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A 2012 survey showed that among a group of adult women with symptoms of interstitial cystitis, 11% reported suicidal thoughts in the past two weeks. [61] Other research has shown that the impact of IC/BPS on quality of life is severe [13] and may be comparable to the quality of life experienced in end-stage kidney disease or rheumatoid ...
First described in 1960 by Gorlin and Goltz, [5] NBCCS is an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma, a type of skin cancer which rarely spreads to other parts of the body. The prevalence is reported to be 1 case per 56,000–164,000 population.
Eosinophilic cystitis is a rare type of interstitial cystitis first reported in 1960 by Edwin Brown. [1] Eosinophilic cystitis has been linked to a number of etiological factors, including allergies, bladder tumors, trauma to the bladder, parasitic infections, and chemotherapy drugs, though the exact cause of the condition is still unknown.
Interstitial granulomatous dermatitis with arthritis commonly presents with symmetrical round-to-oval red or violet plaques on the flanks, armpits, inner thighs, and lower abdomen. [1] The arthritis that coexists with these skin lesions may develop years, months, or even years before the cutaneous lesions first manifest.
Signs and symptoms are not mutually exclusive, for example a subjective feeling of fever can be noted as sign by using a thermometer that registers a high reading. [7] Because many symptoms of cancer are gradual in onset and general in nature, cancer screening (also called cancer surveillance) is a key public health priority. This may include ...
The signs and symptoms depend on the organ involved. [2] Often, no symptoms or only mild symptoms are seen. [2] When it affects the lungs, wheezing, coughing, shortness of breath, or chest pain may occur. [3] Some may have Löfgren syndrome with fever, enlarged hilar lymph nodes, arthritis, and a rash known as erythema nodosum. [2]
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.
Compared to basal cell carcinoma, cSCC is more likely to spread to distant areas. [11] When confined to the epidermis, the outermost layer of the skin, the pre-invasive or in situ form of cSCC is termed Bowen's disease. [12] [13] The most significant risk factor for cSCC is extensive lifetime exposure to ultraviolet radiation from sunlight. [2]
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