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1.
Rheumatol Adv Pract ; 6(2): rkac036, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35663153

RESUMO

Objective: The aim was to assess clinical improvement after US-guided injection of CSs into the SI joint of patients with SpA. Methods: This was an observational, descriptive, retrospective study of patients with SpA and sacroiliitis who received an US-guided injection into the SI joint between 1 June 2020 and 31 May 2021. Means were compared using Student's paired t-test for the variables visual analog scale (VAS), BASDAI, ASDAS, CRP and ESR before and after the procedure. We evaluated the association between these variables and the clinical response using the odds ratio. Results: We analysed 32 patients with SpA [age 42.69 (8.19) years; female sex, 56.25%], with a VAS score of 7.88 (0.79), BASDAI of 5.43 (1.48) and ASDAS of 3.27 (0.86) before the procedure. At 2-3 months, 75% of patients had improved: VAS 3.81 (2.33) (-4.07, P < 0.0001) and BASDAI 3.24 (1.6) (-2.19, P < 0.0001). At 5-6 months, 59.37% had improved: VAS 4.63 (2.31) (-3.25, P < 0.0001), BASDAI 3.57 (1.67) (-1.86, P < 0.0001) and ASDAS 2.27 (0.71) (-1.0, P < 0.0001). Bone marrow oedema resolved in 87.5% of cases compared with the previous MRI scan. No significant association was identified with the clinical response to the injection. Conclusion: US-guided injection of CSs into the SI joint of patients with SpA and active sacroiliitis leads to an improvement in symptoms that is maintained at 5-6 months. The procedure is effective, safe, inexpensive and easy to apply.

2.
Am J Dermatopathol ; 42(12): 956-960, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32809978

RESUMO

Melanomas with complete histological regression have been seen very infrequently. On the other hand, the diagnosis of metastatic melanoma is based on the histopathology and positivity of markers such as S100, Melan-A, and HMB-45 whose sensitivity is 99%, 82%, and 76%, respectively. It is very rare that metastatic melanomas and even more primary melanoma are negative for all of these markers. In these rare cases, there is usually a known primary. We present the case of a 82-year-old woman with a erythematous mass in the left groin and a 1-cm black-bluish irregular nodule on the skin of the ipsilateral foot. This lesion was clinical and dermoscopically compatible with primary melanoma. In the histological evaluation of the skin, a dermis full of melanophages and hemosiderophages were found in a background of fibrosis, scarce lymphocytic infiltrate, and neovascularization. Any cells expressing melanocytic markers were observed. It was diagnosed as tumoral melanosis. Lymph nodes showed a proliferation of atypical epithelioid cells with eosinophilic cytoplasm. Mitosis was conspicuous. Tumoral cells were vimentin and CD99 positive, and S100, CD34, HMB-45, Melan-A, SOX 10, tyrosinase, C-KIT, CD45, and CKAE1/AE3 negative, and BRAF-V600 mutated was detected. During follow-up, atypical vitiligo-like lesions were discovered, suggesting the diagnosis of metastatic melanoma totally regressed in our patient.


Assuntos
Biomarcadores Tumorais/análise , Melanócitos/química , Melanoma/química , Melanose/metabolismo , Neoplasias Cutâneas/química , Idoso de 80 Anos ou mais , Biomarcadores Tumorais/genética , Evolução Fatal , Feminino , Humanos , Metástase Linfática , Melanócitos/patologia , Melanoma/genética , Melanoma/secundário , Melanose/genética , Melanose/patologia , Mutação , Proteínas Proto-Oncogênicas B-raf/genética , Neoplasias Cutâneas/genética , Neoplasias Cutâneas/patologia
3.
Reumatol. clín. (Barc.) ; 16(2,pt.2): 180-182, mar.-abr. 2020. ilus
Artigo em Espanhol | IBECS | ID: ibc-194345

RESUMO

La psoriasis es una frecuente dermatosis inflamatoria que puede asociarse a diversas enfermedades. Estudios recientes señalan que la presencia de enfermedades autoinmunes es mayor, pero es rara la asociación con enfermedades del tejido conectivo. La coexistencia con lupus es infrecuente. Por otra parte, la morfea raramente se ha reportado en pacientes con lupus o psoriasis. Presentamos a una paciente con lupus cutáneo y morfea profunda que posteriormente desarrolló psoriasis, con excelente respuesta a metotrexato y revisamos la literatura


