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1.
Arthritis Rheum ; 43(1): 109-19, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10643706

RESUMO

OBJECTIVE: To retrospectively assess, with a sufficiently long followup (mean 11.6 years; median 9 years), the long-term outcome of chronic recurrent multifocal osteitis (CRMO), a multifocal, inflammatory bone disease. METHODS: Patients included were 8 children/adolescents and 7 adults with no family history of rheumatic disease who had been diagnosed as having CRMO between 1979 and 1995. Ten patients had undergone at least 1 bone biopsy of the lesions, with histologic examination and multiple cultures. In 1996, in addition to an in-depth interview, 12 patients underwent an extensive physical examination, laboratory evaluation, HLA-A, B, C, and DR typing, bone radiography and scintigraphy, and computed tomography scan of the sternoclavicular and sacroiliac joints. RESULTS: Remission was observed in 3 patients. The other 12 patients developed various associations of vertebral (n = 10), sacroiliac (n = 6), anterior thoracic (n = 7), peripheral articular (n = 2), enthesopathic (n = 4), or dermatologic (palmoplantar pustulosis in 3 cases and psoriasis in 2) involvements. Spine involvement was the most common and occurred the earliest (median time to appearance after the onset of osteitis 5.63 years). Clinical sacroiliitis was always unilateral. No patients carried the HLA-B27 haplotype. CRMO responded well to nonsteroidal antiinflammatory drugs. Twelve patients met the European Spondylarthropathy Study Group criteria for spondylarthopathy. CONCLUSION: After 10 years, CRMO had usually evolved to spondylarthropathy, but with certain features not usually seen in the latter: predominantly, unilateral sacroiliitis, no familial form, and no link with HLA-B27.


Assuntos
Osteíte/patologia , Articulação Sacroilíaca/patologia , Espondilite/patologia , Vértebras Torácicas/patologia , Doença Aguda , Adolescente , Adulto , Idade de Início , Anti-Inflamatórios não Esteroides/administração & dosagem , Criança , Doença Crônica , Progressão da Doença , Europa (Continente) , Saúde da Família , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Osteíte/diagnóstico por imagem , Osteíte/tratamento farmacológico , Recidiva , Estudos Retrospectivos , Espondilite/diagnóstico por imagem , Espondilite/tratamento farmacológico , Tomografia Computadorizada por Raios X
2.
Prog Urol ; 8(2): 254-7, 1998 Apr.
Artigo em Francês | MEDLINE | ID: mdl-9615937

RESUMO

Ureteric polyp is a benign lesion, and an uncommon cause of hydronephrosis in children. It is associated with intermittent lumbar pain and haematuria. The diagnosis is usually based on intravenous urography or retrograde urography. Treatment must be conservative and consists of simple resection of the polyp, associated with varying degrees of ureteric resection depending on the size of the lesion. No case of recurrence after treatment has been reported to date. The authors report a case in a 7-year-old boy and present a review of the literature.


Assuntos
Pólipos/diagnóstico , Neoplasias Ureterais/diagnóstico , Criança , Seguimentos , Hematúria/etiologia , Humanos , Hidronefrose/etiologia , Dor Lombar/etiologia , Masculino , Recidiva Local de Neoplasia , Pólipos/complicações , Pólipos/cirurgia , Neoplasias Ureterais/complicações , Neoplasias Ureterais/cirurgia , Urografia
3.
AJR Am J Roentgenol ; 166(6): 1451-5, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8633462

RESUMO

OBJECTIVE: Focal areas of decreased perfusion may be shown by power Doppler sonography in children with acute pyelonephritis. The purposes of this study were to assess the ability of power Doppler sonography to reveal acute pyelonephritis and to compare the sonographic images with enhanced CT images. SUBJECTS AND METHODS: We performed B-mode sonography, power Doppler sonography, and enhanced CT (reference method) of the kidneys of 30 children with symptoms suggesting upper urinary tract infection. All imaging studies were obtained within 24 hr of admission of each child to our hospital. Power Doppler sonography was performed with the same equipment and the same settings for all children. Imaging studies were performed before the results of urine cultures were obtained. Triangular areas of decreased perfusion visible on both longitudinal and axial scans were considered indicative of acute pyelonephritis on power Doppler sonographic images. On CT images, areas of decreased attenuation of the renal parenchyma visible immediately after IV injection of iodinated contrast agent or areas of increased attenuation on delayed scans were considered indicative of acute pyelonephritis. Power Doppler sonography and CT were compared for each renal pole (n = 120). RESULTS: For 17 (89%) of the 19 patients with CT-proven acute pyelonephritis, power Doppler sonography diagnosed this condition on the correct side. Seventeen (77%) of the 22 poles showing acute pyelonephritis on CT scans were also revealed by power Doppler sonography. The two patients in whom acute pyelonephritis was not revealed by power Doppler sonography were an obese 15-year-old girl and a 7-year-old boy with right upper pole pyelonephritis. This boy was one of the first patients to be included in the study. Also, in an obese 11-year-old girl, a false-positive indication of pyelonephritis was given by power Doppler sonography. CONCLUSION: Power Doppler sonography seems to be significantly more sensitive than conventional sonography for the detection of acute pyelonephritis in children. This noninvasive technique should be able to replace CT or dimercaptosuccinic acid scintigraphy in many children with urinary tract infections.


Assuntos
Pielonefrite/diagnóstico por imagem , Tomografia Computadorizada por Raios X , Ultrassonografia Doppler , Doença Aguda , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Estudos Prospectivos
4.
J Radiol ; 65(5): 389-92, 1984 May.
Artigo em Francês | MEDLINE | ID: mdl-6471012

RESUMO

Two cases of intra-articular development of an osteochondroma in the proximal epiphysis of the tibia are reported. The first case, a 3 year old boy, resulted in blocking of the knee. After resection of the mass the diagnosis was confirmed by pathology. The second patient, an 8 year old boy, had no symptoms and surgery was not performed, although ablation was required of an associated astragalian osteochondroma of tibiotarsal intra-articular development. Relations between these epiphyseal osteochondromata and hemimelic epiphyseal dysplasia and metachondromatosis are discussed.


Assuntos
Neoplasias Ósseas/diagnóstico por imagem , Condroma/diagnóstico por imagem , Epífises/diagnóstico por imagem , Tíbia/diagnóstico por imagem , Criança , Pré-Escolar , Humanos , Masculino , Radiografia
6.
Arch Fr Pediatr ; 37(4): 263-5, 1980 Apr.
Artigo em Francês | MEDLINE | ID: mdl-7406643

RESUMO

In a 1 year old child, cyanotic congenital heart disease was complicated by a severe obstruction of the abdominal aorta between the renal arteries and the bifurcation. The surgical treatment consisted of relief of the obstruction in the aorta and a Blalock-Taussig shunt. The general progress was good but there was a ischemia of the left leg for which amputation of the forefoot was required.


Assuntos
Doenças da Aorta/complicações , Cardiopatias Congênitas/complicações , Aorta Abdominal/cirurgia , Doenças da Aorta/diagnóstico , Doenças da Aorta/cirurgia , Humanos , Lactente , Masculino
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