Raras
Buscar doenças, sintomas, genes...
Rabdomiossarcoma, embrionário
ORPHA:99757CID-10 · C49.9OMIM 268210DOENÇA RARA

É uma variação morfológica de rabdomiossarcoma com contornos pouco definidos. É caracterizado pela presença de formação de músculo esquelético ainda em estágio inicial, em qualquer fase do desenvolvimento muscular.

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Introdução

O que você precisa saber de cara

📋

É uma variação morfológica de rabdomiossarcoma com contornos pouco definidos. É caracterizado pela presença de formação de músculo esquelético ainda em estágio inicial, em qualquer fase do desenvolvimento muscular.

Pesquisas ativas
6 ensaios
18 total registrados no ClinicalTrials.gov
Publicações científicas
1.668 artigos
Último publicado: 2026 Mar

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
<1 / 1 000 000
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.048
Austria
Herança
Multigenic/multifactorial
🏥
SUS: Sem cobertura SUSScore: 0%
CID-10: C49.9
Você se identifica com essa condição?
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

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Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Características mais comuns

Rabdomiossarcoma embrionário
Início na idade adulta
Herança autossômica recessiva
3sintomas
Sem dados (3)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 3 características clínicas mais associadas, ordenadas por frequência.

Rabdomiossarcoma embrionárioEmbryonal rhabdomyosarcoma
Início na idade adultaAdult onset
Herança autossômica recessivaAutosomal recessive inheritance

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico1.668PubMed
Últimos 10 anos200publicações
Pico202467 papers
Linha do tempo
2026Hoje · 2026🧪 1991Primeiro ensaio clínico📈 2024Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

4 genes identificados com associação a esta condição. Padrão de herança: Multigenic/multifactorial.

DICER1Endoribonuclease DicerDisease-causing somatic mutation(s) inAltamente restrito
FUNÇÃO

Double-stranded RNA (dsRNA) endoribonuclease playing a central role in short dsRNA-mediated post-transcriptional gene silencing. Cleaves naturally occurring long dsRNAs and short hairpin pre-microRNAs (miRNA) into fragments of twenty-one to twenty-three nucleotides with 3' overhang of two nucleotides, producing respectively short interfering RNAs (siRNA) and mature microRNAs. SiRNAs and miRNAs serve as guide to direct the RNA-induced silencing complex (RISC) to complementary RNAs to degrade them

LOCALIZAÇÃO

CytoplasmCytoplasm, perinuclear region

VIAS BIOLÓGICAS (5)
MicroRNA (miRNA) biogenesisSmall interfering RNA (siRNA) biogenesistRNA-derived small RNA (tsRNA or tRNA-related fragment, tRF) biogenesisM-decay: degradation of maternal mRNAs by maternally stored factorsRegulation of MITF-M-dependent genes involved in apoptosis
MECANISMO DE DOENÇA

Pleuropulmonary blastoma

A rare pediatric intrathoracic neoplasm. The tumor arises from the lung, pleura, or both, and appears to be purely mesenchymal in phenotype. It lacks malignant epithelial elements, a feature that distinguishes it from the classic adult-type pulmonary blastoma. It arises during fetal lung development and is often part of an inherited cancer syndrome. The tumor contain both epithelial and mesenchymal cells. Early in tumorigenesis, cysts form in lung airspaces, and these cysts are lined with benign-appearing epithelium. Mesenchymal cells susceptible to malignant transformation reside within the cyst walls and form a dense layer beneath the epithelial lining. In a subset of patients, overgrowth of the mesenchymal cells produces a sarcoma, a transition that is associated with a poorer prognosis. Some patients have multilocular cystic nephroma, a benign kidney tumor.

EXPRESSÃO TECIDUAL(Ubíquo)
Nervo tibial
46.1 TPM
Tireoide
31.6 TPM
Cervix Endocervix
31.4 TPM
Útero
31.2 TPM
Ovário
30.2 TPM
OUTRAS DOENÇAS (10)
pleuropulmonary blastomaglobal developmental delay - lung cysts - overgrowth - Wilms tumor syndromegoiter, multinodular 1, with or without Sertoli-Leydig cell tumorsrhabdomyosarcoma, embryonal, 2
HGNC:17098UniProt:Q9UPY3
NF1NeurofibrominDisease-causing somatic mutation(s) inAltamente restrito
FUNÇÃO

Stimulates the GTPase activity of Ras. NF1 shows greater affinity for Ras GAP, but lower specific activity. May be a regulator of Ras activity

LOCALIZAÇÃO

NucleusNucleus, nucleolusCell membrane

VIAS BIOLÓGICAS (1)
RAS signaling downstream of NF1 loss-of-function variants
MECANISMO DE DOENÇA

Neurofibromatosis 1

A disease characterized by patches of skin pigmentation (cafe-au-lait spots), Lisch nodules of the iris, tumors in the peripheral nervous system and fibromatous skin tumors. Individuals with the disorder have increased susceptibility to the development of benign and malignant tumors.

EXPRESSÃO TECIDUAL(Ubíquo)
Fibroblastos
17.9 TPM
Cérebro - Hemisfério cerebelar
17.1 TPM
Cerebelo
15.3 TPM
Nervo tibial
14.9 TPM
Tireoide
14.1 TPM
OUTRAS DOENÇAS (12)
neurofibromatosis, familial spinalneurofibromatosis type 1juvenile myelomonocytic leukemiaWatson syndrome
HGNC:7765UniProt:P21359
SLC67A1Solute carrier family 67 member A1Candidate gene tested inTolerante
FUNÇÃO

May act as a transporter of organic cations based on a proton efflux antiport mechanism. May play a role in the transport of chloroquine and quinidine-related compounds in kidney (PubMed:9744804). Plays a role in the regulation of lipid metabolism (By similarity)

LOCALIZAÇÃO

Apical cell membrane

VIAS BIOLÓGICAS (1)
SLC-mediated transport of organic cations
MECANISMO DE DOENÇA

Lung cancer

A common malignancy affecting tissues of the lung. The most common form of lung cancer is non-small cell lung cancer (NSCLC) that can be divided into 3 major histologic subtypes: squamous cell carcinoma, adenocarcinoma, and large cell lung cancer. NSCLC is often diagnosed at an advanced stage and has a poor prognosis.

