| ABK | aphakic bullous keratopathy |
|---|---|
| BIE | bullous ichthyosiform erythroderma |
| BP | Bachelor of Pharmacy; back pressure; barometric pressure; basic protein; bathroom privileges; bed pa... |
| BPAG | bullous pemphigoid antigen |
| CBDC | chronic bullous disease of children |
| bullous oedema | A reddened, swollen appearance of the ureteral orifice in the bladder wall, frequently observed with distal ureteral calculi or in tuberculosis of the ureter. (05 Mar 2000) |
|---|---|
| bullous oedema vesicae | A prominent area of focal oedema involving the bladder mucosa, consisting of elevated masses of edematous tissue or clusters of clear fluid-filled vesicles; often associated with chronic inflammation or irritation secondary to tubes, foreign bodies, or perivesical inflammation. (05 Mar 2000) |
| bullous pemphigoid | <dermatology> Form of pemphigoid (which also affects mucous membranes), in which blisters (bulli) form on the skin. Patients have circulating antibody (usually IgG) to basement membrane of stratified epithelium although the antibody titre does not correlate with the severity of the disease. (18 Nov 1997) |
| bullous pemphiguoid | A disease characterised by tense blistering eruptions of the skin. Caused by antibodies abnormally accumulating in a layer of the skin called the basement membrane. Can be chronic and mild without affecting the general health. It is diagnosed by skin biopsy showing the abnormal antibodies deposited in the skin layer. Treatment is with topical cortisone creams, but sometimes requires high doses of cortisone ( steroids ) taken internally. (12 Dec 1998) |
| bullous syphilid | A rare manifestation of congenital syphilis. Synonym: pemphigoid syphilid. (05 Mar 2000) |
| pemphigoid, bullous | A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. (12 Dec 1998) |
| chronic bullous dermatosis of childhood | A rare self-limiting bullous disease, chiefly of the trunk, perioral, and pelvic areas, with onset in the first decade, successively less severe recurrences, and total remission at adolescence; linear epidermal basement membrane zone deposit of IgA is found in involved and in normal skin. Synonym: linear IgA bullous disease in children. (05 Mar 2000) |
| dermolytic bullous dermatosis | Form of epidermolysis bullosa characterised by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. (12 Dec 1998) |
| linear IgA bullous disease in children | A rare self-limiting bullous disease, chiefly of the trunk, perioral, and pelvic areas, with onset in the first decade, successively less severe recurrences, and total remission at adolescence; linear epidermal basement membrane zone deposit of IgA is found in involved and in normal skin. Synonym: linear IgA bullous disease in children. (05 Mar 2000) |
| acrodynic erythema | Pain in the extremities. (12 Dec 1998) |
| macular erythema | <paediatrics> Also called baby measles. This is a nonserious but common childhood viral infection that starts with a high fever and swollen lymph glands. After 24 hours, the fever breaks and the child develops a red rash on the neck and trunk. (27 Sep 1997) |
| Milian's erythema | An obsolete term for a nontoxic eruption that simulates measles or a toxic erythema, occurring usually on the ninth day of a course of medication; first described as a reaction to arsenical treatment of syphilis. Synonym: Milian's disease, Milian's erythema. (05 Mar 2000) |
| cold erythema | Rash characterised by redness and itching, brought on by exposure to cold. (05 Mar 2000) |
| wheal-and-erythema reaction | The characteristic immediate reaction observed in the skin test; within 10 to 15 minutes after injection of antigen (allergen), an irregular, blanched, elevated wheal appears, surrounded by an area of erythema (flare). Synonym: wheal-and-flare reaction. (05 Mar 2000) |
| haemorrhagic exudative erythema | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
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