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1.
Surg. cosmet. dermatol. (Impr.) ; 14: e20220057, jan.-dez. 2022.
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1369134

ABSTRACT

Corpos riziformes são estruturas que podem ser encontradas no líquido sinovial ou aderidas à sinóvia, que se assemelham macroscopicamente a grãos de arroz. São frequentes em pacientes com artrite reumatoide e decorrem de resposta inflamatória crônica. São encontrados em 25% dos procedimentos de aspiração ou cirurgias das articulações. Porém, ainda não existem publicações relatando sua presença no subcutâneo. Relatamos, pela primeira vez, a ocorrência de corpos riziformes no subcutâneo da região palmar em paciente com artrite reumatoide, confirmados por exames ultrassonográfico e anatomopatológico, tratados com sucesso com drenagem cirúrgica, sem recidivas após dois anos de seguimento


Riziform bodies are structures in the synovial fluid or attached to the synovium, which macroscopically resemble rice grains. They are common in patients with rheumatoid arthritis and result from a chronic inflammation. They are found in 25% of aspiration procedures or joint surgery. However, there are still no publications reporting its presence in the subcutaneous tissue. We report for the first time the occurrence of riziform bodies in the subcutaneous plane of the palmar region in a patient with rheumatoid arthritis, confirmed by sonographic and anatomopathological examination, successfully treated with surgical drainage, without recurrences after two years of follow-up.

2.
Medisur ; 17(2): 278-283, mar.-abr. 2019. ilus
Article in Spanish | LILACS | ID: biblio-1002677

ABSTRACT

RESUMEN Se presenta el caso de una paciente femenina de 29 años de edad, con antecedentes de salud referida que acude a consulta por la presencia de máculas hiperpigmentadas asintomáticas de 21 días de evolución, distribuidas de forma lineal en el miembro superior derecho. Los resultados de laboratorio fueron normales y la histopatología confirmó el diagnóstico de sospecha: dermatosis purpúrica pigmentada (variedad lineal unilateral). Hubo una disminución satisfactoria del número de lesiones durante los dos primeros meses de evolución. La púrpura pigmentada unilateral se presenta con mayor frecuencia en varones adolescentes o pacientes adultos jóvenes, y afecta por lo general las extremidades inferiores y tiene una resolución espontánea.


ABSTRACT The case of a 29 year-old female patient is presented, with a referred health history who came to the consultation due to the presence of asymptomatic hyper-pigmented macules of 21 days of progress, distributed linearly in the right upper limb. Laboratory exams were normal and it was histopathology confirmed the diagnosis of suspicion: pigmented purpuric dermatosis (unilateral linear variety). There was a satisfactory decrease in the number of lesions during the first two months. Unilateral pigmented purpura occurs most frequently in adolescent males or young adult patients, and usually affects the lower extremities and has a spontaneous resolution.


Subject(s)
Humans , Female , Adult , Purpura/diagnosis , Skin Manifestations , Hand Dermatoses/pathology
3.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 1719-1722, 2019.
Article in Chinese | WPRIM | ID: wpr-802671

ABSTRACT

Objective@#To observe the efficacy and safety of 308 nm excimer light combined with compound triamcinolone acetoniazole cream in the treatment of chronic hand eczema.@*Methods@#From February 2016 to August 2017, 62 patients with chronic hand eczema admitted to the First People's Hospital of Taicang were divided into two groups using random digital tables, with 31 cases in each group.The treatment group was given 308nm excimer light combined with compound triamcinolone acetoniazole cream.The control group was treated only with compound triamcinolone acetoniazole cream.The effect after 4 and 8 weeks of treatment were determined in both two groups.@*Results@#After 4 and 8 weeks of treatment, the effective rates in the treatment group were 35.48% and 87.10%, respectively, which in the control group were 29.03% and 61.29%, respectively.After 8 weeks of treatment, the difference between the treatment group and the control group was statistically significant(χ2=5.39, P<0.05).@*Conclusion@#308 nm excimer light combined with triamcinolone acetoniazole cream in the treatment of chronic hand eczema has good clinical effect and less adverse reactions, and the recurrence rate is low.

4.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 1719-1722, 2019.
Article in Chinese | WPRIM | ID: wpr-753681

ABSTRACT

Objective To observe the efficacy and safety of 308 nm excimer light combined with compound triamcinolone acetoniazole cream in the treatment of chronic hand eczema.Methods From February 2016 to August 2017,62 patients with chronic hand eczema admitted to the First People's Hospital of Taicang were divided into two groups using random digital tables,with 31 cases in each group.The treatment group was given 308nm excimer light combined with compound triamcinolone acetoniazole cream. The control group was treated only with compound triamcinolone acetoniazole cream.The effect after 4 and 8 weeks of treatment were determined in both two groups. Results After 4 and 8 weeks of treatment,the effective rates in the treatment group were 35.48% and 87.10%, respectively,which in the control group were 29.03% and 61.29%, respectively. After 8 weeks of treatment, the difference between the treatment group and the control group was statistically significant ( χ2 =5.39, P <0.05 ). Conclusion 308 nm excimer light combined with triamcinolone acetoniazole cream in the treatment of chronic hand eczema has good clinical effect and less adverse reactions,and the recurrence rate is low.