OUTRAS DOENÇAS (3)
lung cancerembryonal rhabdomyosarcomahereditary breast carcinoma
HGNC:10964UniProt:Q96BI1
TP53Cellular tumor antigen p53Disease-causing germline mutation(s) inAltamente restrito
FUNÇÃO

Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence (PubMed:11025664, PubMed:12524540, PubMed:12810724, PubMed:15186775, PubMed:15340061, PubMed:17317671, PubMed:17349958, PubMed:19556538, PubMed:20673990, PubMed:20959462, PubMed:22726440, PubMed:24051492, PubMed:24652652, PubMed:35618207, PubMed:36634798, PubMed:38653238, PubMed:9840937). Acts as a tumor suppressor in many tumor types; induces growth arrest or apop

LOCALIZAÇÃO

CytoplasmNucleusNucleus, PML bodyEndoplasmic reticulumMitochondrion matrixCytoplasm, cytoskeleton, microtubule organizing center, centrosome

VIAS BIOLÓGICAS (10)
TP53 Regulates Metabolic GenesRegulation of TP53 ExpressionRegulation of TP53 DegradationOncogene Induced SenescenceOxidative Stress Induced Senescence
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
73.0 TPM
Skin Sun Exposed Lower leg
37.0 TPM
Skin Not Sun Exposed Suprapubic
35.2 TPM
Fibroblastos
32.9 TPM
Ovário
32.4 TPM
OUTRAS DOENÇAS (29)
Li-Fraumeni syndromenasopharyngeal carcinoma, susceptibility to, 1hepatocellular carcinomafamilial pancreatic carcinoma
HGNC:11998UniProt:P04637

Variantes genéticas (ClinVar)

8,945 variantes patogênicas registradas no ClinVar.

🧬 TP53: NM_000546.6(TP53):c.377del (p.Tyr126fs) ()
🧬 TP53: NM_000546.6(TP53):c.494dup (p.Ser166fs) ()
🧬 TP53: NM_000546.6(TP53):c.184_187dup (p.Ala63fs) ()
🧬 TP53: NM_000546.6(TP53):c.549dup (p.Asp184fs) ()
🧬 TP53: NM_000546.6(TP53):c.43del (p.Ser15fs) ()
Ver todas no ClinVar

Vias biológicas (Reactome)

39 vias biológicas associadas aos genes desta condição.

MicroRNA (miRNA) biogenesis Small interfering RNA (siRNA) biogenesis tRNA-derived small RNA (tsRNA or tRNA-related fragment, tRF) biogenesis M-decay: degradation of maternal mRNAs by maternally stored factors Regulation of MITF-M-dependent genes involved in apoptosis Regulation of RAS by GAPs RAS signaling downstream of NF1 loss-of-function variants SLC-mediated transport of organic cations Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1) Activation of NOXA and translocation to mitochondria Activation of PUMA and translocation to mitochondria Pre-NOTCH Transcription and Translation Oxidative Stress Induced Senescence Formation of Senescence-Associated Heterochromatin Foci (SAHF) Oncogene Induced Senescence DNA Damage/Telomere Stress Induced Senescence SUMOylation of transcription factors Autodegradation of the E3 ubiquitin ligase COP1 Association of TriC/CCT with target proteins during biosynthesis Pyroptosis TP53 Regulates Metabolic Genes Ub-specific processing proteases Ovarian tumor domain proteases Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Interleukin-4 and Interleukin-13 signaling TP53 Regulates Transcription of DNA Repair Genes TP53 Regulates Transcription of Genes Involved in Cytochrome C Release TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain TP53 Regulates Transcription of Caspase Activators and Caspases TP53 Regulates Transcription of Death Receptors and Ligands TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest Regulation of TP53 Expression Regulation of TP53 Activity through Phosphorylation Regulation of TP53 Degradation Regulation of TP53 Activity through Acetylation Regulation of TP53 Activity through Association with Co-factors Regulation of TP53 Activity through Methylation

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

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Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
3Fase 35
2Fase 25
·Pré-clínico5
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 15 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Rabdomiossarcoma, embrionário

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Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

🟢 Recrutando agora

3 pesquisas recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

Outros ensaios clínicos

18 ensaios clínicos encontrados, 6 ativos.

Distribuição por fase
Ver todos no ClinicalTrials.gov
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Publicações mais relevantes

Timeline de publicações
601 papers (10 anos)

Mostrando amostra de 200 publicações de um total de 601

#1

Multimodality Imaging Findings of Primary Embryonal Rhabdomyosarcoma in the Prostate: A Rare Case Report.

Journal of clinical ultrasound : JCU2026 Mar 24

Embryonal rhabdomyosarcoma (ERMS) of the prostate is an extremely rare malignant tumor, which often presents with urinary symptoms. We report a 32-year-old male with recurrent urinary retention diagnosed with prostatic ERMS via surgical pathology. This case analyzes the reasons for initial misdiagnosis and details multimodal imaging features on ultrasound (US), contrast-enhanced ultrasound (CEUS), CT, and MRI. Notably, this report provides the first description of the CEUS enhancement pattern in prostatic ERMS, which may represent a unique imaging characteristic.

#2

Cervical embryonal rhabdomyosarcoma beyond childhood: A case report and literature review.

Radiology case reports2026 Jun

Embryonal rhabdomyosarcoma (ERMS) arising from the uterine cervix is a rare malignancy, predominantly affecting children and adolescents. This case report highlights a rare presentation of cervical ERMS in an adult woman, emphasizing the importance of considering ERMS in the differential diagnosis of a cervical mass in adult women and highlights the critical role of a multidisciplinary treatment approach. A 31-year-old woman presented with acute urinary retention, vaginal bleeding, and postcoital bleeding. Imaging at presentation revealed a large cervical mass exerting a significant mass effect on adjacent structures. Histopathology of the surgically excised mass confirmed the diagnosis of ERMS, with tumor cells arranged in sheets of small, round cells with scant eosinophilic cytoplasm and eccentric, small oval nuclei and inconspicuous nucleoli, supported by immunohistochemical staining positive for desmin, myogenin, and MyoD1. The patient underwent surgical resection; however, she was lost to follow-up, limiting long-term outcome assessment. Cervical ERMS is an aggressive soft tissue sarcoma that rarely occurs in adult women. It can mimic other cervical pathologies, posing diagnostic challenges. Ultrasound and magnetic resonance imaging are key for initial assessment, while early diagnosis, surgery, and adjuvant chemotherapy improve outcomes. Optimal management requires a multidisciplinary team.

