицине
Thoracic outlet syndrome (TOS) comprises a group of clinical syndromes caused by congenital or acquired compression of the brachial plexus or subclavian vessels during their passage through the superior thoracic aperture.Clinical manifestations vary by ...
L. A. Titova, A. A. Gridsay, E. M. Tolstykh, S. I. Marks, N. V. Ischenko, M. V. Anisimov, A. Yu. Goncharova, I. A. Baranov, L. A. Haetskaya   +8 more
doaj   +1 more source

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

Clinical 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, Muhammad Ahsan, Tehreem Farooq, Mirza Daniyal Baig, Mirza Mohammad Ali Baig, Mohammed Hammad Jaber Amin   +5 more
wiley   +1 more source