6,289 results match your criteria: "PA ¶¶¶Cohen Children's Medical Center[Affiliation]"

Association between 99mTc-PSMA SPECT/CT imaging and prostate-specific antigen (PSA) and alkaline phosphatase (ALP) levels post-endocrine therapy in patients with prostate cancer and bone metastases.

Rev Esp Med Nucl Imagen Mol (Engl Ed)

November 2024

Department of Nuclear Medicine, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou 450003, China. Electronic address:

Aim: To investigate the association between positive lesions detected by 99mTc-PSMA SPECT/CT and blood levels of prostate-specific antigen (PSA) and alkaline phosphatase (ALP) in patients with prostate cancer (PCa) and bone metastasis undergoing endocrine therapy.

Methods: A retrospective analysis was performed on 43 patients diagnosed with PCa bone metastasis who underwent endocrine therapy. PSA, ALP, whole body bone imaging and 99mTc-PSMA SPECT/CT imaging were collected from all patients (Among them, 17 cases were re-examined 99mTc-PSMA SPECT/CT imaging).

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Objectives: Pediatric sepsis-associated acute kidney injury (AKI) often requires continuous renal replacement therapy (CRRT), but limited data exist regarding patient characteristics and outcomes. We aimed to describe these features, including the impact of possible dialytrauma (i.e.

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Background: It is unclear whether targeted monitoring of acute adrenal insufficiency (AI) related adverse events (AE) such as sick day episodes (SDEs) and hospitalization rate in congenital adrenal hyperplasia (CAH) is associated with a change in the occurrence of these events.

Aim: Study temporal trends of AI related AE in the I-CAH Registry.

Methods: In 2022, data on the occurrence of AI-related AE in children aged <18 years with 21-hydroxylase deficiency CAH were compared to data collected in 2019.

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Article Synopsis
  • Children with cerebral palsy often experience foot deformities, which require precise evaluation for effective treatment and monitoring.
  • This study tested the reliability of a new photo-based assessment tool called the Modified Foot Posture Index (MFPI) among 13 orthopedic surgeons evaluating foot photographs of 20 children with CP.
  • Results indicated that the MFPI exhibits excellent reliability in measuring foot deformities, making it a noninvasive and practical option for clinical and research settings.
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QSOX1 exerts anti-inflammatory effects in sepsis-induced acute lung injury: Regulation involving EGFR phosphorylation mediated M1 polarization of macrophages.

Int J Biochem Cell Biol

November 2024

Department of Pediatric Nephrology, Children's Hospital of Anhui Medical University, Hefei, Anhui, China.; Department of Pediatric Nephrology, Anhui Provincial Children's Hospital, Hefei, Anhui, China.. Electronic address:

Sepsis is a systemic inflammatory response caused by an infection, which can easily lead to acute lung injury. Quiescin Q6 sulfhydryl oxidase 1 (QSOX1) is a sulfhydryl oxidase involved in oxidative stress and the inflammatory response. However, there are few reports on the role of QSOX1 in sepsis-induced acute lung injury (SALI).

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Analysis of Gene Mutation in Hashimoto's Thyroiditis With Multifocal Papillary Thyroid Carcinoma.

Am Surg

September 2024

Department of Head and Neck Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.

Background: Thyroid cancer (TC) is a highly prevalent malignant tumor of the head and neck. Papillary thyroid carcinoma (PTC) is the primary pathological type of TC, accounting for more than 80% of all TCs. mutations are closely associated with PTC.

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  • Hemolytic disease of the fetus and newborn (HDFN) results from maternal antibodies attacking the fetal red blood cells, but current clinical monitoring practices for it are inconsistent across institutions.
  • A survey of 103 US institutions revealed that while most conduct maternal antibody testing, methods and follow-up practices vary significantly, with only 27% employing cell-free fetal DNA testing to assess fetal risk.
  • The findings indicate a need for standardization in laboratory testing and improved cooperation between blood banks and maternal-fetal medicine services to better manage HDFN risk.
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  • Sacrococcygeal teratoma (SCT) is a rare congenital tumor with unclear risks of malignancy and recurrence, prompting a study to better understand these factors.
  • A global retrospective cohort study analyzed data from 3,612 SCT patients across 145 institutes in 62 countries, focusing on malignant transformation and recurrence rates.
  • Results showed that the risk of malignancy increases with age, plateauing at six years, while 10.2% of patients experienced recurrence, with significant associations related to tumor type and initial histology.
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N6-methyladenosine modification of LATS2 promotes hepatoblastoma progression by inhibiting ferroptosis through the YAP1/ATF4/PSAT1 axis.

