rhabdomyosarcoma (Also rhabdomyosarcomas) : Related Words Words similar in meaning to rhabdomyosarcoma
- rhabdosarcoma«
- rhabdomyosarcoma«
- pleomorphic rhabdomyosarcoma«
- embryonal rhabdomyosarcoma«
- alveolar rhabdomyosarcoma«
- embryonal rhabdosarcoma«
- pleomorphic rhabdosarcoma«
- alveolar rhabdosarcoma«
- myosarcoma«
- tumor«
- sarcoma«
- skeletal«
- patient«
- rhabdomyoblast«
- nonrhabdomyosarcoma«
- muscle«
- metastasis«
- cancerous«
- tumor site«
- disease«
- cancer«
- erms«
- survival rate«
- treatment«
- diagnosis«
- translocation«
- radiation therapy«
- subtypes«
- classification system«
- bladder«
- extremity«
- vincristin«
- rms tumor«
- parameningeal tumor«
- alveolar rms«
- child«
- chemotherapy«
- vac regimen«
- embryonal type«
- presence«
- alveolar type«
- resectability«
- tumor cell«
- anaplastic cell«
- subtype«
- irsg«
- fusion«
- childhood«
- myogenin«
- complete resection«
- cambium layer«
- type«
- prognosis«
- symptom«
- tumor size«
- immune system«
- risk category«
- neck«
- presentation«
- nasopharynx«
- surgical resection«
- primary tumor«
- fusion protein«
- congenital abnormality«
- accurate diagnosis«
- ra«
- myosin«
- loh«
- incidence«
- patient outcome«
- mutation«
- potential role«
- radiation«
- immunotherapy«
- site«
- short arm«
- muscle cell«
- immune cell«
- sign«
- heterogeneity«
- cancer cell«
- surgery«
- vagina«
- weak classification schema«
- undiagnosed sarcoma«
- transactivation site«
- therapy combination«
- strong genetic marker«
- stage rms«
- spindle cell erms«
- specific protein staining«
- special radiation treatment«
- rms. classification«
- rhabdomyosarcogenesis«
- recent treatment modality«
- pseudovascular development«
- pleiomorphic rhabdomyosarcoma«
- pax3-fkhr fusion protein«
- pax3-fkhr fusion product«
- pax3-fkhr fusion gene expression«
- pax3-fkhr«
- paratesticular region«
- paratesticular presentation«
- parameningeal presentation«
- parameningeal«
- paired box family«
- other oncogene«
- oncology group protocol«
- notable rhabdomyoblastic differentiation«
- nonmetastatic disease«
- negative arms.«
- multipolar mitotic figure«
- multiple genetic lesion«
- metastatic rms«
- mediastrium«
- malignant skeletal muscle differentiation«
- malignant rms cell«
- lobate hyperchromatic nucleus«
- leiomyomatous growth pattern«
- iva regimen«
- irsg.«
- irsg study«
- irsg i–iv. pleomorphic rhabdomyosarcoma«
- irsg i–iv«
- irs study iii«
- independent national cancer institute«
- icr system«
- hyaline sclerosis«
- histological subset«
- he& stain«
- genitourinary track«
- genetic feature«
- fourth irsg study«
- forkhead/hnf-3 transcription factor family«
- focused dos«
- fkhr. pax3«
- embryonal variant«
- embryonal rms.«
- embryonal rms tumor«
- embryonal rms«
- discernible separation«
- diffuse variation«
- dense tumor layer«
- definitive classiciation«
- confident elimination«
- common solid tumor«
- common histological variant«
- combined therapeutic approach«
- classic cystic arms.«
- characteristic histology«
- characteristic alveolar spacing«
- boytroid«
- botryoid variant«
- botryoid erms«
- blue cell tumour«
- bladder salvage rate«
- asian child relative«
- arthur stout«
- arm subtype«
- anaplastic rms.«
- alveolar spacing«
- alebit«
- aggressive multimodality treatment«
- actinomyocin d.«
- actinomyocin d«
- cell«
- loss«
- epidemiology«
- extent«
- vaginal mass«
- unusual relative«
- spindle cell rhabdomyosarcoma«
- specific genetic lesion«
- pax3 gene«
- p53 loss«
- orbital swelling«
- open biopsy«
- multiple oncogene«
- modern survival rate«
- leonard wexler«
- investigational technique«
- institutional trial«
- genitourinary tumor«
- folpe«
- extremity tumor«
- erms.«
- current staging system«
- common primary site«
- anaplastic rhabdomyosarcoma«
- common type«
- z band«
- specific genetic abnormality«
- specific actin«
- sarcoma learning center«
- rhabdomyosarcoma patient«
- regional lymph node involvement«
- pink cytoplasm«
- muscle cell development«
