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1. |
BOTRYOMYCOSIS |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 381-388
ALEXANDRO BONIFAZ,
EUGENIO CARRASCO,
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ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03015.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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2. |
ERYTHEMA NODOSUM LEPROSUM |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 389-392
MITCHELL S. MEYERSON,
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ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03016.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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3. |
INFECTION WITHPENICILLIUM MARNEFFEI |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 393-399
PAUL D. WORTMAN,
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ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03017.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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4. |
ADULT T‐CELL LEUKEMIA/LYMPHOMA CUTANEOUS TYPE |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 400-401
TETSUO NAGATANI,
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ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03018.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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5. |
POROKERATOSIS OF MIBELLI AND HIV‐INFECTION |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 402-404
EDUARDO A. RODRÍGUEZ,
SILVIA JAKUBOWICZ,
DANTE A. CHINCHILLA,
ALBERTO CARRIL,
PABLO A. VIGLIOGLIA,
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摘要:
AbstractBackground.The exacerbation of porokeratosis of Mibelli associated with inmunosuppression has been well documented.Materials and Methods.We describe the clinical and histologic data of three cases of HIV‐infected patients, who developed porokeratosis following HIV‐contact.Results.The three reported patients were found to have the clinical and histologic features of porokeratosis of Mibelli. Either the exacerbation or development of the disease followed HIV infection.Conclusion.Although porokeratosis is not a disease indicative of AIDS, its flare‐up or its presence in HIV‐infected patients may serve as a marker of inmunodef
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03019.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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6. |
SKIN DISEASES AMONG ADOLESCENT BOYS IN ABHA, SAUDI ARABIA |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 405-407
KHALED BAHAMDAN,
AHMED A.R. MAHFOUZ,
TALAL TALLAB,
IBRAHIM A. BADAWI,
OMAR M. AL‐AMARI,
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摘要:
AbstractBackground.Adolescence is characterized by a sensitivity to issues of attractiveness. With dermatologic conditions, this may adversely affect early detection and compliance.Methods.A cross‐sectional study was carried out on a multistage stratified random sample of 647 adolescent schoolboys in Abha, Saudi Arabia, to determine the prevalence of skin diseases. The age of the boys ranged from 11 to 19 years with an average of 15.3 ± 1.9 years.Results.It was found that 19.8% of the children were affected by one form or another of transmissible skin diseases (TSD). The most common types were: pediculosis capitis (9.6%), verruca vulgaris (3.9%), and tinea pedis (1.9%). The prevalence of TSD increased significantly as the age decreased and as the crowding index increased. As for nontransmissible skin diseases, acne vulgaris was the most prevalent disease (56.3%). The prevalence and severity of acne increased significantly as the age increased.Conclusions.The findings indicate the need to develop regional intervention programs at the school level. Appropriate continuing medical education programs for school health workers in the region are mandatory to achieve this go
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03020.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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7. |
CUTANEOUS MANIFESTATIONS OF SYSTEMIC LUPUS ERYTHEMATOSUS: STUDY FROM LAHORE, PAKISTAN |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 408-409
NASEEMA KAPADIA,
TAHIR SAEED HAROON,
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摘要:
AbstractBackground.Systemic lupus erythematosus (SLE) is an autoimmune disorder in which cutaneous lesions occur in 85% of patients. This study from Lahore, Pakistan, was conducted to determine the pattern and incidence of such lesions in SLE.Methods.Forty patients with SLE fulfilling the clinical and laboratory criteria of the American Rheumatism Association (ARA) (1982) were examined between October 1992 and September 1993 for the presence of cutaneous manifestations.Results.Skin changes noted were: noncicatricial diffuse alopecia (82.5%), malar rash (60%), mucosal lesions (60%), discoid eruption (57.5%), photosensitivity (60%), nail involvement (55%), vascular lesions (50%), pruritus (45%), and pigmentary changes (37.5%). Peripheral gangrene, chronic ulcers, Raynaud's phenomenon, urticaria, chilblains, thrombophlebitis, palmar erythema, and erythema multiforme were rare. Antinuclear antibody reaction was positive in 80% and anti‐dsDNA antibodies in 70%.Conclusion.A different clinical pattern was noted in our patients than reported previousl
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03021.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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8. |
RECURRENT NONMELANOMA SKIN CANCER IN SOUTHERN AUSTRALIA |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 410-412
