Sujet(s)
Infections à coronavirus/anatomopathologie , Dermatoses du pied/anatomopathologie , Pneumopathie virale/anatomopathologie , Adolescent , Adulte , Betacoronavirus , COVID-19 , Infections à coronavirus/épidémiologie , Érythème/anatomopathologie , Érythème/virologie , Femelle , Dermatoses du pied/virologie , Humains , Italie/épidémiologie , Mâle , Adulte d'âge moyen , Pandémies , Pneumopathie virale/épidémiologie , SARS-CoV-2 , Vascularite/anatomopathologie , Vascularite/virologieRÉSUMÉ
Hidradenoma papilliferum (HP) is a rare, slow-growing, benign adnexal tumour with apocrine differentiation. It usually affects the anogenital region in adult women and is clinically polymorphous, mimicking other benign or malignant neoformations. The dermoscopic features of vulval HP have not been reported yet. We report the clinical and dermoscopic features in a case series of histopathologically proven vulval HPs. Dermoscopy may be a useful tool for the diagnosis of vulval HP. To our knowledge, our paper represents the first report of dermoscopic findings in a series of vulval HPs in a multiracial population.
Sujet(s)
Dermoscopie/méthodes , Cuir chevelu/anatomopathologie , Tumeurs des glandes sudoripares/anatomopathologie , Adénomes tubulaires/diagnostic , Tumeurs de la vulve/anatomopathologie , Adulte , Sujet âgé , Carcinome épidermoïde/diagnostic , Carcinome épidermoïde/anatomopathologie , Choristome/diagnostic , Choristome/épidémiologie , Choristome/anatomopathologie , Dermoscopie/statistiques et données numériques , Diagnostic différentiel , Porocarcinome eccrine/diagnostic , Porocarcinome eccrine/anatomopathologie , Femelle , Humains , Inde/épidémiologie , Italie/épidémiologie , Mâle , Adulte d'âge moyen , Maladie de Paget extramammaire/diagnostic , Maladie de Paget extramammaire/anatomopathologie , Études rétrospectives , Adénomes tubulaires/ethnologie , Adénomes tubulaires/chirurgieRÉSUMÉ
BACKGROUND: Vulvar melanoma (VM) is rare and is often diagnosed late. Dermoscopy may aid in its recognition, differentiating VM from other more common vulvar lesions, such as melanosis and naevi. However, little is known about the dermoscopic features of thin VM. AIM: To retrospectively analyse a series of histopathologically diagnosed thin VMs and to highlight their most suggestive dermoscopic features. METHODS: A multicentre, retrospective study was conducted, including histopathologically proven thin VMs, either intraepidermal or with Breslow thickness ≤ 0.5 mm, diagnosed during the period 2016-2018. We particularly focused on their dermoscopic characteristics to highlight the most suggestive dermoscopic diagnostic clues. RESULTS: In total, 14 cases of early-stage VM were included, in women with a mean age at diagnosis of 64.86 years. The most frequently affected sites were the labia minora. Of these, 11 cases were unifocal. Dermoscopy most often revealed structureless areas, grey globules and areas, irregular black-brown dots, blue and white structures, and red areas. CONCLUSIONS: In our experience, early-stage VM often exhibits dermoscopic features that are more typical of thicker cutaneous melanomas. Dermoscopy may provide useful clues for the prompt diagnosis of thin VM.
Sujet(s)
Dermoscopie , Mélanome/anatomopathologie , Vulve/anatomopathologie , Tumeurs de la vulve/anatomopathologie , Sujet âgé , Sujet âgé de 80 ans ou plus , Dermoscopie/méthodes , Femelle , Système génital de la femme/anatomopathologie , Humains , Mélanome/diagnostic , Adulte d'âge moyen , Études rétrospectives , Tumeurs de la vulve/diagnosticSujet(s)
Carcinome épidermoïde/anatomopathologie , Dermoscopie/méthodes , Tumeurs de la vulve/anatomopathologie , Sujet âgé de 80 ans ou plus , Carcinome épidermoïde/imagerie diagnostique , Carcinome épidermoïde/ultrastructure , Femelle , Humains , Adulte d'âge moyen , Invasion tumorale/anatomopathologie , Tumeurs de la vulve/imagerie diagnostiqueSujet(s)
Épithélioma in situ/diagnostic , Carcinome épidermoïde/diagnostic , Tumeurs de la vulve/diagnostic , Épithélioma in situ/anatomopathologie , Carcinome épidermoïde/anatomopathologie , Couleur , Diagnostic différentiel , Femelle , Humains , Invasion tumorale , Vulve/anatomopathologie , Tumeurs de la vulve/anatomopathologieSujet(s)
dGTPases/génétique , Mélanome/génétique , Protéines membranaires/génétique , Mutation/génétique , Ongles/anatomopathologie , Protéines proto-oncogènes B-raf/génétique , Protéines proto-oncogènes c-kit/génétique , Sujet âgé , Sujet âgé de 80 ans ou plus , Démographie , Femelle , Humains , Mâle , Adulte d'âge moyenRÉSUMÉ
Nail Apparatus Melanoma (NAM) is rare, particularly in Caucasians. Understanding its pathogenesis and collecting epidemiologic data may be difficult due to its location and the exiguity of the case series of this cancer. Cutaneous melanoma has been thought related to UV radiation, and NAM is considered an acral variant of melanoma, even if the nail presents a specific anatomy. Little is reported about pathogenesis, except reports suggesting traumatic injuries as a causal factor. UV exposure is debated in nail melanoma because of its structure. The nail is, in fact, a unique structure with sun-exposed and non exposed melanocytes. NAM arises from the nail melanocytes, located in the nail matrix, which is the germinative part of the nail and composed of a proximal and distal portion. The proximal nail matrix lays under the proximal nail fold that covers it and is non-sun exposed, while the distant nail matrix, clinically visible as the lunula, is sun-exposed, though lying underneath the nail plate. According to these anatomical data, NAM is a distinct melanoma type, and studies need to classify it as acral melanoma or as a particular type of melanoma with its own pathogenesis and prognostic criteria. This study investigates potential risk factors of NAM, emphasizing (i) trauma and (ii) UV exposure among our NAM patients.