- multiple classification system«
- minimal remnant«
- local lymph node involvement«
- late toxicity«
- histopathological characteristic«
- familial cancer syndrome«
- chromosome«
- translocation result«
- sufficient tissue«
- poor differentiation«
- intergroup rhabdomyosarcoma study group«
- earlier sign«
- agent chemotherapy«
- preclinical animal study«
- ear discharge«
- definitive indicator«
- cancer site«
- myogenic differentiation«
- firm mass«
- abdominal ct«
- tissue site«
- rich appearance«
- predisposing risk factor«
- diagnostic significance«
- cross striation«
- cranial nerve dysfunction«
- adult«
- relevant tissue«
- li–fraumeni syndrome«
- histopathological analysis«
- cutaneous syndrome«
- tumor grade«
- pax7«
- obvious nature«
- myod1«
- discernible feature«
- rare presentation«
- function«
- therapy«
- stage classification«
- specific consequence«
- ra activation«
- arms.«
- orbital tumor«
- negative margin«
- histopathological finding«
- histological type«
- children/adolescents«
- rhabdomyoma«
- igf-2«
- urinary tract obstruction«
- multidisciplinary practice«
- digital slide«
- quick diagnosis«
- local invasion«
- ewing sarcoma«
- head«
- costello syndrome«
- stronger muscle«
- protein marker«
- neoadjuvant therapy«
- orbit«
- arm«
- space similar«
- round cell«
- cellular morphology«
- surgical mean«
- prognostic indicator«
- other cancer«
- oncology group«
- foreign cell«
- tissue sarcoma«
- icr.«
- current child«
- cell cancer«
- pulmonary alveolus«
- h stain«
- consistent data«
- affected organ«
- rare subtype«
- lymph node involvement«
- accurate classification«
- malignant form«
- diagnostic trait«
- vast majority«
- p53 gene«
- diseased cell«
- proptosis«
- favorable prognosis«
- genitourinary tract«
- lack«
- lower prevalence«
- gene«
- smooth muscle tissue«
- potential therapeutic target«
- aggressive type«
- wiedemann syndrome«
- ifosfamide«
- fibroblast growth factor receptor«
- retroperitoneum«
- significant morbidity«
- myogenesis«
- facio«
- addition«
- positive diagnosis«
- facial pain«
- genetic sequencing«
- desmin«
- prognostic factor«
- poorer prognosis«
- mucosal«
- leiomyosarcoma«
- soft tissue sarcoma«
- tumor antigen«
- bone scan«
- neurofibromatosis type«
- worse prognosis«
- intensive treatment«
- adjuvant therapy«
- cancer stem cell«
- recurrence rate«
- brachytherapy«
- outcome«
- rare cancer«
- age«
- similar disease«
- system«
- aggressive treatment«
- disease management«
- body«
- aneuploidy«
- system due«
- hematuria«
- lumbar puncture«
- final variant«
- malignant cell«
- heterozygosity«
- dosing«
- organ«
- tumor suppressor«
- chemotherapeutic agent«
- myc«
- location«
- people age«
- doxorubicin«
- neuroblastoma«
- adenovirus«
- cisplatin«
- ultrasonography«
- meninges«
- who.«
- cyclophosphamide«
- aggressive nature«
- light microscopy«
- comprises«
- chemotherapy treatment«
- sinusitis«
- other drug«
- radiation treatment«
- common site«
- specific protein«
- st. jude child«
- mass«
- peritoneum«
- treatment plan«
- resection«
- development«
- genetic marker«
- nci«
- potential loss«
- disfigurement«
- dendritic cell«
- research hospital«
- beckwith«
- recent estimate«
- experimental method«
- actin«
- cardio«
- international classification«
- white child«
- approach«
- additional benefit«
- epithelium«
- main method«
- electron microscopy«
- growth factor«
- histology«
- pax«
- management«
- magnetic resonance imaging«
- effective treatment«
- testicle«
- bone marrow«
- german physician«
- clinical practice«
- transcription factor«
- genitals«
- it origin«
- scattering«
- spindle«
- insulin«
- lymphoma«
- association«
- recruiting«
- osteogenic sarcoma«
- osteosarcoma«
- endothelial myeloma«
- malignant neuroma«
- embryoma of the kidney«
- neurosarcoma«
- nephroblastoma«
- liposarcoma«
- chondrosarcoma«
- adenomyosarcoma«
- 9–15 cycle«
- Kaposi's sarcoma«
- Ewing's sarcoma«
- Wilms tumour«
- Ewing's tumour«
- Wilms' tumor«
- Ewing's tumor«
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