keyword
https://read.qxmd.com/read/38255365/adolescent-idiopathic-scoliosis-surgery-postoperative-functional-outcomes-at-32-years-mean-follow-up
#21
JOURNAL ARTICLE
Giuseppe Barone, Fabrizio Giudici, Francesco Manzini, Pierluigi Pironti, Marco Viganò, Leone Minoia, Marino Archetti, Antonino Zagra, Laura Scaramuzzo
INTRODUCTION: Recent clinical and radiographic studies conducted over short and medium terms have demonstrated positive results in patients undergoing surgery for adolescent idiopathic scoliosis (AIS). However, the absence of long-term data, crucial for comprehending the impact on future quality of life, especially in young patients actively involved in very intense physical activities, remains a gap. This study aims to evaluate long-term functional outcomes in patients who underwent surgery for Adolescent Idiopathic Scoliosis...
December 30, 2023: Children
https://read.qxmd.com/read/38217730/navigating-the-complexities-of-encephalocraniocutaneous-lipomatosis-a-case-series-and-review
#22
JOURNAL ARTICLE
Marco Pavanello, Liliana Piro, Arianna Roggero, Andrea Rossi, Matteo Cataldi, Gianluca Piatelli
INTRODUCTION: Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital syndrome with complex skin, eye, and central nervous system (CNS) symptoms. Diagnosis and treatment are challenging due to its rarity and diverse manifestations. It often involves issues like porencephalic cysts, cortical atrophy, and low-grade gliomas in the CNS, resulting in developmental delays. The spinal cord is frequently affected, leading to problems like medullary compression and radiculopathy, causing back pain and sensory/motor deficits...
January 13, 2024: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/38211554/spondylodiscitis-following-perforated-acute-appendicitis-in-a-14-year-old-female-a-case-report
#23
Marwa AlTarayra, Khalil N M Abuzaina, Ammar W M Hassouneh, Osama Y A Aljabarein
INTRODUCTION AND IMPORTANCE: Acute appendicitis is a common surgical emergency, often resulting in perforation and increased morbidity. Up to 55 % of children with complicated appendicitis may experience a complication such as infection, bowel obstruction, or unplanned hospital re-admission (Blakely et al., 2011 [23]). However, the development of infectious spondylodiscitis following appendectomy is an extremely rare complication, particularly in pediatric patients. We present the first reported case of lumbar spondylodiscitis occurring post-perforated appendicitis in a 14-year-old female, highlighting the importance of recognizing and managing uncommon complications...
February 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38206687/percutaneous-endoscopic-lumbar-discectomy-in-lumbar-disc-herniation-with-posterior-ring-apophysis-fracture-a-case-report-in-a-15-year-old-child
#24
JOURNAL ARTICLE
Baode Zhang, Peikai Chen, Jiaquan Zhong, Michael Kai-Tsun To, Kenneth Man-Chee Cheung, Jianbin Wu
RATIONALE: Lumbar disc herniation (LDH) with posterior ring apophysis fracture (PRAF) is rather rare in children, and in all age-stratified LDH patients, the incidence of RAF was 5.3% to 7.5%. Interestingly, the incidence of LDH with RAF in children (15%-32%) is several times higher than in adults, the mis-diagnosis of which may lead to delayed treatment. PATIENT CONCERNS: Here, we report a 15-year-old schoolboy who suffered from sudden low back pain and radiating pain in both lower limbs after sport activities...
December 29, 2023: Medicine (Baltimore)
https://read.qxmd.com/read/38206487/the-oswestry-disability-index-is-reflective-of-pain-interference-and-mobility-in-children
#25
JOURNAL ARTICLE
Karina A Zapata, Leah Y Carreon, Chan-Hee Jo, Brandon A Ramo
PURPOSE: The 9-item Oswestry Disability Index version 2.1a (ODI-9) has never been formally validated in children. Our primary purpose was to evaluate the ODI-9 using the Patient-Reported Outcomes Measurement Information System (PROMIS) Pediatric Pain Interference (PI) and Mobility Computer Adapted Test (CAT) and Pain Catastrophizing Scale for Children (PCS-C) as anchors to determine concurrent validity in children. METHODS: We retrospectively reviewed cross-sectional patient-reported outcomes data using a convenience sample of children referred to a tertiary pediatric orthopedic institution for any spine condition from April 2021 to April 2022...
