ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00919.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00920.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00921.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00922.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00923.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

摘要:

ABSTRACTSeventy‐eight cases of pilomatricoma are reported. The unexpected findings are new lesions occurring in middle and old age; the lack of association with other diseases; and the large number of lesions located deep in the skin. As contemporary knowledge of the nature of this disorder is advancing, it is suggested that the eponymous title be abandone

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00924.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

摘要:

ABSTRACTPatients with deep mycoses diagnosed in dermatologic clinics of Manaus (state of Amazonas, Brazil) were studied from November 1973 to December 1983. They came from the Brazilian states of Amazonas, Pará, Acre, and Rondônia and the Federal Territory of Roraima. All of these regions, with the exception of Pará, are situated in the western part of the Amazon Basin. The climatic conditions in this region are almost the same: tropical forest, high rainfall, and mean annual temperature of 26C. The deep mycoses diagnosed, in order of frequency, were lorge Lobo's disease, para‐coccidioidomycosis, chromomycosis, sporotrichosis, mycetoma, cryptococcosis, zygomycosis, and histoplasm

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00925.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

摘要:

ABSTRACTA variant of acrodermatitis enteropathica is described that has its onset before weaning and clears when the child starts its normal solid diet. A pedigree with three interrelated families is reported where 10 children were afflicted with this variant. They had symptoms of hypozincemia for a brief period during infancy. At the time of this study, they were symptom‐free and their serum zinc levels were found to be within normal limits. The term “self‐limiting acrodermatitis enteropathica” is proposed for the variant. In one lactating mother, the mammary zinc secretion was determined and was found to be deficient and unresponsive to oral zinc supplements. The possible mode of inheritance is also di

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00926.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

摘要:

ABSTRACTA patient with atrophoderma (Pasini‐Pierini) was studied. Microscopic examination showed small collections of mononuclear cells around dermal blood vessels. Electron microscopic study demonstrated macrophages and lymphocytes around vessels and between fibers in the dermis; the epidermis, dermis, collagen, and elastic fibers appeared normal. Monoclonal antibody studies of the cells in the perivascular infiltrate demonstrated cells reacting with anti‐Leu‐1 (pan‐T‐cell antibody), anti‐Leu‐3a (the helper/inducer T‐cell antibody), and OKM 1 antibody‐reacting cells (macrophages). Direct, immunofluorescent studies showed IgM and C3 staining in the small blood vessels of the papillary dermis, scattered IgM cytoids at the basement membrane, and focal fibrinogen in the mid‐dermis.Mononuclear cells in the perivascular infiltrate, similar in type and percentage concentration, have been demonstrated also in patients with anetoderma, another rare atrophic cutaneous disorder. Macrophages and T lymphocytes around papillary dermal blood vessels may play a role in the pathogenesis of atrophod

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00927.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY

摘要:

ABSTRACTPterygium inversum unguis is a nail abnormality in which the distal aspect of the nail bed/hyponychium is adherent to the ventral surface of the nail plate, resulting in obliteration of the distal groove. We present a 50‐year‐old man who developed this abnormality on his right fingers and toes after a stroke that resulted in paresis of his right side. Unusual features of this case include the association with a neurologic disorder, assymetric distribution, involvement of toes as well as fingers, and occurrence in the male gen

ISSN:0011-9059    

DOI:10.1111/j.1365-4362.1988.tb00928.x

出版商:Blackwell Publishing Ltd    

年代:1988

数据来源: WILEY