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Cancer is a group of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body. [ 3 ] [ 4 ] Cancer can be difficult to diagnose because its signs and symptoms are often nonspecific, meaning they may be general phenomena that do not point directly to a specific disease process.
Neuroendocrine adenoma middle ear. Neuroendocrine adenoma middle ear ( NAME) is a tumor which arises from a specific anatomic site, the middle ear. [1] NAME is a benign glandular neoplasm of middle ear showing histologic and immunohistochemical neuroendocrine and mucin-secreting differentiation (biphasic or dual differentiation). [2] [3]
The following is a list of cancer types. Cancer is a group of diseases that involve abnormal increases in the number of cells , with the potential to invade or spread to other parts of the body. [ 1 ]
Tympanosclerosis. Tympanoesclerosis. Other names. Myringosclerosis, intratympanic tympanosclerosis. Specialty. ENT surgery. Tympanosclerosis is a condition caused by hyalinization and subsequent calcification of subepithelial connective tissue of the tympanic membrane and middle ear, sometimes resulting in a detrimental effect to hearing.
Cancer is caused by genetic changes leading to uncontrolled cell growth and tumor formation. The basic cause of sporadic (non-familial) cancers is DNA damage and genomic instability. [ 1][ 2] A minority of cancers are due to inherited genetic mutations. [ 3] Most cancers are related to environmental, lifestyle, or behavioral exposures. [ 4]
Medical genetics. Birt–Hogg–Dubé syndrome ( BHD ), also Hornstein–Birt–Hogg–Dubé syndrome, Hornstein–Knickenberg syndrome, and fibrofolliculomas with trichodiscomas and acrochordons[ 1] is a human, adult onset, autosomal dominant genetic disorder caused by a mutation in the folliculin ( FLCN) gene. It can cause susceptibility to ...
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Atypical teratoid rhabdoid tumor. An atypical teratoid rhabdoid tumor ( AT/RT) is a rare tumor usually diagnosed in childhood. Although usually a brain tumor, AT/RT can occur anywhere in the central nervous system (CNS), including the spinal cord. About 60% will be in the posterior cranial fossa (particularly the cerebellum ).