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Pachydermoperiostosis (PDP) is a rare genetic disorder manifesting with periostosis, clubbing, and thickened skin. The impact of PDP on bone density and microarchitecture is underexplored despite the potential derangement in bone health due to systemic inflammation. This cross-sectional case-control study was conducted in a tertiary care center in north India from July 2022 to July 2023. We compared treatment naïve PDP patients (n = 8) with age and BMI-matched apparently healthy controls. All participants underwent clinical examination and estimation of biochemical parameters including calcium, phosphorus, alkaline phosphatase, 25(OH)D, and iPTH. Bone turnover markers C-terminal telopeptide of type I collagen (CTX) and procollagen type I N-propeptide (P1NP) were also assessed. All patients underwent areal and volumetric bone density measurements using dual-energy X-ray absorptiometry (DXA) and high-resolution peripheral quantitative computed tomography (HR-pQCT). HR-pQCT analysis revealed diminished cortical volumetric bone mineral density and altered microarchitecture in PDP patients at the radius and tibia, characterized by increased cortical porosity. Bone geometry assessment demonstrated increased cross-sectional bone area both in the cortical and trabecular compartments. Finite element analysis (FEA) indicated a substantial reduction in failure load, cortical and trabecular von Mises stress (VMS) at the tibia and stiffness at the radius in PDP patients compared to controls. PDP patients had similar biochemical and bone turnover parameters to controls. Individuals with PDP show reduced cortical vBMD with disrupted bone microarchitecture. These changes may reflect PGE2-mediated inflammation and bone resorption, suggesting increased fracture risk and the need for ongoing monitoring.
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http://dx.doi.org/10.1007/s00223-025-01427-0 | DOI Listing |
Pediatr Dev Pathol
September 2025
Histopathology Section, Department of Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan.
Introduction: Phyllodes tumor (PT) are rarely seen in young population. Some authors believe that PT behave less aggressively in young patients and the need for aggressive management is questioned.
Objective: We aimed to describe the clinicopathological features of PT in pediatric and adolescent population.
Calcif Tissue Int
August 2025
Department of Endocrinology, NHE, PGIMER, Room: 12, Chandigarh, India.
Pachydermoperiostosis (PDP) is a rare genetic disorder manifesting with periostosis, clubbing, and thickened skin. The impact of PDP on bone density and microarchitecture is underexplored despite the potential derangement in bone health due to systemic inflammation. This cross-sectional case-control study was conducted in a tertiary care center in north India from July 2022 to July 2023.
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August 2025
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) is a rare subtype of B-cell lymphoma. NLPHL is usually indolent, involves lymph nodes and shows a favorable prognosis with high overall survival. In a minority of cases, patients may present and/or progress to advanced disease with involvement of the spleen, liver, and/or bone marrow.
View Article and Find Full Text PDFBackground: Acute postoperative pain (APP) are key factors in the recovery of surgical patients after surgery. This study used the machine learning eXtreme Gradient Boosting (XGBoost) algorithm for the prediction of acute postoperative pain after major noncardiac surgery in older patients.
Methods: This was a secondary analysis of data from a randomized controlled trial containing 1720 older patients undergoing general anesthesia.
Front Pharmacol
August 2025
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Integrating Chinese medicine and biomedicine for treating acute ischemic stroke (AIS) presents a promising strategy. Accurately predicting Traditional Chinese Medicine (TCM) heat syndrome types in AIS patients is crucial for guiding appropriate medication use within this combined treatment strategy. In this study, a clinical cohort including TCM syndromes, laboratory markers, and baseline assessments, were collected from 193 AIS patients.
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