Psoriasis is a common inflammatory dermatosis that may be associated with a number of diseases. Recent studies provide evidence that there is a greater frequency of autoimmune diseases, but association with autoimmune connective tissue diseases is uncommon. The coexistence of psoriasis and lupus erythematosus is rare. Besides, the occurrence of morphea has rarely been reported in patients with lupus or psoriasis. We report a woman with cutaneous lupus and morphea profunda associated with psoriasis, with an excellent response to methotrexate, and review the literature


Assuntos
Humanos , Feminino , Idoso , Lúpus Eritematoso Cutâneo/diagnóstico , Lúpus Eritematoso Cutâneo/patologia , Esclerodermia Localizada/patologia , Psoríase/patologia , Couro Cabeludo/patologia , Lúpus Eritematoso Cutâneo/tratamento farmacológico , Esclerodermia Localizada/tratamento farmacológico , Psoríase/tratamento farmacológico , Autoimunidade , Prednisona/administração & dosagem , Corticosteroides/administração & dosagem , Administração Tópica , Couro Cabeludo/efeitos dos fármacos , Biópsia , Psoríase/etiologia
4.
Reumatol Clin (Engl Ed) ; 16(2 Pt 2): 180-182, 2020.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29625815

RESUMO

Psoriasis is a common inflammatory dermatosis that may be associated with a number of diseases. Recent studies provide evidence that there is a greater frequency of autoimmune diseases, but association with autoimmune connective tissue diseases is uncommon. The coexistence of psoriasis and lupus erythematosus is rare. Besides, the occurrence of morphea has rarely been reported in patients with lupus or psoriasis. We report a woman with cutaneous lupus and morphea profunda associated with psoriasis, with an excellent response to methotrexate, and review the literature.


Assuntos
Lúpus Eritematoso Cutâneo/complicações , Psoríase/complicações , Esclerodermia Localizada/complicações , Idoso , Feminino , Humanos
5.
Rev. Soc. Esp. Dolor ; 26(5): 309-312, sept.-oct. 2019. ilus
Artigo em Espanhol | IBECS | ID: ibc-191382

RESUMO

El pioderma gangrenoso (PG) es una enfermedad cutánea rara y dolorosa con una respuesta de tratamiento impredecible. Las lesiones son recurrentes y ocurren en áreas que han sufrido traumas previos. Algunos casos se han relacionado con diferentes tipos de cirugías y, por lo general, no se diagnostican correctamente y se clasifican erróneamente como un proceso infeccioso. La implantación de un sistema de neuroestimulación es un procedimiento quirúrgico con varias complicaciones posibles, generalmente infecciosas, pero también no infecciosas, como reacciones de hipersensibilidad, pero no hay una descripción de la PG. Presentamos un paciente con un síndrome de dolor regional complejo posquirúrgico en ambos pies que desarrolla una lesión necrótica, pustulosa, eritematosa y dolorosa después del implante de un sistema de neuroestimulación medular que se diagnosticó como PG y se trató correctamente gracias a un enfoque multidisciplinario


Pyoderma gangrenosum (PG) is a rare and painful skin disease with unpredictable treatment response. The lesions are recurrent and occur in areas that have suffered previous trauma. Some cases have been related to different types of surgeries and it is usually underdiagnosed and erroneously classifi ed as an infectious process. The implantation of a neurostimulation system is a surgical procedure with several possible complications, usually infectious but also non-infectious such as hypersensitivity reactions but there is no description of PG. We report a patient with a post-surgical complex regional pain syndrome in both feet that develops a necrotic, pustular, erythematous and painful lesion after the implantation of a spinal cord stimulation which was diagnosed as PG and correctly treated thanks to a multidisciplinary approach


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Pioderma Gangrenoso/etiologia , Estimulação da Medula Espinal/efeitos adversos , Neuroestimuladores Implantáveis/efeitos adversos , Complicações Pós-Operatórias , Síndromes da Dor Regional Complexa/etiologia , Síndrome de Sweet/diagnóstico
6.
An Bras Dermatol ; 92(5 Suppl 1): 76-78, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29267453

RESUMO

We present the case of a 72-year-old Caucasian woman with frontal fibrosing alopecia of one year's duration. Eighteen months later, she presented with sudden hyperpigmentation on the submental area, neck and upper chest. Histopathological examination was consistent with lichen planus pigmentosus. This is the report of a unique case of a FFA and extrafacial lichen planus pigmentosus.


