keyword
https://read.qxmd.com/read/38653794/congenital-agenesis-of-the-common-bile-duct
#1
JOURNAL ARTICLE
Siddhi Chawla, Ashish Swami
No abstract text is available yet for this article.
April 24, 2024: Pediatric Radiology
https://read.qxmd.com/read/38646904/metaizeau-technique-for-treatment-of-paediatric-isolated-radial-neck-fracture-clinical-and-radiological-outcomes-case-control-study
#2
JOURNAL ARTICLE
Maciej Małolepszy, Piotr Buchcic, Andrzej Grzegorzewski
BACKGROUND: Radial neck fractures account for 5-17% of elbow fractures and about 1% of all fractures in children. The subject of the presented research is assesment of clinical and radiological outcomes of the Metaizeau technique for treatment of isolated radial neck fractures in children. MATERIAL AND METHODS: Retrospective analysis of clinical and radiological data of patients treated with the Metaizeau technique in our Department between 2015 and 2020. Twenty children with isolated radial neck fracture met the inclusion criteria...
February 29, 2024: Ortopedia, Traumatologia, Rehabilitacja
https://read.qxmd.com/read/38644086/thyroid-abnormalities-in-patients-with-hodgkin-lymphoma-the-importance-of-close-surveillance
#3
JOURNAL ARTICLE
Cristina Garcés-Visier, Paloma Conejero-Gonzalez, Maitane Andión-Catalán, Alberto Martín-Vega, Diego Muñoz-Hernández, Manuel Leónidas Espinoza-Vega, Ana Lourdes Luis-Huertas, José Lorenzo Alonso-Calderón
INTRODUCTION: Survival in paediatric patients with Hodgkin lymphoma (HL) has increased over the last decades. However, these patients are at increased risk of developing late thyroid sequelae due to the treatment with irradiation and alkylating agents. METHODS: We conducted an observational and retrospective study in patients with a diagnosis of HL between 2007 and 2022, in a hospital that is a paediatric oncology reference centre, through the review of electronic health records...
April 20, 2024: Anales de pediatría
https://read.qxmd.com/read/38642931/preoperative-three-dimensional-modelling-and-virtual-reality-planning-aids-nephron-sparing-surgery-in-a-child-with-bilateral-wilms-tumour
#4
JOURNAL ARTICLE
Avijit Banerjee, Ramesh Babu, Dhaarani Jayaraman, Srinivas Chilukuri
Bilateral Wilms tumour (BWT) is a surgically challenging condition. Virtual reality (VR) reconstruction aids surgeons to foresee the anatomy ahead of Nephron Sparing Surgery (NSS). Three-dimensional (3D) visualisation improves the anatomical orientation of surgeons performing NSS. We herewith report a case of BWT where VR planning and 3D printing were used to aid NSS. Conventional imaging is often found to be inadequate while assessing the tumour-organ-vascular anatomy. Advances like VR and 3D printing help surgeons plan better for complex surgeries like bilateral NSS...
April 19, 2024: BMJ Case Reports
https://read.qxmd.com/read/38641336/clinico-radiologic-spectrum-and-outcome-of-paediatric-acquired-demyelinating-disorders-ads-of-central-nervous-system-a-retrospective-indian-tertiary-care-hospital-cohort
#5
JOURNAL ARTICLE
Prithviraj R Prithviraj, Bidisha Banerjee, Ullas V Acharya, Muhammed Hafis, Sruthi K Sasidharan
UNLABELLED: Paediatric acquired demyelinating syndrome(ADS) constitute group of treatable disorders with acute neurologic dysfunction. Neuroimaging has played significant role in diagnosis of ADS. We describe clinico-radiologic spectrum, outcome and compare the groups Acute disseminated encephalomyelitis (ADEM), Neuromyelitis-optica-spectrum disorder (NMOSD), clinically-isolated-syndrome (CIS), Multiple sclerosis (MS) and Myelin-oligodendrocyte-glycoprotein antibody associated disorders (MOGAD)...
