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1.
Hand Surg Rehabil ; 42(6): 549-552, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37714516

RESUMO

Cutaneous myoepithelioma is a rare neoplasm of the skin that has become more widely recognized in recent years despite significant diagnostic pitfalls. It is a benign neoplasm with a high recurrence rate if not excised radically, and must be distinguished from its malignant counterpart. Few cases have been described so far and, to our knowledge, no cases in the finger of a child exist in the literature. We report the case of a 15 year-old boy affected by a rare form of locally aggressive spindle-cell myoepithelioma, and suggest a new multidisciplinary approach combining surgical excision and custom brachytherapy.


Assuntos
Mioepitelioma , Neoplasias Cutâneas , Masculino , Criança , Humanos , Adolescente , Mioepitelioma/cirurgia , Mioepitelioma/diagnóstico , Mioepitelioma/patologia , Neoplasias Cutâneas/cirurgia , Neoplasias Cutâneas/patologia , Dedos , Extremidade Superior/patologia
2.
Dermatol Ther ; 23 Suppl 1: S20-3, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20136917

RESUMO

Benign skin diseases have seldom been treated with radiotherapy, unless resistant to other treatments. Eccrine syringofibroadenoma (ESFA) is a rare benign eccrine tumor. ESFA very rarely presents bilateral lesions, and seldom a nonsurgical treatment has been proposed. An exceptional case of bilateral ESFA of the foot is presented; radiotherapy was effective in treating both lesions with good cosmetic results.


Assuntos
Glândulas Écrinas , Fibroadenoma/radioterapia , Doenças do Pé/radioterapia , Neoplasias das Glândulas Sudoríparas/radioterapia , Siringoma/radioterapia , Idoso , Feminino , Fibroadenoma/complicações , Fibroadenoma/patologia , Doenças do Pé/complicações , Doenças do Pé/patologia , Humanos , Obesidade/complicações , Neoplasias das Glândulas Sudoríparas/complicações , Neoplasias das Glândulas Sudoríparas/patologia , Siringoma/complicações , Siringoma/patologia
4.
J Cutan Med Surg ; 8(2): 122-5, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15129317

RESUMO

BACKGROUND: Nail psoriasis is a common problem in psoriatic patients and often it is difficult to cure. Several treatments have been proposed in the last decade using new molecules like vitamin-D analog and/or immunosoppressive drugs both systemically and locally. OBJECTIVE: Our goal was to evaluate a combination of cyclosporin and topical calcipotriol cream versus cyclosporin alone in a matched group of patients treated with cyclosporin alone. METHOD: Fifty-four patients affected by severe psoriasis and nail involvement were selected and matched for severity of nail involvement, sex, age, and cyclosporin dosage. Group A included 21 patients treated with cyclosporin alone (3.5 mg/kg/day) for three months. Group B included 33 patients treated with the same cyclosporin dosage plus, for the same time, topical application of calcipotriol cream twice a day. Evaluation for clinical improvement was the personal feeling of the patient after three months, while clinical appearance of the lesions was evaluated by the same dermatologist using digital pictures and who was blind as to the treatment of the patient. A score ranging from + to +++ was used in order to evaluate the improvement, and data were statistically evaluated with the Wilcoxon test. RESULTS: Both cyclosporin alone and a combination of cyclosporin with topical calcipotriol twice a day were useful for treating nail psoriasis after three months of therapy although the combined therapy showed a better overall result in both mild and severe nail psoriasis. Improvement of the clinical appearance of the nail lesions was seen in about 79% of patients in group B (p < or = 0.0004) versus about 47% of patients in group A (p < or = 0.15). CONCLUSIONS: In patients with severe involvement of nail psoriasis we suggest the use of a combination of topical calcipotriol twice a day with systemic treatment such as cyclosporine.