Assuntos
Alopecia/patologia , Hiperpigmentação/patologia , Líquen Plano/patologia , Idoso , Alopecia/complicações , Dermoscopia , Feminino , Testa/patologia , Humanos , Hiperpigmentação/complicações , Líquen Plano/complicações , Pele/patologia
8.
An. bras. dermatol ; 92(5,supl.1): 76-78, 2017. graf
Artigo em Inglês | LILACS | ID: biblio-887058

RESUMO

Abstract We present the case of a 72-year-old Caucasian woman with frontal fibrosing alopecia of one year's duration. Eighteen months later, she presented with sudden hyperpigmentation on the submental area, neck and upper chest. Histopathological examination was consistent with lichen planus pigmentosus. This is the report of a unique case of a FFA and extrafacial lichen planus pigmentosus.


Assuntos
Humanos , Feminino , Idoso , Hiperpigmentação/patologia , Alopecia/patologia , Líquen Plano/patologia , Pele/patologia , Hiperpigmentação/complicações , Dermoscopia , Alopecia/complicações , Testa/patologia , Líquen Plano/complicações
9.
Horiz. méd. (Impresa) ; 16(1): 14-19, Ene.-Mar.2016. tab
Artigo em Espanhol | LILACS, LIPECS | ID: lil-786516

RESUMO

Describir la relación médico-paciente (RMP) y determinar los factores asociados a una buena percepción de está por los pacientes que acuden a consultorios externos del Hospital Carlos Lanfranco La Hoz (HCLLH) del Ministerio de Salud (MINSA), período mayo 2014. Material y Métodos: Estudio transversal-comparativo, realizado en pacientes que acuden a consulta externa de especialidades médicas. Se utilizó el cuestionario estructurado semicerrado, llamado PREMEPA. Los cálculos estadísticos fueron realizados con un nivel de confianza del 95%. Resultados: Un total de 179 pacientes completaron la encuesta, el 64,8%(116) fueron mujeres, el promedio de la edad fue de 42,1 ± 11,9 años. El 23% (41) de los usuarios percibieron una RMP buena, el 52% (93) regular y el 25% (45) mala. Las variables finalmente asociadas con una buena RMP fueron tener entre 18-35 años (OR = 8,1 [IC95%; 1,6-40,1), haber elegido a su médico (OR = 20,5 [IC95%; 5,1-82,5) y ser atendido por una médico mujer (OR = 3,1 [IC 95%; 1,01-9,3]). Conclusiones: Existe un bajo porcentaje (23%) de pacientes que perciben una buena relación médico paciente. El elegir a su médico, ser paciente joven y ser atendido por una médico mujer influyen en tener una buena RMP...


To describe the Physician-patient relationship and to determine the factors associated with a good perception of it by the patients that attend ambulatory care in the Carlos Lanfranco La Hoz Hospital (CLLHH) of the Health Ministry (MINSA), during May 2014. Material and Methods: Transversal-comparative study performed with patients that attend ambulatory care of medical specialties. In this study, a structured semi closed questionnaire called PREMEPA was used and statistical calculations were made with 95% confidence level.Results: A total of 179 patients completed the questionnaire. Of those, 64.8% (116) were women, the average age was 42,1 ± 11,9 years old. 23% (41) of the patients perceived a good physician-patient relationship, 52% (93) regular and 25% (45) a bad relationship. The variables finally associated with a good physician -patient relationship were having between 18-35 years old (OR = 8,1 [IC95%; 1,6-40,1), personally choosing their physicians (OR = 20,5 [IC95%; 5,1-82,5), and be attended by a female physician (OR = 3,1 [IC 95%; 1,01-9,3]). Conclusions: There is a low percentage (23%) of patients that perceive a good physician -patient relationship. Choosing their physician, being a young patient and be attended by a female physician influenced in having a good physician-patient relationship...


