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1.
Int J Mol Sci ; 23(2)2022 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-35055124

RESUMEN

Sézary syndrome is an aggressive leukemic variant of cutaneous T-cell lymphomas, characterized by erythroderma, lymphadenopathy, and peripheral blood involvement by CD4+ malignant T-cells. The pathogenesis of Sézary syndrome is not fully understood. However, the course of the disease is strongly influenced by the tumor microenvironment, which is altered by a combination of cytokines, chemokines, and growth factors. The crosstalk between malignant and reactive cells affects the immunologic response against tumor cells causing immune dysregulation. This review focuses on the interaction of malignant Sézary cells and the tumor microenvironment.


Asunto(s)
Síndrome de Sézary/patología , Neoplasias Cutáneas/patología , Linfocitos T CD4-Positivos/metabolismo , Linfocitos T CD8-positivos/metabolismo , Humanos , Síndrome de Sézary/inmunología , Neoplasias Cutáneas/inmunología , Microambiente Tumoral
3.
An Bras Dermatol ; 98(5): 571-579, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37142464

RESUMEN

Cutaneous metastases from solid tumors are uncommon events in clinical practice. Most of the time, the patient already has the diagnosis of a malignant neoplasm when the cutaneous metastasis is detected. However, in up to one-third of cases, cutaneous metastasis is identified before the primary tumor. Therefore, its identification may be essential for starting treatment, although it is usually indicative of poor prognosis. The diagnosis will depend on clinical, histopathological, and immunohistochemical analysis. Sometimes the identification of the primary site is difficult; however, a thorough analysis using imaging tests and constant surveillance is important.


Asunto(s)
Neoplasias Cutáneas , Humanos , Neoplasias Cutáneas/patología
4.
Transpl Immunol ; 64: 101355, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-33264680

RESUMEN

Solid organ transplant recipients (SOTRs) are susceptible to various cutaneous side effects as a consequence of long-term immunosuppressive therapy. Skin cancers and infections are well-studied complications that can cause death and/or allograft rejection. Other cutaneous drug reactions, such as inflammatory manifestations, have a high prevalence but are rarely studied. We analyzed these manifestations' prevalence and their association with immunosuppressants in transplant recipients from a Brazilian tertiary center. Among 532 SOTRs followed at our dermatology clinic, 60 (11.3%) developed some cutaneous adverse reactions to the immunosuppressants, with a median age at transplantation of 50.5 years and a median life span posttransplantation of seven years. Acneiform eruption was the most common drug reaction found (21 patients, 30.4%), followed by diffuse non-scarring alopecia (16 patients, 23.1%), lymphedema (10 patients, 14.5%), gingival hyperplasia (7 patients, 10.1%), hypertrichosis (6 patients, 8.7%) and sebaceous hyperplasia (9 patients, 13.1%). Adequate immunosuppression is an essential prerequisite for successful organ transplantation. In the immediate post-transplant period, significant immunosuppression is needed, but after that, the complications of excessive immunosuppression outweigh the risk of organ rejection. SORTs may present with a broad spectrum of inflammatory and cosmetic findings due to immunosuppressants that can impair life quality.


Asunto(s)
Erupciones Acneiformes/epidemiología , Alopecia/epidemiología , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/epidemiología , Rechazo de Injerto/tratamiento farmacológico , Inmunosupresores/efectos adversos , Linfedema/epidemiología , Trasplante de Órganos , Piel/patología , Erupciones Acneiformes/etiología , Adolescente , Adulto , Anciano , Brasil/epidemiología , Femenino , Humanos , Inmunosupresores/uso terapéutico , Masculino , Persona de Mediana Edad , Piel/efectos de los fármacos , Adulto Joven
5.
An Bras Dermatol ; 96(3): 324-327, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33781647

RESUMEN

Systemic amyloidosis secondary to psoriatic arthritis is rare, and published data are based mainly on case reports and are associated with increased mortality. This is the report of a patient with long-term psoriatic arthritis and chronic sialadenitis, who showed an inadequate response to therapy. The diagnosis of secondary amyloidosis was attained through biopsies of genital skin lesions. Although very rare, it is important that dermatologists and general practitioners consider the possibility of amyloidosis in patients with chronic inflammatory diseases, since an early intervention can be implemented, and thus, the prognosis of this condition can be improved.


Asunto(s)
Amiloidosis , Artritis Psoriásica , Amiloidosis de Cadenas Ligeras de las Inmunoglobulinas , Psoriasis , Amiloidosis/complicaciones , Amiloidosis/diagnóstico , Artritis Psoriásica/complicaciones , Humanos , Piel
6.
An Bras Dermatol ; 95(2): 241-243, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32165024

RESUMEN

Sporotrichosis is a deep mycosis of subacute or chronic evolution, caused by the dimorphic fungus of the genus Sporothrix. The treatment is carried out with antifungal orally or intravenously. Therapeutic success can be affected by several factors, such as altered gastrointestinal physiology by surgery. More and more patients are submitted to bariatric surgeries and the literature for the alterations of the absorption of medications in this context is very scarce. We intend to contribute to a better understanding with this case report of cutaneous-lymphatic sporotrichosis in a patient after bariatric surgery without response to itraconazole treatment, even at high doses.


