Retinoblastoma

A rare eye tumor disease representing the most common intraocular malignancy in children. It is a life threatening neoplasia but is potentially curable and it can be hereditary or non hereditary, unilateral or bilateral.

Carcinoid tumor

A tumor formed from the endocrine (argentaffin) cells of the mucosal lining of a variety of organs including the stomach and intestine. These cells are from neuroectodermal origin.


Total: 3

                       


(per page)
PMID (PMCID)
8222834
 MALE
An atypical carcinoid tumor of the lung with mutations in the p53 gene and the retinoblastoma gene.
Hiyama K, Hasegawa K, Ishioka S, Takahashi N, Yamakido M.
Chest. 1993;104(5):1606-7.
An atypical carcinoid tumor of the lung with mutations in the p53 gene and the retinoblastoma gene.
8222834
 MALE
An atypical carcinoid tumor of the lung with mutations in the p53 gene and the retinoblastoma gene.
Hiyama K, Hasegawa K, Ishioka S, Takahashi N, Yamakido M.
Chest. 1993;104(5):1606-7.
Molecular analysis of a metastatic lesion of an atypical carcinoid tumor of the lung obtained from a 77-year-old man at autopsy revealed a point mutation in the p53 gene and a deletion in the retinoblastoma (Rb) mRNA.
6204734
 MALE Infant
Metastatic carcinoma involving the testis. Clinical and pathologic distinction from primary testicular neoplasms.
Haupt HM, Mann RB, Trump DL, Abeloff MD.
Cancer. 1984;54(4):709-14.
Neuroblastoma, retinoblastoma, carcinoid tumor, and cancers of the bile duct, ureter, bladder, salivary gland, and thyroid have also involved the testis secondarily.