Assuntos
Humanos , Aceitação pelo Paciente de Cuidados de Saúde , Qualidade da Assistência à Saúde , Empatia , Relações Médico-Paciente , Satisfação do Paciente , Estudos Transversais
11.
Am J Dermatopathol ; 38(2): 135-7, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26825158

RESUMO

Multiple lentiginosis are seen in many multisystemic diseases and during the course of many treatment schemes in the area of application of topical substances, PUVA, or more disseminated reactions in the case of systemic drugs. We report a case of a 67-year-old man with multiple comorbidities including vitiligo, and a recent diagnosis of inflammatory bowel disease, who developed millimeter-size, circular, brown macules in photoexposed areas both affected and not affected by vitiligo while was taken azathioprine, which disappeared after drug withdrawal. Biopsy showed groups of apoptotic keratinocytes, basal hyperpigmentation, and slight dermal inflammation. The authors describe "eruptive lentiginosis" as an adverse event of azathioprine not previously described in the literature.


Assuntos
Anti-Inflamatórios/efeitos adversos , Azatioprina/efeitos adversos , Toxidermias/etiologia , Fármacos Gastrointestinais/efeitos adversos , Doenças Inflamatórias Intestinais/tratamento farmacológico , Lentigo/induzido quimicamente , Pele/efeitos dos fármacos , Vitiligo/complicações , Idoso , Apoptose/efeitos dos fármacos , Biópsia , Toxidermias/diagnóstico , Humanos , Doenças Inflamatórias Intestinais/complicações , Doenças Inflamatórias Intestinais/diagnóstico , Queratinócitos/efeitos dos fármacos , Queratinócitos/patologia , Lentigo/diagnóstico , Masculino , Pele/patologia , Pigmentação da Pele/efeitos dos fármacos , Vitiligo/diagnóstico
13.
Reumatol. clín. (Barc.) ; 11(6): 395-397, nov.-dic. 2015. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-146766

RESUMO

La sarcoidosis es una enfermedad granulomatosa sistémica con un gran abanico de manifestaciones clínicas, siendo la afectación cutánea una de las más precoces, frecuentes y accesible de un estudio histopatológico. En la actualidad, se han descrito varios factores de riesgo que determinarán la probable afectación sistémica de una aparente afectación cutánea única. Esta correcta valoración establecerá el inicio de un tratamiento sistémico, previniendo de esta forma futuras complicaciones. Se presenta a continuación una serie de 3 casos de sarcoidosis cutánea como primera manifestación de una enfermedad sistémica paucisintomática y se hace una revisión del tema (AU)


Sarcoidosis is a systemic granulomatous disease with a wide range of clinical manifestations. Skin involvement is an early, frequent and accessible location for a histopathological study. Several risk factors have been described to determine the likelihood of systemic involvement of an apparent cutaneous condition. Early diagnosis and systemic treatment could prevent future complications. A series of three cases is presented in which the initial diagnosis was cutaneous sarcoidosis, but it was actually the first manifestation of a systemic disease. A review of this topic is also presented (AU)


Assuntos
Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Sarcoidose/diagnóstico , Dermatopatias/diagnóstico , Doença Granulomatosa Crônica/diagnóstico , Mediastinite/etiologia , Doenças Linfáticas/etiologia
14.
Rev. esp. patol ; 48(3): 159-162, jul.-sept. 2015. ilus
Artigo em Espanhol | IBECS | ID: ibc-139259

