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1.
Radiographics ; 44(10): e240035, 2024 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-39264836

RESUMEN

Sinonasal neoplasms are a remarkably heterogeneous group, reflecting the numerous tissue types present in the nasal cavity and paranasal sinuses. These entities can be relatively benign (ie, respiratory epithelial adenomatoid hamartoma) or can be exceedingly aggressive (ie, NUT carcinoma). Certain sinonasal tumors have a propensity to spread through local invasion and destruction, while others have a high likelihood of perineural spread. The genetic and molecular mechanisms underlying sinonasal tumor behavior have recently become better understood, and new tumor types have been described using these genetic and molecular data. This has prompted an expansion in the number of tumors included in the World Health Organization fifth edition classification system for head and neck tumors, along with a new classification structure. Radiologists' familiarity with this classification structure is crucial to understanding the expected behavior of these tumors and to collaboration with the multidisciplinary cancer care board in making decisions for optimal patient care. ©RSNA, 2024.


Asunto(s)
Neoplasias de los Senos Paranasales , Humanos , Neoplasias de los Senos Paranasales/diagnóstico por imagen , Neoplasias de los Senos Paranasales/terapia , Grupo de Atención al Paciente , Neoplasias Nasales/diagnóstico por imagen , Neoplasias Nasales/terapia
2.
J Am Acad Dermatol ; 82(3): 628-633, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31325552

RESUMEN

BACKGROUND: Vitiligo is associated with medical conditions, primarily autoimmune disorders; however, only a few studies in the United States have investigated these associations. OBJECTIVE: Our purpose was to investigate the diseases associated with vitiligo in the New York, New York, population and evaluate if these associations differ by race/ethnicity and sex. METHODS: In this retrospective study, we analyzed data collected from the medical records of 1487 vitiligo patients seen at New York University during a 10-year period. RESULTS: Vitiligo patients had a statistically significant higher prevalence of hypothyroidism, multiple sclerosis, rheumatoid arthritis, idiopathic thrombocytopenic purpura, seronegative arthritis, pernicious anemia, myasthenia gravis, inflammatory bowel disease, lymphoma, and systemic lupus erythematosus. Rates of comorbid autoimmune diseases varied by race and sex. LIMITATIONS: Medical charts did not consistently report race/ethnicity, type of vitiligo, and total body surface area affected. Information from nondermatology medical visits was also included. CONCLUSION: This study revealed multiple new disease associations for vitiligo, including multiple sclerosis, idiopathic thrombocytopenic purpura, and lymphoma, as well as confirmed previously reported associations with other autoimmune diseases, the most common being hypothyroidism followed by rheumatoid arthritis. Associations did vary by race/ethnicity and sex.


Asunto(s)
Vitíligo/complicaciones , Estudios Transversales , Femenino , Humanos , Masculino , New York/epidemiología , Prevalencia , Grupos Raciales/estadística & datos numéricos , Estudios Retrospectivos , Factores de Tiempo , Salud Urbana , Población Urbana , Vitíligo/epidemiología
3.
Adv Anat Pathol ; 26(1): 40-55, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30418180

RESUMEN

Inflammatory skin diseases encompass a vast array of conditions. The field continues to expand and evolve with resurgence of conditions, through newly recognized medication adverse effects, and via more detailed descriptions of known dermatoses. The importance of clinicopathologic correlation and an up to date knowledge of dermatologic conditions cannot be overstated. This review focuses on an array of recent important developments in the histologic diagnosis of inflammatory conditions that affect the skin.


Asunto(s)
Enfermedades Autoinmunes/patología , Inflamación/patología , Enfermedades de la Piel/patología , Piel/patología , Anticuerpos/uso terapéutico , Enfermedades Autoinmunes/tratamiento farmacológico , Antígeno B7-H1/inmunología , Antígeno CTLA-4/inmunología , Humanos , Inflamación/tratamiento farmacológico , Enfermedades de la Piel/diagnóstico , Enfermedades de la Piel/tratamiento farmacológico
4.
Am J Dermatopathol ; 41(5): 347-349, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30422830

