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1.
Am J Dermatopathol ; 45(6): 388-390, 2023 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-36939134

RESUMO

ABSTRACT: Halo nevus is a benign type of melanocytic nevi commonly found in children and manifests as a central pigmented part surrounded by a well-defined hypopigmented area. Halo nevi are commonly located on the trunk. The central nevus may show partial or complete regression, whereas the associated halo may persist or enlarge. The term 'agminated nevus' refers to a cluster of melanocytic nevi restricted to an area of the body and commonly reported with acquired melanocytic nevi, blue nevi, and Spitz nevi. To the best of our knowledge, agminated halo nevus has not been previously described. We hereby report 2 cases with clinical and histopathologic findings consistent with the diagnosis of agminated halo nevus.


Assuntos
Nevo de Células Epitelioides e Fusiformes , Nevo com Halo , Nevo Pigmentado , Nevo , Neoplasias Cutâneas , Criança , Humanos , Neoplasias Cutâneas/patologia , Nevo Pigmentado/patologia
2.
Am J Dermatopathol ; 44(1): 7-16, 2022 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-34783707

RESUMO

ABSTRACT: Granular cell tumors (GCTs) are rare soft tissue tumors of Schwann cell origin that manifest as papulonodular lesions and occur mainly in adults. The diagnosis is usually confirmed by histopathology. Most of GCTs are benign, but some lesions may exhibit malignant criteria. This study is a retrospective case series including all children with histopathologically documented multiple GCTs who attended the dermatology department of the university hospitals between February 2008 and March 2021. The objective of our study was to raise awareness to this unrecognized and rare entity in such age group. The study included 9 patients (6 girls and 3 boys) with multiple GCTs. Their age ranged between 5 and 13 years. The lesions were skin-colored to light brown, firm, smooth-surfaced nodules. Most of the lesions were on the extremities, and their mean diameter was 160.5 mm2. None of the lesions exhibited any malignant criteria on histopathology. No extracutaneous or mucosal lesions were detected. Dermatologists should be aware of this rare condition in children because early recognition allows more conservative resection of the tumor and less invasive reconstruction of the defect. Our study highlights that multifocality does not necessarily indicate malignancy or other systemic comorbidities.


Assuntos
Tumor de Células Granulares/patologia , Neoplasias Cutâneas/patologia , Adolescente , Idade de Início , Criança , Pré-Escolar , Feminino , Tumor de Células Granulares/cirurgia , Humanos , Masculino , Estudos Retrospectivos , Neoplasias Cutâneas/cirurgia
3.
J Cutan Pathol ; 48(7): 925-927, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33595129

RESUMO

Spotted grouped pigmented nevus is a distinct form of non-giant congenital melanocytic nevi. Histopathologically, it tends to proliferate around the skin appendages. We report a case of a 10-year-old boy with clinical and pathological findings consistent with the diagnosis of spotted grouped pigmented nevus of more than 20 cm diameter, which is considered giant.


Assuntos
Melanócitos/patologia , Melanoma/prevenção & controle , Nevo Pigmentado/diagnóstico , Neoplasias Cutâneas/patologia , Biópsia/métodos , Criança , Diagnóstico Diferencial , Seguimentos , Humanos , Masculino , Melanoma/patologia , Nevo Pigmentado/congênito
5.
Arch Dermatol Res ; 316(8): 556, 2024 Aug 23.
Artigo em Inglês | MEDLINE | ID: mdl-39177703

RESUMO

Entrustable professional activities (EPAs) are units of professional practice that could be observed, assessed, monitored, documented, and entrusted. EPAs when entrusted, outline the physician's qualifications, and shape the scope of practice. This insight highlights the importance of development of EPAs in all medical specialties including dermatology to ensure the best standards for patient's care. Development of EPAs-based training program is considered a challenge for clinical educators. In this paper, we describe practical tips and reflections on our experience in developing EPAs in dermatology doctoral training program that could be a guide for dermatology educators to implement EPAs in dermatology training programs.


Assuntos
Competência Clínica , Dermatologia , Educação de Pós-Graduação em Medicina , Dermatologia/educação , Humanos , Educação de Pós-Graduação em Medicina/métodos , Currículo , Docentes de Medicina/educação
6.
J Cutan Pathol ; 40(4): 397-404, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23379648

