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pseudoallergy 601 psoriasis vulgaris<br />

P selection (NMR).<br />

pseudoallergy<br />

An anaphylaxis-like reaction that occurs suddenly, frequently<br />

following food ingestion, and represents an anaphylactoid<br />

reaction. It may be induced by a psychogenic factor, a metabolic<br />

defect, or other nonimmunological cause. This is not an<br />

immune reaction and is classified as an anaphylactoid reaction.<br />

pseudogene<br />

A sequence of DNA that is similar to a sequence of a true<br />

gene but does not encode a protein due to defects that<br />

inhibit gene expression. Pseudogenes represent nonusable or<br />

junk DNA. They may result from duplicated genes and have<br />

several defects as mutations accumulate.<br />

pseudolymphoma<br />

Hyperplasia of lymphoid tissue involving a uniform accumulation<br />

of lymphocytes. Unlike lymphomas, the cells are polyclonal.<br />

The architecture of the lymph nodes is well preserved,<br />

with distinct cortical germinal centers showing little or minimal<br />

capsular infiltration by lymphocytes. Inflammatory cells<br />

are detectable between germinal centers, but mitoses occur<br />

only within the centers. The reticular framework remains<br />

intact. The lymphoid hyperplasia that characterizes pseudolymphoma<br />

may be found in various locations such as gastrointestinal<br />

tract, lung, breast, salivary gland, mediastinum, skin,<br />

Stratum<br />

corneum<br />

Basement<br />

membrane Dermal<br />

vessels<br />

Chondro-fibrous<br />

junction<br />

Marginal cartilage<br />

Fluorescent<br />

deposits<br />

Psoriasis vulgaris.<br />

soft tissue, and other areas. Pseudolymphomas may occur in<br />

individuals who later develop lymphomas.<br />

pseudolymphomatous lymphadenitis<br />

Hyperplasia of lymphoid organs that is similar to lymphoma<br />

except that the hyperplasia is reversible.<br />

Pseudomonas aeruginosa immunity<br />

Pseudomonas aeruginosa infection is followed by the<br />

development of antibodies that facilitate opsonophagocytosis<br />

and protection against subsequent infections. An<br />

adequate antibody response is required for protection.<br />

Antibody alone may be insufficient because the lungs of<br />

patients with cystic fibrosis continue to be chronically<br />

colonized even in the presence of potent serum antibody<br />

responses to several antigens of this microorganism.<br />

Active vaccination is made less desirable by the fact that<br />

P. aeruginosa infections cannot be reliably predicted;<br />

thus, passively administered hyperimmune intravenous<br />

immunoglobulin from immunized volunteers has been<br />

used to confer protection. Nevertheless, contemporary<br />

investigations show that antibodies against lipopolysaccharide<br />

(LPS) serotypes and to exotoxin A do not significantly<br />

protect recipients.<br />

pseudoparaproteinemia<br />

An elevation of transferrin to levels at least twice normal<br />

(200 to 400 mg/dL). Profound iron deficiency anemia leads<br />

to this increase. The one molecular form of transferrin in<br />

the serum is concentrated into a single band that travels in<br />

the β region in serum electrophoresis, giving the appearance<br />

of a paraproteinemia. However, a real paraproteinemia<br />

is characterized by a spike on serum electrophoresis representing<br />

a monoclonal gammopathy.<br />

pseudopodia<br />

Membrane extensions from motile and phagocytic cells.<br />

psoriasis vulgaris<br />

A chronic, recurrent, papulosquamous autoimmune disease<br />

attributed to improper functioning of keratinocytes. Marked<br />

P

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