Pathology - Von Hippel-Lindau disease
This is an autosomal dominant condition that causes the deletion of the von Hippel-Lindau (VHL) gene, which is a tumor suppressor gene located on chromosome 3p. Study of diseases and their effects on the body. Hemangioblastomas, which are vascular tumors accompanied by massive cysts, or cavernous hemangiomas, can occur in the cerebellum, brain stem, and retina. Liver, kidney, and pancreas adenomas and cysts. Symptoms and signs Manifests first with symptoms such as migraines, ataxia, or loss of eyesight. Linked to a higher occurrence of renal cell carcinoma, pheochromocytoma, and hemangioblastomas in the eyes and central nervous system. Administration Tumor excision and radiotherapy. A capillary hemangioma is a noncancerous abnormality characterized by a group of blood-filled channels that resemble capillaries. It is the predominant neoplasm in infancy and is accountable for the development of port wine stain birthmarks. Cavernous hemangioma is characterized by a substantial vascular cavity that is filled with blood. Furthermore, these abnormalities typically exhibit a benign nature.
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