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1.
J Dermatolog Treat ; 33(2): 1047-1062, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32705920

RESUMO

INTRODUCTION: Penile intraepithelial neoplasia (PeIN) is a histological term for precancerous penile lesions. PeIN is important due to the high morbidity and mortality associated with progression to penile squamous cell carcinoma (PSSC). But PeIN is rare, contributing to a limited evidence-base for the relative efficacy of available treatment options. OBJECTIVES & METHODS: To consolidate and expand knowledge about PeIN and its treatment, we describe the clinical and histological characteristics, treatments and outcomes of 345 patients with PeIN, managed by our multidisciplinary team. Our results are compared and contrasted with those in the literature, following comprehensive review. RESULTS: 8.7% of patients had concomitant, invasive PSCC, whilst 91.3% demonstrated PeIN alone. 84% had undifferentiated PeIN, and 10.7% differentiated PeIN (5.2%, not specified). Clinical or histological evidence of HPV alone was present in 58%; features of lichen sclerosus alone in 12%; features of both in 29.4%. Only 14.4% of patients could be treated solely with topical agents or cryotherapy, whereas the remaining 85.6% underwent some form of surgical intervention, circumcision being the mainstay. Just 2.6% progressed to PSCC. CONCLUSIONS: Clinical management of PeIN can be rationally optimized with excellent outcomes. Circumcision is important. Topical treatments alone are disappointing.


Assuntos
Carcinoma in Situ , Líquen Escleroso e Atrófico , Neoplasias Penianas , Neoplasias Cutâneas , Carcinoma in Situ/patologia , Carcinoma in Situ/terapia , Humanos , Líquen Escleroso e Atrófico/patologia , Líquen Escleroso e Atrófico/terapia , Masculino , Neoplasias Penianas/patologia , Neoplasias Penianas/terapia , Pênis/patologia , Neoplasias Cutâneas/patologia
3.
Br J Dermatol ; 184(1): 25-33, 2021 01.
Artigo em Inglês | MEDLINE | ID: mdl-32163590

RESUMO

BACKGROUND: Erosive pustular dermatosis of the scalp (EPDS) is a chronic condition characterized by erosive plaques and subsequent scarring alopecia as a result of local trauma or inflammation. A number of therapeutic approaches have been described in the literature but there is no consensus of opinion on optimal treatment of the disease. OBJECTIVES: To provide evidence-based recommendations for topical and systemic treatment of adult patients with EPDS by performing a systematic review. METHODS: The MEDLINE, MEDLINE In-Process, Embase and Cochrane databases were searched from inception to 26 June 2019 in accordance with the PRISMA guidelines for studies involving adult patients treated for EPDS with at least one reported response to treatment. The study was registered on PROSPERO. Texts were reviewed independently by two authors. The risk of bias and quality of the studies were assessed using the Quality Appraisal Checklist for Case Series Studies. RESULTS: In total 75 studies were included, involving 168 patients. Many treatments have been reported in the literature, with varying degrees of therapeutic success. The results were highly heterogeneous and methodological quality was very low. We were unable to perform a meta-analysis on the data. CONCLUSIONS: The limited available evidence supports use of topical corticosteroids, with or without oral zinc, followed by maintenance therapy with topical calcineurin inhibitors as being effective in managing this condition. Topical photodynamic therapy is also potentially beneficial in the management of EPDS. Prospective, comparative, randomized controlled trials are required in order to provide further evidence to guide treatment.


Assuntos
Dermatoses do Couro Cabeludo , Couro Cabeludo , Alopecia , Inibidores de Calcineurina , Humanos , Estudos Prospectivos , Dermatoses do Couro Cabeludo/tratamento farmacológico
8.
Trop Med Int Health ; 22(8): 994-999, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28609809

RESUMO

OBJECTIVE: To describe characteristics, presentation, time to diagnosis and diagnostic findings of patients with intestinal tuberculosis (ITB) in a low-burden country. METHOD: Retrospective study of 61 consecutive ITB patients diagnosed between 2008 and 2014 at a large East London hospital. RESULTS: Forty of sixty-one patients were male. Mean age was 34.6 years. 93% of patients were born abroad, mostly from TB-endemic areas (Indian subcontinent: 88%, Africa: 9%). 25% had concomitant pulmonary TB. Median time from symptom onset to ITB diagnosis was 13 weeks (IQR 3-26 weeks). Ten patients were initially treated for IBD, although patients had ITB. The main sites of ITB involvement were the ileocaecum (44%) or small bowel (34%). Five patients had isolated perianal disease. Colonoscopy confirmed a diagnosis of ITB in 77% of those performed. 42 of 61 patients had a diagnosis of ITB confirmed on positive histology and/or microbiology. CONCLUSION: Diagnosis of ITB is often delayed, which may result in significant morbidity. ITB should be excluded in patients with abdominal complaints who come from TB-endemic areas to establish prompt diagnosis and treatment. Diagnosis is challenging but aided by axial imaging, colonoscopy and tissue biopsy for TB culture and histology.


Assuntos
Intestinos/patologia , Tuberculose Gastrointestinal/diagnóstico , Dor Abdominal/diagnóstico , Dor Abdominal/etiologia , Adulto , África/etnologia , Doenças do Ânus/etiologia , Demografia , Diagnóstico Diferencial , Emigrantes e Imigrantes , Feminino , Humanos , Índia/etnologia , Intestinos/microbiologia , Londres/epidemiologia , Masculino , Estudos Retrospectivos , Migrantes , Tuberculose Gastrointestinal/complicações , Tuberculose Gastrointestinal/epidemiologia , Tuberculose Gastrointestinal/microbiologia , Tuberculose Pulmonar/complicações
9.
Clin Exp Dermatol ; 42(2): 189-191, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28052370

RESUMO

We report the case of a 24-year-old woman with an 8-month history of deep pelvic pain and postcoital bleeding. Examination revealed desquamation of the vaginal epithelium with tender fissured plaques in the vagina, initially thought to be vaginal intraepithelial neoplasia. Histology showed squamous mucosa with suprabasal acantholysis and hyperkeratosis, and no evidence of viral infection, dysplasia or malignancy. These findings were consistent with acantholytic dermatosis (AD), a rare lesion that resembles Hailey-Hailey and Darier disease histopathologically, but can be distinguished on a clinical basis. Vulval cases of AD are well recognized, but to our knowledge, this is the first reported case involving the vaginal epithelium alone.


Assuntos
Acantólise/diagnóstico , Doenças Vaginais/diagnóstico , Acantólise/patologia , Biópsia , Colposcopia , Diagnóstico Diferencial , Epitélio/patologia , Feminino , Humanos , Vagina/patologia , Doenças Vaginais/patologia , Adulto Jovem
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