#3

Laparoscopic Resection of Vaginal Embryonal Rhabdomyosarcoma in a 16-Month-Old Girl: An Organ-Preserving Surgical Approach.

Journal of pediatric and adolescent gynecology2026 Mar 20

Vaginal rhabdomyosarcoma is a rare malignant soft tissue tumor in pediatric patients, and optimal management aims to achieve tumor control while preserving pelvic organs. We report the case of a 16-month-old girl who presented with a protruding vaginal mass. Imaging studies revealed a vaginal tumor near the cervix without evidence of metastatic disease. Histopathological examination confirmed embryonal rhabdomyosarcoma. The patient received 12 weeks of neoadjuvant VAC/VA chemotherapy followed by laparoscopic tumor resection, which was chosen to address the limited pelvic space in infancy and to preserve surrounding organs. The postoperative course was uneventful, and adjuvant chemotherapy was completed. At 32 months of follow-up, no local recurrence or distant metastasis was observed. This case suggests that laparoscopic resection combined with chemotherapy may represent a feasible and organ-preserving treatment option for selected infants with vaginal rhabdomyosarcoma, although long-term follow-up remains necessary.

#4

Adult embryonal rhabdomyosarcoma (botryoid subtype) of the ureter: A case report.

Urology case reports2026 May

Embryonal rhabdomyosarcoma arising from the ureter is exceedingly rare. We report the case of a 20-year-old female who presented with flank pain and hematuria, initially attributed to ureteral stones. Subsequent evaluation revealed an embryonal rhabdomyosarcoma (botryoid subtype) of the ureter. Following surgical resection and chemotherapy, the patient achieved remission and experienced minor complications including neuropathy and bladder irritation. This case highlights the classification and management of ureteral rhabdomyosarcoma. While the prognosis for ureteral rhabdomyosarcoma appears favorable based on limited literature, long-term surveillance is crucial for monitoring recurrence and managing potential complications.

#5

A rare presentation of uterine cavity embryonal rhabdomyosarcoma in a preschool girl: a case report.

International journal of surgery case reports2026 Mar

Rhabdomyosarcoma (RMS) is a malignant soft tissue sarcoma arising from primitive mesenchymal cells. It is rare in childhood and adolescence but is one of the more common pediatric soft tissue sarcomas. Hence, clinical presentation and prompt treatment strategies of such cases should be known for better management. A 3-year-old girl presented with a one-and-a-half-year history of progressive vaginal mass protrusion and serosanguinous discharge. Abdominal examination revealed a large suprapubic mass extending above the umbilicus. MRI revealed a lesion involving the entire uterus. She underwent a Wertheim-Meigs hysterectomy. Histopathology confirmed embryonal RMS, botryoid variant, originating from the uterine cervix with vaginal extension. RMS originates from rhabdomyoblasts, immature skeletal muscle cells. Botryoid RMS typically presents as multiple grape-like vaginal masses with serosanguinous discharge. Prognosis depends on tumor site, size, extent, residual disease, and histologic sub type. Vaginal lesions generally have better outcomes than cervical ones.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC825 artigos no totalmostrando 198

2026

Multimodality Imaging Findings of Primary Embryonal Rhabdomyosarcoma in the Prostate: A Rare Case Report.

Journal of clinical ultrasound : JCU
2026

Cervical embryonal rhabdomyosarcoma beyond childhood: A case report and literature review.

Radiology case reports
2026

Laparoscopic Resection of Vaginal Embryonal Rhabdomyosarcoma in a 16-Month-Old Girl: An Organ-Preserving Surgical Approach.

Journal of pediatric and adolescent gynecology
2026

Adult embryonal rhabdomyosarcoma (botryoid subtype) of the ureter: A case report.

Urology case reports
2026

A rare presentation of uterine cavity embryonal rhabdomyosarcoma in a preschool girl: a case report.

International journal of surgery case reports
2026

DICER1 Syndrome With Embryonal Rhabdomyosarcoma of the Uterine Cervix and Retroperitoneal Metastasis: A Case Report and Literature Review.

Case reports in obstetrics and gynecology
2026

Embryonal Rhabdomyosarcoma of the Diaphragm in a Two-Year-Old Boy.

Cureus
2026

DICER1-Related Primitive Polyphenotypic Neoplasm: A Report of 15 Cases of an Underrecognized Tumor of the Gynecologic Tract and Peritoneum.

The American journal of surgical pathology
2026

Early recurrence and prognosis in patients undergoing resection of primary retroperitoneal sarcoma: an international, retrospective cohort study.

EClinicalMedicine
2026

Primary peritoneal embryonal rhabdomyosarcoma in a 6-year-old girl with rapid post-surgical peritoneal recurrence possibly due to surgical tumor seeding: a case report and review of the literature.

Journal of medical case reports
2026

Primary Embryonal Rhabdomyosarcoma of the Breast: A Case Report and Literature Review.

Case reports in oncology
2025

Case of primary digital embryonal rhabdomyosarcoma in a cat.

The Canadian veterinary journal = La revue veterinaire canadienne
2026

Predictors of survival in alveolar rhabdomyosarcoma in the US.

Annals of medicine and surgery (2012)
2026

[Malignant embryonal rhabdomyosarcoma with heterologous differentiation in gastric stromal tumors: report of a case].

Zhonghua bing li xue za zhi = Chinese journal of pathology
2025

Rare Presentations of Embryonal Rhabdomyosarcoma in the Middle Ear of a 3-Year-Old Boy and Girl.

