ABSTRACT
Fracture-classification systems are used to recommend treatment and predict outcomes. In this study, a modified Gartland classification system of supracondylar humerus fractures in children was assessed for intraobserver and interobserver variability. Five observers classified radiographs of 50 consecutive children with extension supracondylar humerus fractures on three separate occasions. After a 2-week interval, 90% of fractures were classified the same on both readings, with and intraobserver kappa value of 0.84. After a 36-week interval, 89% of the fractures were classified the same, with a kappa value of 0.81. Interobserver reliability was evaluated by pairwise comparison among observers, resulting in an overall kappa value of 0.74. The reliability of the Gartland classification for supracondylar humerus fractures in children is better than that published for other fracture-classification systems. However, 10% of the time, a second reading by the same observer is different. This makes treatment recommendations based only on fracture type imprecise.
Subject(s)
Humeral Fractures/classification , Child , Diagnosis, Differential , Humans , Humeral Fractures/diagnostic imaging , Observer Variation , Radiography , Reproducibility of ResultsABSTRACT
Precocious puberty is caused by a heterogeneous group of disorders, which range from idiopathic to malignant tumours. The radiologist's role is to help: (1) differentiate precocious puberty from pubertal variants; (2) identify the underlying cause of precocity if present; and (3) assess for effectiveness of treatment. This pictorial review discusses the types of precocious puberty and their underlying aetiologies, differentiates precocious puberty from pubertal variants and illustrates the appropriate imaging evaluation for the patient diagnosed with precocious puberty.
Subject(s)
Puberty, Precocious/diagnostic imaging , Algorithms , Brain Injuries/complications , Brain Injuries/diagnosis , Brain Neoplasms/complications , Brain Neoplasms/diagnosis , Child , Child, Preschool , Clinical Protocols , Diagnosis, Differential , Female , Humans , Hydrocephalus/complications , Hydrocephalus/diagnosis , Hypothalamo-Hypophyseal System/physiology , Infant , Infant, Newborn , Magnetic Resonance Imaging , Male , Pituitary-Adrenal System/physiology , Puberty, Precocious/etiology , Tomography, X-Ray Computed , Treatment OutcomeABSTRACT
As advances in cancer therapy improve the prognosis of patients with childhood malignancies, awareness of the consequences of treatment methods assumes increasing importance. All cancer treatment modalities are associated with toxic effects, and the spectrum of therapy-induced complications involves all organ systems. Radiologists have a pivotal role in detecting these sequelae, which can be categorized by the affected organ system and by whether they occur (a) at diagnosis or during initial therapy or (b) after the completion of treatment. The first group consists of oncologic emergencies, infectious complications, and irritant effects. Oncologic emergencies can be further categorized as space-occupying lesions (e.g., superior vena cava syndrome or spinal cord compression), vascular abnormalities (e.g., hyperleukocytosis, anemia, coagulopathy), and metabolic emergencies (e.g., tumor lysis syndrome). Common complications developing after completion of treatment include leukoencephalopathy and neurocognitive defects; cataract formation; cardiomyopathy and congestive heart failure; hepatic dysfunction, fibrosis, and cirrhosis; radiation enteritis; renal dysfunction or failure; scoliosis and short stature; hypothyroidism; gonadal dysfunction; graft-versus-host disease; and development of secondary malignancies. Physician awareness of these complications will permit more effective patient surveillance, which may afford patients the opportunity for earlier intervention in these situations and improved quality of life.
Subject(s)
Neoplasms/complications , Neoplasms/therapy , Adolescent , Antineoplastic Agents/adverse effects , Child , Child, Preschool , Combined Modality Therapy , Humans , Infant , Neoplasms/diagnostic imaging , Quality of Life , Radiography , Radiotherapy/adverse effectsABSTRACT
Perlman syndrome is a rare entity characterized by hypotonia, facial dysmorphism, gigantism, and visceromegaly including nephromegaly. The current case illustrates the ultrasonographic and computed tomographic appearances of renal abnormalities in this condition. Findings in Perlman syndrome can overlap with and need to be distinguished from two more common clinical entities: prune-belly and Beckwith-Wiedemann syndromes. Additional cranial findings previously unreported are also described.
Subject(s)
Abnormalities, Multiple/diagnosis , Beckwith-Wiedemann Syndrome/diagnosis , Kidney/abnormalities , Prune Belly Syndrome/diagnosis , Diagnosis, Differential , Face/abnormalities , Face/diagnostic imaging , Fatal Outcome , Follow-Up Studies , Gigantism/diagnosis , Humans , Hypotension/diagnosis , Infant, Newborn , Kidney/diagnostic imaging , Male , Syndrome , Tomography, X-Ray Computed , UltrasonographyABSTRACT
Lengthening of the psoas tendon commonly is performed for various conditions of the hip including developmental dysplasia and neuromuscular contractures and instability. Anecdotal reports of injury to surrounding neurovascular structures suggest an investigation of the local anatomy is warranted. Using magnetic resonance images from 54 children younger than 10 years, the authors examined the anatomic relationship between major neurovascular structures (femoral artery and vein, external iliac artery and vein, femoral nerve) and the psoas tendon. The mean distance between the neurovascular structures and the psoas tendon in the over the brim position is 1 cm, although it may be as close as 4 mm in a child. The mean distance is 3.1 cm at the tendon's insertion at the lesser trochanter. Surgeons performing psoas over the brim lengthenings should be aware that major neurovascular structures may be only 4 mm from the psoas tendon. The recommended surgical technique is presented.
Subject(s)
Magnetic Resonance Imaging , Psoas Muscles , Tendons/anatomy & histology , Tendons/surgery , Cadaver , Child, Preschool , Dissection/methods , Femoral Artery/anatomy & histology , Femoral Nerve/anatomy & histology , Femoral Vein/anatomy & histology , Hip Dislocation, Congenital/surgery , Humans , Iliac Artery/anatomy & histology , Iliac Vein/anatomy & histology , InfantABSTRACT
The fetal kidneys and bladder are usually visible by 15 weeks' gestation on sonograms. The authors present their experience with the diagnosis of renal abnormalities in the fetus.