5.
An. bras. dermatol ; 93(5): 730-732, Sept.-Oct. 2018. graf
Article in English | LILACS | ID: biblio-949940

ABSTRACT

Abstract: Neutrophilic dermatosis of the dorsal hands is considered a rare and localized variant of Sweet's syndrome. Although the etiology is unknown, there are reports of association with infections, neoplasias, autoimmune diseases and medications. Histopathology shows a dense neutrophilic inflammatory infiltrate in the dermis. Treatment is based on the administration of systemic corticosteroids; however, a combination of medications is useful, given the frequency of relapses. The authors report a classic and clinically exuberant case of neutrophilic dermatosis of the dorsal hands, with excellent response to oral dapsone treatment, and offer a brief literature review.


Subject(s)
Humans , Female , Middle Aged , Sweet Syndrome/drug therapy , Dapsone/therapeutic use , Hand Dermatoses/drug therapy , Anti-Infective Agents/therapeutic use , Sweet Syndrome/complications , Hand Dermatoses/etiology
6.
Surg. cosmet. dermatol. (Impr.) ; 9(4): 285-289, out.-dez. 2017. graf.
Article in English, Portuguese | LILACS | ID: biblio-880495

ABSTRACT

Introdução: Os sinais da idade costumam se evidenciar mais intensamente na face, no pescoço e nas mãos revelando perda considerável de volume, um indicador comum de envelhecimento. Objetivo: Comparar o tempo de duração e os efeitos adversos de dois tipos de preenchedores subcutâneos para o tratamento do envelhecimento volumétrico de mão. Métodos: Estudo prospectivo e comparativo, onde os pacientes foram divididos aleatoriamente em 3 grupos: Grupo A, composto por 4 pacientes que utilizaram o mesmo volume de hidroxiapatita de cálcio e ácido hialurônico em ambas as mãos; Grupo B, composto por 4 pacientes que utilizaram maior volume de hidroxiapatita de cálcio tambem em uma das maõs e Grupo C, composto por 4 pacientes que utilizaram maior volume de ácido hialurônico. Os pacientes foram avaliados através de mudanças em escala validada para envelhecimento de mãos, registradas por fotografias digitais antes e 1,3,6,9,12,15 e 18 meses após o procedimento. Resultados: No Grupo A os pacientes apresentaram o mesmo tempo de duração de ambos os preenchedores; no Grupo B os pacientes tratados com hidroxiapatita de cálcio apresentaram maior tempo de duração; no Grupo C os pacientes tratados com ácido hialurônico apresentaram maior tempo de duração. Os efeitos adversos foram mais frequentes com o uso de hidroxiapatita de cálcio. Conclusões: Pode-se concluir que o tempo de duração é proporcional ao volume injetado para ambos os preenchedores, e que o ácido hialurônico é mais seguro para o tratamento dessa irregularidade cosmética.


Introduction: Signs of aging usually arise more intensely on the face, neck, and hands, in the form of considerable loss of volume, which is a common indicator of aging. Objective: To compare the duration, and adverse effects of two types of subcutaneous fillers in the treatment of the volumetric aging of hands. Methods: Group A: four patients who used the same amount of the products in both hands; Group B: four patients who used greater amounts of calcium hydroxyapatite in one of the hands and Group C: four patients who used greater amounts of hyaluronic acid also in one of the hands. The patients were evaluated through changes in a validated scale for hand aging, recorded by digital photographs before and 1,3,6,9,12,15 and 18 months after the procedure. Results: In Group A the patients had the same duration for both fillers; in Group B patients treated with hydroxyapatite calcium had longer duration; in Group C, the patients treated with hyaluronic acid presented longer duration. Adverse effects were more frequent with the use of calcium hydroxyapatite. Conclusions: It can be concluded that the filler duration is proportional to the volume injected for both fillers, and that hyaluronic acid is safer for the treatment of this cosmetic irregularity.

7.
Surg. cosmet. dermatol. (Impr.) ; 9(2): 173-176, abr.-jun. 2017. ilus.
Article in English, Portuguese | LILACS | ID: biblio-880319

ABSTRACT

Paquidermodactilia é forma rara, benigna e adquirida de fibromatose digital caracterizada por espessamento de partes moles nas regiões laterais das articulações interfalangeanas proximais, tipicamente dos II, III e IV dedos de ambas as mãos. É associada, em grande parte dos casos, a microtraumas digitais repetidos. Relatamos o caso de um paciente de 22 anos de idade, com apresentação clínica típica da doença. O tratamento com infiltrações de triancinolona levou a redução parcial do espessamento, além de hipopigmentação e hiperemia, não tendo sido uma boa opção. Apesar de rara e benigna, essa condição clínica típica deve ser considerada, evitando-se investigações desnecessárias e onerosas, assim como tratamentos inapropriados.


