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1.
Clin Exp Dermatol ; 29(2): 159-60, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14987274

ABSTRACT

Cryptococcus neoformans is an opportunistic yeast with a worldwide distribution. Although well recognized as a cause of cutaneous disease in immunocompromised patients, this rarely occurs in healthy hosts. In this article, we present the case of a farmer who developed cutaneous cryptococcosis at the site of an injury he sustained while cleaning out his barn. Despite an extensive work-up, no evidence of disseminated disease or underlying immunosuppression was found. The patient recovered completely several weeks after beginning treatment with oral fluconazole.


Subject(s)
Antifungal Agents/administration & dosage , Arm Injuries/complications , Cryptococcosis/drug therapy , Dermatomycoses/drug therapy , Fluconazole/administration & dosage , Administration, Oral , Aged , Aged, 80 and over , Cryptococcosis/etiology , Dermatomycoses/etiology , Humans , Male
3.
J Am Acad Dermatol ; 43(2 Pt 2): 329-32, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10901714

ABSTRACT

A patient with clinical findings of dermatitis herpetiformis (DH), negative direct immunofluorescent (DIF) findings for junctional IgA deposits in 2 biopsy specimens, and positive for IgA endomysial (AEmA) and tissue transglutaminase (tTG) antibodies responded initially to dapsone. After dapsone had to be discontinued because of side effects, a gluten-free diet and supportive therapy controlled the disease; the AEmA and tTG antibodies became negative. Our data on 10 consecutive DH cases examined by DIF and by serum studies for AEmA and antibodies to tTG, point to frequencies of 90% DIF positive and 70% AEmA and tTG positive cases. The use of both DIF and serum tests for AEmA and tTG reveals DH cases not detected by DIF alone that respond to gluten-free diet. Findings on autoantibodies to tTG, an enzyme that metabolizes gliadin, points to a role of tTG in the immunopathology of gluten-sensitive enteropathy and helps to explain the need for a gluten-free diet in the management of DH cases.


Subject(s)
Autoantibodies/analysis , Dermatitis Herpetiformis/pathology , Fluorescent Antibody Technique, Direct , Immunoglobulin A/analysis , Transglutaminases/immunology , Celiac Disease/diet therapy , Celiac Disease/immunology , Celiac Disease/pathology , Dermatitis Herpetiformis/diet therapy , Dermatitis Herpetiformis/immunology , Diagnosis, Differential , Female , Glutens/administration & dosage , Glutens/immunology , Humans , Middle Aged , Skin/immunology , Skin/pathology
4.
J Am Acad Dermatol ; 42(5 Pt 2): 907-13, 2000 May.
Article in English | MEDLINE | ID: mdl-10767703

ABSTRACT

Dermatofibrosarcoma protuberans (DFSP) occurs most commonly on the trunk, affects all races, and often develops between the second and fifth decades of life. It is uncommon in childhood and is sometimes mistaken for a vascular lesion, as it often presents as a blue macule or small nodule. Review of the English literature revealed approximately 152 cases of DFSP developing before 16 years of age and only 19 claimed congenital cases. A case of congenital dermatofibrosarcoma protuberans is presented with a literature review and discussion of congenital and childhood presentations of the tumor.


Subject(s)
Dermatofibrosarcoma/congenital , Skin Neoplasms/congenital , Age Factors , Child, Preschool , Dermatofibrosarcoma/pathology , Female , Humans , Skin Neoplasms/pathology
5.
Cutis ; 63(4): 223-5, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10228751

ABSTRACT

Drug-induced pseudoporphyria cutanea tarda has been attributed to many different medications including several nonsteroidal anti-inflammatory drugs (NSAIDs). Often the patients taking these anti-inflammatory medications became part of a treatment dilemma when one of the drugs is deemed the cause of a blistering disease. We present a prototypical case of NSAID-induced pseudoporphyria cutanea tarda and suggest alternative NSAIDs that may be safely used in these patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Porphyria Cutanea Tarda/chemically induced , Drug-Related Side Effects and Adverse Reactions , Humans , Porphyria Cutanea Tarda/pathology
7.
Am J Dermatopathol ; 20(4): 413-6, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9700384