RESUMO

La inmunodeficiencia variable común es una inmunodeficiencia primaria por hipogamaglobulinemia de IgG e IgA poco frecuente en la población. Clásicamente se presenta durante la juventud y se diagnostica durante la investigación de infecciones respiratorias y gastrointestinales a repetición. Estos pacientes pueden además presentar enfermedades autoinmunes, inflamatorias, neoplásicas, malabsorción y problemas granulomatosos no infecciosos, que afectan el pulmón, ganglios, bazo, hígado, y menos usualmente la piel. Presentamos el caso de una paciente diagnosticada de inmunodeficiencia variable común que se presenta en la consulta dermatológica con múltiples nódulos eritemato-costrosos en miembros, donde se hallaron únicamente granulomas asépticos (AU)


Common variable immunodeficiency is a rare, primary immunodeficiency characterized by hypogammaglobulinemia of IgG and IgA. It classically presents as recurrent respiratory and gastrointestinal infections in young patients, who may also have autoimmune and inflammatory disease, malignancies, malabsorption and non-infectious granulomas, mainly located in the lung, lymph nodes, spleen, liver and, less frequently, in the skin. We report the case of a patient diagnosed with common variable immunodeficiency who presented in the dermatology clinic with multiple, erythematous, crusted nodules on the limbs. Only aseptic granulomas were found (AU)


Assuntos
Feminino , Humanos , Granuloma/patologia , Imunodeficiência de Variável Comum/complicações , Imunodeficiência de Variável Comum/diagnóstico , Imunodeficiência de Variável Comum/patologia , Imunoglobulina A/isolamento & purificação , Infecções Respiratórias/patologia , Diagnóstico Diferencial , Antígenos CD4 , Síndromes de Imunodeficiência/patologia , Imunoglobulina G , Linfócitos B/patologia , Tomografia Computadorizada de Emissão , Antígenos CD8
15.
Reumatol Clin ; 11(6): 395-7, 2015.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-25823568

RESUMO

Sarcoidosis is a systemic granulomatous disease with a wide range of clinical manifestations. Skin involvement is an early, frequent and accessible location for a histopathological study. Several risk factors have been described to determine the likelihood of systemic involvement of an apparent cutaneous condition. Early diagnosis and systemic treatment could prevent future complications. A series of three cases is presented in which the initial diagnosis was cutaneous sarcoidosis, but it was actually the first manifestation of a systemic disease. A review of this topic is also presented.


Assuntos
Sarcoidose/diagnóstico , Dermatopatias/diagnóstico , Adulto , Feminino , Humanos , Pessoa de Meia-Idade
18.
Reumatol. clín. (Barc.) ; 9(5): 319-321, sept.-oct. 2013. ilus
Artigo em Espanhol | IBECS | ID: ibc-115103

RESUMO

La meralgia parestésica es una mononeuropatía del nervio femorocutáneo con una presentación clínica característica, usualmente secundaria a lesión o atrapamiento en algún punto de su recorrido, siendo más habitual las producidas a nivel inguinal. Sin embargo, se publican casos excepcionales asociados a compresiones originadas por masas ocupantes de espacio a nivel retroperitoneal, por lo que se debería ampliar su estudio con pruebas de imagen ante dicho cuadro clínico. A continuación presentamos un caso asociado a un tumor renal(AU)


Meralgia paresthetica is a mononeuropathy of the femoral cutaneous nerve with characteristic findings, usually secondary to injury or compression, being most common in the inguinal area. Exceptional cases associated with compressions caused by abdominal or pelvic tumors have been published, so it is always advisable to extend the study with imaging tests. We present a case associated with a renal tumor(AU)


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Parestesia/complicações , Parestesia/diagnóstico , Mononeuropatias/complicações , Mononeuropatias/diagnóstico , Neoplasias Renais/complicações , Neoplasias Renais/diagnóstico , Diagnóstico Diferencial , Parestesia/fisiopatologia , Parestesia , Mononeuropatias/fisiopatologia , Mononeuropatias , Neoplasias Renais/fisiopatologia , Neoplasias Renais
19.
Reumatol Clin ; 9(5): 319-21, 2013.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-23608051

RESUMO

Meralgia paresthetica is a mononeuropathy of the femoral cutaneous nerve with characteristic findings, usually secondary to injury or compression, being most common in the inguinal area. Exceptional cases associated with compressions caused by abdominal or pelvic tumors have been published, so it is always advisable to extend the study with imaging tests. We present a case associated with a renal tumor.


