Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
1.
Clin Infect Dis ; 22(2): 331-5, 1996 Feb.
Article in English | MEDLINE | ID: mdl-8838192

ABSTRACT

We report the second case of chromoblastomycosis caused by Exophiala spinifera; this is the first known case in the United States. Examination of biopsied tissue showed thick-walled, internally septated, chestnut brown muriform cells (sclerotic bodies) within multinucleated giant cells present in the dermis that were characteristic of chromoblastomycosis. The individual cells within the muriform cells disarticulated from the outer wall of the parent cell and from each other to form endoconidia within the outer walls of the parent cells. After fracture of the outer walls, the endoconidia were released. This unique process of endoconidial formation in vivo for the propagation of muriform cells was observed for the first time. Initial treatment with itraconazole and 5-fluorocytosine followed by treatment with itraconazole and heat resulted in marked improvement in the patient's lesions. This infection reiterates the fact that the dematiaceous fungus E. spinifera, a well-known etiologic agent of phaeohyphomycosis, can cause more than one type of infection and supports earlier observations that chromoblastomycosis and phaeohyphomycosis represent extremes of a continuum of infections.


Subject(s)
Chromoblastomycosis/microbiology , Exophiala/isolation & purification , Antifungal Agents/therapeutic use , Chromoblastomycosis/drug therapy , Exophiala/growth & development , Humans , Itraconazole/therapeutic use , Male , Middle Aged , Skin/microbiology , United States
2.
Am J Dermatopathol ; 17(1): 48-52, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7695010

ABSTRACT

Dermatitis herpetiformis has a characteristic histologic pattern consisting of subepidermal blisters often containing fibrin, infiltrates of neutrophils and nuclear dust at tips of dermal papillae, and papillary dermal edema. These are features of early and evolving lesions. We present two cases of clinically typical dermatitis herpetiformis with previously unreported histologic features that may provide a significant diagnostic clue. In each of these cases there were focal collections of nuclear dust in the cornified layer of the epidermis, a finding that may represent a resolving phase of dermatitis herpetiformis, beyond the usual papillary dermal neutrophilic microabscesses seen in early lesions. Biopsy material was available for immunofluorescent studies in one of the cases presented. In addition to the granular pattern of IgA positivity at the dermal-epidermal junction, which is diagnostic of dermatitis herpetiformis, this biopsy also showed similar IgA positivity in the intracorneal nuclear dust aggregates. In the second case, initial sections showed only intracorneal nuclear dust, but at deeper levels there were more typical diagnostic microabscesses at the tips of dermal papillae.


Subject(s)
Cell Nucleus/ultrastructure , Dermatitis Herpetiformis/diagnosis , Dermatitis Herpetiformis/pathology , Skin/ultrastructure , Abscess/pathology , Adult , Blister/pathology , Edema/pathology , Epidermis/ultrastructure , Female , Fibrin/analysis , Fibrinogen/analysis , Follow-Up Studies , Humans , Immunoglobulin A/analysis , Male , Middle Aged , Neutrophils/pathology
4.
Pediatr Dermatol ; 7(3): 208-13, 1990 Sep.
Article in English | MEDLINE | ID: mdl-2247390

ABSTRACT

Preschool sarcoidosis is characterized by the triad of skin, joint, and eye disease without pulmonary involvement. Arthritis and uveitis are also frequently seen together in juvenile rheumatoid arthritis. We report two patients with preschool sarcoidosis, both of whom were initially diagnosed and treated as having juvenile rheumatoid arthritis. Skin biopsy is an important early diagnostic procedure to differentiate the conditions. The uveitis in both diseases can have serious sequelae.


Subject(s)
Arthritis, Juvenile/diagnosis , Sarcoidosis/diagnosis , Skin Diseases/diagnosis , Child , Child, Preschool , Diagnosis, Differential , Female , Humans , Infant , Male , Sarcoidosis/complications , Sarcoidosis/pathology , Skin Diseases/pathology , Uveitis/etiology
6.
Prostate ; 2(4): 337-58, 1981.
Article in English | MEDLINE | ID: mdl-7329871

ABSTRACT

The mechanism by which estrogens inhibit castration atrophy has been investigated morphologically and biochemically utilizing ventral prostate from Copenhagen rats. The suppression of weight loss and gross edematous appearance of the prostate associated with the in vivo effect of 17 beta-estradiol (E2) could not be accounted for by DNA and protein synthesis. Increase in the fluid content in the tissues was confirmed by demonstration of significant increase in the ratio of wet/dry tissue weights. Light microscopy demonstrated that the main effects were on the stroma, characterized by large interglandular areas almost totally devoid of collagen resulting in an edematous appearance. Electron microscope studies showed an abundance of fluid localized adjacent to the capillary endothelium and some red blood cells indicating disturbances in capillary permeability. The combination of a prolactin secretion inhibiting agent with E2 alone, indicating an involvement of prolactin the estrogen effect. Differences in blood prolactin concentration between the strains of rats may influence the sensitivity of the prostate to estrogens.


Subject(s)
Castration , Ergolines/pharmacology , Estrogens/pharmacology , Prostate/anatomy & histology , Animals , DNA/analysis , Estradiol/pharmacology , Male , Organ Culture Techniques , Organ Size/drug effects , Prolactin/blood , Prostate/drug effects , Prostate/pathology , Proteins/analysis , Rats , Rats, Inbred Strains
SELECTION OF CITATIONS
SEARCH DETAIL
...