Nigerian medical journal : journal of the Nigeria Medical Association
2025

Clinicopathological observation of adult malignant ectodermal mesenchymoma: A case report and literature review.

Medicine
2026

GREB1-rearranged uterine tumour shares a common DNA methylation signature with ESR1-rearranged UTROSCT.

Histopathology
2026

Malignant Transformation of a Pediatric Intracranial Nongerminomatous Germ Cell Tumor to Embryonal Rhabdomyosarcoma: Case Report and Literature Review.

Journal of pediatric hematology/oncology
2025

[Clinical and pathological characteristics of pediatric tumors with DICER1 mutations detected by Sanger sequencing].

Zhonghua bing li xue za zhi = Chinese journal of pathology
2025

Neurolysis of the Sphenopalatine Ganglion for Refractory Facial Pain in a Paediatric Cancer Patient: A Case Report.

Indian journal of palliative care
2025

[Antibodies against VP3 protein of echovirus 30 (Picornaviridae: Enterovirus: Enterovirus betacoxsackie) neutralize virus in vitro].

Voprosy virusologii
2025

Clinicopathological Features and Therapeutic Outcomes of Head and Neck Sarcomas: A 14-Year Retrospective Study.

Cureus
2025

Functional Analysis and Clinical Data Reclassify the DICER1 c.4206+1G>C Variant, Leading to Exon 22 Skipping, as Likely Pathogenic.

Clinical genetics
2026

DICER1 -Associated Gynecologic Neoplasms: An Update and Review.

Advances in anatomic pathology
2025

Vesicovaginal Leiomyoma at 20 Years of Age-A Rare Clinical Entity: Case Report and Literature Review.

Diagnostics (Basel, Switzerland)
2025

Orbital Rhabdomyosarcoma in a Pediatric Patient With Costello Syndrome.

Ophthalmic plastic and reconstructive surgery
2025

Embryonal rhabdomyosarcoma of the uterine corpus in a postmenopausal Woman: A case report and literature Review.

Gynecologic oncology reports
2025

Imaging Progress and Treatment of Malignant Triton Tumor of the Skull Base.

The Journal of craniofacial surgery
2025

[Clinicopathological and molecular genetic characteristics of embryonal rhabdomyosarcoma in the middle ear: an analysis of 11 cases].

Zhonghua bing li xue za zhi = Chinese journal of pathology
2025

A Horrific Case of Proptosis: Salvaging Vision in a Pediatric Patient With Rapidly Growing Orbital Rhabdomyosarcoma.

Cureus
2025

Marked Prolongation of Capillary Refill Time in the Right Foot of a 20-Month-Old Female Infant With Rhabdomyosarcoma.

Cureus
2025

DICER1 Syndrome: What Do We Know of the Pathogenetic Mechanisms?

Cancers
2025

Embryonal Rhabdomyosarcoma of the Uterine Cervix in a Patient With Xeroderma Pigmentosum: An Exceptional Association.

Cureus
2025

Rhabdomyosarcoma: A Case Report and Comprehensive Literature Review.

Cureus
2025

Pediatric Embryonal Rhabdomyosarcoma: An Integrated Study of Clinicopathological Features, Pan-cancer Targeted Next-generation Sequencing, and Chromosomal Microarray Analysis from a Single Institution.

Virchows Archiv : an international journal of pathology
2025

A Rare Case of Uterine Embryonal Rhabdomyosarcoma.

CRSLS : MIS case reports from SLS
2025

[DICER1-syndrome with manifestation of genital embryonal rhabdomyosarcoma in the first year of life: case report].

Problemy endokrinologii
2025

Recombinant Human GH in Managing Refractory Hypoglycemia in a Young Patient With Embryonal Rhabdomyosarcoma.

JCEM case reports
2025

Case Report: A case of uterine embryonal rhabdomyosarcoma in adult female-navigating the complexities of the diagnostic journey.

Frontiers in oncology
2025

A Rare Case of Adult Embryonal Rhabdomyosarcoma of the Uterus in a Postmenopausal Woman.

Indian journal of surgical oncology
2025

Ovarian Rhabdomyosarcoma in Children.

Cureus
2025

Identification of germline mutations in DICER1 through routine somatic NGS analysis in various neoplasms.

Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia
2025

Cyano-containing Daphniphyllum alkaloids with antienteroviral activity from the leaves and stems of Daphniphyllum calycinum Benth.

Phytochemistry
2025

Proton beam therapy for a patient with prostatic rhabdomyosarcoma: a case report and review of the literature.

Frontiers in oncology
2025

Auricular Embryonal Rhabdomyosarcoma With Parotid Gland and Cervical Infiltration in a Pediatric Patient With Congenital Ichthyosis Vulgaris: A Case Report.

Ear, nose, &amp; throat journal
2025

[Detection of MYOD1-mutation of rhabdomyosarcoma and its clinicopathological characteristics].

Zhonghua bing li xue za zhi = Chinese journal of pathology
2025

Vaginal and cervical tumors in children and adolescents: a SEER population-based study.

Pediatric surgery international
2025

Emergency Radiation Therapy for Hemorrhage in Botryoides Sarcoma: A Pediatric Case Report.

The American journal of case reports
2025

EHMT1 mediates cellular motility in embryonal rhabdomyosarcoma by activating SOX8 expression.

British journal of cancer
2025

Genitourinary rhabdomyosarcoma in a child with urinary incontinence as the initial symptom: A case report and literature review.

Urology case reports
2025

A rare case of giant hepatic mesenchymal hamartoma in a pediatric patient: diagnostic and surgical challenges.

Journal of surgical case reports
2025

The Histological Spectrum of DICER1-Associated Neoplasms.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
2025

Utility of Protein Kinase C Beta II Immunohistochemistry in Differential Diagnosis of Ewing Sarcoma.

The American journal of surgical pathology
2025

Evaluation of pediatric prostatic and retroperitoneal embryonal rhabdomyosarcoma with high Ki-67-case series study.

Turkish journal of surgery
2025

A Report of Two Cases of Embryonal Rhabdomyosarcoma: Diagnostic Insights From Pathology.