RESUMEN

"Eosinophils are absent in psoriasis" has been dogma for generations; yet, there is little published to support this statement. Two recent studies examining the presence of eosinophils in psoriasis came to contrasting conclusions. We reviewed skin biopsies from 50 patients with clinically confirmed cases of psoriasis vulgaris to characterize the histologic features, with a focus on the number of eosinophils in the dermis. We noted the presence of eosinophils in nearly half of our study population (n = 23, 46.0%). There was no significant association between the presence of eosinophils and degree of spongiosis (P = 0.405). Eosinophil density ranged from 0 to 8 per tissue section. The mean average eosinophil density was 1.04 (range: 0-8) per tissue section. Among cases with eosinophils, there were 73.9% (n = 17/23) of cases with 1-2 eosinophils, and 26.1% (n = 6) with 3-8 eosinophils. Mild to moderate spongiosis was noted in the majority of cases (n = 48; 96.0%). Eosinophils were only present in psoriasis cases with evidence of spongiosis (n = 23; 47.9%). We conclude that eosinophils are not an uncommon finding in the dermis of psoriasis vulgaris, although the number is often few. The presence of eosinophils should not preclude a diagnosis of psoriasis, particularly if other histologic features are supportive.


Asunto(s)
Eosinófilos/patología , Psoriasis/patología , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad
5.
J Cutan Pathol ; 45(2): 118-121, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-29086985

RESUMEN

BACKGROUND: Calciphylaxis and pseudoxanthoma elasticum (PXE) are rare, clinically distinct disorders that share a common feature of cutaneous calcification and that vary widely in their cutaneous presentation. METHODS: We conducted a descriptive, retrospective review of biopsy specimens collected over a 2-year period. Only specimens with a histologic and clinical diagnosis of calciphylaxis were included in the review. Specimens were then histologically examined for features of PXE in the dermis and/or subcutaneous fat, utilizing hematoxylin and eosin staining. Von Kossa and Verhoeff-Van Gieson special stains were also performed to examine calcification and elastic fibers, respectively. RESULTS: We reviewed 13 biopsy specimens from 9 patients with known clinical and histologic evidence of calciphylaxis, both uremic and non-uremic types. Upon re-examination, we found that 46.2% (n = 6/13) of the specimens showed concomitant PXE-like changes uniquely localized to the subcutaneous fat. CONCLUSION: The presence of PXE-like changes in the subcutis may heighten suspicion for a diagnosis of calciphylaxis in the appropriate clinical setting and be helpful when classic histologic features are subtle or absent.


Asunto(s)
Calcifilaxia/patología , Seudoxantoma Elástico/patología , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Grasa Subcutánea/patología
6.
Dermatol Online J ; 24(12)2018 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-30677798

RESUMEN

We present a case of necrobiosis lipoidica (NL) of the right abdomen in a 75-year-old man. A skin biopsy performed showed a layered infiltrate of mono and multinucleated histiocytes palisaded around degenerated collagen bundles. Laboratory workup was unremarkable. The patient was treated with topical corticosteroids with cessation of progression of his disease, although the eruption did not resolve. There are a number of treatments for NL reported in the literature, all with varying efficacy. Although NL lesions are usually asymptomatic, patients with NL must be monitored closely for signs of ulceration or malignant transformation, in which case more aggressive treatment options may be warranted.


Asunto(s)
Histiocitos/patología , Necrobiosis Lipoidea/patología , Piel/patología , Administración Cutánea , Anciano , Biopsia , Glucocorticoides/uso terapéutico , Humanos , Masculino , Necrobiosis Lipoidea/diagnóstico , Necrobiosis Lipoidea/tratamiento farmacológico , Triamcinolona/uso terapéutico
7.
Dermatol Online J ; 24(12)2018 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-30677795

RESUMEN

The pathophysiology of generalized essential telangiectasia is not well understood. Generalized essential telangiectasia is an uncommon disorder in which widespread telangiectasias of unknown cause develop without associated systemic or antecedent dermatologic disease. We report a case of generalized essential telangiectasia in an otherwise healthy 49-year-old man.


Asunto(s)
Dermatosis del Pie/patología , Dermatosis de la Pierna/patología , Telangiectasia/patología , Dermatosis del Pie/diagnóstico , Humanos , Dermatosis de la Pierna/diagnóstico , Masculino , Persona de Mediana Edad , Telangiectasia/diagnóstico
9.
Dermatol Online J ; 24(8)2018 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-30677850

RESUMEN

Cutaneous Crohn disease (CCD) is a rare dermatologic manifestation of Crohn disease and is defined as noncaseating, granulomatous skin lesions noncontiguous with the gastrointestinal tract. It most commonly affects the skin of the legs, although genital CCD is the most common presentation in children. Diagnosis of CCD is made by a combination of clinical and histopathological findings. Therapeutic options include topical, intralesional, and systemic corticosteroids as well as topical and systemic immunosuppressants and immunomodulators. Surgical excision may be considered for refractory cases. We report CCD in a 9-year old boy with penile swelling, granulomatous cheilitis-like lesions, and perianal plaques.


