Pathological processes of the testis are very frequently found, and include non-tumoral and tumoral lesions. Ultra-sonography performed with a high-frequency transducer has become the imaging modality of choice for examination of these organs. This method is of help to improve intratesticular lesions characterization, and in many instances the findings suggest a more specific diagnosis, especially in the presence of similar clinical manifestations such as pain, swelling and local increase in volume. Color Doppler is an invaluable tool for demonstrating anomalous patterns of testicular perfusion and aids in the diagnosis of acute clinical conditions. In the present iconographic essay, the authors summarize the most frequent clinical, pathological findings as well as the main diagnostic features of benign intratesticular lesions such as microlithiasis, simple cysts, spermatocele, varicocele, tubular ectasia of the rete testis, orchitis, hematomas and more rare conditions. Familiarity with clinical and sonographic features is essential for the correct diagnosis and starting of the most effective therapy, as necessary.

Keywords: Testis, Benign testicular lesions, Ultrasonography, Color Doppler

The authors present a case of a 2-month-old infant affected by the recessive form of chondrodysplasia punctata, a rare condition radiologically characterized by severe proximal shortening and anomalous ossification (epiphyseal stippling) of the limbs. Clinical and radiological findings as well as main differential diagnoses are emphasized on the basis of data originating from a brief literature review.

Keywords: Chondrodysplasia punctata, Bone dysplasia, Peroxisomal disorders

A wide spectrum of congenital anomalies may affect the gastrointestinal tract at any level from the esophagus to the anus. Atresia is an important cause of gastrointestinal obstruction with high morbidity rate in neonates. Different pathogenetic mechanisms could cause this malformation and the two classical explanations are: a defect of recanalization of the intestinal tube or an interruption of blood supply during intrauterine life. The authors present a literature review with an iconographic essay of imaging findings in children with gastrointestinal atresia.

Keywords: Atresia, Children, Pediatrics, Imaging

Intussusception is a medical emergency that occur with higher frequency in children under 2 years of age. Diagnosis can be difficult as the classical triad of abdominal pain, jelly stools and palpable abdominal mass is seen in less than 50% of the patients. However, the diagnosis of intussusception can be established with variable degree of accuracy using plain abdominal x-ray films, ultrasound, computed tomography or barium (or air/saline) enema. Some of these imaging methods are also useful during treatment of this condition. The authors present a review of the literature and a pictorial essay of the imaging findings in patients with intussusception. In addition, a discussion on the current and controversial issues related to the treatment of intussusception is presented.

Keywords: Intussusception, Children, Pediatrics, Imaging

Leukokoria is an abnormal pupillary reflex most commonly seen in children that usually results from an intra-ocular abnormality. The evaluation of a child with leukokoria should be performed particularly to rule out a retinoblastoma (the cause of leukokoria in half of the cases). The authors present the main clinical and imaging features for the diagnosis of the most common causes of leukokoria.

Keywords: Eye, Leukokoria, Childhood, Ultrasonography, Computed tomography, Magnetic resonance imaging

The melanotic neuroectodermal tumor of infancy, also known as progonoma, is a rare benign disease of neural crest origin that occurs within the first year of life and affects mainly the maxilla. The authors report a case of a 10-month-old child presenting with this uncommon tumor in the maxilla, emphasizing the diagnostic findings on computed tomography, and present a literature review.

Keywords: Neoplasia, Neural crest, Maxilla, Infancy, Computed tomography

Hypertrophic pyloric stenosis is a common condition in infants with 2 - 12 weeks of postnatal life. The cause of this disease remains obscure. Clinical diagnosis is based on the history of projectile, nonbilious vomiting, gastric hyperperistalsis and a palpable pyloric "tumor". The authors review the typical findings seen on upper gastrointestinal x-ray series and abdominal ultrasonography. The diagnostic criteria for hypertrophic pyloric stenosis are presented and the applications of these two methods are established on the basis of the current literature.

Keywords: Hypertrophic pyloric stenosis, Pylorus, Vomiting, Ultrasonography, Infants

Persistent hyperplastic primary vitreous (PHPV) is a congenital developmental anomaly of the eye that primarily affects premature infants. PHPV results from failure of regression of the embryogenic primary vitreous and hyaloid vasculature, and proliferation of connective tissue. Three types of PHPV may be found: anterior, posterior and a combination of anterior and posterior. The clinical findings include leukocoria (white pupillary reflex) and microphthalmic eye. This anomaly is usually unilateral and unassociated with other systemic findings. The differential diagnosis between PHPV and other ocular diseases may be difficult due to similar features such as leukocoria, detached retina, retinal folds and cataract. Other diseases with similar features include retinoblastoma, isolated congenital cataract, retinopathy of prematurity and pseudogliomas or leukocorias. Direct visualization of the remnants of the fetal hyaloid vascular system offers the best evidence of PHPV. However, diagnosis using the ophthalmoscope is sometimes impossible because of opaque tissues. In this circumstance an indirect visualization by ultrasound, computed tomography or magnetic resonance imaging may be useful. These imaging methods provide valuable information for the differentiation from other diseases, particularly retinoblastoma. The authors present a review of the literature and an iconographic study of the imaging findings in patients with PHPV.

Keywords: Persistent hyperplastic primary vitreous, Leukocoria, Hyaloid artery, Cloquet's canal

Sarcomatoid renal carcinoma is an aggressive neoplasm with clinical and radiological features similar to those of clear cell renal sarcomas. The tumor is formed by layers of malignant spindle cells that show immunohistochemical and ultrastructural characteristics of both stromal and epithelial cells, and may also contain mixoid areas of osteoclast-like giant cells, rhabdomyoblast-like pleomorphic cells as well as other rare sarcomatoid components. The authors report a case of sarcomatoid renal carcinoma in a 54-year-old male patient presenting with the classic clinical triad seen on patients with renal cell carcinomas. The typical macroscopic and microscopic features, imaging findings and differential diagnosis with true renal sarcomas are discussed.

Keywords: Renal cell carcinoma, Sarcomatoid renal carcinoma, Tumor metaplasia, Computed tomography, Ultrasonography

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

The authors report two cases of pulmonary alveolar microlithiasis affecting monozygotic twins. The main findings observed on plain x-ray films and high-resolution computed tomography are discussed and compared with data from a brief literature review.

Keywords: Lungs, Pulmonary alveolar microlithiasis, Computed tomography

Fibrovascular polyp of the esophagus is a rare, pedunculated, intraluminal, benign tumor. We describe a case of a patient with a fibrovascular polyp of the esophagus and discuss the esophagogram and computed tomography findings. Due to the excellent correlation between pathology and imaging findings, computed tomography and magnetic resonance imaging are considered specific and useful in its diagnosis.

Keywords: Fibrovascular polyp, Esophagus, Computed tomography

We report a case of a 2 years and 8 months-old child with the recessive form of craniometaphyseal dysplasia. Clinical and radiological features as well as the main differential diagnosis are discussed and compared with data from a brief literature review.

Keywords: Craniometaphyseal dysplasia, Bone dysplasia, Bone sclerosis, Nasal obstruction