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Dive into the research topics where Helen Saunders is active.

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Featured researches published by Helen Saunders.


Contact Dermatitis | 2008

The validity and reliability of the occupational contact dermatitis disease severity index

Nathan Curr; Shyamali C. Dharmage; Tessa Keegel; Adriene Lee; Helen Saunders; Rosemary Nixon

Background:  The occupational contact dermatitis disease severity index (ODDI) was designed to assess the severity and importantly the functional disability caused by occupational contact dermatitis (OCD) of the hands in patients attending our occupational dermatology clinic.


Australasian Journal of Dermatology | 2003

Pedigree of multiple benign adnexal tumours of Brooke–Spiegler type

Helen Saunders; Paul Tucker; Tricia Saurine; Frances Watkins

A pedigree of autosomal dominant expression of multiple benign adnexal tumours is presented. Seven cases spanning three generations are discussed. The clinical manifestations of these tumours are quite variable, including multiple papules concentrated on the face, scalp nodules and a large turban tumour. One member of the family had a linear papular eruption involving one half of his body. Histopathology of all lesions demonstrated benign adnexal characteristics, including well‐characterized eccrine spiradenomas, trichoepitheliomas and an eccrine cylindroma. The cutaneous tumours occurring in these patients have continued to develop during their lifetimes. The authors propose that this pedigree has phenotypic characteristics consistent with Brooke–Spiegler syndrome.


Australasian Journal of Dermatology | 2010

Hidradenitis suppurativa responding to treatment with infliximab

Anita Lasocki; Rodney Sinclair; Peter Foley; Helen Saunders

A series of four cases of severe recalcitrant hidradenitis suppurativa treated with infliximab is presented. All patients had failed to respond to prior medical and surgical management. Baseline Quantiferon‐TB Gold and chest radiograph were carried out before commencement of treatment. No patients had associated Crohns disease. All patients received induction infusions of infliximab 5 mg/kg at weeks 0, 2 and 6, followed by eight weekly maintenance infusions. The total number of infusions varied between 4 and 6. Skin photography with Sartorius scoring was used to evaluate response to treatment. All patients experienced marked improvement in their disease activity, with a mean 48% improvement in Sartorius score after one infusion (week 2, P < 0.01), and 70% improvement after three infusions (week 14, P < 0.01). Time to relapse following cessation of therapy ranged from 6 weeks to 4 months. Further studies examining the efficacy of infliximab and its effect on the course of the disease, particularly relating to long‐term management, are required.


Contact Dermatitis | 2004

Topical corticosteroid allergy in an urban Australian centre

Tessa Keegel; Helen Saunders; Roger L. Milne; Praneet Sajjachareonpong; Ashley Fletcher; Rosemary Nixon

The reported prevalence of allergic contact dermatitis from topical corticosteroids in clinical populations, in the period 1993–2002, varied from 0.55 to 5.98%. This study is a retrospective analysis of 1153 individuals undergoing routine patch testing in an Occupational Dermatology Clinic in Melbourne, Australia. We report a rate of 0.52% for positive patch test reactions to 5 corticosteroids. Corticosteroids tested were betamethasone‐17‐valerate, budesonide, Diprosone® cream (betamethasone diproprionate 0.05%) (Essex‐Pharma, a division of Schering‐Plough Pty Ltd, Sydney, Australia), tixocortol‐21‐pivalate and triamcinolone acetonide. Population characteristics were described using the MOAHL (M = percentage of males tested; O = occupational; A = atopics; H = patients with hand eczema; L = patients with leg ulcers or stasis eczema) index. Prescribing patterns, rate of referral and rate of relevant positive patch test reactions were characterized for the region. These results were compared to the rates of corticosteroid allergy and patch testing methodologies from published international studies. It was noted that many high‐sensitization potential corticosteroids were not available in our region. Although a low percentage of leg ulcers and stasis dermatitis may be associated with a lower rate of corticosteroid allergy, this association may be confounded by regional factors such as prescribing habits and the local availability of corticosteroids. We conclude that the low rate of topical corticosteroid contact allergy reported by our clinic is associated with regional availability and prescribing practices and the scarcity of stasis dermatitis and leg ulcers in our clinic population.