ABSTRACT

The authors report a case of Lhermitte-Duclos disease, or dysplastic cerebellar gangliocytoma, in which a cutaneous sclerotic fibroma was found incidentally during the second resection of a recurrent cerebellar hamartoma. The association of Lhermitte-Duclos disease and sclerotic fibroma with Cowden's syndrome led to a dermatologic examination and confirmation of the diagnosis of Cowden's syndrome. The combination of both Lhermitte-Duclos disease and sclerotic fibroma with Cowden's syndrome has not previously been reported. A review of the 15 cases of Lhermitte-Duclos disease associated with Cowden's syndrome shows no significant gender predilection. Sclerotic fibromas, once thought to be specific for Cowden's syndrome, also are reviewed.


Subject(s)
Cerebellar Neoplasms/pathology , Fibroma/pathology , Ganglioneuroma/pathology , Hamartoma Syndrome, Multiple/pathology , Skin Diseases/pathology , Skin Neoplasms/pathology , Adult , Cerebellar Neoplasms/complications , Diagnosis, Differential , Fibroma/complications , Ganglioneuroma/complications , Hamartoma Syndrome, Multiple/complications , Humans , Male , Skin Diseases/complications , Skin Neoplasms/complications
8.
Arch Dermatol ; 134(5): 595-8, 1998 May.
Article in English | MEDLINE | ID: mdl-9606329

ABSTRACT

The possibility that there is an increased risk of melanoma in patients with psoriasis treated with psoralen-UV-A (PUVA) therapy has raised concern on the part of physicians and patients about the long-term safety of this treatment. In response to this concern, the National Psoriasis Foundation sponsored a workshop at which invited participants with expertise in PUVA therapy, psoriasis treatment, melanoma and nonmelanoma skin cancer, and epidemiological and clinical trials were asked to develop a consensus on the following 3 issues: the risk of long-term adverse effects of PUVA therapy with emphasis on nonmelanoma and melanoma skin cancer; the guidelines for physicians and patients for selection and use of PUVA therapy with consideration of the risk-benefit ratio of this treatment compared with the risk-benefit ratios of alternative treatments; and the directions for further evaluation of the long-term effects Of PUVA therapy.


Subject(s)
Melanoma/chemically induced , PUVA Therapy/adverse effects , Skin Neoplasms/chemically induced , Humans , Psoriasis/drug therapy , Risk , Time Factors
10.
Pediatr Dermatol ; 14(5): 387-90, 1997.
Article in English | MEDLINE | ID: mdl-9336813

ABSTRACT

We report a 15-year-old primagravida female with a history of chronic plaque psoriasis who developed impetigo herpetiformis at 28 weeks gestation. Culture of a needle aspirate from a tender, enlarged cervical lymph node grew Staphylococcus aureus. The patient improved rapidly on wet dressings, topical midpotency corticosteroids, and intravenous nafcillin. The remainder of her pregnancy was uncomplicated. We speculate that both pregnancy and infection led to this pustular flare of her psoriasis.


Subject(s)
Dermatitis Herpetiformis/complications , Impetigo/complications , Lymphadenitis/microbiology , Pregnancy Complications , Staphylococcal Infections , Adolescent , Female , Humans , Lymph Nodes/microbiology , Lymphadenitis/drug therapy , Nafcillin/therapeutic use , Penicillins/therapeutic use , Pregnancy , Pregnancy Complications/drug therapy , Psoriasis/complications
12.
J Am Acad Dermatol ; 33(1): 44-52, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7601945

ABSTRACT

BACKGROUND: Etretinate is an aromatic retinoid given orally to treat severe psoriasis, a chronic disease that often requires long-term therapy. OBJECTIVE: We assessed the safety of long-term therapy with etretinate for psoriasis. METHODS: This 5-year prospective study of a cohort of 956 patients with psoriasis treated with etretinate assessed the frequency of adverse events in relation to total use and in relation to the frequency of these events in control populations. RESULTS: Our data do not provide evidence for an increased risk of cardiovascular disease, cancer, diabetes, or inflammatory bowel disease in association with long-term etretinate use. Although some patients reported that joint problems improved with the use of etretinate, a greater number associated the use of etretinate with joint problems. CONCLUSION: With proper patient selection and monitoring, long-term etretinate therapy (up to 4 years) does not appear to be accompanied by a substantial increased risk of major adverse effects.


