DICER1 Mutations Do Not Always Indicate Dismal Prognosis in Pediatric Poorly Differentiated Thyroid Carcinomas
Authors (first, second and last of 8)
Collection
Pediatric Endocrine Pathology
Pathology of pediatric endocrine neoplasms is an area of interest with respect to its clinical, pathologic and molecular characteristics. This topical collection includes original articles, reviews, brief reports and case series on recently identified clinicopathologic and molecular correlates of pediatric endocrine neoplasia. Future published submissions on the spectrum of pediatric endocrine pathology will be added to this collection. Endocrine Pathology, the Official journal of Endocrine Pathology Society welcome your contribution.
Articles (10 in this collection)
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Pediatric Adrenocortical Neoplasms: A Study Comparing Three Histopathological Scoring Systems
Authors (first, second and last of 10)
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DICER1 Mutations Occur in More Than One-Third of Follicular-Patterned Pediatric Papillary Thyroid Carcinomas and Correlate with a Low-Risk Disease and Female Gender Predilection
Authors (first, second and last of 13)
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Alternative Lengthening of Telomeres (ALT) and Telomerase Reverse Transcriptase Promoter Methylation in Recurrent Adult and Primary Pediatric Pituitary Neuroendocrine Tumors
Authors (first, second and last of 8)
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High Prevalence of DICER1 Mutations and Low Frequency of Gene Fusions in Pediatric Follicular-Patterned Tumors of the Thyroid
Authors (first, second and last of 8)
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Clinical Impact of Pathological Features Including the Ki-67 Labeling Index on Diagnosis and Prognosis of Adult and Pediatric Adrenocortical Tumors
Authors (first, second and last of 7)
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Frequent BRAF V600E and Absence of TERT Promoter Mutations Characterize Sporadic Pediatric Papillary Thyroid Carcinomas in Japan
Authors (first, second and last of 11)
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Classic Architecture with Multicentricity and Local Recurrence, and Absence of TERT Promoter Mutations are Correlates of BRAF V600E Harboring Pediatric Papillary Thyroid Carcinomas
Authors (first, second and last of 10)
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Monomorphous Plurihormonal Pituitary Adenoma of Pit-1 Lineage in a Giant Adolescent with Central Hyperthyroidism
Authors (first, second and last of 6)