April 19, 2024: Neuropediatrics
https://read.qxmd.com/read/38635846/evaluation-of-radiological-capacity-and-usage-in-paediatric-tb-diagnosis-a-mixed-method-protocol-of-a-comparative-study-in-mozambique-south-africa-and-spain
#6
JOURNAL ARTICLE
Isabelle Munyangaju, Benedita José, Ridwaan Esmail, Megan Palmer, Begoña Santiago, Alicia Hernanz-Lobo, Crimenia Mutemba, Patricia Perez, Liebe Hendrietta Tlhapi, Vanessa Mudaly, Richard D Pitcher, Andreas Jahnen, Eliseo Vañó Carruana, Elisa López-Varela, Isabelle Thierry-Chef
INTRODUCTION: Tuberculosis remains one of the top ten causes of mortality globally. Children accounted for 12% of all TB cases and 18% of all TB deaths in 2022. Paediatric TB is difficult to diagnose with conventional laboratory tests, and chest radiographs remain crucial. However, in low-and middle-income countries with high TB burden, the capacity for radiological diagnosis of paediatric TB is rarely documented and data on the associated radiation exposure limited. METHODS: A multicentre, mixed-methods study is proposed in three countries, Mozambique, South Africa and Spain...
2024: PloS One
https://read.qxmd.com/read/38623139/successful-stent-implantation-into-the-patent-ductus-arteriosus-in-complex-cyanotic-congenital-heart-disease
#7
Kunal Bhugaonkar, Kshitij Balwaik, Neha Masne
Birth-associated structural issues with the heart are known as congenital heart disorders or defects. They might alter the heart's regular blood flow. A 10-month-old female child presented to a tertiary care hospital with symptoms of recurrent cyanotic spells with episodes of desaturation a few months after birth. ECG findings depicted a normal sinus rhythm with a right axis deviation along the right ventricular forces. Two-dimensional echocardiography showed a tetralogy of Fallot with pulmonary atresia with a patent ductus arteriosus from the undersurface of the arch with confluent small pulmonary arteries...
March 2024: Curēus
https://read.qxmd.com/read/38616820/brain-magnetic-resonance-imaging-review-suggests-unrecognised-hypoglycaemia-in-childhood
#8
JOURNAL ARTICLE
Chris Worth, Pon Ramya Gokul, Katie Ramsden, Sarah Worthington, Maria Salomon-Estebanez, Amit Maniyar, Indraneel Banerjee
INTRODUCTION: Neonatal and early-life hypoglycaemia, is a frequent finding but is often non-specific and asymptomatic, making detection and diagnosis challenging. Hypoglycaemia-induced cerebral injury can be identified by magnetic resonance imaging (MRI) changes in cerebral white matter, occipital lobes, and posterior parietotemporal regions. It is unknown if children may have hypoglycaemic brain injury secondary to unrecognised hypoglycaemia in early life. We have examined retrospective radiological findings of likely brain injury by neuroimaging to investigate the existence of previous missed hypoglycaemic events...
2024: Frontiers in Endocrinology
https://read.qxmd.com/read/38615503/imaging-of-pediatric-gastrointestinal-tumors-a-tertiary-center-experience-over-19%C3%A2-years
#9
JOURNAL ARTICLE
Mareen S Kraus, Swathi Selvam, Iram Siddiqui, Jeanette A Reyes, Govind B Chavhan
PURPOSE: Gastrointestinal tract (GIT) tumors in children are rare and there is a scarcity of data on their imaging features. The purpose of this study was to determine thefrequency of various GIT tumor types in children and to identify key imaging characteristics. METHODS: This retrospective, single-center study was approved by the local ethics committee. Children with histologically proven GIT tumours (malignantand benign) who had imaging available on the institutional PACS between May 1, 2000 and Dec 31, 2019 were included...
April 10, 2024: European Journal of Radiology
https://read.qxmd.com/read/38614533/paediatric-interventional-radiology-it-s-not-child-s-play
#10
JOURNAL ARTICLE
J Alonso Sánchez, D A Parra, C Parra-Fariñas
Pediatric interventional radiology is a dynamic and growing subspecialty. The new training pathways in interventional radiology, the maintenance of skills with a small volume of cases or complex procedures, the limited availability of specific pediatric equipment and materials pose significant challenges and opportunities.
2024: Radiología
https://read.qxmd.com/read/38602555/routine-ultrasound-screening-for-hip-dysplasia-in-children-with-clubfoot-is-not-supported
#11
JOURNAL ARTICLE
Dell McLaughlin, Sara De Salvo, Kathryn Brewerton, Caitlyn Hui, Maryse Bouchard
PURPOSE: Despite the existence of guidelines for screening for developmental dysplasia of the hip (DDH), there remains controversy regarding the need for routine ultrasound screening for DDH in patients with clubfoot due to an unclear correlation between the two conditions. The purpose of this study is to determine whether ultrasound screening for DDH in this population improved the diagnostic accuracy of DDH over standard assessment for patient risk factors and physical exam. METHODS: This is a retrospective cross-sectional review of infants diagnosed with idiopathic clubfoot who underwent hip ultrasounds to assess for DDH as identified by keyword search in an institutional radiological database at a tertiary care paediatric hospital...
