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1.
J Am Acad Dermatol ; 75(2): 347-55, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-27245278

RESUMEN

BACKGROUND: It is generally accepted that folliculotropic mycosis fungoides (FMF) is usually typified by indurated plaques and tumors mainly on the head/neck and an aggressive course. However, its clinical manifestations have long been recognized to be quite variable, and some studies indicate a better prognosis for certain presentations. OBJECTIVE: We sought to summarize our experience with the clinicopathological presentations of FMF and impact on prognosis. METHODS: Data were collected retrospectively for adults with FMF followed up prospectively at a tertiary medical center in 1995 through 2014. RESULTS: In all, 34 patients presented with follicle-based patch/flat plaques, keratosis pilaris-like lesions, and/or acneiform lesions, defined clinically as early stage (IA, IB), and 15 presented with follicle-based infiltrated plaques and/or tumors, defined as advanced stage (IIB). The head/neck was involved in all tumor-stage cases, whereas early-stage lesions involved mainly the trunk/limbs. The tumor stage was characterized by more pruritus, heavier perifollicular infiltrates, greater vertical depth, and more frequent presence of eosinophils. On multivariate analysis, infiltrate density was the only significant histopathological discriminator between the stages. Estimated 5-year survival was 0.94 in the early-stage group and 0.69 in the tumor-stage group. LIMITATIONS: Lack of long-term follow-up and relatively small sample are limitations. CONCLUSION: FMF presents with 2 distinct patterns of clinicopathologic features, early stage and advanced stage, each with different prognostic implications.


Asunto(s)
Micosis Fungoide/patología , Neoplasias Cutáneas/patología , Adulto , Anciano , Progresión de la Enfermedad , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Micosis Fungoide/complicaciones , Estadificación de Neoplasias , Pronóstico , Prurito/etiología , Estudios Retrospectivos , Neoplasias Cutáneas/complicaciones , Adulto Joven
2.
Lasers Med Sci ; 31(7): 1397-405, 2016 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-27311768

RESUMEN

Given that the pigment particles in tattoos have a relaxation time of <10 ns, picosecond lasers would be expected to be more effective than nanosecond lasers in tattoo removal. To systematically review the evidence regarding the effectiveness and safety of picosecond lasers for tattoo removal, Pubmed, Cochrane Central Register of Controlled Trials (CENTRAL), ClinicalTrials.gov, and reference lists were searched for relevant trials. The primary outcome was >70 % clearance of tattoo pigment. Secondary outcomes were 90-100 % clearance of tattoo pigment, number of laser sessions required, and adverse effects. Eight trials were included, six with human participants (160 participants) and 2 with animal models. Seven of the eight trials explored the usage of either 755, 758, 795, 1064, or 1064/532-nm picosecond lasers for black and blue ink tattoos. In the human trials, 69-100 % of tattoos showed over 70 % clearance of pigment after 1-10 laser treatments. Reported side effects included pain, hyperpigmentation and hypopigmentation, blister formation and transient erythema, edema, and pinpoint bleeding. Included articles varied in type of laser investigated, mostly non-comparative studies and with a medium to high risk of bias. There is sparse evidence that picosecond lasers are more effective than their nanosecond counterparts for mainly black and blue ink tattoo removal, with minor side effects.


Asunto(s)
Rayos Láser , Tatuaje , Adulto , Animales , Vesícula/etiología , Ensayos Clínicos como Asunto , Cobayas , Humanos , Hiperpigmentación/etiología , Hipopigmentación/etiología , Tinta , Masculino , Persona de Mediana Edad , Dolor/etiología , Tatuaje/efectos adversos , Adulto Joven
5.
Alcohol Clin Exp Res ; 35(5): 804-5, 2011 May.
Artículo en Inglés | MEDLINE | ID: mdl-21284670

RESUMEN

Treatment of alcoholic liver disease is for the most part based on the stage of the disease and the pathogenic event that is being targeted. The primary treatment modalities that are considered in the treatment of alcoholic liver disease include abstinence, agents that suppress inflammation, anticytokine therapy, nutritional support, modifiers of alcohol metabolism, anti-oxidants, and inhibitors of hepatic fibrosis. Future therapeutic options include exploration of new pathways such as the patatin-like phospholipase domain containing 3 protein (PNPLA-3).