January 11, 2024: Spine Deformity
https://read.qxmd.com/read/38196410/dandy-walker-syndrome-delayed-acute-presentation-with-unusual-symptoms
#26
Fakhar Hayat, Mohamed Ismail, Muhanned M Alqhtani, Talal Almayman, Noor Sardar, Abdullah Ismaeel, Mohammed AlJohani, Rayan S Alruwaili
Dandy-Walker syndrome (DWS) is a rare congenital brain malformation defined by the presence of an expanded posterior fossa, full or partial absence of the cerebellar vermis, and a cystic expansion of the fourth ventricle. We report an 18-month-old girl with DWS presenting with atypical clinical manifestations and unusual symptoms. She initially presented with persistent vomiting and abdominal pain for four days, not responding to antiemetic medication. In addition, she was found to have abnormal postural arching of the back, extension of the lower limbs, and neck extension...
December 2023: Curēus
https://read.qxmd.com/read/38192660/pediatric-h3k27m%C3%A2-mutant-diffuse-midline-glioma-with-vertebral-metastasis-a-case-report-and-literature-review
#27
Xiaohui Ge, Yu Yang, Wenyan Wang, Lei Tian, Ge Zhang, Zhesen Tian, Xiaoying Xue
H3K27M-mutant diffuse midline glioma (DMG) is a type of high-grade glial tumor, which occurs in the midline structure and develops mostly in children. Extraneural metastases (ENM) are exceedingly rare in patients with H3K27M-mutant DMG. A 9-year-old male patient presented with a headache, nausea and vomiting. Following magnetic resonance imaging and immunohistochemical molecular testing examination, the patient was diagnosed with H3K27M-mutant DMG and received chemoradiotherapy plus five cycles of chemotherapy with temozolomide intermittently as an adjuvant therapy...
February 2024: Oncology Letters
https://read.qxmd.com/read/38181242/the-green-bad-omen-in-blood-smear-and-the-potential-of-blood-purification-therapy-a-case-report
#28
JOURNAL ARTICLE
Yanhui Chen, Wenpeng Ni, Guanghong Gu
RATIONALE: Green inclusions (GI) are distinct morphological features found in phagocytic cells like neutrophils and monocytes. These intracellular structures exhibit bright green color with unclear boundaries, and their origin and clinical significance are still not fully understood. GI carriers, often middle-aged to elderly with liver dysfunction, face higher mortality rates, earning them the nickname "inclusions of death." This report presents a rare GI-related pediatric case, demonstrating a favorable response to blood purification therapy...
January 5, 2024: Medicine (Baltimore)
https://read.qxmd.com/read/38180406/an-uncommon-cause-of-nocturnal-crying-and-discomfort-a-case-of-a-15-month-old-girl-with-spondylodiscitis
#29
JOURNAL ARTICLE
Lotje A Hoogervorst, Janne L Punski-Hoogervorst, Amoe Baktash, Danielle M C Brinkman, Pieter Bas de Witte
Nocturnal crying in toddlers has a broad spectrum of causes, including psychosocial and somatic causes, whereby the majority are self-limiting and do not need referral to specialist medical care. Although uncommon, atypical presentations of nocturnal crying-such as spondylodiscitis-require referral to specialist medical care, especially when combined with discomfort. In this case report, we present a case of a 15-month-old girl with an atypical presentation of nocturnal crying in combination with back pain.
January 3, 2024: Journal of Pediatric Health Care
https://read.qxmd.com/read/38179394/a-pediatric-case-of-spinal-intradural-epidermoid-cyst-a-rare-encounter
#30
Fahad N Alsulami, Fahad M Alotaibi, Layan S Alfraidi, Nasser F Alotaibi, Razan E Alnami, Mohammed F Alotaibi, Reema M Musllet, Ahlam Alharbi
Intradural epidermoid cysts of the spine are rare congenital lesions. Their etiology is thought to stem from ectodermal remnants during embryonic development. They result in a diverse clinical presentation, often marked by an insidious onset and variable neurological deficits. Timely diagnosis is crucial for optimizing patient outcomes. We present the case of a 10-year-old male child presenting a six-month history of worsening back pain, intermittent leg weakness, and urinary incontinence. The physical examination revealed tenderness over the lower thoracic and lumbar spine, lower limb weakness, hyperreflexia, and sensory deficits...