Assuntos
Calcitriol/análogos & derivados , Calcitriol/administração & dosagem , Ciclosporina/administração & dosagem , Fármacos Dermatológicos/administração & dosagem , Doenças da Unha/tratamento farmacológico , Psoríase/tratamento farmacológico , Administração Oral , Administração Tópica , Adulto , Quimioterapia Combinada , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Método Simples-Cego
5.
J Am Acad Dermatol ; 50(5): 657-75; quiz 676-8, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-15097948

RESUMO

UNLABELLED: Interleukin 10 (IL-10) is a key cytokine produced by a multitude of immune effector cells and possesses distinct regulatory effects on immune functioning in the skin. In this article we report the current understanding of the immunobiology of IL-10 and identify the role of IL-10 in cutaneous infection as well as in autoimmune and neoplastic processes. We reviewed the literature to examine the function of IL-10 in different cutaneous disorders. IL-10 can influence and potentially treat T1/T2 differentiation, antigen-presenting cell functioning, antigen-presenting cell-mediated T-cell activation, and T-cell, B-cell, and mast cell growth and differentiation that is aberrant in various disease processes. The literature consensus is that the multitude of effects of IL-10 contribute to the pathogenesis of different skin disorders. In certain circumstances IL-10 could represent novel therapeutic approaches to treating cutaneous diseases. LEARNING OBJECTIVE: At the conclusion of this learning activity, participants should be acquainted with the role of IL-10 in many infectious diseases, autoimmune skin disease, inflammatory processes, and malignancy. Its possible role in the resolution of various skin diseases should be better understood.


Assuntos
Interleucina-10/fisiologia , Dermatopatias/fisiopatologia , Animais , Doenças Autoimunes/imunologia , Doenças Autoimunes/fisiopatologia , Dermatite/imunologia , Dermatite/fisiopatologia , Humanos , Interleucina-10/imunologia , Interleucina-10/uso terapêutico , Psoríase/imunologia , Psoríase/fisiopatologia , Pele/imunologia , Dermatopatias/imunologia , Dermatopatias/terapia , Dermatopatias Infecciosas/imunologia , Dermatopatias Infecciosas/fisiopatologia , Neoplasias Cutâneas/imunologia , Neoplasias Cutâneas/fisiopatologia
6.
Exp Dermatol ; 12(4): 466-71, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12930304

RESUMO

The role of urokinase type plasminogen activator (uPA) has been well documented in the pathogenesis of pemphigus vulgaris (PV). Activation of plasminogen into active serine protease plasmin initiates extracellular proteolysis leading to acantholysis but the mechanisms underlying this process are not clearly understood. We have previously shown that keratinocyte derived cytokines IL-1alpha and TNF-alpha are involved in PV-induced acantholysis. In the present study we sought to examine whether keratinocyte-derived IL-1alpha and TNF-alpha are correlated with uPA induction in keratinocytes during acantholysis. Normal human keratinocytes were incubated with diluted PV serum. mRNAs for IL-1alpha, TNF-alpha and uPA were examined with RT-PCR at various time points and acantholysis was measured. IL-1alpha, TNF-alpha and uPA mRNAs were all induced in keratinocytes following PV serum stimulation; IL-1alpha/TNF-alpha mRNAs' expression was earlier than the expression of uPA mRNA. To further examine the role of IL-1alpha, TNF-alpha and uPA in acantholysis, we performed antibody blocking studies. Anti-IL-1alpha, anti-TNF-alpha and anti-uPA antibodies suppressed acantholysis by 76%, 80% and 90%, respectively. In addition, anti-IL-1alpha and anti-TNF-alpha antibodies inhibited uPA mRNA induction, whereas anti-uPA antibodies did not alter IL-1alpha/TNF-alpha mRNAs' expression. Our results confirm the role of uPA in acantholysis and suggest an involvement of IL-1alpha/TNF-alpha in uPA induction.


Assuntos
Acantólise/etiologia , Interleucina-1/genética , Queratinócitos/imunologia , Queratinócitos/metabolismo , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Fator de Necrose Tumoral alfa/genética , Ativador de Plasminogênio Tipo Uroquinase/genética , Acantólise/genética , Acantólise/imunologia , Acantólise/metabolismo , Anticorpos Bloqueadores/farmacologia , Sequência de Bases , Linhagem Celular , DNA Complementar/genética , Humanos , Imunoglobulina G/farmacologia , Técnicas In Vitro , Interleucina-1/antagonistas & inibidores , Pênfigo/etiologia , Pênfigo/genética , Pênfigo/imunologia , Pênfigo/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Necrose Tumoral alfa/antagonistas & inibidores
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