Congenital Gastric Teratoma Presenting with Gastrointestinal Bleeding: Case Report and Review of Literature
CONCLUSION: Owing to the unique characteristics and the extreme rarity of this entity, accurate preoperative diagnosis has remained elusive.PMID:38647426 | DOI:10.1080/15513815.2024.2341235 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 22, 2024 Category: Pathology Authors: Khadiga M Ali Gena Abdel-Azeem Tarik Barakat Sherine M Elzeiny Mohammed Albishbishy Ahmed Megahed Source Type: research
Immunohistochemical and Histopathological Characterization of Spina Bifida Defect Tissues Removed After Prenatal and Postnatal Surgical Repair
Conclusion: Tissues harvested from prenatal and postnatal spina bifida repair surgeries appear as normal skin near the defect site. However, cystic tissues consist of highly dense fibrous connective tissue with complete absence of normal epidermal development.PMID:38634787 | DOI:10.1080/15513815.2024.2326834 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 18, 2024 Category: Pathology Authors: James R Bardill Melissa R Laughter Jaclyn B Anderson Hilary Hoffman Ahmed Gilani Maranke I Koster Ahmed I Marwan Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
Fibrocartilaginous Dysplasia of the Proximal Femur in Two Pediatric Patients, Including a Pathologic Fracture in a Patient With McCune-Albright Syndrome
We report the clinical presentation, imaging findings, and management of two pediatric patients with fibrocartilaginous dysplasia of the proximal femur to (1) highlight that recognition that fibrous dysplasia may contain cartilage upon frozen section will avoid overly aggressive therapy, and (2) FCD can occur in the McCune-Albright syndrome.PMID:38587471 | DOI:10.1080/15513815.2024.2320341 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Adam Haydel Randall Craver Matthew Cable Source Type: research
Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias
CONCLUSION: Beckwith-Wiedemann syndrome anomalies may include multifocal developmental dysplastic chondromatous lesions and cerebral neuronal heterotopias, lateralized, and corpus callosum aplasia.PMID:38587479 | DOI:10.1080/15513815.2024.2337639 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - April 8, 2024 Category: Pathology Authors: Stephanie Collier Ewa M Wasilewska Randall Craver Source Type: research