D. CZARNECKI,
M. STAPLES,
A. MAR,
G. GILES,
C. MEEHAN,
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摘要:
AbstractBackground and Objective.In retrospective studies of nonmelanoma skin cancers, the recurrence rates were relatively high. This study had as its aim to determine the recurrence rate of nonmelanoma skin cancer (NMSC) and prospectively, risk factors for recurrence in southern Australia.Study Design.This is a prospective study of outpatients with histologically confirmed NMSC. All patients seen by a dermatologist between November 1988 and November 1989 were entered into the study and followed for at least 3 years. Any recurrent NMSCS were removed and recorded.Results.Four hundred and eighty‐one patients were entered and 420 followed for at least 3 years. A recurrent NMSC developed in 8% (adjusted for losses). A multivariate analysis determined that the main risk factor for recurrence within the first 3 years of follow‐up was the number of NMSC a patient had when entering into the study. Those with 3 to nine NMSC were five times more likely to develop a recurrence than those with less than three NMSC. Those with 10 or more NMSC were 25 times more likely to develop a recurrence. Age, sex, and types of skin cancers removed were not risk factors within the first 3 years of follow‐up.Conclusions.Patients who have had multiple skin cancers require careful follow‐up because of the risk of developing recu
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03022.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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9. |
TREATMENT OF ACTINIC PRURIGO IN CHIMILA INDIANS |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 413-416
MARIA M. DURÁN,
CLARA P. ORDOÑEZ,
JUAN C. PRIETO,
JAIME BERNAL,
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摘要:
AbstractBackground.Actinic prurigo has a high prevalence in women of child‐bearing age. Its treatment has been, among others, with thalidomide. To avoid the deleterious effects of this drug on the embryo, therapeutic alternatives have been sought. Among these, tetracycline and vitamin E have been investigated as to their influence on the symptoms of actinic prurigo. Both these drugs affect superoxide radicals that are thought to be involved in the pathogenesis of actinic prurigo.Materials and Methods.Patients (Chimila Indians with a high prevalence of actinic prurigo) received either (a) tetracycline, 500 mg three times daily, for 6 months, or (b) vitamin E, 100 IU daily, for 6 months. The patients were seen once monthly. There were eight patients in each group.Results.Both drugs used were effective. Pruritus was remarkably improved by either treatment. None of the side effects were severe enough to lead to interruption of treatment, but the observation period posttreatment was relatively short, 4 months for tetracycline and 2 months for vitamin E. The improvement occurred in spite of the continuation of extensive exposure to the sun.Conclusions.Tetracycline and vitamin E are efficacious in relieving the pruritus of actinic prurigo. Preliminary trials of a combination treatment with these two drugs is a new avenue which has shown in preliminary trials to yield synergistic effects which might allow the dosage of tetracycline to be reduce
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03023.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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10. |
CORNEOCYTES IN SCALY PARAKERATOTIC DISEASES |
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International Journal of Dermatology,
Volume 35,
Issue 6,
1996,
Page 417-421
MOHAMED AMER,
FAWZIA FARAG MOSTAFA,
ZENAB TOSSON,
AWATIF NAGIB NASR,
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摘要:
AbstractBackground and Objectives.The stratum corneum of some of the scaly (parakeratotic) diseases was examined with light and scanning electron microscopy (SEM) with the purpose to reveal the importance of this layer in the diagnosis of some of the diseases associated with the formation of scales.Materials and Methods.Two biopsies of the skin surface were taken: one, obtained from 80 patients with various parakeratotic scaly diseases and from 25 control subjects, was processed for light microscopy; the other biopsy for SEM was taken from 10 control subjects and 25 patients. The diagnoses of these patients were: psoriasis (5 patients), erythrodermic psoriasis (2 subjects), parapsoriasis (5 patients), pityriasis rubra pilaris (5 subjects), pityriasis rosea (3 subjects), and seborrheic dermatitis (5 subjects).Results.The light microscopic studies showed that normal corneocytes are of polygonal shape with their largest diameter measuring 42 μm; these cells lacked nuclei. All parakeratotic cells appeared bizarre in shape, smaller than normal, and the cells contained a nucleus. With SEM, normal cells appeared relatively regular in size and shape, trabeculated, and had a flat surface. Cells examined in all the diseases revealed various sizes, outlines, and trabeculae. Specific surface patterns (print) of diseased cells were: “fish‐scale” in psoriasis; “marbled” in parapsoriasis, “rocky stone” in pityriasis rubra pilaris; “heart‐shaped” in seborrheic dermatitis, and semi‐crystalloid in pityriasis rosea.Conclusions.Parakeratosis is characterized not only by the retention of the nucleus in keratinocytes, but is also characterized by a cell of smaller size. The specific print of a disease helps in the diagnosis. The print will change with differe
ISSN:0011-9059
DOI:10.1111/j.1365-4362.1996.tb03024.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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