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[Treatment of pruritus and vulvitis, especially in pregnancy, with Delmeson foam].
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[VULVITIS AND VULVOVAGINITIS IN CHILDHOOD].
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NON-SPECIFIC VULVITIS.
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[A RARE CASE OF DEEPLY INFILTRATING VULVITIS].
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Vaginitis and vulvitis. Clinical diagnosis and treatment.
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[Treatment of chronic vulvitis and vulvar pruritus].
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Plasma cell vulvitis: a rare cause of intractable vulvar pruritus.
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[Gabapentin as therapy for vulvitis].
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Vulvitis granulomatosa and unilateral hypertrophy of the vulva related to Crohn's disease: a case report.
We report the case of a patient with voluminous unilateral hypertrophy of vulvar labia and pseudocondylomata in the fossa navicularis associated with intestinal Crohn's disease. No fistulas were observed. The patient has had Crohn's disease for 8 years. Interrelationship of genital alterations and Crohn's disease are discussed.
[Is non IgE-dependent sensitization to cow's milk proteins responsible for resistant idiopathic vulvitis of young girls?].
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Imiquimod treatment of vulvitis circumscripta plasmacellularis.
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Squamous cell carcinoma of the bladder presenting as vulvitis and cliteromegaly.
INTRODUCTION: Clitoral metastases are exceptionally rare. We present a case of a squamous cell carcinoma of the bladder presenting with a clitoral metastasis. CASE REPORT: We report the case of an 84-year-old lady with frequency, dysuria and a clitoral mass, which was found to be a poorly differentiated carcinoma on fine needle aspiration cytology. Cystoscopy revealed a moderate to poorly differentiated squamous cell carcinoma of the bladder. CONCLUSION: This is the first reported case of a squamous cell carcinoma of the bladder with clitoral metastasis. Clitoral metastases are exceptionally rare, with only seven previous cases reported in the literature. Although the commonest cause of cliteromegaly is hormonal, a metastatic carcinoma should be considered as part of the differential diagnosis in the elderly female.
Vulvitis and vulvovaginitis: cutaneous considerations.
Vulvar dermatoses (previously dystrophies) include psoriasis, allergic or irritant reactions, lichen sclerosus, lichen simplex chronicus, lichen planus, and tinea. Some of these have bullous or erosive forms, but they differ from the immune-mediated vesiculobullous disease group, which includes vulvar pemphigus, benign familial pemphigus, pemphigoid, linear IgA disease, and dermatitis herpetiformis. Vulvar ulcers can occur in dermatoses resulting from systemic disease (Behçet's syndrome, lupus, pellagra, and Reiter's disease) or malignancies resembling dermatoses (extramammary Paget's disease, squamous cell carcinoma, and vulvar intraepithelial neoplasia). Many vulvar dermatoses itch or burn. Vulvodynia occurs with irritant and allergic dermatitis, vulvar dermatoses, complications of steroid use, candidiasis, papillomatosis, vestibulitis, or essential (dysesthetic) vulvodynia. Diagnostic tests (potassium hydroxide, cultures, and biopsy) should establish the diagnosis and therapy should be specific. Few skin diseases are curable but all are treatable; effective management is defined by whether a medication reliably controls outbreaks or symptoms when it is used. Patience is recommended, because treatment may take weeks or months.
Etretinate: therapy for plasma cell vulvitis.
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A case of vulvitis circumscripta plasmacellularis positive for herpes simplex type II antigen.
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[Ulcerating vulvitis--a rare complication in abdominal typhus].
This article describes the clinical pattern and course of an ulcerating vulvovaginitis occurring within the overall clinical picture of a case of typhus abdominalis as a now rare complication of that severe infectious disease.
Ulcerative vulvitis in atypical Reiter's syndrome.
We report a case of atypical Reiter's syndrome occurring in a female patient who had severe, ulcerative vulvar disease develop in association with conjunctivitis, low back pain, stomatitis, and psoriasiform skin lesions. Vulvar lesions have rarely been described in Reiter's syndrome and are not well characterized.