WilmsGerm cell tNeuroblastomaDifferential diagnosisMedulloblastomaCommonPrimaryFemaleOriginPatientsDesmoplastic SmallNeoplasmTumoursPeripheralMalignantSarcomaEmbryonalImmunohistochemicalBoneClinicalAlveolarAbundantDiagnosticLiterature ReviewChildrenCentral nervouApproximatelyGenerallyStudyCasesAnalysis
Wilms3
- The differential diagnosis of a malignant effusion is accordingly broad, especially for the small round blue cell tumors that includes not only mesenchymal tumors, but also non-mesenchymal tumors, such as neuroblastoma and Wilms tumor. (cytojournal.com)
- Other rare non-epithelial malignancies that may be encountered in effusion cytology include neuroblastoma, Wilms tumor, and metastatic brain tumors. (cytojournal.com)
- Studies in experimental incidence and multiplicity of tumours to Wilms tumour in humans - in the animals increase and the latency period de adult rat after perinatal exposure to a creases with increasing dose. (who.int)
Germ cell t6
- While most tumors metastatic to the serous membranes are of epithelial origin, cytologists should be aware that non-epithelial neoplasms can also cause malignant effusions including sarcomas, melanomas, germ cell tumors, and, more rarely, brain tumors. (cytojournal.com)
- Common non-epithelial neoplasms that may cause malignant effusions include malignant melanoma, sarcomas, and other neoplasms including germ cell tumors [ Figure 1 ]. (cytojournal.com)
- In clinical practice, she concentrates on germ cell tumors, while her epidemiologic research primarily focuses on colorectal cancer screening and prevention. (dana-farber.org)
- and (3) treatment of germ cell tumors in pediatric patients. (dana-farber.org)
- In clinical care, Dr. Frazier is the national expert on germ cell tumors in pediatric patients and oversees the care of these patients referred to DFCI. (dana-farber.org)
- In addition, she is cochair of two national protocols that opened in 1999 for the treatment of low-risk and high-risk pediatric germ cell tumors and chair of the COG Germ Cell subcommittee in COG Rare Tumors. (dana-farber.org)
Neuroblastoma1
- The histologic appearance of MNTI is usually that of a small, dark, cell neoplasm suggestive of neuroblastoma, rhabdomyosarcoma, Ewing sarcoma, lymphoma, desmoplastic small round cell tumor, and peripheral primitive neuroectodermal tumor. (medscape.com)
Differential diagnosis1
- Consider clinical, radiographic, laboratory, and histologic findings when establishing a proper differential diagnosis for melanotic neuroectodermal tumor of infancy (MNTI). (medscape.com)
Medulloblastoma1
- 1 - 3 Intracranial brain tumors, most commonly medulloblastoma [ Figure 2 ], can metastasize to the peritoneal cavity via ventriculo-peritoneal shunts used to divert excess cerebrospinal fluid. (cytojournal.com)
Common1
- The same age differential is noted with respect to the more common odontogenic tumors (eg, ameloblastoma, odontoma, adenomatoid odontogenic tumor, calcifying epithelial odontogenic tumor, ameloblastic fibroma, odontogenic myxoma, odontogenic fibroma). (medscape.com)
Primary1
- A new technique has been presented that results in an acceleration of delayed primary healing with full thickness skin and subcutaneous tissue coverage. (who.int)
Female1
- ENU during the final week of gestat the rapidly changing patterns of gene In both the fetus and the pregnant ion is approximately 50 times that of expression in fetal target tissues, female rat, the target organ for single the mother. (who.int)
Origin2
- Melanotic neuroectodermal tumor of infancy--a neoplasm of neural crese origin. (medscape.com)
- Most tumors metastatic to the serous membranes are of epithelial origin. (cytojournal.com)
Patients1
- Evaluation of prevalence and outcomes of serial tyrosine kinase inhibitor use in pediatric patients with advanced solid tumors. (dana-farber.org)
Desmoplastic Small2
- 2. Desmoplastic Small Round Cell Tumor of the Submandibular Gland: A Case Report and Literature Review. (nih.gov)