Contact Dermatitis | 2005

Incidence and prevalence rates for occupational contact dermatitis in an Australian suburban area

Tessa Keegel; Jennifer Cahill; Amanda Noonan; Shyamali C. Dharmage; Helen Saunders; Kathryn Frowen; Rosemary Nixon

Occupational contact dermatitis (OCD) regularly causes high levels of worker morbidity; however, this is often not reflected in available statistics. This study aimed to collect and verify OCD reports/referrals and generate disease estimates for a defined geographical area in Melbourne, Australia. Two methods of data collection were used. In the first method, 30 general practitioners (GPs), 2 dermatologists and 1 dermatology outpatient clinic within a defined area reported each worker with suspected OCD seen as part of routine practice. With the second method, workers living in the area who were referred to a tertiary referral OCD clinic were included in the study. An occupational dermatologist used a gold standard process that included diagnostic patch testing to verify suspected cases. The incidence rate for confirmed cases was 20.5 per 100 000 workers [95% confidence interval (CI): 13–32.1]. The 1‐year‐period prevalence rate was 34.5 per 100 000 (95% CI: 24.4–48.7). The positive predictive value (PPV) was highest for the occupational dermatology clinic referrals [63% (95% CI: 49–76%)] compared with reports from the dermatologists/dermatology outpatient clinic [55% (95% CI: 36–74%)] and from GPs [43% (95% CI: 29–59%)]. This study utilizes reports from GPs and dermatologists to provide OCD disease estimates and validation data for an OCD disease register.


Australasian Journal of Dermatology | 2006

Multiple periungual pyogenic granulomas following systemic 5-fluorouracil

Nathan Curr; Helen Saunders; Anand Murugasu; Prasad Cooray; Max Schwarz; Douglas L. Gin

A 65‐year‐old man presented with a 7‐month history of eight bleeding periungual lesions on both feet. The clinical diagnosis of multiple pyogenic granulomas was confirmed by histological examination. Historically, the pyogenic granulomas appeared 3 months after commencing 5‐fluorouracil chemotherapy for rectal carcinoma, suggesting a possible causative relationship. Chemotherapy was ceased by the supervising oncologist. Resolution occurred after two lesions had been treated with curettage and diathermy, and the remaining lesions with occlusive dressings over Kenacomb ointment (triamcinolone acetonide 0.1%, neomycin sulphate 0.25%, gramicidin 0.025%, nystatin 100 000 U/g) topically twice daily for a period of 3 months.


Contact Dermatitis | 2007

Are material safety data sheets (MSDS) useful in the diagnosis and management of occupational contact dermatitis

Tessa Keegel; Helen Saunders; Anthony D. LaMontagne; Rosemary Nixon

Objectives:  This study assesses both the success of medical practitioners in accessing hazardous substances’ information from product manufacturers and the accuracy and clinical usefulness of Material Safety Data Sheets (MSDS) presented by workers with suspected occupational contact dermatitis (OCD).


Contact Dermatitis | 2004

Persistent post‐occupational dermatitis

Praneet Sajjachareonpong; Jennifer Cahill; Tessa Keegel; Helen Saunders; Rosemary Nixon


Australasian Journal of Dermatology | 2004

Textile dye allergic contact dermatitis following paraphenylenediamine sensitization from a temporary tattoo.

Helen Saunders; Timothy J O'Brien; Rosemary Nixon


Contact Dermatitis | 2003

Career counsellors and occupational contact dermatitis

Helen Saunders; Tessa Keegel; Rosemary Nixon; Kath Frowen

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Tessa Keegel

University of Melbourne

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Jennifer Cahill

University of Southern Denmark

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Anita Lasocki

Peter MacCallum Cancer Centre

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Peter Foley

University of Melbourne

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