Assuntos
Neoplasias Renais/complicações , Síndromes de Compressão Nervosa/etiologia , Idoso , Neuropatia Femoral , Humanos , Masculino
20.
Dermatol. peru ; 23(1): 26-30, ene.-mar. 2013. tab
Artigo em Espanhol | LILACS, LIPECS | ID: lil-765193

RESUMO

Objetivo. Determinar los factores de riesgo para la ocurrencia de melasma en pacientes adultos del servicio de Dermatolog¡a del Hospital Nacional Daniel A. Carri¢n durante el a¤o 2011. Methodolog¡a. Estudio de casos y controles. La poblacion de estudio estuvo conformada por pacientes atendidos en el Servicio de Dermatolog¡a del Hospital Nacional Daniel A. Carri¢n en el Callao. Per£. Se evalu¢ la presencia de factores de riesgo para la ocurrencia de meelasma tales como edad, sexo fototipo cut neo, lugar de procedencia, lugar de nacimiento del paciente, antecedentes de fotoexposici¢n, gestaciones previas y uso de hormonas sexuales femeninas. Se calcularon odds ratios (OR) crudos y ajustados con un nivel de confianza de 95%, mediante el uso del programa estad¡stico Stata12. Resultados. Se evalu¢ 78 casos y 76 controles. El an lisi bivariado mostr¢ que tanto el sexo femenino (OR, 10,2; IC95% 3,3-30,9), el haber nacido en Lima a Callao (OR, 2,7; IC95%, 1,2-160,4) asi como la procedencia de los padres de Lima o Callao (OR padre, 16; IC95%. 1.9-136; OR madre, 18,7; IC95%, 2,2-160,4) estuvieron asociados a la presencia de melasma. el uso de fotoprotector fue mayor entre los casos (p<0,01). el uso de hormonas sexuales femeninas estuvo fuertemente asociado al aumento de melasma (OR, 43,3; IC95%, 3,7 a 505). El an lisis multivariado encontr¢ que el sexo femenino(OR, 10,9; IC95%, 3,3-30,9) y el uso de anticonceptivos orales (OR, 44,9; IC95%, 3,35-603,9) constituyeron factores de riesgo para la presencia de melasma, con ajuste para variables potencialmente confusoras como el sexo del producto de la £¤tima gestaci¢n, lugar de nacimiento as¡ como de la procedencia del padre y la madre. Conclusion. El sexo femenino y el uso de anticonceptivos orales contituyen factores de riesgo para melasma en pacientes del Hospital Daniel A. Carri¢n.


Objective. Evaluated the factors associated with the ocurrence of melasma in adult patients of the Dermatology Department of the Hospital Nacional Daniel A. Carrion in 2011. Methods. We conducted a case-control study. The study population consisted of patients attending the Dermatology Department of the Hospital Nacional Daniel A. Carri¢n in Callao, Per£. We evaluated the presence of factors associated with the ocurrence of melasma such as age, sex, skin phototype, place of origin and birth of the patient, history of photo exposure, previous pregnancies, and use of sesual hormones. We calculated crude and adjusted ORs with a confidence level of 95% using the statistical software stata 12. Results. We evaluated 78 cases and 76 controls. The bivariate analysis showed that female sex (OR, 10,2; 95%CI, 3,3-30,9), being born in Lima and Callao (OR, 2,7;95%CI, 1,2-6,2) and parents origin of Lima and Callao (father OR, 16; 95% CI, 2,2-160,4) were associated with the presence of melasma. The use of sunscreen was higher among cases (p<0,01). The use of secual hormones was strongly associated with melasma (OR, 43,3; 95%CI, 3,35-603,9) as the only factor associated with the occurrence of melasma, adjusted by the sex of the baby, place of birth and origin of the father and the mother. Role of female gender was not evaluated because of dependency among variables. conclusion. Melasma is a highly prevalent entity in our environment female gender and the uso of hormonal medication were identified as only factors associated to this condition in our population.


Assuntos
Humanos , Masculino , Feminino , Anticoncepcionais Orais , Fatores de Risco , Melanose , Melanose/prevenção & controle
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