Patients with completely resected nongenitourinary low‐risk embryonal rhabdomyosarcoma are candidates for reduced duration low‐intensity chemotherapy
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DOI: 10.1002/cncr.34497
Abstract: The survival of patients with localized embryonal rhabdomyosarcoma (RMS) completely resected at diagnosis is greater than 90%. Most patients have paratesticular, uterine, or vaginal RMS, limiting specific analyses of RMS localized in other anatomic regions.… read more here.
Keywords: patients completely; completely resected; nongenitourinary low; embryonal rhabdomyosarcoma ... See more keywords
Embryonal rhabdomyosarcoma of breast, pleura, and retroperitoneum diagnosed from pleural fluid cytology
Sign Up to like & getrecommendations! Published in 2020 at "Diagnostic Cytopathology"
DOI: 10.1002/dc.24677
Abstract: Embryonal rhabdomyosarcoma (ERMS) is a malignant small blue round cell tumor which is commonly seen in head and neck region. Breast and pleural involvement are uncommon. Rhabdomyosarcoma has been rarely reported in the body fluids… read more here.
Keywords: pleural fluid; cytology; embryonal rhabdomyosarcoma; rhabdomyosarcoma breast ... See more keywords
Cytologic diagnosis of metastatic embryonal rhabdomyosarcoma in cerebrospinal fluid: A case report
Sign Up to like & getrecommendations! Published in 2021 at "Diagnostic Cytopathology"
DOI: 10.1002/dc.24742
Abstract: Rhabdomyosarcoma (RMS) originates from a differentiation block in muscle progenitors. Leptomeningeal metastasis is a rare but devastating complication of RMS which can be caused by dissemination of cancer cells in cerebrospinal fluid (CSF). Here, we… read more here.
Keywords: diagnosis metastatic; report; rhabdomyosarcoma; embryonal rhabdomyosarcoma ... See more keywords
Adult embryonal rhabdomyosarcoma in the nasal cavity; a case report with a review of the literature
Sign Up to like & getrecommendations! Published in 2022 at "Annals of Medicine and Surgery"
DOI: 10.1016/j.amsu.2022.103424
Abstract: Introduction Rhabdomyosarcoma (RMS) is a primitive malignant soft tissue tumor arising from premature mesenchymal cells. The current study presents a rare case of embryonal rhabdomyosarcoma in the nasal cavity of an adult patient. Case presentation… read more here.
Keywords: case; nasal cavity; cavity; embryonal rhabdomyosarcoma ... See more keywords
Embryonal rhabdomyosarcoma in a patient with a germline CBL pathogenic variant.
Sign Up to like & getrecommendations! Published in 2019 at "Cancer genetics"
DOI: 10.1016/j.cancergen.2018.12.006
Abstract: Germline pathogenic variants in CBL are associated with an autosomal dominant RASopathy and an increased risk for malignancies, particularly juvenile myelomonocytic leukemia. Herein, we describe a patient with clinical features of a Noonan-spectrum disorder who… read more here.
Keywords: germline cbl; pathogenic variant; embryonal rhabdomyosarcoma; germline ... See more keywords
Management of neonatal retro-auricular embryonal rhabdomyosarcoma – Case report
Sign Up to like & getrecommendations! Published in 2020 at "International Journal of Surgery Case Reports"
DOI: 10.1016/j.ijscr.2020.09.076
Abstract: Highlights • RMS is a fast-growing malignant and aggressive tumor originating from skeletal muscle.• Diagnosis can be performed with CT-scan or MRI and confirmed by biopsy.• The treatment is based on chemotherapy followed by radiotherapy… read more here.
Keywords: case; neonatal retro; management neonatal; embryonal rhabdomyosarcoma ... See more keywords
When Chemotherapy Is Not Enough-Management of Prostatic Embryonal Rhabdomyosarcoma in an Infant.
Sign Up to like & getrecommendations! Published in 2018 at "Urology"
DOI: 10.1016/j.urology.2017.10.044
Abstract: A baby boy was diagnosed with embryonal rhabdomyosarcoma causing left hydroureteronephrosis. A loop ureterostomy was performed, and the infant was treated per the RMS13 protocol. After 3 months of chemotherapy, the infant's tumor burden increased,… read more here.
Keywords: enough management; chemotherapy enough; management prostatic; rhabdomyosarcoma ... See more keywords
An uncommon perineal embryonal rhabdomyosarcoma in adult: A case report
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DOI: 10.1097/md.0000000000032529
Abstract: Rationale: Embryonal rhabdomyosarcoma (ERMS) is a major subtype of rhabdomyosarcoma, mainly affect children. There is seldom report for perineal ERMS in adults, since its rare location and the age. Patient concerns: A 20-year old male… read more here.
Keywords: rhabdomyosarcoma adult; perineal embryonal; adult; embryonal rhabdomyosarcoma ... See more keywords
The Value of DICER1 Mutation Analysis in "Subtle" Diagnostically Challenging Embryonal Rhabdomyosarcomas of the Uterine Cervix.
Sign Up to like & getrecommendations! Published in 2020 at "International Journal of Gynecological Pathology"
DOI: 10.1097/pgp.0000000000000718
Abstract: Embryonal rhabdomyosarcoma of the uterine cervix is a rare neoplasm which is almost invariably associated with pathogenic somatic or germline DICER1 mutations; patients with germline mutations have DICER1 syndrome. We report 2 subtle cervical embryonal… read more here.
Keywords: uterine cervix; dicer1; dicer1 syndrome; embryonal rhabdomyosarcoma ... See more keywords
Response to the combination use of pazopanib with olaratumab in a patient with lung-metastatic embryonal rhabdomyosarcoma: a case report.
Sign Up to like & getrecommendations! Published in 2021 at "Translational lung cancer research"
DOI: 10.21037/tlcr-19-644
Abstract: Embryonal rhabdomyosarcoma (ERMS) is associated with a low prevalence, poor prognosis, and limited treatment efficacy. Here, we report a case of a 21-year-old male whose disease relapsed in the thoracic cavity following traditional chemotherapy. The… read more here.
Keywords: combination; pazopanib olaratumab; case; report ... See more keywords
DICER1 syndrome and embryonal rhabdomyosarcoma of the cervix: a case report and literature review
Sign Up to like & getrecommendations! Published in 2023 at "Frontiers in Pediatrics"
DOI: 10.3389/fped.2023.1150418
Abstract: Background Embryonal rhabdomyosarcomas (ERMS) of the uterine cervix and corpus are rare pediatric tumors usually associated with a late age of onset and frequent somatic DICER1 mutation. It may also develop in the context of… read more here.
Keywords: syndrome embryonal; embryonal rhabdomyosarcoma; case; cervix ... See more keywords