Asunto(s)
Nalgas/patología , Enfermedad de Crohn/patología , Granuloma/patología , Enfermedades del Pene/patología , Enfermedades de la Piel/patología , Niño , Colonoscopía , Enfermedad de Crohn/diagnóstico , Edema/diagnóstico , Granuloma/diagnóstico , Humanos , Masculino , Enfermedades del Pene/diagnóstico , Enfermedades de la Piel/diagnóstico
11.
J Drugs Dermatol ; 15(11): 1420-1426, 2016 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-28095557

RESUMEN

BACKGROUND: Photodynamic therapy (PDT) is an FDA approved treatment for actinic keratoses (AK's) although multiple off-label indi- cations are reported. Despite frequent use for AK's, no clear consensus exists regarding protocols for overall treatment parameters. METHODS: Retrospective chart review of 1,491 subjects who underwent PDT between 2007 and 2011 at a high volume laser surgery center. Demographic information, clinical history, treatment data, and subsequent diagnosis of skin cancers were recorded. An ex- ploratory subgroup analysis was performed for patients treated for AK and/or squamous cell carcinoma (SCC) that developed SCC or remained SCC-free one year after treatment. RESULTS: The most common indications for PDT were actinic keratoses (n=1404, 94.9%) then NMSC (n=45, 3.0%) The most common treatment site was the head and neck (n=1274, 86.1%). Blue light activation (405-420nm) was used more frequently than red light and visible light. (73.8% vs. 22.8% vs. 6.8%). The most commonly used photosensitizer was aminolevulinic acid (ALA) (98.6%, n=1456). Topical application (97.7% n=1437) of photosensitizer was used more frequently than intralesional administration (2.0%, n=29). 580 patients met subgroup analysis criteria. 66 developed SCC at treatment site (11%). Factors associated with developing SCC were older age, SCC history, Fitzpatrick skin-type 1, and sixty-minute or less incubation times (P less than 0.05 for all factors). The SCC subgroup had a unique distribution of treatment sites (P less than.001). No statistically significant differences were observed for gender or wavelength. CONCLUSION: There are differences in protocols based on indication and location of lesion. Blue light is preferable for superFIcial lesions and red light for deeper lesions. Intralesional delivery is used more commonly for NMSC. Extremities require longer incubation times. PDT may be more effective with younger patients and longer than sixty-minute incubation times. PDT chemoprevention is independent of light source used. J Drugs Dermatol. 2016;15(11):1420-1426..


Asunto(s)
Procedimientos Quirúrgicos Dermatologicos/métodos , Queratosis Actínica/cirugía , Terapia por Láser/métodos , Fotoquimioterapia/métodos , Neoplasias Cutáneas/cirugía , Anciano , Anciano de 80 o más Años , Estudios de Cohortes , Procedimientos Quirúrgicos Dermatologicos/tendencias , Femenino , Humanos , Queratosis Actínica/diagnóstico , Queratosis Actínica/epidemiología , Terapia por Láser/tendencias , Masculino , Persona de Mediana Edad , Fotoquimioterapia/tendencias , Estudios Retrospectivos , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/epidemiología
12.
Dermatol Online J ; 22(12)2016 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-28329552

RESUMEN

Diffuse sebaceous-gland hyperplasia is a rarevariant of sebaceous-gland hyperplasia that isdistinct from the well-known circumscribed type.The term presenile sebaceous hyperplasia has beenutilized to describe this entity that is distinguishedby specific features, which include confluence oflesions that results in the formation of large plaqueson the face, the sparing of periorificial regions, andhighly functional glandular hyperplasia that resultsin excessive sebaceous secretion. We present a43-year-old woman with monomorphous, skincoloredand yellow, smooth 1- to-3-mm papules,some with central umbilication, that spare theperiorificial zones. Histopathologic examination wassuggestive of diffuse sebaceous-gland hyperplasia.Differential diagnosis of this condition is broad andincludes syndromes that are associated with multiplefacial papules and malignant conditions, such asMuire-Torre syndrome and Cowden syndrome. Itis important to be aware of this condition in orderto consider appropriate treatment options, such asisotretinoin and to avoid unnecessary diagnostictests.


