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2.
Eur Radiol ; 10(11): 1832-5, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11097416

RESUMEN

A rare case of progressive pseudorheumatoid dysplasia (PPD) in a 9-year-old girl is presented. Clinically, chronic painless swollen joints, accompanied by progressive motion restriction and progressive walking difficulties, were found. Radiologically, there was enlargement of the epimetaphyseal portions of the large joints, metacarpal heads, and phalanges, and generalized platyspondyly with irregular delineation of the endplates of the vertebral bodies. The radioclinical features at the peripheral joints were originally misdiagnosed as juvenile rheumatoid arthritis (JRA), and the structural spinal abnormalities were neglected and interpreted as Scheuermann's disease. However, the absence of active inflammatory parameters argues against JRA, whereas the low age of onset of the irregularities at the vertebral endplates is an argument against the diagnosis of Scheuermann's disease. The combination of the dysplastic abnormalities of the spine, with platyspondyly and Scheuermann-like lesions at an unusually low age of onset, and radiological features mimicking JRA of the peripheral joints, is the clue to the diagnosis of this rare autosomal-recessive disease. This case is the first to document the MRI features of PPD of the spine.


Asunto(s)
Osteocondrodisplasias/diagnóstico , Osteocondrodisplasias/genética , Artritis Juvenil/diagnóstico por imagen , Niño , Diagnóstico Diferencial , Femenino , Genes Recesivos , Humanos , Imagen por Resonancia Magnética , Radiografía , Enfermedad de Scheuermann/diagnóstico por imagen , Columna Vertebral/diagnóstico por imagen , Columna Vertebral/patología
3.
JBR-BTR ; 83(5): 263-70, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11201543

RESUMEN

Pulmonary embolism is a relative common, potentially fatal disorder that clinicians have difficulty detecting and difficulty diagnosing. Deep venous thrombosis (DVT) is the most important source of thrombi. Early and accurate diagnosis is essential for efficient therapy. Therapy is based on long-term anticoagulation and has an important impact on the mortality and morbidity of pulmonary embolism. For the diagnosis of pulmonary embolism, the ventilation/perfusion (V/Q) scan is still the first examination in many instances. A normal V/Q scan or the combination of a low probability scan and a low clinical suspicion are associated with a prevalence of pulmonary embolism of 4%. The combination of a high-probability V/Q scan and a strong clinical suspicion has a prevalence of pulmonary embolism of 96%. All other results should be considered as non-diagnostic. However, the number of non-diagnostic V/Q examinations can be as high as 70%. Nevertheless, an additional pulmonary angiography will be performed in only in 15% of these cases. In the low pre-test probability group (poor clinical suspicion, absence of risk factors and no medical history) the V/Q scan is useful as a screening test ("rule-out" strategy). When the pre-test probability is higher or in other cases in which early diagnosis is necessary ("rule-in" strategy), a contrast-enhanced spiral CT of the pulmonary arteries (possibly in combination with ultrasonography of the lower limbs) is the most accurate examination.


Asunto(s)
Embolia Pulmonar/diagnóstico por imagen , Tomografía Computarizada por Rayos X/métodos , Enfermedad Aguda , Árboles de Decisión , Humanos , Embolia Pulmonar/prevención & control , Factores de Riesgo , Ultrasonografía
4.
Eur Radiol ; 9(1): 96-8, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-9933389

RESUMEN

We present a case of Langerhans' cell histiocytosis (LCH) of the liver and spleen in an adult. The imaging features are different from those in the few previously reported cases of individual organ involvement by LCH.


Asunto(s)
Histiocitosis de Células de Langerhans/diagnóstico , Hepatopatías/diagnóstico , Enfermedades del Bazo/diagnóstico , Tomografía Computarizada por Rayos X , Ultrasonografía , Adulto , Diagnóstico Diferencial , Histiocitosis de Células de Langerhans/patología , Humanos , Hígado/patología , Hepatopatías/patología , Masculino , Bazo/patología , Enfermedades del Bazo/patología
5.
Eur Radiol ; 13 Suppl 4: L40-4, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15018164

RESUMEN

Two cases of pseudotumoral peliosis hepatis are presented with emphasis on MRI findings. One patient had four individual lesions, the other had two. Image characteristics in both were: heterogeneic signal intensity on T1-weighted images (T1WI) with areas of high-, intermediate, and low signal intensity; heterogeneic signal intensity on T2WI with presence of numerous intralesional "cystic" hyperintense areas with a hypointense border. Signal intensities on T1WI were iso- to hypointense in one case and mild central hyperintensities were demonstrated in the other case, probably due to intra-lesional hemorrhage or diffuse accumulation of fresh clotting within the sinusoids. One case demonstrated early enhancement of the peripheral borders in the arterial phase, and both demonstrated enhancement in the portovenous and late phases. One case was studied with Gd-BOPTA and iron oxides and demonstrated enhancement with both products, suggestive for the presence of hepatocytes and Kupffer cells. This is the first report of the use of hepato-specific contrast agents in this entity. Spontaneous regression of the lesions was demonstrated on a follow-up MR examination in one case.


Asunto(s)
Granuloma de Células Plasmáticas/diagnóstico , Neoplasias Hepáticas/diagnóstico , Imagen por Resonancia Magnética/métodos , Peliosis Hepática/diagnóstico , Anciano , Biopsia con Aguja , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Gadolinio DTPA , Humanos , Inmunohistoquímica , Masculino , Medición de Riesgo , Sensibilidad y Especificidad
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