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 - 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 -