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.

31. Phenotypic similarities within the morphologic spectrum of DICER1-associated sarcomas and pleuropulmonary blastoma: Histopathologic features guide diagnosis in the LMIC setting / Roy, Paromita; Das, Anirban; Singh, Angad; Panda, Joyshree; Bhattacharya, Arpita; Gehani, Anisha; Parihar, Mayur; K S, Reghu; Achari, Rimpa; Alaggio, Rita; Field, Amanda; Ashley Hill, D; P Dehner, Louis; P Schultz, Kris Ann. - In: PEDIATRIC BLOOD & CANCER. - ISSN 1545-5017. - (2021). [10.1002/pbc.29466]

31. Phenotypic similarities within the morphologic spectrum of DICER1-associated sarcomas and pleuropulmonary blastoma: Histopathologic features guide diagnosis in the LMIC setting.

Rita Alaggio;
2021

Abstract

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.
2021
DICER1 syndrome; DICER1-associated sarcoma; rhabdomyosarcoma.
01 Pubblicazione su rivista::01a Articolo in rivista
31. Phenotypic similarities within the morphologic spectrum of DICER1-associated sarcomas and pleuropulmonary blastoma: Histopathologic features guide diagnosis in the LMIC setting / Roy, Paromita; Das, Anirban; Singh, Angad; Panda, Joyshree; Bhattacharya, Arpita; Gehani, Anisha; Parihar, Mayur; K S, Reghu; Achari, Rimpa; Alaggio, Rita; Field, Amanda; Ashley Hill, D; P Dehner, Louis; P Schultz, Kris Ann. - In: PEDIATRIC BLOOD & CANCER. - ISSN 1545-5017. - (2021). [10.1002/pbc.29466]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1704314
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