- The histologic appearance of MNTI is usually that of a small, round blue cell neoplasm suggestive of neuroblastoma, rhabdomyosarcoma, Ewing sarcoma, lymphoma, desmoplastic small round cell tumor, and peripheral primitive neuroectodermal tumor. (medscape.com)
Neoplasm2
- 18. Malignant peripheral neuroectodermal tumours of bone other than Askin's neoplasm: characterization of 14 new cases with immunohistochemistry and electron microscopy. (nih.gov)
- Melanotic neuroectodermal tumor of infancy--a neoplasm of neural crese origin. (medscape.com)
Tumours1
- 19. Malignant peripheral neuroectodermal tumours of childhood and adolescence. (nih.gov)
Peripheral1
- 11. [A case of peripheral-type primitive neuroectodermal tumor arising in the dura mater at the frontal base]. (nih.gov)
Malignant2
- 16. Malignant rhabdoid tumor. (nih.gov)
- Malignant C8495 Hereditary Retinoblastoma Familial Retinoblastoma An inherited malignant tumor that originates in the nuclear layer of the retina. (nih.gov)
Sarcoma2
Embryonal2
- This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development. (nih.gov)
- The lack of PAX3-FOXO1 fusions in most of these tumors suggests that are biologically and clinically related to embryonal rhabdomyosarcoma. (nih.gov)
Immunohistochemical1
- 12. Aberrant immunohistochemical expression in nonrhabdomyosarcoma soft tissue sarcomas of infancy: retrospective review of clinical material. (nih.gov)
Bone1
- However, this entity can be differentiated from the MNTI by its strong female predilection and involvement exclusively of the gingival soft tissues without destruction of the underlying maxillary bone. (medscape.com)
Clinical1
- Consider clinical, radiographic, laboratory, and histologic findings when establishing a proper differential diagnosis for melanotic neuroectodermal tumor of infancy (MNTI). (medscape.com)
Alveolar3
- 20. [Alveolar soft part sarcomas . (nih.gov)
- The radiographic appearance of a maxillary alveolar low-density radiolucency is consistent with any of the odontogenic cysts or tumors. (medscape.com)
- These tumors were previously considered variants of alveolar rhabdomyosarcoma. (nih.gov)
Abundant1
- It is characterized by the presence of invasive and anaplastic trophoblastic tissue composed of intermediate trophoblastic cells, cytotrophoblasts and syncytiotrophoblasts, abundant vascularity, and secretion of human chorionic gonadotropin. (nih.gov)
Diagnostic1
- The cytokeratin 17 expression in primary ovarian tumors has diagnostic but not prognostic significance. (patologia.ro)
Literature Review1
- Cutler LS, Chaudhry AP, Topazian R. Melanotic neuroectodermal tumor of infancy: an ultrastructural study, literature review, and reevaluation. (medscape.com)
Children1
- Approximately 5% of all children with NBCCS develop medulloblastoma (primitive neuroectodermal tumor), generally the desmoplastic subtype. (nih.gov)
Central nervou1
- Five cancer types account for the majority of LFS tumors: adrenocortical carcinomas, breast cancer, central nervous system tumors, osteosarcomas, and soft-tissue sarcomas. (nih.gov)
Approximately1
- ENU during the final week of gestat the rapidly changing patterns of gene In both the fetus and the pregnant ion is approximately 50 times that of expression in fetal target tissues, female rat, the target organ for single the mother. (who.int)
Generally1
- Tumour the fetus via the maternal circulation utero, but when the reactive metab multiplicity rises to a maximum in must have crossed the placenta, and olites formed in maternal tissues are offspring exposed at approximate consequently are generally referred too unstable to circulate in the mater ly 21 days of gestation, a few days to as transplacental carcinogens. (who.int)
Study1
- Horizontal tumor extent (HZTE) has limited prognostic significance in 2018 FIGO stage I endocervical adenocarcinoma (ECA): a retrospective study of 416 cases. (patologia.ro)
Cases1
- Clear Cell Carcinoma (CCC) of the Cervix Is a Human Papillomavirus (HPV)-independent Tumor Associated With Poor Outcome: A Comprehensive Analysis of 58 Cases. (patologia.ro)
Analysis1
- 9. [Clinicopathology analysis of mesenchymal chondrosarcoma in soft tissue]. (nih.gov)