Asunto(s)
Antifúngicos/uso terapéutico , Cirugía Bariátrica/efectos adversos , Itraconazol/uso terapéutico , Esporotricosis/tratamiento farmacológico , Adulto , Femenino , Absorción Gastrointestinal , Humanos , Esporotricosis/patología , Insuficiencia del Tratamiento
7.
Rev Assoc Med Bras (1992) ; 66(10): 1391-1395, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-33174932

RESUMEN

OBJECTIVE: The relationship between the clinicopathological and sociodemographics characteristics of acral melanomas diagnosed at the Hospital do Servidor Público Estadual de São Paulo was analyzed and traced between 1997 and 2016. METHODS: An observational, descriptive, and retrospective study of patients diagnosed with acral melanoma was performed at Hospital do Servidor Público Estadual de São Paulo. Sociodemographic and clinicopathological characteristics were collected and analyzed. RESULTS: Forty-five patients with acral melanomas were found during the evaluation period. Thirty-one were females, and 14 were males (68.89% and 31.3%, respectively). Most of the cases were invasive (88.37%), and the predominant histological subtype was the acral lentiginous (91.11%). The plantar region was the most prevalent (64.44%). The median Breslow index was 3 mm, and there was a tendency towards greater severity in male patients. CONCLUSIONS: Acral site melanomas are detected diagnosed when they reach more advanced stages, which leads to a worse prognosis for patients. Late detection assumes even greater importance in highly mixed and black populations, such as the Brazilian population.


Asunto(s)
Melanoma , Neoplasias Cutáneas , Brasil/epidemiología , Femenino , Humanos , Masculino , Melanoma/epidemiología , Pronóstico , Estudios Retrospectivos , Neoplasias Cutáneas/epidemiología
8.
An Bras Dermatol ; 95(1): 95-97, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31932162

RESUMEN

The Borst-Jadassohn phenomenon is a morphological finding that consists of the presence of well-defined nests of cells located in the spiny stratum of an acanthotic epidermis. One of the neoplasms where this phenomenon is found is hidroacanthoma simplex. This neoplasm is considered the intraepidermal form of the eccrine poroma. Despite its benign nature, malignant transformations are reported. The present article reports a case of hidroacanthoma simplex and discusses the dermoscopy of this phenomenon.


Asunto(s)
Acantoma/diagnóstico por imagen , Acantoma/patología , Neoplasias Cutáneas/diagnóstico por imagen , Neoplasias Cutáneas/patología , Anciano de 80 o más Años , Biopsia , Dermoscopía/métodos , Epidermis/diagnóstico por imagen , Epidermis/patología , Femenino , Humanos
9.
Int J Trichology ; 11(1): 31-33, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30820131

RESUMEN

We report a case of trigeminal trophic syndrome (TTS) on the scalp of a 69-year-old woman. Initially, the diagnosis of pityriasis amiantacea was considered. The review of pathological antecedents and knowledge of TTS were fundamental for the diagnosis of this illness. We performed a brief review on TTS and differential diagnoses.

10.
An. bras. dermatol ; 98(5): 571-579, 2023. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1505673

RESUMEN

Abstract Cutaneous metastases from solid tumors are uncommon events in clinical practice. Most of the time, the patient already has the diagnosis of a malignant neoplasm when the cutaneous metastasis is detected. However, in up to one-third of cases, cutaneous metastasis is identified before the primary tumor. Therefore, its identification may be essential for starting treatment, although it is usually indicative of poor prognosis. The diagnosis will depend on clinical, histopathological, and immunohistochemical analysis. Sometimes the identification of the primary site is difficult; however, a thorough analysis using imaging tests and constant surveillance is important.

11.
An Bras Dermatol ; 93(6): 893-895, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30484539

RESUMEN

Squamoid eccrine ductal carcinoma is a cutaneous malignancy that originates from the eccrine sweat gland. A 76-year-old woman presented with an asymptomatic papule on her nose that had been present for one year. Dermoscopy showed pseudocysts, irregular linear crown vessels, and yellowish-brown globules surrounded by white halos. This is the first dermoscopic description of squamoid eccrine ductal carcinoma. Studies with more cases are needed to confirm the dermoscopic characterization of this tumor.


