OBJECTIVE: The purpose of this study was to evaluate the interobserver variability of ultrasound in the measurement of subcutaneous, visceral and perirenal fat through standard technique. MATERIALS AND METHODS: From November 2006 to January 2007, 50 patients were evaluated. The subcutaneous fat thickness was measured with a 7.5 MHz linear transducer transversely positioned 1 cm above the umbilical scar. For the visceral fat, a 3.5 MHz transducer was also positioned 1 cm above the umbilical scar, considering the distance between the internal surface of the abdominal rectus muscle and the posterior aortic wall in the abdominal midline. The perirenal fat was measured in the middle third of the right kidney, with the transducer positioned at the axillary midline. RESULTS: The t-Student test was utilized to analyze the interobserver reproducibility with significance level of 95%. No statistically significant difference was observed among mean values for subcutaneous, visceral and perirenal fat (p = 0.7141, 0.7286 and 0.6368, respectively). Mean and standard deviation corresponded to 2.64 ± 1.37 for subcutaneous thickness, 6.84 ± 2.38 for visceral fat, and 4.89 ± 2.6 for perirenal fat. CONCLUSION: Ultrasound presented a good interobserver reproducibility in the evaluation of abdominal fat based on measurement of subcutaneous, visceral and perirenal fat as parameters.

Keywords: Abdominal fat, Ultrasound, Metabolic syndrome

OBJECTIVE: To describe the clinical, imaging and pathological findings of SAPHO syndrome and to point out that although considered rare this syndrome may be under-diagnosed by clinicians and radiologists, probably due to unfamiliarity with its features. MATERIALS AND METHODS: A retrospective study of six cases diagnosed in the last six years, with emphasis on clinical findings (age, sex and symptoms) and imaging findings (bone scintigraphy, conventional x-ray, computed tomography and magnetic resonance imaging) was conducted. RESULTS: The initial clinical presentation in all patients was pain in the upper anterior chest wall for at least four months. Imaging findings of all these patients indicated inflammatory process and/or hyperostosis and osteitis in the joints of the upper anterior chest wall. Skin manifestations of the syndrome, such as palmoplantar pustulosis, were identified in five of the patients. In none of the cases the diagnosis was suggested either at the initial clinical medical appointment or after imaging assessment by radiologists not specialized in musculoskeletal system. CONCLUSION: Our clinical and imaging findings are in line with the ones described in the literature. This diagnosis must be considered for each patient presenting with pain in the upper anterior chest wall associated with skin lesions and/or osteitis.

Keywords: Acquired hyperostosis syndrome, Sternocostoclavicular hyperostosis, Psoriasis, Osteitis

A choking patient was admitted with dyspnea, cyanosis, and loss of consciousness, which initially improved after suction of the airways. The patient presented worsening of the clinical parameters until the introduction of supportive treatment, after which she rapidly recovered. Chest x-ray taken on day of hospitalization showed bilateral diffuse alveolar filling pattern, and computed tomography showed ground glass areas. The aim of this paper is to show the radiological features of this syndrome.

Keywords: Mendelson syndrome, Chest x-ray, Computed tomography

Elongated styloid process or Eagle's syndrome is a multifactorial disease with unspecific characteristics on clinical and imaging examinations. The use of imaging methods in combination with the signs and symptoms are valuable in the confirmation of the diagnosis since they show the extension of the styloid complex, the muscles and ligaments, and adjacent structures. The diagnosis can be established when there is an association of clinical information and imaging findings. The authors report two cases of elongated styloid process including the imaging findings, mainly obtained using computed tomography.

Keywords: Eagle's syndrome, Diagnosis, Computed tomography

The authors report two cases of gastrocolic fistula caused by chronic therapy with indometacin in patients with Bartter's syndrome followed at the outpatients clinic of "Instituto da Criança do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo", Brazil. The diagnosis was suggested by a barium meal that showed a gastrocolic fistula between the greater curvature of the stomach and the transverse colon. Treatment was surgical in the both cases.

Keywords: Bartter's syndrome, Gastrocolic fistula, Indometacin, Barium meal

Tracheobronchomegaly is a rare condition of uncertain etiology characterized by marked dilatation of the trachea and main bronchi, bronchiectasis and recurrent respiratory tract infections. Clinical presentation is nonspecific and the diagnosis is usually made by imaging methods. We report a case of a patient with tracheobronchomegaly. Diagnosis was confirmed by plain x-ray films and computed tomography of the chest.

Keywords: Tracheobronchomegaly, Mounier-Kuhn syndrome, Computed tomography

We report the radiographic findings in the long bones of a newborn with confirmed diagnosis of congenital syphilis and discuss the differential diagnosis with battered child syndrome. The radiographic findings in the long bones from birth to the fourth month of life are presented. Clinical and laboratory data, the serial x-ray films and the characteristic radiological signs were essential to establish the correct diagnosis.

Keywords: Congenital syphilis, Battered child syndrome, Bone fractures

The author reports the radiological findings in two siblings with mucopolysaccharidosis type VI (mucopolysaccharide VI). Conventional radiographs of the skeleton and magnetic resonance imaging examination of the central nervous system were performed. Skeletal abnormalities in patients with mucopolysaccharidosis type VI have already been well described by other authors and are generally similar to other mucopolysaccharides. Magnetic resonance imaging of the central nervous system may be helpful in the differential diagnosis, assessment of extension, and follow-up of these diseases.

