ABSTRACT
Bacteroidales 16S rRNA gene markers were evaluated for their use as a microbial source tracking tool in a well characterized 750 ha agricultural watershed in Nova Scotia, Canada. Water quality monitoring was conducted following the validation of host-specific and universal Bacteroidales (AllBac) markers for their proficiency in this particular geographic region, which provided further evidence that these markers are geographically stable. Increasing Escherichia coli concentrations were positively correlated (p < 0.01) with concentrations of the AllBac marker in water samples, suggesting that this universal marker is more suited as a positive DNA control rather than as an indicator of recent fecal contamination. Ruminant (BacR) and bovine (CowM2) specific marker detection was associated with increased runoff due to precipitation in sub-watersheds putatively impacted by cattle farming, demonstrating that the BacR and CowM2 markers can be used to detect the recent introduction of fecal matter from cattle farming activities during rainfall events. However, the human associated marker (BacH) was only detected once in spite of numerous on-site residential wastewater treatment systems in the watershed, suggesting that this assay is not sensitive enough to detect this type of human sewage source. E. coli O157:H7 and Salmonella spp. DNA was not detected in any of the 149 watershed samples; however, 114 (76.5%) of those samples tested positive for Campylobacter spp. No significant correlation (p > 0.05) was found between Campylobacter spp. presence and either E. coli or AllBac marker levels. Further studies should be conducted to assess the origins of Campylobacter spp. in these types of watersheds, and to quantify pathogen cell numbers to allow for a human health risk assessment.
Subject(s)
Bacteroidetes/isolation & purification , Environmental Monitoring , Water Microbiology , Water Quality , Water Wells/microbiology , Animals , Animals, Domestic/microbiology , Bacteria/genetics , Bacteria/isolation & purification , Bacteroidetes/genetics , Biomarkers/analysis , Cattle , DNA, Bacterial/genetics , Feces/microbiology , Female , Humans , Male , Mammals/microbiology , Nova Scotia , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , RainABSTRACT
Lichen sclerosus (LS) is a skin condition that affects genital and extra genital epithelia in both males and females of all ages and it may occur in association with other autoimmune disease. Currently, the first line effective treatment is an ultra-potent topical corticosteroid. The long-term sequelae of LS include scarring, malignancy, which is rare, and psychosexual disfunction, which is common.
Subject(s)
Anti-Inflammatory Agents/therapeutic use , Clobetasol/analogs & derivatives , Clobetasol/therapeutic use , Lichen Sclerosus et Atrophicus/drug therapy , Administration, Topical , Anus Diseases/drug therapy , Anus Diseases/psychology , Anus Diseases/surgery , Female , Glucocorticoids , Humans , Lichen Sclerosus et Atrophicus/psychology , Lichen Sclerosus et Atrophicus/surgery , Male , Penile Diseases/drug therapy , Penile Diseases/psychology , Penile Diseases/surgery , Sexual Dysfunctions, Psychological/etiology , Sexual Dysfunctions, Psychological/therapy , Vulvar Diseases/drug therapy , Vulvar Diseases/psychology , Vulvar Diseases/surgeryABSTRACT
BACKGROUND: Vulval carcinoma is a relatively rare disorder that may have various aetiologies. Objectives To document the features and outcome in a series of patients with this disorder. METHODS: Retrospective analysis of patients presenting to a vulval clinic over a 5-year period. RESULTS: Twenty-one women presented with a squamous cell carcinoma (SCC) and two with a verrucous carcinoma (VC). The age range was 43-83 years. Twenty-one had well-established (1-30 years) vulval symptoms prior to developing their tumour. Specific tumour-related symptoms ranged from 3 weeks to 11 months. Eight had had a prior diagnosis of lichen sclerosus (LS) or lichen planus (LP), only two of whom were on regular treatment and follow-up. At presentation, 12 patients had clinical signs of LS, three of LP, and five had some changes of both LS and LP. Two patients had multifocal vulval intraepithelial neoplasia (VIN3). Only one had no evidence of any background vulval skin disease. The commonest histological changes noted in the epithelium either adjacent to or distant from the SCC were those of atrophic LS (n = 8), LS with squamous cell hyperplasia (n = 3), LS with hyperplastic foci and lichenoid infiltrate (n = 4), and LS with differentiated VIN3 (n = 1). Four cases demonstrated the changes of LP, and three showed VIN3. All patients were treated surgically and, in those who had lymphadenectomy, four had positive nodes. There have been two deaths due to metastatic disease, and one further patient has developed a second primary SCC at a different site. CONCLUSIONS: An underlying skin disorder prior to the development of their carcinoma was found in 22 of 23 patients with vulval SCC and is therefore an important risk factor.
Subject(s)
Carcinoma, Squamous Cell/pathology , Vulvar Neoplasms/pathology , Adult , Aged , Aged, 80 and over , Carcinoma, Squamous Cell/secondary , Carcinoma, Squamous Cell/surgery , Female , Humans , Lichen Sclerosus et Atrophicus/complications , Lichen Sclerosus et Atrophicus/pathology , Middle Aged , Precancerous Conditions/pathology , Retrospective Studies , Risk Factors , Skin Neoplasms/secondary , Vulvar Neoplasms/etiology , Vulvar Neoplasms/surgeryABSTRACT
Vulvodynia, defined as vulval pain, soreness or burning as opposed to itching or pruritus, is a common and important problem. Although not a sexually transmitted disease, it often presents to physicians working in that field. The main groups of vulvodynia are those where the symptoms are the consequence of an active dermatosis or infection, and those where it is not attributable to such conditions. In the latter group, the patients fall into two main categories: those of dysesthetic vulvidynia, with constant unprovoked pain, and vulval vestibulitis, with pain provoked by attempted vaginal entry. The recent realization that dysesthetic vulvodynia and vulval vestibulitis may be regarded as pain syndromes is proving a fruitful concept as regards both theory and management of these troublesome conditions.
