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Mastoiditis is the result of an infection that extends to the air cells of the skull behind the ear. Specifically, it is an inflammation of the mucosal lining of the mastoid antrum and mastoid air cell system inside [ 1 ] the mastoid process .
Human infectious diseases may be characterized by their case fatality rate (CFR), the proportion of people diagnosed with a disease who die from it (cf. mortality rate).It should not be confused with the infection fatality rate (IFR), the estimated proportion of people infected by a disease-causing agent, including asymptomatic and undiagnosed infections, who die from the disease.
The mastoid cells (also called air cells of Lenoir or mastoid cells of Lenoir) are air-filled cavities within the mastoid process of the temporal bone of the cranium. The mastoid cells are a form of skeletal pneumaticity. Infection in these cells is called mastoiditis. The term cells here refers to enclosed spaces, not cells as living ...
Cholesteatoma is a destructive and expanding growth consisting of keratinizing squamous epithelium in the middle ear and/or mastoid process. [1] [2] Cholesteatomas are not cancerous as the name may suggest, but can cause significant problems because of their erosive and expansile properties.
Mastoiditis* Children History of URI >10 days Recent history of URI or ear infection Fevers/chills May see signs of otitis media on exam Pain is located behind the ear with postauricular (i.e. near mastoid process) swelling* Diagnose with CT Chronic suppurative otitis media: Conductive hearing loss Relapsing/remitting or chronic discharge
Gradenigo's syndrome, also called Gradenigo-Lannois syndrome, [1] [2] is a complication of otitis media and mastoiditis involving the apex of the petrous temporal bone. It was first described by Giuseppe Gradenigo in 1904. [3]
As more young people are diagnosed with breast cancer, they worry about returning stage 4, metastatic breast cancer. Experts share emerging research, what's known.
Mastoiditis; Mastroiacovo–De Rosa–Satta syndrome; Mastroiacovo–Gambi–Segni syndrome; MAT deficiency; Maternal hyperphenylalaninemia; Maternally inherited diabetes and deafness; Mathieu–De Broca–Bony syndrome; Matsoukas–Liarikos–Giannika syndrome; Matthew–Wood syndrome; Maturity onset diabetes of the young; Maumenee syndrome ...