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There is very rare expression of NTRK fusion but in various adult and pediatric solid tumors, including infantile fibrosarcoma, glioma, glioblastoma, diffuse intrinsic pontine glioma (DIPG), congenital mesoblastic nephroma, melanoma, inflammatory myofibroblastic tumor (IMT), uterus sarcoma, soft tissue tumor, gastrointestinal stromal tumor (GIST), secretory carcinoma of breast, secretory carcinoma of salivary gland, cancer of unknown primary, lung cancer, colorectal cancer, appendiceal cancer, breast cancer, gastric cancer, ovarian cancer, thyroid cancer, cholangiocarcinoma, pancreatic cancer, head and neck cancer, and various sarcomas.
Cystic nephroma is a mixed mesenchymal and epithelial neoplasm of the kidney which has a benign nature and tends to grow slowly (1).
Two cases each of urothelial carcinoma of the renal pelvis, squamous cell carcinoma and one case of mesoblastic nephroma were the other tumours recorded in the study.
A new species of Nephroma (Nephromataceae) from the Tibetan Plateau.
Tumor types included 10 distinct soft tissue sarcomas, salivary gland, infantile fibrosarcoma, thyroid, lung, melanoma, colon, gastrointestinal stromal tumor, breast, bone sarcoma, cholangiocarcinoma, carcinoma of unknown primary, congenital mesoblastic nephroma, appendiceal, and pancreas cancers.
Detection of the ETV6-NTRK3 chimeric RNA of infantile fibrosarcoma/cellular congenital mesoblastic nephroma in paraffin-embedded tissue: application to challenging pediatric renal stromal tumors.
Different types of pediatric renal tumors are known, the commonest of which is Wilms tumor or nephroblastoma, other less common tumors are nephroblastomatosis, rhabdoid malignant tumor, clear cell sarcoma, congenital mesoblastic nephroma and multilocular cystic nephroma3.
Previously, the ETV6-NTRK3 translocation has been described in infantile fibrosarcoma (11), congenital mesoblastic nephroma, and acute myelogenous leukaemia (2, 7, 8).
Four benign renal tumours were found, made up of oncocytoma (n=2), cystic nephroma (n=1) and angiomyolipoma (n=1).
amplissima, Nephroma laevigatum and Pannaria conoplea provide information on agglomeration forest age, Lobaria pulmonaria is also an indicator of the purity of the environment.
While differential diagnosis included a blastemal predominant Wilms Tumor and congenital mesoblastic nephroma, the tumor was determined to be most consistent with a rare ossifying renal tumor of infancy.
DICER1 syndrome is a familial tumour susceptibility syndrome associated with pleuropulmonary blastoma; ovarian sex cord-stromal tumours; cystic nephroma; thyroid gland neoplasia; and other rare benign and malignant tumours.
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- Nephritic stone
- nephrogenic diabetes insipidus
- Nephrolepis exaltata
- Nephrolepis exaltata bostoniensis
- Nephrolepis pectinata
- Nephrops norvegicus
- nephrotic syndrome
- Nephthytis afzelii
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- nephronophthisis type 11
- nephronophthisis type 9
- nephronophthisis-like nephropathy type 1