Asunto(s)
Carcinoma de Células Escamosas/diagnóstico , Glándulas Ecrinas/patología , Neoplasias Cutáneas/patología , Anciano , Carcinoma de Células Escamosas/patología , Carcinoma de Células Escamosas/cirugía , Dermoscopía , Diagnóstico Diferencial , Diagnóstico Precoz , Glándulas Ecrinas/cirugía , Femenino , Humanos , Inmunohistoquímica , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/cirugía
13.
An Bras Dermatol ; 92(6): 836-837, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29364442

RESUMEN

Nevus sebaceous of Jadassohn is a congenital hamartoma that usually affects the scalp and face. Several benign or malignant neoplasias may develop in the lesion and the most common are trichoblastoma, syringocystadenoma papilliferum, and basal cell carcinoma. Trichilemmoma is a benign solid tumor originating from external sheath cells of pilosebaceous follicles. When it is characterized by a central zone of desmoplasia, it is called desmoplastic trichilemmoma. We report a case of a 58-year-old patient who developed a tumor in a sebaceous nevus. We performed a total excision of the lesion. Histopathological diagnosis was compatible with desmoplastic trichilemmoma. Our literature review reveals that the occurrence of trichilemmoma desmoplastic is unusual. Moreover, it can mimic an invasive carcinoma on histological and clinical examinations. This fact confirms the importance of reporting the occurrence of this rare cancer in a nevus sebaceous of Jadassohn.


Asunto(s)
Enfermedades del Cabello/etiología , Enfermedades del Cabello/patología , Folículo Piloso/patología , Nevo Sebáceo de Jadassohn/complicaciones , Nevo Sebáceo de Jadassohn/patología , Carcinoma Basocelular/patología , Femenino , Humanos , Persona de Mediana Edad , Enfermedades Raras , Cuero Cabelludo/patología , Neoplasias Cutáneas/patología
15.
An. bras. dermatol ; 96(3): 324-327, May-June 2021. graf
Artículo en Inglés | LILACS | ID: biblio-1285063

RESUMEN

Abstract Systemic amyloidosis secondary to psoriatic arthritis is rare, and published data are based mainly on case reports and are associated with increased mortality. This is the report of a patient with long-term psoriatic arthritis and chronic sialadenitis, who showed an inadequate response to therapy. The diagnosis of secondary amyloidosis was attained through biopsies of genital skin lesions. Although very rare, it is important that dermatologists and general practitioners consider the possibility of amyloidosis in patients with chronic inflammatory diseases, since an early intervention can be implemented, and thus, the prognosis of this condition can be improved.


Asunto(s)
Humanos , Psoriasis , Artritis Psoriásica/complicaciones , Amiloidosis de Cadenas Ligeras de las Inmunoglobulinas , Amiloidosis/complicaciones , Amiloidosis/diagnóstico , Piel
17.
An. bras. dermatol ; 95(2): 241-243, Mar.-Apr. 2020. graf
Artículo en Inglés | LILACS, Coleciona SUS (Brasil) | ID: biblio-1130855

RESUMEN

Abstract Sporotrichosis is a deep mycosis of subacute or chronic evolution, caused by the dimorphic fungus of the genus Sporothrix. The treatment is carried out with antifungal orally or intravenously. Therapeutic success can be affected by several factors, such as altered gastrointestinal physiology by surgery. More and more patients are submitted to bariatric surgeries and the literature for the alterations of the absorption of medications in this context is very scarce. We intend to contribute to a better understanding with this case report of cutaneous-lymphatic sporotrichosis in a patient after bariatric surgery without response to itraconazole treatment, even at high doses.


Asunto(s)
Humanos , Femenino , Adulto , Esporotricosis/tratamiento farmacológico , Itraconazol/uso terapéutico , Cirugía Bariátrica/efectos adversos , Antifúngicos/uso terapéutico , Esporotricosis/patología , Insuficiencia del Tratamiento , Absorción Gastrointestinal
18.
An. bras. dermatol ; 95(1): 95-97, Jan.-Feb. 2020. graf
Artículo en Inglés | LILACS | ID: biblio-1088711

RESUMEN

Abstract The Borst-Jadassohn phenomenon is a morphological finding that consists of the presence of well-defined nests of cells located in the spiny stratum of an acanthotic epidermis. One of the neoplasms where this phenomenon is found is hidroacanthoma simplex. This neoplasm is considered the intraepidermal form of the eccrine poroma. Despite its benign nature, malignant transformations are reported. The present article reports a case of hidroacanthoma simplex and discusses the dermoscopy of this phenomenon.


Asunto(s)
Humanos , Femenino , Anciano de 80 o más Años , Neoplasias Cutáneas/patología , Neoplasias Cutáneas/diagnóstico por imagen , Acantoma/patología , Acantoma/diagnóstico por imagen , Biopsia , Dermoscopía/métodos , Epidermis/patología , Epidermis/diagnóstico por imagen
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