December 2023: Curēus
https://read.qxmd.com/read/38167502/pediatrics-severe-low-back-pain-by-disc-herniation-an-uncommon-entity
#31
JOURNAL ARTICLE
Wendlassida Joelle Stéphanie Tiendrebeogo/Zabsonre, Denlewende Sylvain Zabsonre, Fulgence Kabore, Abdoulaye Sanou, Yakouba Haro, Inoussa Zoungrana, Dieu-Donné Ouedraogo
BACKGROUND: Common severe back pain due to disc herniation is rare in the paediatric population which involves children under eighteen years of age. Paediatric lumbar disc herniation (LDH) cannot be considered the same disease as in adults, as it has potentially different natural and clinical backgrounds. The treatment of pediatric LDH is the other particularity of this condition. Indeed, in children, delaying surgery for a conservative treatment is justified. We report 3 cases treated in 8 years...
January 2, 2024: Pediatric Rheumatology Online Journal
https://read.qxmd.com/read/38161897/valid-and-invalid-indications-for-osteopathic-interventions-a-systematic-review-of-evidence-based-practices-and-french-healthcare-society-recommendations
#32
REVIEW
Zeinab M Khalaf, Pierre Margulies, Mohamad K Moussa, Yoann Bohu, Nicolas Lefevre, Alexandre Hardy
The main aim of this study was to determine the level of evidence in the literature for the main indications of osteopathy as recommended by the French osteopathy societies. This systematic review followed the 2020 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and evaluated articles published between January 2012 and January 2022 with one modification: when level one evidence studies were available, level two to five studies were excluded. Sources included PubMed, the Cochrane library, the French National Health Authority (HAS) and its affiliates...
November 2023: Curēus
https://read.qxmd.com/read/38161162/cushing-syndrome-in-childhood
#33
REVIEW
Anthony Parish, Clement Cheung, Anna Ryabets-Lienhard, Paul Zamiara, Mimi S Kim
We describe a 15-year-old boy who presented with low back pain due to vertebral compression fractures, growth deceleration, excessive weight gain, rounded facies, dorsocervical fat pad, and hypertension. He was diagnosed as having Cushing syndrome (CS) due to primary pigmented nodular adrenocortical disease resulting in excess cortisol produced by the adrenal glands, leading to disruption of the hypothalamic-pituitary-adrenal axis. The most common cause of CS is exogenous glucocorticoids, with endogenous causes being extremely rare, often leading to delay in diagnosis or misdiagnosis...
January 1, 2024: Pediatrics in Review
https://read.qxmd.com/read/38083935/intraocular-medulloepithelioma-an-unusual-and-challenging-entity-in-paediatric-population
#34
Uzma Imam, Marya Hameed, Irma Anis, Israr Bhutto, Syed Habib Ahmed, Attiya Rizvi, Zubair Ahmad
Intraocular medulloepithelioma is a rare, congenital tumour of the non-pigmented ciliary epithelium. It most frequently arises from the ciliary body but can also have its origin from the retina, iris and optic nerve. The age when lesion first appears is typically around 2-10 years. Nearly 50-60% of patients having this lesion may also have secondary features such as cataract and neovascular glaucoma. Those with extrascleral medulloepithelioma are at risk for metastasis. Systemic correlation of the tumour with pleuropulmonary blastoma/DICER1 gene is reported in the literature...
December 2023: JPMA. the Journal of the Pakistan Medical Association
https://read.qxmd.com/read/38072858/disparities-in-indications-and-outcomes-reporting-for-pediatric-tethered-cord-surgery-the-need-for-a-standardized-outcome-assessment-tool
#35
JOURNAL ARTICLE
Matthew C Findlay, Samuel Tenhoeve, Skyler A Terry, Rajiv R Iyer, Douglas L Brockmeyer, Michael P Kelly, John R W Kestle, David Gonda, Vijay M Ravindra
PURPOSE: Tethered cord syndrome (TCS) is characterized by abnormal attachment of the spinal cord neural elements to surrounding tissues. The most common symptoms include pain, motor or sensory dysfunction, and urologic deficits. Although TCS is common in children, there is a significant heterogeneity in outcomes reporting. We systematically reviewed surgical indications and postoperative outcomes to assess the need for a grading/classification system. METHODS: PubMed and EMBASE searches identified pediatric TCS literature published between 1950 and 2023...