April 11, 2024: International Orthopaedics
https://read.qxmd.com/read/38599741/enteric-duplication-cysts-in-paediatric-population-along-with-literature-review
#12
JOURNAL ARTICLE
Sana Ahuja, Rashi Maheshwari, Saba Naaz, Sufian Zaheer
The clinical presentation of enteric duplication cysts is dependent on the location of the cyst with symptoms varying from nausea and vomiting to abdominal distension, pain and perforation. Four patients were identified who were diagnosed with enteric duplication cysts within the period from 2019 to 2023. Three of the patients presented with signs of intestinal obstruction-abdominal distension and pain, while one had an antenatally detected abdominal mass. There were three boys and one girl with ages ranging from 4 months to 14 years...
2024: Revista Española de Patología
https://read.qxmd.com/read/38589235/denosumab-and-sclerotherapy-for-recurrent-spinal-aneurysmal-bone-cyst-in-a-child
#13
JOURNAL ARTICLE
Raj Singh, Sreekumar Madasswery, Matt Colman, Paul McKeegan Kent
Aneurysmal bone cyst (ABC) is a non-malignant, locally destructive, blood-filled lesion in the bone that tends to grow aggressively. A young girl presented with a rapid recurrence after aggressive surgery of a large symptomatic sacral-spinal ABC. After a multidisciplinary tumour board, she was successfully treated with sclerotherapy and monthly intravenous denosumab. The patient has maintained asymptomatic for over 36 months now and has returned to full activity and strength. She never required surgery and has had radiologic resolution of the lesions...
April 8, 2024: BMJ Case Reports
https://read.qxmd.com/read/38580747/paediatric-hepatic-angiosarcoma-with-consumptive-hypothyroidism-an-important-diagnostic-pitfall-to-avoid-during-evaluation-of-hepatic-vascular-tumours
#14
JOURNAL ARTICLE
Dickson Fenn, Kin Fen Kevin Fung, Anthony Pak-Yin Liu, Wai Fu Ng, Yee-Ling Elaine Kan
Hepatic angiosarcoma is an extremely rare primary malignant vascular tumour in children with very poor prognosis. Radiological diagnosis of hepatic angiosarcoma is challenging due to overlapping imaging features with other benign vascular hepatic tumours, particularly infantile hepatic haemangioma. Consumptive hypothyroidism is a condition that is almost exclusively associated with infantile hepatic haemangioma and has never been reported in angiosarcoma. We present a case of hepatic angiosarcoma in a 20-month-old girl, associated with consumptive hypothyroidism and, as a result, initially misdiagnosed as infantile hepatic haemangioma...
April 6, 2024: Pediatric Radiology
https://read.qxmd.com/read/38578371/partial-splenic-embolization-in-paediatric-sickle-cell-disease-patients-with-hypersplenism
#15
JOURNAL ARTICLE
Jacques A Bazeboso, Didier Mbuyi Mukendi, Cissé-Luc Mbongo, Wilfrid Mbombo, Michel Lelo Tshikwela, Antoine Molua, Benjamin Longo, Léon Tshilolo, José I Bilbao
PURPOSE: To assess the safety and efficacy of partial splenic embolization (PSE) to reduce the need of transfusions and improve hematologic parameters in patients with hypersplenism and sickle cell disease (SCD). MATERIAL AND METHODS: This prospective study includes 35 homozygous hemoglobin S patients with SCD and hypersplenism who underwent PSE from 2015 until 2021 in Kinshasa. Patients were evaluated, before and after PSE (1, 3 and 6 months), using clinical, laboratory and ultrasonographic methods...