Keywords: Mucopolysaccharidoses, Maroteaux-Lamy syndrome, Gargoylism

Short bowel syndrome is defined as the small bowel functional absorptive surface inability to provide adequate nutrition, leading to intestinal failure and chronic malnutrition. In adult individuals the main etiologies for short bowel syndrome are related to extensive or multiple surgical bowel resections secondary to mesenteric ischemia, Crohn’s disease and actinic enteritis. Besides evaluating the transit time through the large bowel, barium follow through may be utilized in the measurement of bowel remnants length as well as in the follow-up of structural adaptation phenomena of small bowel and colonic loops. In patients with short bowel syndrome, structural small bowel adaptation consists in hyperplasia of villi and mucosal folds, which become more numerous, deeper and larger in diameter, as well as remnant segment dilation. Such morphological findings are more prominent and best established in the ileal loops, whose remarkable adaptive capacity has been well documented. Therefore, the knowledge of imaging findings regarding morphological and adaptive characteristics of the small bowel is extremely relevant in the multidisciplinary approach to short bowel syndrome.

Keywords: Short bowel syndrome; Radiology; Adaptation.

The authors report the case of mixed approach for endovascular treatment of occlusive disease of the anterior tibial artery by retrograde pedal artery access where the traditional antegrade approach failed to overcome a segmental occlusion. The technique seems to offer an option for endovascular procedures aimed at treating occlusion of the anterior tibial artery in cases where the conventional antegrade approach demonstrates to be inappropriate.

Keywords: Angioplasty; Arterial occlusive disease; Percutaneous transluminal angioplasty; Tibial arteries; Endovascular procedures.

The present report describes the case of a 43-year-old diabetic patient with facial pain, protruding eyes, nasal congestion and decreased right vision (involvement of the ipsilateral cranial nerves III, IV and V). Computed tomography showed diffuse sinusitis at right, cribriform plate erosion and presence of a hypodense collection in the frontal lobe with peripheral enhancement. Magnetic resonance imaging confirmed the presence of a cerebral abscess. Samples were collected from the lesion, confirming hyphae compatible with mucormycosis.

Keywords: Syndrome; Cavernous sinus; Mucormycosis.

The present report is aimed at describing a rare case of cranial malformation - cloverleaf skull syndrome -, whose presence was noticed after the birth of a child with signs of abnormality. Imaging diagnosis methods such as computed tomography and conventional radiography were used to characterize the syndrome.

Keywords: Syndrome; Malformation; Computed tomography.

The authors report the case of a 55-year-old female, hypertensive, smoker patient presenting with dysphonia, dysphagia and persistent dry cough. Laryngoscopy diagnosed left vocal cord paralysis. Computed tomography demonstrated saccular aneurysm of the inferior wall of the aortic arch, stretching the left recurrent laryngeal nerve, a finding compatible with Ortner's syndrome.

Keywords: Ortner's syndrome; Aortic arch aneurysm; Recurrent laryngeal nerve; Dysphonia; Dry cough.

OBJECTIVE: To describe the prevalence of carpal tunnel syndrome in a sample of 200 healthy hospital workers, establishing the respective epidemiological associations. MATERIALS AND METHODS: Two hundred individuals were submitted to wrist ultrasonography to measure the median nerve area. They were questioned and examined for epidemiological data, body mass index, carpal tunnel syndrome signs and symptoms, and submitted to the Boston carpal tunnel questionnaire (BCTQ) to evaluate the carpal tunnel syndrome severity. A median nerve area > 9 mm² was considered to be diagnostic of carpal tunnel syndrome. RESULTS: Carpal tunnel syndrome was diagnosed by ultrasonography in 34% of the sample. It was observed the association of carpal tunnel syndrome with age (p < 0.0001), paresthesia (p < 0.0001), Tinel's test (p < 0.0001), Phalen's test (p < 0.0001), BCTQ score (p < 0.0001), and years of formal education (p < 0.0001). Years of formal education was the only variable identified as an independent risk factor for carpal tunnel syndrome (95% CI = 1.03 to 1.24). CONCLUSION: The prevalence of carpal tunnel syndrome in a population of hospital workers was of 34%. The number of years of formal education was the only independent risk factor for carpal tunnel syndrome.

Keywords: Carpal tunnel syndrome; Ultrasonography; Median nerve area; Hand pain; Hand paresthesia.

Tarsal tunnel syndrome results from compression or damage to the tibial nerve or its branches as they pass through the tarsal tunnel beneath the flexor retinaculum. Diagnosing tarsal tunnel syndrome is challenging because of nonspecific symptoms that overlap with those of other lower limb pathologies. Vascular disorders are common causes but are often overlooked. High-resolution ultrasonography has emerged as a valuable diagnostic tool, offering advantages over other imaging methods. This technique allows real-time assessment, identifying the factors that cause vascular compression and improving diagnostic accuracy. Increased awareness of the vascular contributions to tarsal tunnel syndrome can promote early diagnosis and improve treatment outcomes.

Keywords: Ultrasonography; Tarsal tunnel syndrome; Tibial nerve; Vascular diseases.