Cureus
2025

Embryonal rhabdomyosarcoma at an unusual age and in an atypical site: a case report.

Journal of medical case reports
2025

Parameningeal embryonal rhabdomyosarcoma with leptomeningeal metastasis in a young adult female: illustrative case.

Journal of neurosurgery. Case lessons
2025

Clinicopathological analysis of 13 patients with embryonal rhabdomyosarcoma of the female reproductive system in the Chinese population.

Frontiers in oncology
2025

A 15-year-old male with embryonal rhabdomyosarcoma of the testis-a rare tumor with unusual presentation.

Journal of surgical case reports
2025

The Emerging Role and Clinical Significance of PI3K-Akt-mTOR in Rhabdomyosarcoma.

Biomolecules
2025

A case of multiple embryonal rhabdomyosarcoma in left atrium.

European heart journal
2025

Preclinical Activity of the Type II RAF Inhibitor Tovorafenib in Tumor Models Harboring Either a BRAF Fusion or an NF1 Loss-of-Function Mutation.

Cancer research communications
2025

Case Report on Rhabdomyosarcoma of Middle Ear in A 4 Year Old Child: A Rare Case.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
2025

DICER1 associated cervical embryonal rhabdomyosarcoma in a 59-year-old woman.

Gynecologic oncology reports
2025

Embryonal Rhabdomyosarcoma Arising From the Buccal Mucosa in a Child: Imaging Findings.

Ear, nose, &amp; throat journal
2025

Loss of H3K27me3 Is Not Specific to Malignant Triton Tumor: Immunohistochemical Analysis of 23 Cases of Embryonal Rhabdomyosarcoma.

Archives of pathology &amp; laboratory medicine
2025

Spinal rhabdomyosarcoma in a child at the site of a lumbosacral lipoma: a rare entity.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
2025

Nephrostomy tubes for management of a bladder occupying embryonal rhabdomyosarcoma in a 2-year-old: A case report and review of the literature.

Urology case reports
2025

The Diagnostic Yield of Panel Versus Exome Sequencing to Identify Hereditary Cancer Disorders in Pediatric Cancer.

Journal of pediatric hematology/oncology
2025

Malignant Ectomesenchymoma in a 6-Month-Old: A Rare Pediatric Tumor Case Report.

Urology
2025

Embryonal Rhabdomyosarcoma of the Abdominal Wall in a Pregnant Woman: Magnetic Resonance Imaging and Pathology Findings.

Journal of clinical ultrasound : JCU
2025

Adult Embryonal Rhabdomyosarcoma of the Prostate Presented on 18 F-FDG and Al 18 F-FAPI-74 PET/CT.

Clinical nuclear medicine
2024

Rhabdomyosarcoma of the Middle Ear Case Report.

Children (Basel, Switzerland)
2024

Primary Esophageal Rhabdomyosarcoma: An Exceptionally Rare Cause of Pediatric Dysphagia.

Case reports in gastrointestinal medicine
2024

Maintenance therapy with trofosfamide, idarubicin and etoposide in patients with rhabdomyosarcoma and other high-risk soft tissue sarcomas (CWS-2007-HR): a multicentre, open-label, randomised controlled phase 3 trial.

EClinicalMedicine
2024

Pineal gland metastatic embryonal rhabdomyosarcoma: A case report.

Asian journal of surgery
2024

A Nose Bleed Reveals Rhabdomyosarcoma's Seed.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
2025

Management and Long-term Follow-up of Vaginal Rhabdomyosarcoma in a 3-Year-Old Female.

Urology
2025

Maternal illnesses during pregnancy and the risk of childhood cancer: A medical-record based analysis (UKCCS).

International journal of cancer
2024

Wide-Excision Choice in Orbital Rhabdomyosarcoma on an 8-Year-Old Patient in a Low-Resource Setting: A Case Report.

Case reports in ophthalmology
2024

Embryonal rhabdomyosarcoma of prostate combined with prostatic abscess in an adult patient: a case report and literature review.

Translational andrology and urology
2024

Cardiac embryonal rhabdomyosarcoma in a domestic shorthair cat.

Topics in companion animal medicine
2024

Unveiling the Rare: Retroauricular Subcutaneous Embryonal Rhabdomyosarcoma: Answer.

The American Journal of dermatopathology
2024

Anlotinib treatment for rapidly progressing pediatric embryonal rhabdomyosarcoma in the maxillary gingiva: a case report.

Diagnostic pathology
2024

Imaging Insights Suggesting a Sinister Cause of a Breast Mass in Adolescents: A Case of Rhabdomyosarcoma in a Teenager.

European journal of case reports in internal medicine
2024

Orbital embryonal rhabdomyosarcoma: a case-based update.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
2024

Phospholipase Cδ-4 (PLCδ4) Acts as a Nuclear Player to Influence Cyclin B Expression in the Embryonal Rhabdomyosarcoma Cell Lines RD and A204.

Biomolecules
2024

Successful treatment of rare case of rhabdomyosarcoma of urinary bladder in adult, experience from tertiary hospital. Case report.

International journal of surgery case reports
2024

Embryonal Rhabdomyosarcoma of the Bile Ducts Causing Obstructive Jaundice in a Child: A Case Report.

Acta medica Philippina
2024

Botryoid-type Embryonal Rhabdomyosarcoma: A Comprehensive Clinicopathologic and Molecular Appraisal With Cross-comparison to its Conventional-type Counterpart.

The American journal of surgical pathology
2024

Perianal embryonal rhabdomyosarcoma: A case report.

Oncology letters
2024

Results of the JRS-I LRA0401 and LRB0402 Japan Rhabdomyosarcoma Study Group trials for low-risk embryonal rhabdomyosarcoma.

International journal of clinical oncology
2024

Entinostat as a combinatorial therapeutic for rhabdomyosarcoma.

Scientific reports
2024

Novel PAX3::MAML3 Fusion Identified in Alveolar Rhabdomyosarcoma, Using DNA Methylation Profiling to Expand the Genetic Spectrum of "Fusion-Positive" Cases.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
2024

A rare case of metastatic prostatic rhabdomyosarcoma in a young adult: Clinical challenges and therapeutic perspectives.