April 5, 2024: Cardiovascular and Interventional Radiology
https://read.qxmd.com/read/38577960/infantile-osteopetrosis-with-delayed-development-organomegaly-and-wandering-eyes-case-report
#16
JOURNAL ARTICLE
Ashwini Prithvi, Dhrithi Kodethoor, Sushma K, Sanjiv Lewin
Osteopetrosis encompasses rare inherited metabolic bone disorders with defect in the osteoclast activity. Severe forms of presentation such as malignant infantile osteopetrosis are seen in infants and milder forms in older children. The clinical presentation includes failure to thrive, severe pallor, optic atrophy and hepatosplenomegaly. The disorder is characterised by dense bone on radiography, hence the name marble bone disease. A 10-month-old boy who presented with developmental delay, failure to thrive, nystagmus (which the mother described as wandering eye movements), splenomegaly of 16 cm and hepatomegaly of 8 cm...
April 5, 2024: Paediatrics and International Child Health
https://read.qxmd.com/read/38558695/unveiling-enigma-navigating-the-diagnostic-labyrinth-of-an-atypical-medial-clavicular-enchondroma
#17
Adarsh Jayasoorya, Sandeep Shrivastava, Ankit M Jaiswal, Hardik Patel, Rohan Chandanwale
Benign cartilaginous lesions called enchondromas usually appear in the long bones of the limbs. This case report, however, draws attention to an uncommon and unusual appearance of enchondroma near the medial end of clavicle. Because of the unusual location, the diagnostic process was very complex, which presented a challengefor the physicians. We provide the clinical, radiological and histological results that finally allowed for an accurate diagnosis. This example highlights the need of taking into account atypical location for benign lesions and highlights the necessity of a thorough diagnostic approach in unexpected clinical settings...
February 2024: Curēus
https://read.qxmd.com/read/38546944/a-phase-1-study-of-intravenous-egfr-erbituxedvsmit-in-children-with-solid-or-cns-tumours-expressing-epidermal-growth-factor-receptor
#18
JOURNAL ARTICLE
Louise Evans, Rick Walker, Jennifer MacDiarmid, Himanshu Brahmbhatt, Antoinette Anazodo, Geoffrey McCowage, Andrew J Gifford, Maria Kavallaris, Toby Trahair, David S Ziegler
BACKGROUND: Recurrent or refractory solid and central nervous system (CNS) tumours in paediatric patients have limited treatment options and carry a poor prognosis. The EnGeneIC Dream Vector (EDV) is a novel nanocell designed to deliver cytotoxic medication directly to the tumour. The epidermal growth factor receptor is expressed in several CNS and solid tumours and is the target for bispecific antibodies attached to the EDV. OBJECTIVE: To assess the safety and tolerability of EGFR-Erbitux receptor EnGeneIC Dream Vector with mitoxantrone (E EDVsMit ) in children with recurrent / refractory solid or CNS tumours expressing EGFR...
March 28, 2024: Targeted Oncology
https://read.qxmd.com/read/38546282/paediatric-endoscopic-endonasal-middle-skull-base-reconstruction-retrospective-analysis-of-78-patients-treated-in-a-single-tertiary-care-paediatric-center
#19
JOURNAL ARTICLE
Danilo Di Giorgio, Filippo Giovannetti, Paolo Priore, Mirko Scagnet, Federico Mussa, Ingrid Raponi, Valentino Valentini, Lorenzo Genitori
INTRODUCTION: Skull base pathologies in the paediatric population are rare and require treatment by multiple qualified specialists. The endoscopic endonasal approach has revolutionized surgical treatment because it is less invasive than existing treatments.The goal of this study was to retrospectively review our experience with the reconstruction of paediatric skull middle base defects and associated complications. MATERIALS AND METHODS: We analysed medical records from patients aged ≤ 18 years who were treated at our centre between 2013 and 2021...
March 28, 2024: British Journal of Neurosurgery
https://read.qxmd.com/read/38546253/gastric-teratoma-in-children-a-report-of-two-cases-and-review-of-literature
#20
JOURNAL ARTICLE
Md Mokarram Ali, Ram Raj, Ram Jeewan Singh, Rashi Rashi, Amit Kumar, Amit Kumar Sinha, Bindey Kumar
Gastric teratomas are very rare tumours. They present with upper abdomen distension which can easily be confused with other common conditions with mass per abdomen in the paediatric age group. Surgical excision is curative for gastric teratomas. The diagnosis is confirmed by radiological evaluation followed by histopathological analysis of excised specimen. We are reporting two such cases of gastric teratomas who presented with complaints of upper abdomen distension. They were evaluated with radiological imaging and successfully managed by surgical excision...
April 1, 2024: African Journal of Paediatric Surgery: AJPS
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