نتایج جستجو برای: chronic multifocal osteomyelitis crmo

تعداد نتایج: 512001  

2015
A Daia V Kini RZ Taha H El-Shanti B Fathalla

Introduction Patients with more than one autoinflammatory disorder are rarely reported in the literature [1]. Additionally, rare reports suggest that MEFV mutations might be associated with atypical manifestations for familial Mediterranean fever (FMF), such as isolated recurrent muscle pain in one patient [2] and chronic recurrent multifocal osteomyelitis (CRMO) responsive to colchicine in ano...

2013
C Galeotti I Koné-Paut

Introduction The syndrome of synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) is a rare autoinflammatory syndrome, affecting essentially the adults. Osteitis with Propionibacterium Acnes reported in the literature is generally connected to the presence of a foreign body or with the SAPHO syndrome. Chronic recurrent multifocal osteomyelitis (CRMO) is a disease related to the SAPHO ...

2016
Matthias Christian Wurm Ines Brecht Michael Lell Kathrin Brunner Konstantinos Theodorou Mitsimponas Martin Chada Julia Jahn Friedrich-Wilhelm Neukam Cornelius von Wilmowsky

BACKGROUND Chronic recurrent multifocal osteomyelitis (CRMO) is a rare acquired inflammatory skeletal disorder of unknown origin. CRMO was first described by Gideon in 1972 and mainly affects children and young adults of female gender. The CRMO is part of the clinical picture of non-bacterial Osteomyelitis (NBO) and typically presents a relapsing recurring course with both remission and spontan...

2013
C Galeotti I Koné-Paut

Introduction The syndrome of synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) is a rare autoinflammatory syndrome, affecting essentially the adults. Osteitis with Propionibacterium Acnes (P.Acnes) reported in the literature is generally connected to the presence of a foreign body or with the SAPHO syndrome. Chronic recurrent multifocal osteomyelitis (CRMO) is a disease related to ...

Journal: :Pediatric rheumatology online journal 2015
M Barrani F Massei M Scaglione A Paolicchi S Vitali E M Ciancia S Crovella M C Caparello R Consolini

BACKGROUND Chronic recurrent multifocal osteomyelitis (CRMO) is a rare condition that commonly affects the clavicle and pelvis. CASE PRESENTATION We report here a case a 12 years old girl with CRMO arising with recurrent episodes of left supraorbital headache, followed by the appearance of a periorbital dyschromia. Magnetic resonance imaging (MRI) of the skull and orbits revealed an important...

Journal: :British Journal of Surgery 2021

Abstract Introduction Chronic recurrent multifocal osteomyelitis (CRMO) is a paediatric inflammatory bone condition requiring close monitoring by multi-disciplinary team throughout childhood. Many UK patients are seen at the Royal National Orthopaedic Hospital, Stanmore for more than decade of specialist management. Prior to recent COVID crisis, we recognised need frequent without inconvenience...

2013
Mohammadhassan Aelami Hamid Ahanchian Reza Jafarzadeh Esfehani Yasmin Davoudi Mohammad Gharedaghi Vahid Reza Dabbagh Kakhki Vahid Reza Dabbagh

Chronic recurrent multifocal osteomyelitis (CRMO) is an inflammatory bone disease usually affecting children. A 9-year old boy presented with recurrent lower extremities pain and discomfort lasting for two years. In every time, symptoms vanished after several weeks. The patient received antibiotics only in one period of bone pain. In other occasions the patient didn’t received any antibiotics. ...

Journal: :Journal of the Pediatric Orthopaedic Society of North America 2023

Background: Chronic Recurrent Multifocal Osteomyelitis (CRMO) is a rare aseptic autoinflammatory disease with wide and vague clinical presentation that often mimics infection, malignancy, or benign conditions, leading to delayed diagnosis. Methods: Children diagnosed CRMO at single tertiary pediatric hospital in the United States between 2012 2022 who were evaluated by orthopaedic surgeon retro...

2009
Saadiya A. Haque Aziza Shad Metin Ozdemirli Victoria K. Shanmugam Bhaskar Kallakury

Primary lymphoma of the bone (PLB) accounts for 2% of all non-Hodgkin's lymphomas, and until recently it had not been well characterized in literature. Most cases present in adulthood (average age 50), with localized painful lesions in the long bones, cranium, or axial skeleton.We describe a case of multifocal PLB in an adolescent female. In this case, the initial presentation, with migratory l...

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