DICER1‐associated embryonal rhabdomyosarcoma and adenosarcoma of the gynecologic tract: pathology, molecular genetics, and indications for molecular testing

M Apellaniz‐Ruiz, WG McCluggage… - Genes …, 2021 - Wiley Online Library
Gynecologic sarcomas are uncommon neoplasms, the majority occurring in the uterus. Due
to the diverse nature of these, the description of “new” morphological types and the rarity of …

Update on pediatric rhabdomyosarcoma: A report from the APSA Cancer Committee

DS Rhee, DA Rodeberg, RM Baertschiger… - Journal of pediatric …, 2020 - Elsevier
Abstract Background/Purpose Rhabdomyosarcoma is the most common soft tissue sarcoma
in children and young adults and requires multimodality treatment. The purpose of this …

Cancer of the vagina: 2021 update

TS Adams, LJ Rogers, MA Cuello - International Journal of …, 2021 - Wiley Online Library
Diagnosis of a primary vaginal cancer is rare, as most vaginal tumors are metastatic from
another primary site. Although cancer of the vagina is more common in postmenopausal …

Cancer of the vagina

TS Adams, MA Cuello - International Journal of Gynecology & …, 2018 - Wiley Online Library
Diagnosis of a primary vaginal cancer is rare because most of these lesions will be
metastatic from another primary site. Although cancer of the vagina is more common in …

Epidemiology, incidence, and survival of rhabdomyosarcoma subtypes: SEER and ICES database analysis

KM Amer, JE Thomson, D Congiusta… - Journal of …, 2019 - Wiley Online Library
Rhabdomyosarcoma is the most common soft‐tissue sarcoma in children and adolescents
and accounts for 3% of all pediatric tumors. Subtypes include alveolar, spindle cell …

[HTML][HTML] Clinicopathologic and molecular analysis of embryonal rhabdomyosarcoma of the genitourinary tract: evidence for a distinct DICER1-associated subgroup

FKF Kommoss, D Stichel, J Mora, M Esteller… - Modern …, 2021 - nature.com
Embryonal rhabdomyosarcoma (ERMS) of the uterus has recently been shown to frequently
harbor DICER1 mutations. Interestingly, only rare cases of extrauterine DICER1-associated …

[HTML][HTML] Significantly greater prevalence of DICER1 alterations in uterine embryonal rhabdomyosarcoma compared to adenosarcoma

L de Kock, JY Yoon, M Apellaniz-Ruiz, D Pelletier… - Modern Pathology, 2020 - Elsevier
Embryonal rhabdomyosarcomas (ERMS) account for 2–3% of cancers in pediatric and
adolescent populations. They are rarer in adults. We and others have reported that ERMS …

Sarcomatoid renal cell carcinoma: population-based study of 879 patients

M Alevizakos, A Gaitanidis, D Nasioudis… - Clinical genitourinary …, 2019 - Elsevier
Background Sarcomatoid renal cell carcinoma (sRCC) constitutes a rare and aggressive
subtype of renal cell carcinoma. We aimed to investigate its clinicopathologic characteristics …

Local treatment of rhabdomyosarcoma of the female genital tract: expert consensus from the Children's Oncology Group, the European Soft‐Tissue Sarcoma Group …

TB Lautz, H Martelli, J Fuchs, C Chargari… - Pediatric Blood & …, 2023 - Wiley Online Library
Abstract The International Soft‐Tissue Sarcoma Consortium (INSTRuCT) was founded as an
international collaboration between different pediatric soft‐tissue sarcoma cooperative …

Embryonal rhabdomyosarcoma of the uterine cervix: a clinicopathologic study of 94 cases emphasizing issues in differential diagnosis staging, and prognostic factors

KM Devins, RH Young, M Ghioni… - The American Journal …, 2022 - journals.lww.com
Embryonal rhabdomyosarcoma of the uterine cervix (cERMS) is rare and frequently
associated with DICER1 mutations. We report 94 tumors that arose in patients aged 7 to 59 …