December 11, 2023: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/38050600/is-sagittal-spinopelvic-alignment-a-cause-of-low-back-pain-in-pediatric-spine-pathologies-a-review
#36
REVIEW
Czubak-Wrzosek Maria, Wrzosek Patryk, Żebrowski Mateusz, Tyrakowski Marcin
PURPOSE: Altered spinopelvic morphology is observed in many spine pathologies occurring during growth. The aim of the study is to better understand the sagittal compensatory mechanisms and their possible influence on the occurrence of pain in selected pediatric spine pathologies. METHODS: A bibliographic search in the PubMed database included articles published between September 1965 and July 2023. The keywords contained in the search were "spondylolysis," "spondylolisthesis," "scoliosis," "kypho," "sagittal," "pediatric," "child," "adolescent," "grow," "development," and "pain...
December 2023: Journal of Children's Orthopaedics
https://read.qxmd.com/read/38050596/tumors-and-infections-of-the-growing-spine
#37
REVIEW
Barbara Jasiewicz, Ilkka Helenius
The growing spine differs from the adult spine in several ways. Although tumors and infections cause only a small percentage of pediatric back pain incidences, delayed proper diagnosis and treatment may be disastrous. Benign lesions, such as osteoid osteoma, osteoblastoma, and aneurysmal bone cyst in the spine, are predominant during the first two decades of life, whereas malignant bony spinal tumors are rare. In the pediatric population, malignant spine tumors include osteosarcoma, Ewing's sarcoma, lymphoma, and metastatic neuroblastoma...
December 2023: Journal of Children's Orthopaedics
https://read.qxmd.com/read/38050588/clinical-examination-and-imaging-resources-in-children-and-adolescent-back-pain
#38
REVIEW
Ana León-Domínguez, Rocío Cansino-Román, Jose M Martínez-Salas, David M Farrington
Back pain is a relatively common complaint in children and adolescents. The pediatric patient presenting with back pain can often be challenging, and there are many well-known organic diagnoses that should not be missed. In younger children, an organic cause of back pain can often be found. However, back pain in older children and adolescents is often "non-specific." The differential diagnosis of back pain in children includes neoplasms, developmental, and inflammatory conditions. Basic steps should include an in-depth anamnesis, a systematic physical examination, and standard spine radiographs (anteroposterior and lateral)...
December 2023: Journal of Children's Orthopaedics
https://read.qxmd.com/read/38050509/pediatric-rehabilitation-of-acute-hyperextension-induced-myelopathy-after-surfing
#39
Stephen E Ritter, Katee O'Malley, Kaycee Nguyen, Yousef Darwish, Nancy Yeh, Jace C Bradshaw, Adam Kenet
This case is a unique pediatric presentation of a surfer's myelopathy, now referred to as acute hyperextension-induced myelopathy (AHIM), that provides an optimistic rehabilitation outcome. A 13-year-old boy presented to the emergency department with back pain, paraplegia, urinary retention, and dysesthesia following his first surfing lesson while visiting Hawaii. MRI of the thoracic spine without contrast showed a significant T2 hyperintense signal in the T9-T12 distal thoracic cord, consistent with AHIM. He completed a 10-day inpatient rehabilitation program and experienced exceptional improvement in functional mobility...
November 2023: Curēus
https://read.qxmd.com/read/38027301/case-report-guanfacine-and-methylphenidate-improved-chronic-lower-back-pain-in-autosomal-dominant-polycystic-kidney-disease-with-comorbid-attention-deficit-hyperactivity-disorder-and-autism-spectrum-disorder
#40
Satoshi Kasahara, Shoichiro Kanda, Miwako Takahashi, Mao Fujioka, Taito Morita, Ko Matsudaira, Naoko Sato, Motoshi Hattori, Toshimitsu Momose, Shin-Ichi Niwa, Kanji Uchida
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited renal disease characterized by the bilateral development of multiple cysts in the kidneys. Pain management is a clinically important issue, especially because approximately 60% of patients with ADPKD experience chronic pain related to hemorrhage from renal cysts, which significantly reduces their daily life. The cystic fibrosis transmembrane conductance regulator, the molecule responsible for cyst formation in ADPKD, is also the cause of cystic fibrosis...
2023: Frontiers in Pediatrics
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