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.

Hypertension

The presence of chronic increased pressure in the systemic arterial system.


Total: 1

                      


(per page)
PMID (PMCID)
15136974
MALE Middle Aged
A rare combination consisting of aldosterone-producing adenoma and adrenal myelolipoma in a patient with heterozygosity for retinoblastoma (RB) gene.
Caliumi C, De Toma G, Bossini A, Cianci R, Bosman C, Genuardi M, Cerci S, Letizia C.
J Renin Angiotensin Aldosterone Syst. 2004;5(1):45-8.
In this report, a case of adrenal myelolipoma (a rare non-functioning tumour composed of mature adipose tissue and normal haematopoietic elements similar to bone marrow cells), aldosterone-producing adenoma and a pituitary microadenoma coexisting in a 62-year-old man with a 15-year history of arterial hypertension, previous ablation of an autonomously-functioning thyroid adenoma, multiple lipomas and an heterozygosity of the retinoblastoma (RB) susceptibility gene is reported.