RESUMO

Hypopigmented mycosis fungoides (HMF) is uncommon clinical variant that was commonly observed in dark-skinned individuals. We described the clinical characteristics, pathological features, immunohistochemical profile and prognosis of HMF in Egyptian patients. During the period from January 2004 to December 2011, we were able to diagnose and follow up 27 patients with HMF. The study included 18 males (66.7%) and 9 females (33.3%) with a mean age of 35.39 ±13.13 years. The duration ranged from 1 to 6 years with a mean of 3.26 ±1.7 years. The majority of patients were skin type IV (63%) and presented with multiple (88.9%), asymptomatic (74.1%), ill-defined (70.4%) and non-scaly (77.8%) lesions distributed on the trunk (81.5%). Histologically, epidermotropic lymphocytes were observed in 100%, basal alignment of lymphocytes in 81.5%, Pautrier's microabscesses in 29% and folliculotropism in 18.5%. Immunostaining showed predominance of epidermal CD8+ cells in 51.9% while in 29.6% CD4+ cells were predominant. Phototherapy was effective in 86.7% of patients with success rate 66.7% of narrow band (NB) ultraviolet-B and 80% of psoralen ultraviolet-A. HMF among Egyptians could be classified as non-aggressive epidermotropic cytotoxic CD8+ variant. It is common among middle age males with skin type IV and mostly well respond to phototherapy.


Assuntos
Micose Fungoide/patologia , Transtornos da Pigmentação/patologia , Neoplasias Cutâneas/patologia , Adulto , Comorbidade , Egito/epidemiologia , Feminino , Humanos , Masculino , Micose Fungoide/epidemiologia , Micose Fungoide/terapia , Fototerapia , Transtornos da Pigmentação/epidemiologia , Transtornos da Pigmentação/terapia , Neoplasias Cutâneas/epidemiologia , Neoplasias Cutâneas/terapia , Pigmentação da Pele , Resultado do Tratamento
7.
Arch Dermatol Res ; 315(6): 1649-1654, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-36781459

RESUMO

Syringoma is rare disease that in classical variant occurs mainly on lower eyelids. In previously published researches, there is increasing evidence that eruptive syringomas must be discussed as an inflammatory dermal reaction pattern. And there was a proposal to change a name from eruptive syringoma to reactive syringomatous proliferation in appropriate cases. We conduct retrospective study on histopathological archived material to study the histopathological findings in cases of eruptive syringomas and correlate it with hypothesis that eruptive syringomas is not true adnexal neoplasms "de novo" but a hyperplastic response of the acrosyringium to an inflammatory process.According to obtained data and literature correlation, we can conclude that there is apparent diversity in eruptive syringomas. Part of cases can be calculated as neoplastic lesions arising "de novo," and another part as reactive syringomatous proliferation due to preceding cutaneous inflammatory process. Thus, term "eruptive syringoma" may be changed in appropriate cases to a "reactive syringomatous proliferation."Clinical variants of eruptive syringoma with evidence of underlying inflammatory process may be more responsive on types of treatments used for inflammatory disorders. Thus, more global clinicopathological correlative researches should be conducted and classification with terminology should be appropriately changed.


Assuntos
Dermatite , Neoplasias das Glândulas Sudoríparas , Siringoma , Humanos , Siringoma/diagnóstico , Siringoma/patologia , Neoplasias das Glândulas Sudoríparas/diagnóstico , Neoplasias das Glândulas Sudoríparas/patologia , Estudos Retrospectivos , Pele/patologia , Inflamação
8.
J Cancer Res Clin Oncol ; 149(7): 3121-3129, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-35870014

RESUMO

PURPOSE: Basal cell carcinoma (BCC) is the most diagnosed type of cancer accounting for 80% of all keratinocyte malignancies. However, the exact demographic properties and clinicopathological criteria for BCC in Egyptians are not clearly reported. Our aim is to report and analyze the epidemiological and clinicopathological features of BCC in Egyptians. METHODS: We retrospectively reviewed the medical records for patients diagnosed pathologically with BCC during the period from January 2017 to December 2021. Data were recruited from four dermatology centers with different geographical distributions. RESULTS: We registered 544 patients. Their age ranged between 22-91 years with a mean of 61.6 ± 13.2 years. Females showed younger age of onset. The mean duration of the tumor was 3.9 ± 3.8 years. The most common involved region was the head (79.4%), and about one third of patients (32.2%) had a giant lesion (> 5 cm). The most common clinical presentation was ulcerative lesions (44.9%). Pathologically, the nodular type represented the most common variant (50.4%). CONCLUSION: Our results proposed that the annual incidence of BCC is increasing among Egyptians. Ultraviolet radiation is considered a high-risk factor of BCC leading to a higher affection of the head region and more prevalence in men. This study also highlights some criteria of BCC in Egyptians such as the long duration of the tumor, the early onset in females, the higher percentage of giant types, and the predominance of nodular type. To our knowledge, this is the first report describing the characteristic features of BCC among Egyptians.


Assuntos
Carcinoma Basocelular , Neoplasias Cutâneas , Masculino , Feminino , Humanos , Adulto Jovem , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Neoplasias Cutâneas/epidemiologia , Neoplasias Cutâneas/patologia , Estudos Retrospectivos , Raios Ultravioleta , Egito/epidemiologia , Carcinoma Basocelular/epidemiologia , Carcinoma Basocelular/patologia
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