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1.
Rev Med Liege ; 67(12): 619-22, 2012 Dec.
Article in French | MEDLINE | ID: mdl-23342871

ABSTRACT

A 27-year-old-man was diagnosed as having ankylosing spondylitis (AS) in 2003 and received a treatment by etanercept. Typical symptoms of active Crohn's disease (CD) developed 11 months after initiation of etanercept therapy. At colonoscopy, lesions compatible with CD were found endoscopically and histologically. Etanercept was interrupted and CD responded to standard treatment. A switch to infliximab was decided to treat a flare up ofAS. New onset CD may be considered an immune mediated injury induced by etanercept, but the causative role of the latter has not been demonstrated at this stage.


Subject(s)
Crohn Disease/chemically induced , Immunoglobulin G/adverse effects , Immunologic Factors/adverse effects , Adult , Antibodies, Monoclonal/therapeutic use , Colonoscopy , Etanercept , Humans , Immunoglobulin G/therapeutic use , Immunologic Factors/therapeutic use , Infliximab , Male , Receptors, Tumor Necrosis Factor/therapeutic use , Spondylitis, Ankylosing/drug therapy
2.
Rheumatol Int ; 32(4): 1075-8, 2012 Apr.
Article in English | MEDLINE | ID: mdl-21331571

ABSTRACT

We report a new case of polyostotic fibrous dysplasia (FD). A 26-year-old woman was referred to our department complaining of pain in her left arm. She had suffered for tow fractures in left leg and arm previously. Plain radiographs showed osteolytics lesions at the left humerus and radius. Histological examination of the surgical specimens showed FD. She has beneficed with zoledronic acid perfusion.


Subject(s)
Fibrous Dysplasia, Polyostotic/diagnostic imaging , Humerus/diagnostic imaging , Radius/diagnostic imaging , Adult , Bone Density Conservation Agents/therapeutic use , Diphosphonates/therapeutic use , Female , Fibrous Dysplasia, Polyostotic/drug therapy , Fibrous Dysplasia, Polyostotic/pathology , Humans , Humerus/pathology , Imidazoles/therapeutic use , Radiography , Radius/pathology , Zoledronic Acid
3.
Med Trop (Mars) ; 71(1): 87-9, 2011 Feb.
Article in French | MEDLINE | ID: mdl-21585104

ABSTRACT

The purpose of this report is to describe the case of a 13-year-old boy presenting typical sciatica leading to the discovery of primary pelvic hydatid cyst extending to the ischiatic bone. Diagnosis was suspected based on echography and magnetic resonance imaging and confirmed by surgical exploration.


Subject(s)
Echinococcosis/complications , Sciatica/parasitology , Adolescent , Humans , Male , Pelvis , Tunisia
6.
BMJ Case Rep ; 20112011 Mar 24.
Article in English | MEDLINE | ID: mdl-22699469

ABSTRACT

Hydatidosis, also known as echinococcosis, is a rare but serious parasitic disease in endemic areas. Primary spinal location is extremely rare. This case report describes a rare instance of hydatid cyst that caused severe and progressive low-back pain and neurologic dysfunction. Spine MRI showed a unique vertebral collapse of Th12 body with multicystic lesions filling the spinal canal. In addition, hydatidosis serodiagnostic test was positive at 1/725. Treatment depended on the actual surgical removal of the cysts. Surgery consisted in excision and extirpation of the cysts, associated with decompressive laminectomy. The diagnosis was confirmed on the basis of histological results. No coincidental hydatid visceral involvement was found. Antihelminthic drugs (Albendazole) were promptly given before surgery for a long period. The outcome was satisfactorily marked by total regression of the motor deficit and sphincter disorders.


Subject(s)
Echinococcosis/diagnosis , Fractures, Compression/etiology , Low Back Pain/etiology , Spinal Fractures/etiology , Thoracic Vertebrae/injuries , Echinococcosis/complications , Fractures, Compression/diagnosis , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Spinal Fractures/diagnosis
7.
BMJ Case Rep ; 20112011 Mar 25.
Article in English | MEDLINE | ID: mdl-22700074

ABSTRACT

Brucellosis is a zoonosis that affects several organs. The spine is the most common site of musculoskeletal involvement. However, multiple-level spinal involvement is rare in brucella spondylodiscitis. The authors report a case of a 56-year-old male shepherd who had developed a spondylodiscitis affecting simultaneously the cervical, thoracic and lumbar regions. The diagnosis was established by using MRI after the brucella-agglutination test was found to be positive. A high degree of suspicion in the diagnosis of brucellar spondylodiscitis is essential to reduce the delay for the treatment. Thus, it should be essentially included in the differential diagnosis of longstanding cervical, thoracic or back pain, particularly in regions where brucellosis is endemic. Screening serological tests for brucella should be used more widely in cases with low index of suspicion, especially in endemic areas.


Subject(s)
Brucellosis/diagnosis , Cervical Vertebrae , Discitis/microbiology , Lumbar Vertebrae , Magnetic Resonance Imaging , Thoracic Vertebrae , Brucellosis/complications , Discitis/diagnosis , Humans , Male , Middle Aged
8.
BMJ Case Rep ; 20112011 Feb 02.
Article in English | MEDLINE | ID: mdl-22714601

ABSTRACT

Sweet's syndrome (SS) is an acute neutrophilic dermatosis characterised by abrupt onset of fever, leukocytosis and cutaneous eruption, with dermal neutrophilia on skin biopsy. Most cases are idiopathic but SS can be associated with various affections, especially neoplastic, inflammatory and infectious diseases. The authors report the case of an SS occurring in a patient with a known rheumatoid arthritis associated with a secondary Sjögren's syndrome, with incidental finding of concurrent lymph node tuberculosis. In case of SS, an associated disease (malignant, inflammatory or infectious diseases) must imperatively be searched for, knowing that two or more of these affections can coexist.


Subject(s)
Arthritis, Rheumatoid/complications , Sjogren's Syndrome/complications , Sweet Syndrome/etiology , Tuberculosis, Lymph Node/complications , Adult , Female , Humans
11.
Med Trop (Mars) ; 70(5-6): 537-9, 2010 Dec.
Article in French | MEDLINE | ID: mdl-21520662

ABSTRACT

Tabetic arthropathy (TA) is a type of neuropathic arthropathy that has become rare. The purpose of this report is to describe a case of tabetic arthropathy involving the knee. A 53-year-old man was hospitalized for painless right knee arthropathy. Clinical examination demonstrated hydarthrosis of the right knee, peripheral neuropathic syndrome of the lower limbs, and paralysis of the IXth and Xth cranial pairs. Plain radiography showed the presence of lytic lesions in the internal femoral condyle and tibial plateau. Syphilitic serology tests were positive in the blood and cerebrospinal fluid.


Subject(s)
Arthropathy, Neurogenic/diagnosis , Tabes Dorsalis/diagnosis , Arthropathy, Neurogenic/microbiology , Humans , Knee Joint/pathology , Male , Middle Aged , Tabes Dorsalis/complications , Tunisia
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