Urology case reports
2024

DICER1-sarcomas of GYN tract: Expanding on an emerging entity.

Human pathology
2024

A rare adult case of primary uterine rhabdomyosarcoma with mixed pattern: a clinicopathological & immunohistochemical study with literature review.

Diagnostic pathology
2024

Bladder Embryonal Rhabdomyosarcoma Presenting in the Perinatal Period: Report of Two Consecutive Cases.

Urology
2024

Left testicular giant embryonal rhabdomyosarcoma.

Asian journal of surgery
2024

Crizotinib therapy for congenital embryonal rhabdomyosarcoma associated with an ATIC-ALK gene fusion.

Pediatric blood &amp; cancer
2024

The mitochondrial calcium uniporter: Balancing tumourigenic and anti-tumourigenic responses.

The Journal of physiology
2024

Developmental and therapeutic implications of IL4ra expression for rhabdomyosarcoma.

Transgenic research
2024

Radiological features of multifocal embryonal rhabdomyosarcoma affecting the vagina and the urinary bladder in a pediatric patient.

BMJ case reports
2024

Cytological diagnosis of patients with embryonal rhabdomyosarcoma of the cervix: case report and literature review.

Diagnostic pathology
2024

18F-fluorodeoxyglucose Positron Emission Tomography/Computed Tomography and 68Ga-prostate-specific Membrane Antigen Positron Emission Tomography/Computed Tomography Imaging in the Evaluation of Rare Entity Adult Embryonal Rhabdomyosarcoma of Prostate.

Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
2024

BOTRROID Embryonal Rhabdomyosarcoma with Uterine Cervix in a Postmenopausal Woman: An Unusual Case Report.

Journal of mid-life health
2024

A challenging diagnosis and treatment of embryonal rhabdomyosarcoma in the cervix of an adult woman: A surgical case report.

International journal of surgery case reports
2024

A 16-Year-Old Girl with Sinonasal Cutaneous Fistula Following Excision and Radiotherapy for Rhabdomyosarcoma Requiring Reconstructive Surgery Using an Expanded Forehead Flap.

The American journal of case reports
2024

Genomic profiling of pleomorphic rhabdomyosarcoma reveals a genomic signature distinct from that of embryonal rhabdomyosarcoma.

Genes, chromosomes &amp; cancer
2024

The Effect of Socioeconomic Status and Race/Ethnicity on the Risk of Presenting With Advanced Stage at Diagnosis in Embryonal Tumors.

Journal of pediatric hematology/oncology
2024

Embryonal and alveolar rhabdomyosarcoma in adolescents/young adults, adults and older adults: a population-based cohort study.

Japanese journal of clinical oncology
2024

Bone marrow disease in rhabdomyosarcoma visualized by 2-[18F]fluorodeoxyglucose positron emission tomography/computed tomography.

Pediatric radiology
2025

Assessment of Stiffness-Dependent Autophagosome Formation and Apoptosis in Embryonal Rhabdomyosarcoma Tumor Cells.

Methods in molecular biology (Clifton, N.J.)
2024

Corrigendium: Effects of RAS on the genesis of embryonal rhabdomyosarcoma.

Genes &amp; development
2024

Non-surgical Fertility Sparing Management of Cervical Embryonal Rhabdomyosarcoma.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC
2024

The "Other" Uterine Mesenchymal Neoplasms: Recent Developments and Emerging Entities.

Advances in anatomic pathology
2024

NF1-Driven Rhabdomyosarcoma Phenotypes: A Comparative Clinical and Molecular Study of NF1-Mutant Rhabdomyosarcoma and NF1-Associated Malignant Triton Tumor.

JCO precision oncology
2024

Cytomorphological Insights into Embryonal Rhabdomyosarcoma: A Rare Case in the Middle Ear.

Acta cytologica
2024

Embryonal rhabdomyosarcoma of the testis in a 17-year-old male.

Urology case reports
2024

Embryonal Rhabdomyosarcoma of the Prostate: Clinico-Pathological Highlights with Review of Literature.

Journal of the West African College of Surgeons
2024

Primary Conjunctival Embryonal Rhabdomyosarcoma in an 8-Year-Old Girl.

Case reports in ophthalmology
2024

Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma: A Report From the Children's Oncology Group.

JAMA network open
2024

Spindle cell embryonal rhabdomyosarcoma of the prostate in an adult patient: a case report and review of the literature.

The Journal of international medical research
2024

Unraveling the Clinicopathological Diversity and Subtypes of Rhabdomyosarcoma: A Study From a Tertiary Care Center.

Cureus
2024

Final report of the phase II NEXT/CNS-GCT-4 trial: GemPOx followed by marrow-ablative chemotherapy for recurrent intracranial germ cell tumors.

Neuro-oncology practice
2023

Small bowel metastasis from embryonal rhabdomyosarcoma of the extremity- a case report.

South African journal of surgery. Suid-Afrikaanse tydskrif vir chirurgie
2024

Prostatic embryonal rhabdomyosarcoma in an adult.

British journal of hospital medicine (London, England : 2005)
2024

Rhabdomyosarcoma of the tongue in a neonatal calf.

Journal of comparative pathology
2024

In silico identification of chikungunya virus replication inhibitor validated using biochemical and cell-based approaches.

The FEBS journal
2024

Adolescents and young adults with rhabdomyosarcoma: A report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.

Pediatric blood &amp; cancer
2024

Nocardiosis in an infant with spindle cell rhabdomyosarcoma treated with mild immunosuppressive chemotherapy.

Pediatric blood &amp; cancer
2024

Successful management strategy for giant primary hepatic rhabdomyosarcoma in 15-year-old male: a case report.

Journal of surgical case reports
2024

Oral rhabdomyosarcoma, a rare malignant tumor mimicking an endodontic-periodontal lesion in an adult patient: a case report.

BMC oral health
2024

BRD4 isoforms have distinct roles in tumour progression and metastasis in rhabdomyosarcoma.

EMBO reports
2023

A rare case of embryonal rhabdomyosarcoma with tumor cells in peripheral blood mimicking acute leukemia.

