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
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
Primary Intraosseous Granular Cell Tumor of the Sphenoid and Central Skull Base in a Pediatric Patient
We present a primary intra-osseous granular cell tumor of the sphenoid and central skull base arising in a 12- year- old girl.CASE REPORT: A 12-year-old female with sickle cell disease and Jeavons syndrome presented with seizures. Imaging and partial resection revealed an expansile benign granular cell tumor (GCT) involving the sphenoid body, pterygoid process, and central skull base. The disease has remained stable after 36-month follow up.DISCUSSION: GCT primarily involving the osseous sphenoid/skull base has not been previously reported in a child. Although mostly benign, some are aggressive, with malignant transformati...
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Delaney Sheehan Belinda Mantle Ashley Kraft Randall Craver Christopher Arcement Renee Gardner Ellen Zakris Daniel Nuss Source Type: research
Cell Free Microbial DNA Utilization at a Children's Hospital
Conclusions: Efficiency of cfDNA was 30.4-41.8.PMID:38345066 | DOI:10.1080/15513815.2024.2315434 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - February 12, 2024 Category: Pathology Authors: Randall Craver Stephanie Collier Margot Anderson Source Type: research