Subject(s)
Vulvar Diseases/diagnosis , Bacterial Infections/diagnosis , Coitus , Diagnosis, Differential , Female , Humans , Pain/diagnosis , Pain Management , Sensation Disorders/diagnosis , Sexually Transmitted Diseases/diagnosis , Skin Diseases/complications , Tampons, Surgical/adverse effects , Vulvar Diseases/etiology , Vulvar Diseases/microbiology , Vulvar Diseases/therapy , Vulvitis/diagnosis , Vulvitis/etiologyABSTRACT
Women with vulval intraepithelial neoplasia (VIN), lichen sclerosus (LS) and Paget's disease are referred either to gynaecologists or to dermatologists. We have ascertained the caseloads, referral patterns and treatment modalities used in the two specialties. A postal questionnaire was sent to 540 consultant gynaecologists and 225 consultant and senior registrar members of the British Association of Dermatologists. 350 gynaecologists and 161 dermatologists returned completed questionnaires. The workload of LS and Paget's disease was evenly distributed, with 54% of dermatologists and 58% of gynaecologists seeing more than six cases of LS per annum and less than 1% seeing more than five cases of Paget's disease. 92% of responding gynaecologists saw at least one case of VIN per year whereas 43% of dermatologists saw no cases. Patients with VIN and Paget's were referred to gynaecologists for treatment by 66% of dermatologists. Both groups are equally prepared to treat LS. Indications for treatment of VIN and LS were suspicion of invasion and symptoms. Local excision of VIN is the treatment of choice by both gynaecologists and dermatologists. LS is predominantly treated with topical steroids but gynaecologists also use topical oestrogen and testosterone. The great majority of responders favoured establishing a national register to study the outcome of vulval lesions.
Subject(s)
Carcinoma in Situ/therapy , Lichen Sclerosus et Atrophicus/therapy , Paget Disease, Extramammary/therapy , Vulvar Neoplasms/therapy , Dermatology , Female , Gynecology , Health Care Surveys , Humans , Practice Patterns, Physicians' , Referral and Consultation/statistics & numerical data , Surveys and Questionnaires , United KingdomABSTRACT
A study of 350 women with lichen sclerosus, originally made to elucidate the relationship between lichen sclerosus and autoimmunity, led to the amassing of a considerable amount of clinical material. Our review is confined to those with anogenital lesions (342), supplemented by some new cases (15), giving a total of 357 women with biopsy proven lichen sclerosus. It demonstrates the wide age range of the condition, the association with morphoea and lichen planus and the occurrence of squamous cell carcinoma in some cases. It also shows that inappropriate surgery has continued to be carried out for benign disease.
Subject(s)
Anus Diseases/complications , Lichen Sclerosus et Atrophicus/complications , Vulvar Diseases/complications , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Anus Diseases/etiology , Anus Diseases/therapy , Autoimmune Diseases/complications , Carcinoma, Squamous Cell/etiology , Female , Humans , Lichen Sclerosus et Atrophicus/etiology , Lichen Sclerosus et Atrophicus/therapy , Middle Aged , Vulvar Diseases/etiology , Vulvar Diseases/therapy , Vulvar Neoplasms/etiologySubject(s)
Vulvar Diseases/etiology , Child , Diagnosis, Differential , Female , Hair Diseases/diagnosis , Hair Diseases/etiology , Hair Diseases/therapy , Humans , Infant , Skin Diseases/diagnosis , Skin Diseases/etiology , Skin Diseases/therapy , Vulvar Diseases/diagnosis , Vulvar Diseases/therapySubject(s)
Nevus, Pigmented/pathology , Skin Neoplasms/pathology , Follow-Up Studies , Humans , Infant , MaleSubject(s)
Societies, Medical , Vulvar Diseases , Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Lichen Planus/diagnosis , Organizational Policy , Outpatient Clinics, Hospital , Sclerosis/diagnosis , Vulva/pathologyABSTRACT
Lichen sclerosus is a skin condition affecting all areas of the body at all ages and in both sexes. It appears to be a histologic and clinical entity, although in very many respects it is close to lichen planus and morphea. Its cause and pathogenesis are not established, but a link with autoimmune disease is recognized. Its predilection for the anogenital area in women has led to an unfortunate dichotomy between dermatologists and gynecologists. This was a potent source of confusion for many years but has now been resolved with a the recent formulation of a classification acceptable to the ISSVD (representing gynecologists, dermatologists, and pathologists) and the ISGyP (see Appendices). It is hoped that management will now be more logical, with the mainstay being emollients and topical corticosteroids, and that the vulvectomies sometimes performed for benign disease have become a thing of the past. There is almost certainly an increased risk of malignancy in lichen sclerosus, albeit at present an unquantifiable one, and for that reason patients should be kept under review.