Journal of hematopathology
2023

Embryonal rhabdomyosarcoma of the uterine cervix.

Medical ultrasonography
2023

Clinicopathologic characteristics, treatment, prognosis and pregnancy outcomes in rhabdomyosarcoma of the uterine cervix: a case series.

Ginekologia polska
2024

Isolated embryonal rhabdomyosarcoma of the anterior petrous bone in a young child: Focusing on the intra-operative diagnosis and differentials.

Clinical neuropathology
2024

Embryonal rhabdomyosarcoma of the testis in a young male.

Asian journal of surgery
2024

Massive primary pulmonary artery rhabomyosarcoma: A case report.

Romanian journal of internal medicine = Revue roumaine de medecine interne
2023

Primary paratesticular embryonal rhabdomyosarcoma - An unusual presentation.

Journal of family medicine and primary care
2024

The Broad Spectrum of Paediatric Pancreatic Disease: A Single-center 26-years Retrospective Review.

Journal of pediatric surgery
2024

The RRAS2 pathogenic variant (c.67G>T; p. Gly23Cys) produces Noonan syndrome with embryonal rhabdomyosarcoma.

Molecular genetics &amp; genomic medicine
2024

A case of spindle cell rhabdomyosarcoma with a ZFP64::NCOA3 fusion.

Genes, chromosomes &amp; cancer
2023

Staufen1 controls mitochondrial metabolism via HIF2α in embryonal rhabdomyosarcoma and promotes tumorigenesis.

Cellular and molecular life sciences : CMLS
2023

Patient-derived organoids facilitating individual therapy in an adolescent with embryonal rhabdomyosarcoma of the cervix: a case report and literature review.

Frontiers in oncology
2023

Multifocal, biatrial, primary cardiac embryonal rhabdomyosarcoma.

Przeglad menopauzalny = Menopause review
2024

[Diagnosis of uterine sarcomas and rare uterine mesenchymal tumours with malignant potential. Guidelines of the French Sarcoma Group and Rare Gynaecological Tumours].

Bulletin du cancer
2023

Simultaneous Occurrence of Multiple Neoplasms in Children with Cancer Predisposition Syndromes: Collaborating with Abnormal Genes.

Genes
2023

Unique manifestation of primary renal rhabdomyosarcoma in patient with autosomal polycystic kidneys: Case report and review of literature.

Urology case reports
2024

A retrospective study of conjunctival lesions in the Paediatric Eye Clinic over 12 years.

Eye (London, England)
2023

DICER1-mutated rhabdomyosarcoma of the ovary with teratoid features.

Genes, chromosomes &amp; cancer
2023

A case of primary embryonal rhabdomyosarcoma of the right breast in a 17-year-old girl.

Asian journal of surgery
2023

In-utero Diagnosis of Prostatic Embryonal Rhabdomyosarcoma.

Urology
2023

Successful pregnancy in a female with embryonal rhabdomyosarcoma of the cervix who received biopsy and chemotherapy alone without recurrence after 16 years: a case report and literature review.

BMC women's health
2023

A systematic review of the prevalence of pathogenic or likely pathogenic germline variants in individuals with FOXO1 fusion-positive rhabdomyosarcoma.

Pediatric blood &amp; cancer
2023

Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation.

Frontiers in genetics
2023

Epithelioid and spindle cell rhabdomyosarcoma with EWSR1::TFCP2 fusion mimicking metastatic lung cancer: A case report and literature review.

Pathology, research and practice
2023

Complete loss of TP53 and RB1 is associated with complex genome and low immune infiltrate in pleomorphic rhabdomyosarcoma.

HGG advances
2023

Mesenteric embryonal rhabdomyosarcoma in an adolescent: a case report.

Journal of surgical case reports
2023

BRD4 isoforms have distinct roles in tumor progression and metastasis in embryonal rhabdomyosarcoma.

bioRxiv : the preprint server for biology
2023

Magnetic resonance imaging analysis of embryonal rhabdomyosarcoma of the prostate.

Technology and health care : official journal of the European Society for Engineering and Medicine
2023

Changes on chromosome 11p15.5 as specific marker for embryonal rhabdomyosarcoma?

Genes, chromosomes &amp; cancer
2023

Similar additive effects of doxorubicin in combination with photon or proton irradiation in soft tissue sarcoma models.

Frontiers in oncology
2023

Pediatric laryngeal embryonal rhabdomyosarcoma.

Brazilian journal of otorhinolaryngology
2023

PRAME immunohistochemistry in soft tissue tumors and mimics: a study of 350 cases highlighting its imperfect specificity but potentially useful diagnostic applications.

Virchows Archiv : an international journal of pathology
2023

Use of Perirectal Hyaluronic Acid Spacer Prior to Radiotherapy in a Pediatric Patient With Bladder Rhabdomyosarcoma: A Case Report.

Urology
2023

A dysfunctional miR-1-TRPS1-MYOG axis drives ERMS by suppressing terminal myogenic differentiation.

Molecular therapy : the journal of the American Society of Gene Therapy
2023

Detailed molecular and pathological analyses of primary intracranial embryonal rhabdomyosarcoma with a BRAF mutation: illustrative case.

Journal of neurosurgery. Case lessons
2023

Biliary Embryonal Rhabdomyosarcoma: A Case Report.

Mymensingh medical journal : MMJ
2023

Embryonal Rhabdomyosarcoma of the Tongue in Adults.

Life (Basel, Switzerland)
2024

Diagnostic Utility of GATA3 and ISL1 in Differentiating Neuroblastoma From Other Pediatric Malignant Small Round Blue Cell Tumors.

International journal of surgical pathology
2023

Defining function of wild-type and three patient-specific TP53 mutations in a zebrafish model of embryonal rhabdomyosarcoma.

eLife
2023

Facial deformation following treatment for pediatric head and neck rhabdomyosarcoma; the difference between treatment modalities. Results of a trans-Atlantic, multicenter cross-sectional cohort study.

Pediatric blood &amp; cancer
2023

Single-cell transcriptomics reveals immune suppression and cell states predictive of patient outcomes in rhabdomyosarcoma.