Int J Biol Sci

September 2024

Clinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, P. R. China.

Article Synopsis
  • Ferroptosis, a type of cell death, is gaining attention in cancer research as a potential treatment target, particularly in hepatoblastoma (HB).
  • The study reveals that LATS2, a key player in the Hippo pathway, is decreased in HB cells and its overexpression can trigger ferroptosis, thereby inhibiting tumor cell growth.
  • The mechanism for reduced LATS2 involves m6A modification, which promotes its degradation and links the YAP1/ATF4/PSAT1 pathway to HB progression, suggesting LATS2 as a viable therapeutic target for HB.
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N1-methyladenosine (mA) is a reversible epigenetic modification of RNAs. Aberrant mA modification levels due to dysregulation of mA regulators have been observed in multiple cancers. tRNA methyltransferase 10C (TRMT10C) can install mA in RNAs; however, its role in hepatoblastoma remains unknown.

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Purpose: Malnutrition is common in children with cancer. While multiple validated malnutrition screens exist, there is no universal, standardized approach to screen or diagnose malnutrition. The Multinational Association of Supportive Care in Cancer (MASCC) Pediatric Study Group is focused on oncologic supportive care for children and young adults.

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A comparative study between EMG uroflowmetry with and without a catheter in children.

BMC Urol

September 2024

Urology Unit - Schneider Children's Medical Center of Israel, Affiliated to Sackler Faculty of Medicine, Tel Aviv University, Petach Tikva, Tel Aviv, 4941492, Israel.

Objectives: To evaluate the effect of urethral catheterization on the accuracy of EMG uroflowmetry in children with non-neurogenic voiding disorders during pressure-flow (PF) studies compared to the non-invasive EMG uroflowmetry test.

Methods: A retrospective study of children undergoing a urodynamic evaluation at our institution between 8/2018 and 7/2022 was employed. Urination curves and pelvic floor muscle activity were compared between PF studies and non-invasive EMG uroflowmetry test.

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MAPK signaling pathway induced LOX-1 polymorphonuclear myeloid-derived suppressor cells in biliary atresia.

Clin Immunol

November 2024

Guangdong Provincial Key Laboratory of Research in Structure Birth Defect Disease and Department of Pediatric Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou 510623, China. Electronic address:

Biliary atresia (BA) is a severe pediatric liver disease characterized by progressive bile duct destruction and fibrosis, leading to significant liver damage and frequently necessitating liver transplantation. This study elucidates the role of LOX-1 polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) in BA pathogenesis and assesses their potential as non-invasive early diagnostic biomarkers. Using flow cytometry, immunofluorescence, and molecular profiling, we analyzed the expression and activity of these cells in peripheral blood and liver tissues from BA patients and controls.

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A dendritic cell-recruiting, antimicrobial blood clot hydrogel for melanoma recurrence prevention and infected wound management.

Biomaterials

February 2025

Department of Dermatology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, People's Republic of China. Electronic address:

Surgical resection, the mainstay for melanoma treatment, faces challenges due to high tumor recurrence rates and complex postoperative wound healing. Chronic inflammation from residual disease and the risk of secondary infections impede healing. We introduce an innovative, injectable hydrogel system that integrates a multifaceted therapeutic approach.

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Article Synopsis
  • The study classified 111 pediatric gliomas using the WHO's latest classification, analyzing clinical, imaging, and molecular features observed from January 2020 to June 2023 at a medical center in China.
  • Mixed gender distribution was noted among patients (56 males and 55 females), with ages ranging from 10 days to 13 years, and common clinical signs included increased intracranial pressure and neurological impairments.
  • Different types of pediatric gliomas were identified, with pediatric diffuse low-grade glioma (pDLGG) and circumscribed astrocytoma glioma (CAG) being less common in the infratentorial region compared to pediatric diffuse high-grade glioma (pDHGG), which tended
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Proteomic analysis of serum small extracellular vesicles identifies diagnostic biomarkers for neuroblastoma.

Front Oncol

August 2024

Department of Clinical Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Background: Neuroblastoma (NB) primarily arises in children who are <10 years of age, and originates from developing sympathetic nervous system, which results in tumors in adrenal glands and/or sympathetic ganglia. The diagnosis of NB involves a combination of laboratory and imaging tests, and biopsies. Small extracellular vesicles (sEVs) have gained attention as potential biomarkers for various types of tumors.

