TY - JOUR
T1 - Phenotypic similarities within the morphologic spectrum of DICER1-associated sarcomas and pleuropulmonary blastoma
T2 - Histopathologic features guide diagnosis in the LMIC setting
AU - Roy, Paromita
AU - Das, Anirban
AU - Singh, Angad
AU - Panda, Joyshree
AU - Bhattacharya, Arpita
AU - Gehani, Anisha
AU - Parihar, Mayur
AU - Reghu, K. S.
AU - Achari, Rimpa
AU - Alaggio, Rita
AU - Field, Amanda
AU - Hill, D. Ashley
AU - Dehner, Louis P.
AU - Schultz, Kris Ann P.
N1 - Funding Information:
Dr. Stefan Rutkowski, Dr. Jonas Ecker, Dr. Kerstin Grund, and the Pediatric Targeted Therapy 2.0 program at the German Cancer Research Center (DKFZ), Heidelberg University, Germany. Testing for DICER1 was supported by the International Pleuropulmonary Blastoma/DICER1 Registry. Courier charges were borne by Tata Medical Center.
Funding Information:
Dr. Stefan Rutkowski, Dr. Jonas Ecker, Dr. Kerstin Grund, and the Pediatric Targeted Therapy 2.0 program at the German Cancer Research Center (DKFZ), Heidelberg University, Germany. Testing for DICER1 was supported by the International Pleuropulmonary Blastoma/DICER1 Registry. Courier charges were borne by Tata Medical Center.
Publisher Copyright:
© 2021 Wiley Periodicals LLC
PY - 2022/3
Y1 - 2022/3
N2 - Extrapulmonary DICER1-associated sarcomas (DS) can harbor morphological features overlapping with pleuropulmonary blastoma. We report three children with intracranial and genital tract sarcomas, suspected to have DS based on a heterogeneous yet defining combination of spindle-cell sarcomatous and blastemal morphology, with rhabdomyomatous differentiation. Foci of immature cartilage at diagnosis (n = 2/3) and increased neuroepithelial differentiation at recurrence (n = 1) were noted. Morphological suspicion prompted somatic testing at reference centers, confirming likely biallelic, loss-of-function, and “hotspot” missense DICER1 variants in all three tumors. This can serve as a model for this diagnosis in resource-limited settings and has implications for germline testing, surveillance, and tumor management.
AB - Extrapulmonary DICER1-associated sarcomas (DS) can harbor morphological features overlapping with pleuropulmonary blastoma. We report three children with intracranial and genital tract sarcomas, suspected to have DS based on a heterogeneous yet defining combination of spindle-cell sarcomatous and blastemal morphology, with rhabdomyomatous differentiation. Foci of immature cartilage at diagnosis (n = 2/3) and increased neuroepithelial differentiation at recurrence (n = 1) were noted. Morphological suspicion prompted somatic testing at reference centers, confirming likely biallelic, loss-of-function, and “hotspot” missense DICER1 variants in all three tumors. This can serve as a model for this diagnosis in resource-limited settings and has implications for germline testing, surveillance, and tumor management.
UR - http://www.scopus.com/inward/record.url?scp=85121381763&partnerID=8YFLogxK
U2 - 10.1002/pbc.29466
DO - 10.1002/pbc.29466
M3 - Article
C2 - 34913555
AN - SCOPUS:85121381763
SN - 1545-5009
VL - 69
JO - Pediatric Blood and Cancer
JF - Pediatric Blood and Cancer
IS - 3
M1 - e29466
ER -