Asunto(s)
Dermatosis Facial/diagnóstico , Enfermedades de las Glándulas Sebáceas/diagnóstico , Glándulas Sebáceas/patología , Adulto , Dermatosis Facial/patología , Femenino , Humanos , Hiperplasia , Enfermedades de las Glándulas Sebáceas/patología
13.
Dermatol Online J ; 21(12)2015 Dec 16.
Artículo en Inglés | MEDLINE | ID: mdl-26990335

RESUMEN

Eosinophilic dermatosis of hematologic malignancy is a rare, paraneoplastic phenomenon that presents as a pruritic papular or vesicular eruption that is clinically and histopathologically similar to insect bites. We present a 56-year-old man with multiple relapses of diffuse large B cell lymphoma with a typical presentation of pruritic papules and vesicles on the extremities that correlate with a recent relapse of his lymphoma.


Asunto(s)
Dermatitis/etiología , Eosinofilia/etiología , Linfoma de Células B Grandes Difuso/complicaciones , Piel/patología , Biopsia , Dermatitis/diagnóstico , Eosinofilia/diagnóstico , Humanos , Linfoma de Células B Grandes Difuso/diagnóstico , Masculino , Persona de Mediana Edad
14.
Am J Public Health ; 104(11): e92-9, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25211764

RESUMEN

Although personal melanoma risk factors are well established, the contribution of socioeconomic factors, including clothing styles, social norms, medical paradigms, perceptions of tanned skin, economic trends, and travel patterns, to melanoma incidence has not been fully explored. We analyzed artwork, advertisements, fashion trends, and data regarding leisure-time activities to estimate historical changes in UV skin exposure. We used data from national cancer registries to compare melanoma incidence rates with estimated skin exposure and found that they rose in parallel. Although firm conclusions about melanoma causation cannot be made in an analysis such as this, we provide a cross-disciplinary, historical framework in which to consider public health and educational measures that may ultimately help reverse melanoma incidence trends.


Asunto(s)
Melanoma/epidemiología , Baño de Sol/estadística & datos numéricos , Adolescente , Adulto , Vestuario/historia , Cultura , Femenino , Conocimientos, Actitudes y Práctica en Salud , Historia del Siglo XX , Humanos , Incidencia , Masculino , Melanoma/etiología , Piel/efectos de la radiación , Baño de Sol/historia , Bronceado , Estados Unidos , Adulto Joven
16.
J Am Acad Dermatol ; 71(6): 1241-9, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25267379

RESUMEN

Pigmented vulvar lesions are present in approximately 1 in 10 women and include melanocytic and nonmelanocytic proliferations. Vulvar nevi, melanosis, and melanoma are particularly challenging because of the similarity of their clinical and/or histopathological presentation. As a result, they are often difficult to diagnose, may result in patient and physician anxiety, and can lead to unneeded, potentially disfiguring surgical procedures. Because it is often detected late, vulvar melanoma carries a poor prognosis with associated significant morbidity and mortality, underscoring the importance of prompt recognition and treatment. In this review, we analyze the distinct epidemiologic, clinical, and histopathologic characteristics of vulvar nevi, melanosis, and melanoma, discuss treatment options, and propose a practical, systematic approach to facilitate formulation of a differential diagnosis and initiation of appropriate management.


Asunto(s)
Melanoma , Nevo Pigmentado , Neoplasias Cutáneas , Neoplasias de la Vulva , Diagnóstico Diferencial , Femenino , Humanos , Melanoma/epidemiología , Melanoma/patología , Melanoma/cirugía , Nevo Pigmentado/epidemiología , Nevo Pigmentado/patología , Nevo Pigmentado/cirugía , Neoplasias Cutáneas/epidemiología , Neoplasias Cutáneas/patología , Neoplasias Cutáneas/cirugía , Neoplasias de la Vulva/epidemiología , Neoplasias de la Vulva/patología , Neoplasias de la Vulva/cirugía
17.
Semin Ultrasound CT MR ; 45(2): 139-151, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38373671

RESUMEN

The field of Radiology is continually changing, requiring corresponding evolution in both medical student and resident training to adequately prepare the next generation of radiologists. With advancements in adult education theory and a deeper understanding of perception in imaging interpretation, expert educators are reshaping the training landscape by introducing innovative teaching methods to align with increased workload demands and emerging technologies. These include the use of peer and interdisciplinary teaching, gamification, case repositories, flipped-classroom models, social media, and drawing and comics. This publication aims to investigate these novel approaches and offer persuasive evidence supporting their incorporation into the updated Radiology curriculum.


Asunto(s)
Curriculum , Radiólogos , Radiología , Humanos , Radiólogos/educación , Radiología/educación
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