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[Coccidioidomycosis in children].

Coccidioides immitis is the cause of coccidioidomycosis, the fungus has been found extensively in the Southwestern United States, and Mexico, and certain areas of Central and South America. Some climatic conditions, such as hot summers with little winter frost, combined with arid, alkaline soils produce ideal circumstances for preservation of the arthroconidia. Children and other human groups are infected by dustbone arthroconidia or by contact with infected soils. There has been limited epidemics of infantile coccidioidomycosis, however, only very few have been verified as to the source of the outbreak by the soil-culture of the fungus. The primary pulmonary infection is usually asymptomatic, but it may resemble influenza with cough, fever, and chest pain. Chronic pulmonary lesions are rare in children. Erythema multiforme an erythema nodosum have been described, namely in females. Arthralgias occurs in some patients. The disseminated form is similar to tuberculosis with lungs, lymph nodes, bones, joints, abdominal organs and skin being the frequently affected sites. Meningitis and limited dissemination to one of few sites is more common in mexican children than adults. Serologic tests are very useful in moderate to severe illnesses. Precipitins can be easily detected by immunodifusion. Higher and persistent complement fixation titers are observed in severe and disseminated infection. Conversion of a skin test with coccidioidin or spherulin from negative to positive strongly suggest coccidioidomycosis. Most cases do not require treatment, but amphotericin B or ketoconazol, are the standard therapy in severe pulmonary disease or disseminated forms, and surgery has been advocated for localized, persistent or drug-resistant, progressive lesions.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗

Two drug-induced dermatological syndromes among employees of a Polish construction site in a tropical country.

The two rare cases of exudative multiform erythema were described in its heavier alterations of Fiessinger-Rendu-Leroy as well as of Stevens-Johnson syndrome, most likely of drug-induced origin, at the employees of a Polish construction site in a tropical country, taking under consideration the causing reasons, diagnostic features as well as conditions of course and principles of treatment.

Acetaminophen↗

[Kawasaki disease: report of 6 cases].

Six cases of children between 20 months and 6 years old, who suffer Kawasaki disease are presented. All of them had diagnostic parameters required by the Investigation Committee of this disease, with similar clinical symptoms as in other countries but with an upper average age (3 years old) to Japanese patients and nearer to that of the North American patients. It is important to emphasize the appearance of exanthema in one case, as well as a multiforme erythema exudative, a rare fact, and the observation, up to now not shown, of a positive rheumatoid factor in another two of the patients. All have undergone a good evolution without cardiovascular complications.

Child↗

Cutaneous erythematous reaction patterns.

Cutaneous erythematous reaction patterns are signs of hypersensitivity to inciting agents, both endogenous and exogenous. They include erythema multiforme, toxic epidermal necrolysis, erythema nodosum and the figurate erythemas. A thorough evaluation is often necessary to identify the provocative agent. When the cause is not discovered, it is imperative that the physician perform repeat examinations, since serious internal disorders may be associated with some of these reactions.

Adult↗

Erythema multiforme-like manifestations and arthritis in a 3-year-old child with leukocytoclastic vasculitis.

A 3-year-old boy with erythema multiforme-like manifestations and severe articular involvement is reported. Because of the unusual onset of the cutaneous lesion a skin biopsy was performed, revealing the typical features of a leukocytoclastic vasculitis. A direct immunofluorescent study revealed C3 and IgM deposition within the wall and around the small vessels. The clinical and immunopathological findings in this patient were similar to those reported for the acute hemorrhagic edema of infancy (AHE) described in children younger than 2 years of age. The present case supports the hypothesis that AHE is a distinctive leukocytoclastic vasculitis of childhood, irrespective of the age at onset.

Arthritis↗

Systemic lupus erythematosus with erythema multiforme-like lesions and histiocytic necrotizing lymphadenitis--a case report.

A 9-year-old Chinese girl with systemic lupus erythematosus presented initially with persistent cervical lymphadenopathy without any constitutional symptoms. The histology of the involved lymph node showed histiocytic necrotizing lymphadenitis and the initial clinical diagnosis of Kikuchi-Fujimoto disease was made. The patient subsequently developed fever, oral ulcerations, epistaxis, generalised myalgia and erythema multiforme-like skin lesions over the face and upper arms. Investigations showed anaemia, leucopenia, hypocomplementemia, a positive antinuclear antibody and a positive anti-double-stranded DNA antibody test. The clinical diagnosis was revised to systemic lupus erythematosus. The histological picture of histiocytic necrotizing lymphadenitis can occur in systemic lupus erythematosus and may be indistinguishable from that seen in Kikuchi-Fujimoto disease. The diagnosis of Kikuchi-Fujimoto disease should be confined to a benign clinical subset of histiocytic necrotizing lymphadenitis which resolves spontaneously without treatment. The occurrence of erythema multiforme-like lesions in lupus erythematosus is unusual and together with the characteristic serologic abnormalities, fits Rowell's syndrome.

Child↗

Epidemiology of erythema exsudativum multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis in Germany (1990-1992): structure and results of a population-based registry.

The severe skin reactions erythema exsudativum multiforme majus (EEM with mucosal involvement, EEMM), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN) are difficult to study as they are very rare diseases with an incidence of about two cases per 1 million inhabitants per year. We report on the structure of a registry with the aim of ascertaining all hospitalized cases of EEMM, SJS, and TEN in western Germany and Berlin. The registry is structured as an intensive reporting system, regularly contacting more than 1500 departments including 100% of the burn units (n = 34), departments of pediatrics (n = 241), departments of dermatology (n = 106), and 100% of all internal medicine departments in hospitals with intensive care facilities or with more than 200 beds (n = 1161). With a coverage rate up to 95% based on the number of responding departments between April 1, 1990 and December 31, 1992, from a total of 767 reported cases 353 patients with EEMM, SJS, and TEN were finally included in the registry. Most of these patients were directly reported to the registry; only 2.54% (9 of 353) were primarily registered by the German spontaneous reporting systems. Assuming an average population of 64.5 million for western Germany and Berlin an incidence up to 1.89 per 1 million inhabitants per year could be calculated for SJS and TEN.

Epidemiologic Methods↗