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Cow's milk allergy (CMA) is one of the most common presentations of food allergy in early childhood. Management of CMA involves individualized avoidance of cow's milk and other mammalian milk and foods containing these. Optimal elimination of cow's milk avoidance includes: label reading; information about safe and nutritious substitute foods; appropriate choice of infant formula or a plant-based food; establishing tolerance to baked milk and monitoring nutritional intake and growth.

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Lipid metabolism reprogramming stands as a fundamental hallmark of cancer cells. Unraveling the core regulators of lipid biosynthesis holds the potential to find promising therapeutic targets in pancreatic ductal adenocarcinoma (PDAC). Here, it is demonstrated that platelet-derived growth factor C (PDGFC) orchestrated lipid metabolism, thereby facilitated the malignant progression of PDAC.

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Article Synopsis
  • Cobalamin C defect, caused by pathogenic variants in the MMACHC gene, disrupts vitamin B12 metabolism, leading to high homocysteine and low methionine levels in patients.
  • A study at AKUH analyzed 33 Pakistani patients, revealing a median age of symptom onset at 300 days and common issues like cognitive impairment and seizures.
  • Gene analysis showed a predominant pathogenic variant, highlighting late diagnoses and the need for better awareness and diagnostic resources in Pakistan.
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  • The prognosis for patients with central nervous system retinoblastoma (RB) after high-dose chemotherapy and stem cell transplant remains poor, and the effects of radiation therapy used afterward are unclear.
  • A study reviewed data from 16 patients with CNS RB who received chemotherapy followed by high-dose stem cell transplant, observing a 75% response rate to initial treatment.
  • Patients who received radiation therapy post-transplant had a 62.5% survival rate at 5 years, while those who did not only had a 28.6% survival rate, suggesting that radiation could improve outcomes and warrants further clinical trials.
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The deubiquitinase USP44 enhances cisplatin chemosensitivity through stabilizing STUB1 to promote LRPPRC degradation in neuroblastoma.

Neuro Oncol

August 2024

Department of Pathology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, National Children's Medical Center for South Central Region, Guangzhou, 510623, P. R. China.

Article Synopsis
  • Researchers studied a specific enzyme called USP44 to understand its role in a type of cancer called neuroblastoma, especially in patients with advanced disease.
  • They found that low levels of USP44 were linked to worse outcomes, but when USP44 was increased, cancer cells became more sensitive to a treatment called cisplatin.
  • The study showed that USP44 works with another protein, STUB1, to break down a different protein, LRPPRC, which helps cancer cells die faster when treated with cisplatin, making it a possible target for future treatments.
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Identification of clinical prognosis features and significant DNA methylation regulation in pineoblastoma.

Int J Clin Oncol

November 2024

Department of Hematology & Oncology, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.

Background: Pineoblastoma (PB) represents a great challenge for clinical management due to lack of a specific therapeutic regimen. This study aims to identify relevant prognostic factors and potential treatment targets by mining public databases.

Methods: The clinical characteristics and survival data of PB patients were obtained from the SEER database between 2000 and 2019 for Cox regression analysis and nomogram construction.

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Currently, the oncogenic mechanism of endoplasmic reticulum stress-CAF (ERS-CAF) subpopulation in chordoma remains unknown. Here, single-cell RNA sequencing, spatial transcriptomics, GeoMx Digital Spatial Profiler, data-independent acquisition proteomics, bulk RNA-seq, and multiplexed quantitative immunofluorescence are used to unveil the precise molecular mechanism of how ERS-CAF affected chordoma progression. Results show that hypoxic microenvironment reprograms CAFs into ERS-CAF subtype.

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Predictors of Radial Head Dislocation in Patients with Multiple Hereditary Exostoses.

J Hand Surg Asian Pac Vol

October 2024

Department of Orthopaedic Surgery, Yodogawa Christian Hospital, Kunizima, Higashiyodogawa-ku, Osaka, Japan.

Radial head dislocation in patients with multiple hereditary exostoses (MHE) is associated with loss of function and cosmetic problems. The treatment of the deformity with radial head dislocation is difficult and the timing of surgical intervention is important. The aim of this study was to evaluate the factors predictive of radial head dislocation in patients with MHE.

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