Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
Ann Dermatol ; 28(4): 470-8, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27489430

ABSTRACT

BACKGROUND: A small subset of adolescents atopic dermatitis (AD) tends to persist. This also leads to get more antibiotics exposure with advancing years. Antibiotic resistance has been regarded as a serious problem during Staphylococcus aureus treatment, especially methicillin-resistant S. aureus (MRSA). OBJECTIVE: It was investigated the S. aureus colonization frequency in the skin lesions and anterior nares of adolescent AD patients and evaluated the changes in S. aureus antimicrobial susceptibility for years. METHODS: Patients who visited our clinic from September 2003 to August 2005 were classified into group A, and patients who visited from August 2010 to March 2012 were classified into group B. To investigate the differences with regard to patients' age and disease duration, the patients were subdivided into groups according to age. Lesional and nasal specimens were examined. RESULTS: Among the 295 AD patients, the total S. aureus colonization rate in skin lesions was 66.9% (95/142) for group A and 78.4% (120/153) for group B. No significant changes in the systemic antimicrobial susceptibilities of S. aureus strains isolated from adolescent AD patients were observed during about 10-year period. The increased trend of MRSA isolation in recent adolescent AD outpatients suggest that the community including school could be the source of S. aureus antibiotic resistance and higher fusidic acid resistance rates provides evidence of imprudent topical use. CONCLUSION: Relatively high MRSA isolation and fusidic acid resistance rates in recent AD patients suggest that the community harbors antibiotic-resistant S. aureus.

4.
Pediatr Dermatol ; 22(5): 476-9, 2005.
Article in English | MEDLINE | ID: mdl-16191006

ABSTRACT

Cutaneous infection arising from Mycobacterium scrofulaceum, a nontuberculous mycobacteria, has rarely been reported, and most of the reported infections were disseminated forms in patients with AIDS or other immunocompromising illness. We describe an occurrence of localized mycobacterial skin infection caused by M. scrofulaceum in a previously healthy child that manifested as a red nodule on the cheek. A biopsy specimen of the lesion demonstrated granulomatous infiltration in the dermis. M. scrofulaceum was isolated from culture of a tissue specimen. Polymerase chain reaction amplified specific fragments for M. scrofulaceum. The patient was treated successfully with clarithromycin as monotherapy for 6 months, leading to complete healing without recurrence during a follow-up period of 2 years.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Clarithromycin/therapeutic use , Mycobacterium Infections, Nontuberculous/drug therapy , Mycobacterium scrofulaceum/isolation & purification , Skin Diseases, Bacterial/drug therapy , Child, Preschool , Female , Humans , Mycobacterium Infections, Nontuberculous/complications , Skin Diseases, Bacterial/microbiology
5.
Dermatol Surg ; 31(8 Pt 1): 973-6, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16042947

ABSTRACT

BACKGROUND: Trichilemmal carcinoma (TLC) is a rare cutaneous neoplasm that occurs in the sun-exposed skin of the elderly. Although the clinical behavior of TLC appears to be relatively indolent, wide excision or Mohs micrographic surgery is the recommended treatment owing to its locally aggressive growth. Recently, imiquimod has become an important part of the armamentarium in the treatment of nonmelanoma skin cancer. OBJECTIVE: This article serves to remind dermatologists that in addition to Mohs micrographic surgery and surgical excision, imiquimod 5% cream may have a role in the treatment of TLC. METHODS: In addition to a review of the literature, we present a case of TLC successfully treated with 5% imiquimod cream. CONCLUSION: Its nonsurgical approach and excellent cosmetic result make imiquimod 5% cream another promising therapeutic option for TLC, even though it is histologically infiltrative.


Subject(s)
Aminoquinolines/administration & dosage , Antineoplastic Agents/administration & dosage , Hair Follicle/pathology , Skin Neoplasms/diagnosis , Administration, Cutaneous , Aged , Aged, 80 and over , Diagnosis, Differential , Face/pathology , Female , Humans , Imiquimod , Skin Neoplasms/drug therapy , Skin Neoplasms/pathology
6.
Contact Dermatitis ; 52(3): 142-4, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15811028

ABSTRACT

Zinc pyrithione is a shampoo ingredient that has been shown to be safe and effective for dandruff and scalp psoriasis. It is thought to decrease the cell turnover rate in hyperproliferative dermatoses such as psoriasis, and also has fungistatic and antimicrobial activity, although its exact mode of action is unknown. In psoriasis, external factors, such as trauma, infection and drugs, may provoke aggravated manifestations of psoriatic skin lesions. Rarely, irritant or allergic mechanisms are likely causes of psoriatic flare and Kobnerization. A patient had had stable psoriasis for 25 years and no any other skin disease. Within 20 days, she developed an aggravated scaly erythematous patch on the scalp, where a shampoo had been applied, and simultaneously developed pustular psoriasis on both forearms. Patch testing showed a relevant sensitization to zinc pyrithione, and we observed symptomatic aggravation by provocation testing with zinc pyrithione shampoo. We report a rare case of psoriasis aggravated by the induction of allergic contact dermatitis from zinc pyrithione after using antidandruff shampoo.


Subject(s)
Dermatitis, Allergic Contact/etiology , Hair Preparations/adverse effects , Psoriasis/chemically induced , Pyridines/adverse effects , Scalp Dermatoses/chemically induced , Zinc Compounds/adverse effects , Adult , Cyclosporine/therapeutic use , Dermatitis, Allergic Contact/drug therapy , Female , Humans , Immunosuppressive Agents/therapeutic use , Psoriasis/drug therapy , Psoriasis/physiopathology , Risk Factors , Scalp Dermatoses/drug therapy
SELECTION OF CITATIONS
SEARCH DETAIL
...