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Synonyms for mesoblastic

relating to or derived from the mesoderm


References in periodicals archive ?
Congenital mesoblastic nephroma (leiomyomatous hamartoma): first adult case.
Calficiation and ossification in a congenital mesoblastic nephroma.
Congenital mesoblastic nephroma: cytogenetic comparison to leiomyoma.
The ETV6-NTRK3 gene fusion has previously been detected in pediatric malignant mesenchymal tumors (congenital fibrosarcoma and congenital cellular mesoblastic nephroma).
Congenital fibrosarcoma is another spindle cell sarcoma associated with a characteristic cytogenetic change, the t(12;15)(p13;q26) translocation, not found in adult fibrosarcomas or other sarcomas (123,124) and identical to that described for congenital mesoblastic nephroma.
Other possible diagnoses for antenatal suprarenal cysts include benign entities, such as adrenal hemorrhage, retropleural pulmonary sequestration, neurogenic cysts, enteric duplication cysts and malignant diseases, including Wilm's tumour and congenital mesoblastic nephroma.
3-11) These tumors have been published under the following names in the literature: leiomyomatous renal hamartomas, congenital mesoblastic nephroma in an adult, cystic hamartoma of renal pelvis, solitary multilocular cysts of the kidney, multilocular renal cyst with mullerian-like stroma, and adult metanephric stromal tumor.
2) Other renal tumors of childhood have been associated with recurring genetic abnormalities: deletion or mutations of WT1 and p53 in some Wilms tumors, t (12;15) creating the ETV6-NTRK3 fusion gene in congenital mesoblastic nephroma, and INI1 deletions or mutations in malignant rhabdoid tumors.
The differential diagnosis for mesoblastic nephroma includes (Figure 1): a.
Pathologic Diagnosis: Mesoblastic Nephroma, Classic Type