Dr. Shiel received a Bachelor of Science degree with honors from the University of Notre Dame. There he was involved in research in radiation biology and received the Huisking Scholarship. After graduating from St. Louis University School of Medicine, he completed his Internal Medicine residency and Rheumatology fellowship at the University of California, Irvine. He is board-certified in Internal Medicine and Rheumatology.
Serious rashes are usually caused by allergic reactions, disorders of the immune system, or by poisonous byproducts of an infection. Blisters in these disorders are usually caused when the proteins that connect layers of skin are attacked. Because the proteins holding them together aren't working, the layers of skin come apart, and fluid fills the space between them, thus forming the blister.
PV is a disorder of the immune system (an autoimmune disorder). As in all autoimmune disorders, the body's natural immune system mistakenly identifies proteins within the body as foreign and begins the natural response to get rid of these foreign proteins producing antibodies to attack the foreign intruder.
In PV, the targets of these antibodies are anchoring proteins within the skin.
Certain medications have been linked with the development of PV, including D-penicillamine (Cuprimine, Depen), captopril (Capoten), enalapril (Vasotec), penicillin, interleukin 2, nifedipine (Adalat CC, Procardia, Procardia XL), and rifampicin (Rifadin).
Stevens-Johnson syndrome (SJS)
The exact cause of SJS is unknown, but it is thought to be a severe form of allergic reaction to certain medications or infections.
Antibiotics, typically sulfa-containing and penicillin-containing antibiotics, and medications given for seizures (phenytoin [Dilantin, Dilantin Infatabs, Dilantin Kapseals, Dilantin-125, Phenytek, Phenytoin Sodium, Prompt], phenobarbital [Solfoton], carbamazepine [Carbatrol, Equetro, Tegretol, Tegretol XR], and lamotrigine [Lamictal]) have been linked to SJS, as have the nonsteroidal anti-inflammatory drugs.
Other possible causes of SJS include viral infections with hepatitis, herpes simplex, Epstein-Barr, cytomegalovirus, and influenza viruses; bacterial infections with streptococcal-type and tuberculous bacteria; vaccination, particularly with the smallpox vaccination; and cancers.
HIV-infected individuals have a higher risk of developing skin reactions when compared to the general population. Medications used in the treatment of human immunodeficiency virus infection can have skin reactions
as a side effect, including Stevens-Johnson syndrome. These medications include the protease inhibitors (PI) (atazanivir), the nucleoside reverse transcriptase inhibitors (NRTI) (efavirenz
[Sustiva]), and the nonnucleoside reverse transcriptase inhibitors (NNRTI) (abacavir [Ziagen], nevirapine [Viramune]).
Toxic epidermal necrolysis (TEN)
TEN is thought to be a severe form of SJS.
Causes are similar but include penicillin-type antibiotics, radiation
therapy, collagen vascular disease, and recent bone marrow
transplantation or blood transfusions.
HIV-infected individuals are at higher risk for the development of both SJS and TEN, with a combined incidence of 1/1000 person-years.
TSS is caused by an underlying infection with specific Staphylococcus bacteria.
Certain strains of bacteria produce poisons that are released into the bloodstream and cause disease throughout the body.
TSS became a public health issue in the 1970s with the introduction of super-absorbent tampons. These tampons caused menstruating women to be more easily infected with the staphylococcal infections that led to TSS.
Other infections that may lead to TSS include superficial skin infections, surgical wound infections, infections after delivering a baby, or infected nasal packings after nasal surgery or nosebleeds.