Asunto(s)
Hepatopatías Alcohólicas/terapia , Templanza , Alcoholismo/genética , Alcoholismo/patología , Alcoholismo/terapia , Animales , Antiinflamatorios/uso terapéutico , Manejo de la Enfermedad , Terapia Genética/tendencias , Humanos , Lipasa/genética , Hepatopatías Alcohólicas/genética , Hepatopatías Alcohólicas/patología , Proteínas de la Membrana/genética , Apoyo Nutricional/métodos
6.
J Dermatolog Treat ; 30(3): 258-263, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-29889596

RESUMEN

BACKGROUND: Retinoids exert their biologic effects by binding to intracellular retinoic-acid receptors (RARs) and/or retinoid X receptors (RXRs). Early-stage mycosis fungoides (MF) has been effectively treated with bexarotene, an RXR-agonist, with overall response (OR) rates 54-67% and complete response (CR) rates 7-27%. Data on RAR-agonist monotherapy are limited. OBJECTIVE: To analyze the effectiveness of RAR-agonist monotherapy for early-stage MF. METHODS: Data on patients with early-stage MF treated with acitretin/isotretinoin monotherapy at a tertiary cutaneous lymphoma clinic in 2010-2017 were collected retrospectively from the medical files. RESULTS: Thirty-five patients (26 males) of median age 50 years (range 8-83) with early-stage MF (IA 9, IB 26) underwent 37 treatment events: 25 acitretin and 12 isotretinoin at a median dosages of 0.3 mg/kg (range 0.2-0.9) and 0.2 mg/kg (range 0.1-0.7), respectively. Median time to maximal response was 6 months for both (range 1-10 for acitretin, 3-16 for isotretinoin); median treatment duration was 10 months (range 3-46) for acitretin, and 9 months (range 3-55) for isotretinoin. OR was 64% for acitretin and 80% for isotretinoin, and CR, 4% and 8%, respectively. Side-effect profiles were as previously reported for retinoids. CONCLUSIONS: Early-stage MF patients may benefit from low dose RAR-agonist monotherapy, although the CR rate is low.


Asunto(s)
Acitretina/uso terapéutico , Fármacos Dermatológicos/uso terapéutico , Isotretinoína/uso terapéutico , Micosis Fungoide/tratamiento farmacológico , Neoplasias Cutáneas/tratamiento farmacológico , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Receptores X Retinoide/agonistas , Estudios Retrospectivos , Adulto Joven
7.
Am J Clin Dermatol ; 18(5): 697-704, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28389891

RESUMEN

BACKGROUND: Dermatophytes are the most common cause of superficial fungal infections in humans. Deep dermatophytosis, however, is rare, described to date only in isolated case reports, usually in the setting of systemic immunosuppression. OBJECTIVE: To present the 15-year experience of a tertiary dermato-mycology clinic with the diagnosis and treatment of deep dermatophytosis. METHODS: Patients were identified by database search. Clinical, mycological, histological, and treatment data were collected from the medical files. RESULTS: Ten patients were identified: nine after solid-organ transplantation and one undergoing chemotherapy, all diagnosed within 3 years after beginning immunosuppression (average 7.5 months). The infective agent in nine cases was Trichophyton rubrum. All patients presented with concurrent superficial fungal infections. Complete resolution was noted in response to systemic antifungal agents. There was no histological evidence of hair-follicle involvement. LIMITATIONS: The limitations of the study were the retrospective design and the small cohort size. CONCLUSION: This case-series study suggests that deep dermatophytosis is a separate entity, distinct from Majocchi's granuloma. It occurs only in immunocompromised patients and is characterized by discrete nodules, an indolent course, the absence of follicular invasion, and proximity to a superficial dermatophyte infection. Systemic antifungal treatment leads to complete resolution. The urgent need for the treatment of superficial fungal infections in immunocompromised patients is emphasized.