Subject(s)
Etretinate/adverse effects , Psoriasis/drug therapy , Adult , Etretinate/therapeutic use , Eye Diseases/chemically induced , Eye Diseases/epidemiology , Female , Follow-Up Studies , Humans , Incidence , Joint Diseases/chemically induced , Joint Diseases/epidemiology , Male , Middle Aged , Myocardial Infarction/chemically induced , Myocardial Infarction/epidemiology , Neoplasms/chemically induced , Neoplasms/epidemiology , PUVA Therapy , Pregnancy , Pregnancy Complications/drug therapy , Pregnancy Complications/epidemiology , Prospective Studies , Psoriasis/mortality , Time Factors
13.
Arch Dermatol ; 131(5): 561-8, 1995 May.
Article in English | MEDLINE | ID: mdl-7741543

ABSTRACT

BACKGROUND AND DESIGN: Patient preferences for health outcomes can be explicitly assessed and expressed in quantitative terms known as utilities. Three standard methods for utility assessment have been used to quantify patient preferences, but these methods have not previously been applied to skin disease. Eighty-seven patients with psoriasis from a tertiary medical center were interviewed, using an interactive, computer-based utility assessment questionnaire, U-Titer. Utilities for three categories of psoriasis severity and potential adverse outcomes of methotrexate therapy were assessed by the vertical rating scale, time trade-off, and standard gamble. RESULTS: Patients assigned a broad range of utilities for each of the health states. Utilities obtained by the vertical rating scale did not correlate well with utilities obtained by standard gamble or time trade-off methods. However, utilities assessed by standard gamble and time trade-off were not significantly different. Patient characteristics such as age, gender, and education were not correlated with utility and did not explain the variation. Indicators of the patients' disease severity were not predictive of utilities for the assessed health states. The relatively high utility for liver biopsy suggests that there is less patient aversion to the procedure than suspected. CONCLUSIONS: Utilities, or quantitative measures of patient preferences for health states, are measurable and vary widely for mild, moderate, and severe psoriasis and possible adverse outcomes of methotrexate treatment. The process of elucidating individual patient utilities for various health outcomes can be used to incorporate patient preferences into the process of clinical decision making. Guidelines that are based solely on severity of symptoms, without input from patients on how they value such symptoms, must be questioned.


Subject(s)
Attitude to Health , Methotrexate/therapeutic use , Psoriasis/psychology , Adult , Aged , Biopsy , Chemical and Drug Induced Liver Injury , Decision Making , Female , Forecasting , Health Status , Humans , Liver/drug effects , Liver Diseases/pathology , Male , Methotrexate/administration & dosage , Middle Aged , Patient Satisfaction , Psoriasis/drug therapy , Quality of Life , Time Factors , Treatment Outcome
16.
Arch Dermatol ; 125(9): 1209-17, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2774596

ABSTRACT

To determine whether liver function tests and clinical and demographic information would predict methotrexate-associated hepatotoxicity, we identified 78 patients who had undergone 147 liver biopsies associated with methotrexate therapy for psoriasis. The joint sensitivity of aspartate aminotransferase, alkaline phosphatase, and total bilirubin values in detecting abnormal results from a biopsy specimen obtained after treatment was .86; the predictive value of negative test results was .93. A logistic regression model significantly predicted the presence of abnormal (grade III or higher) liver biopsy specimen results. The concordance index was .92 (perfect, 1.0). Regression coefficients may be used along with information from a specific patient to calculate the predicted probability of an abnormal result from a liver biopsy specimen after treatment. We conclude that this multivariate risk estimation model significantly predicts the likelihood of positive findings from liver biopsy specimens in this patient population. The clinical use of this model awaits further validation.


Subject(s)
Chemical and Drug Induced Liver Injury/pathology , Liver Cirrhosis/pathology , Liver/pathology , Methotrexate/adverse effects , Psoriasis/drug therapy , Biopsy , Chemical and Drug Induced Liver Injury/etiology , Cholecystitis/pathology , Female , Humans , Liver/drug effects , Liver Cirrhosis/chemically induced , Liver Function Tests , Male , Middle Aged , Predictive Value of Tests , ROC Curve , Retrospective Studies , Risk Factors , Time Factors
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