Nature communications
2023

Diagnosis and Treatment of Rare Adult Embryonal Rhabdomyosarcoma in Maxillary Sinus.

The Journal of craniofacial surgery
2023

DICER1 syndrome and embryonal rhabdomyosarcoma of the cervix: a case report and literature review.

Frontiers in pediatrics
2023

A report of a rare case of paratesticular spindle cell rhabdomyosarcoma in an adult patient.

Urology case reports
2023

New concept in urologic surgery: The total extended genital sparing radical cystectomy in women.

Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica
2023

Case Report: An NTRK1 fusion-positive embryonal rhabdomyosarcoma: clinical presentations, pathological characteristics and genotypic analyses.

Frontiers in oncology
2023

Uterine embryonal rhabdomyosarcoma in adult women: a case report on the challenging diagnosis and treatment.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
2023

Embryonal rhabdomyosarcoma of the prostate in a young male: A rare case report.

International journal of surgery case reports
2023

Survival and Analysis of Prognostic Factors for Bladder Malignancies in Children and Adolescents: A Population-based Study.

Urology
2023

Complete mimicry: Rhabdomyosarcoma with FUS::TFCP2 fusion masquerading as carcinoma-diagnostic challenge and report of two cases.

Genes, chromosomes &amp; cancer
2023

Alveolar rhabdomyosarcoma has superior response rates to vinorelbine compared to embryonal rhabdomyosarcoma in patients with relapsed/refractory disease: A meta-analysis.

Cancer medicine
2023

Botryoid-type of embryonal rhabdomyosarcoma of the proximal and mid ureter in an adult woman.

Urology case reports
2023

Radiation-induced intracranial rhabdomyosarcoma- A rare complication: Report of a case with literature review.

Medical journal, Armed Forces India
2023

Rhabdomyosarcoma Arising in Inflammatory Rhabdomyoblastic Tumor: A Genetically Distinctive Subtype of Rhabdomyosarcoma.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
2023

Rhabdomyosarcoma with isolated lung metastases: A report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.

Pediatric blood &amp; cancer
2023

Sarcoma Botryoides: Optimal Therapeutic Management and Prognosis of an Unfavorable Malignant Neoplasm of Female Children.

Diagnostics (Basel, Switzerland)
2023

Loss of Nf1 and Ink4a/Arf Are Associated with Sex-Dependent Growth Differences in a Mouse Model of Embryonal Rhabdomyosarcoma.

Current issues in molecular biology
2023

Embryonal rhabdomyosarcoma of the uterine cervix in an adult female.

Autopsy &amp; case reports
2023

Adaptive Proton Therapy for Pediatric Parameningeal Rhabdomyosarcoma: On-Treatment Anatomic Changes and Timing to Replanning.

Clinical oncology (Royal College of Radiologists (Great Britain))
2022

Baseline Characteristics, Prognostic Factors, and Treatment Outcomes for Adult Patients With Rhabdomyosarcoma (RMS).

Cureus
2023

Botryoid embryonal rhabdomyosarcoma of the cervix: A case report.

International journal of surgery case reports
2022

An uncommon perineal embryonal rhabdomyosarcoma in adult: A case report.

Medicine
2022

The botanical drug PBI-05204, a supercritical CO2 extract of Nerium oleander, sensitizes alveolar and embryonal rhabdomyosarcoma to radiotherapy in vitro and in vivo.

Frontiers in pharmacology
2023

National assessment of lymph node status indicators & predictors in pediatric head and neck rhabdomyosarcomas in the US.

International journal of pediatric otorhinolaryngology
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Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Multimodality Imaging Findings of Primary Embryonal Rhabdomyosarcoma in the Prostate: A Rare Case Report.
    Journal of clinical ultrasound : JCU· 2026· PMID 41876358mais citado
  2. Cervical embryonal rhabdomyosarcoma beyond childhood: A case report and literature review.
    Radiology case reports· 2026· PMID 41868466mais citado
  3. Laparoscopic Resection of Vaginal Embryonal Rhabdomyosarcoma in a 16-Month-Old Girl: An Organ-Preserving Surgical Approach.
    Journal of pediatric and adolescent gynecology· 2026· PMID 41866106mais citado
  4. Adult embryonal rhabdomyosarcoma (botryoid subtype) of the ureter: A case report.
    Urology case reports· 2026· PMID 41852850mais citado
  5. A rare presentation of uterine cavity embryonal rhabdomyosarcoma in a preschool girl: a case report.
    International journal of surgery case reports· 2026· PMID 41837097mais citado
  6. myoActivation® for Chronic Pain Care That Changes the Biotensegral Properties of the Human Body: A Motion Laboratory Case Report.
    Cureus· 2026· PMID 41994784recente
  7. Embryonal Rhabdomyosarcoma of the Prostate in a Young Adult.
    Acta Med Indones· 2026· PMID 41978295recente
  8. Rhabdomyosarcoma of the temporal bone in children - a systematic review.
    Int J Pediatr Otorhinolaryngol· 2026· PMID 41946032recente
  9. A Rare Case of Uterine Embryonal Rhabdomyosarcoma in a Postmenopausal Woman.
    Cureus· 2026· PMID 41939651recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:99757(Orphanet)
  2. OMIM OMIM:268210(OMIM)
  3. MONDO:0009993(MONDO)
  4. GARD:4702(GARD (NIH))
  5. Variantes catalogadas(ClinVar)
  6. Busca completa no PubMed(PubMed)
  7. Q5370233(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Rabdomiossarcoma, embrionário
Compêndio · Raras BR

Rabdomiossarcoma, embrionário

ORPHA:99757 · MONDO:0009993
Prevalência
<1 / 1 000 000
Herança
Multigenic/multifactorial
CID-10
C49.9 · Neoplasia maligna do tecido conjuntivo e tecidos moles, não especificados
Ensaios
6 ativos
Prevalência
0.048 (Austria)
MedGen
UMLS
C0206656
Repurposing
2 candidatos
actinomycin-dRNA polymerase inhibitor
dactinomycin
EuropePMC
Wikidata
Papers 10a
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