Asunto(s)
Antifúngicos/uso terapéutico , Huésped Inmunocomprometido/inmunología , Terapia de Inmunosupresión/efectos adversos , Tiña/inmunología , Trichophyton/inmunología , Adulto , Anciano , Femenino , Folículo Piloso/patología , Humanos , Incidencia , Israel/epidemiología , Masculino , Persona de Mediana Edad , Trasplante de Órganos/efectos adversos , Estudios Retrospectivos , Centros de Atención Terciaria/estadística & datos numéricos , Tiña/tratamiento farmacológico , Tiña/epidemiología , Tiña/microbiología , Trichophyton/aislamiento & purificación
8.
Autoimmun Rev ; 13(4-5): 477-81, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24424192

RESUMEN

Pemphigus and bullous pemphigoid represent the two major groups of autoimmune blistering diseases. Pemphigus has three major variants: pemphigus vulgaris, pemphigus foliaceus and paraneoplastic pemphigus and is characterized by autoantibodies directed against the cell surface of keratinocytes, producing acantholysis that in turn leads to intraepithelial blisters in the skin and/or mucous membranes. In bullous pemphigoid, the autoantibodies are present at the dermo-epidermal junction and attack the hemidesmosomes, causing subepidermal blister formation. The classification of the major variants of both the pemphigus group and bullous pemphigoid can be based on the combination of clinical, histopathological and immunopathological criteria. Many tools are available for the diagnosis of these entities including biopsy, direct and indirect immunofluorescence, immunoprecipitation, immunoblotting and ELISA. However, currently there are no generally accepted criteria for the diagnosis of these disorders. The present review provides a proposal for diagnostic criteria.


Asunto(s)
Enfermedades Autoinmunes/diagnóstico , Penfigoide Ampolloso/diagnóstico , Pénfigo/diagnóstico , Autoanticuerpos/inmunología , Enfermedades Autoinmunes/inmunología , Enfermedades Autoinmunes/patología , Biopsia , Humanos , Penfigoide Ampolloso/inmunología , Penfigoide Ampolloso/patología , Pénfigo/inmunología , Pénfigo/patología
9.
Fertil Steril ; 92(3): 835-848, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19631936

RESUMEN

The objective of this review was to examine the role of the various spermatozoal components suspected of actively participating in early human development. The contributions of the fertilizing spermatozoon to the oocyte include, as a minimum, the delivery of the DNA/chromatin, a putative oocyte-activating factor (OAF), and a centriole. Recent data indicate that spermatozoa may also provide the zygote with a unique suite of paternal mRNAs; some transcripts might be crucial for early and late embryonic development and deficient delivery, or aberrant transcription might contribute to abnormal development and arrest. Clinical evidence from assisted reproduction suggests that failure to complete the fertilization process, syngamy, or early cleavage might be the result of an early paternal effect. It is speculated that an abnormal release of a putative OAF and/or dysfunctions of the centrosome and cytoskeletal apparatus may mediate these effects. On the other hand, a later paternal effect resulting in embryonic failure to achieve implantation, pregnancy loss, and/or developmental abnormalities resulting from "carried over" sublethal effects may be associated with sperm nuclear/chromatin defects, including the presence of aneuploidy, genetic anomalies, DNA damage, and possibly other causes. These findings highlight the need for continuous monitoring of clinical results.


Asunto(s)
Desarrollo Embrionario/fisiología , Fertilización/fisiología , Espermatozoides/fisiología , Animales , Centriolos/fisiología , ADN Mitocondrial/fisiología , Femenino , Humanos , Masculino , Técnicas Reproductivas Asistidas , Interacciones Espermatozoide-Óvulo/fisiología
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