Pachydermodactyly is a rare, benign and acquired form of digital fibromatosis characterized by the thickening of soft tissues in the lateral regions of the proximal interphalangeal joints, typically of the digiti II, III and IV of both hands. In most cases it is associated with repeated digital microtraumas. The authors of the present article report the case of a 22-year-old patient with a typical clinical presentation of the condition. The treatment with triamcinolone injections led to a partial reduction of the thickening, in addition to hypopigmentation and hyperemia, meaning it was an unfavorable option. Although rare and benign, this typical clinical condition deserves attention, and unnecessary and costly investigations, as well as inappropriate treatments should be avoided.

8.
Rev. bras. med. trab ; 13(1)jan.-jun. 2015. tab
Article in Portuguese | LILACS | ID: lil-771367

ABSTRACT

Contexo: O trabalhador em sua atividade laboral está em contato frequente com diversos agentes que em determinadas situações podem comprometer as unhas, a eficiência e produtividade do trabalho exercido. Objetivos: Este estudo constitui-se de uma revisão da literatura com uma breve discussão acerca da distrofia ungueal ocupacional, abordando etiologias, tratamento e prevenção. Métodos: Foi realizada uma consulta por normas e artigos científicos selecionados através de busca no banco de dados do SciELO e da Bireme, a partir das fontes Medline e Lilacs, entre dezembro de 2013 e janeiro de 2014. Resultados: Distrofias são alterações ungueais e em seus anexos, causadas ou agravadas por agentes biológicos, químicos e/ou físicos presentes no ambiente de trabalho. O diagnóstico se baseia em uma anamnese minuciosa, a qual é passível de elucidar a etiologia da doença, e a terapêutica da mesma pode exigir o afastamento do trabalho. A retirada do agente causal e o uso correto dos equipamentos de proteção individual são as melhores formas de prevenção de tal doença ocupacional. Conclusões: O médico do trabalho, detendo condições de observação e avaliação do ambiente de trabalho, deve reconhecer riscos potenciais e reais para o empregado e propor medidas que neutralizem esses riscos.


Context: Worker in their labor activity is in frequent contact with many agents in certain situations that may affect the nails and the efficiency and productivity of their occupation. Objectives: This study consisted of a literature review with a brief discussion of occupational nail dystrophy, addressing causes, treatment and prevention. Methods: A query for standards and selected by searching the database SciELO/Bireme and scientific articles from Medline and Lilacs sources between December 2013 and January 2014. Results: Dystrophies are nail changes and its annexes, caused or aggravated by biological, chemical and/or physical agents in the workplace. The diagnosis is based on a thorough medical history, which is likely to elucidate the etiology of the disease, and its therapy may require absence from work. The withdrawal of the causative agent and the correct use of personal protective equipment are the best ways to care involvement. Conclusions: The occupational physician, in conditions of observation and evaluation of the work environment should know actual and potential risks to the employee and propose measures to neutralize these risks.


Subject(s)
Working Conditions/legislation & jurisprudence , Onychomycosis/etiology , Hand Dermatoses , Occupational Diseases/prevention & control
9.
An. bras. dermatol ; 89(5): 835-836, Sep-Oct/2014. graf
Article in English | LILACS | ID: lil-720788

ABSTRACT

Focal acral hyperkeratosis is a rare genodermatosis with an autosomal dominant pattern of inheritance. It is characterized by usually asymptomatic keratotic papules along the borders of the hands and/or feet. The main differential diagnosis is acrokeratoelastoidosis of Costa, which differs from the former only by not presenting elastorrhexis in histopathological examination, thus requiring this exam for a correct diagnosis.


Subject(s)
Humans , Female , Adult , Keratoderma, Palmoplantar/pathology , Biopsy , Dermis/pathology , Diagnosis, Differential
10.
An. bras. dermatol ; 88(6,supl.1): 206-208, Nov-Dec/2013. graf
Article in English | LILACS | ID: lil-696781

ABSTRACT

Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis, which manifests in infants and becomes more evident in adulthood. Its mode of inheritance is autosomal dominant with mutation in loricrin and Connexin 26 genes. Patients with this mutation present hyperkeratosis of the palms and soles, constricting bands of the digits, usually on the fifth, and starfish-shaped hyperkeratosis on the dorsal aspects of the hands and feet. The disease mostly occurs in white women, where constricting fibrous bands appear on the digits and can lead to progressive strangulation and auto-amputation (pseudo-ain-hum).The authors report a rare case of a patient with a clinical ichthyosiform variant of Vohwinkel syndrome.


A síndrome de Vohwinkel ou queratodermia hereditária mutilante é uma queratose palmo-plantar rara, autossômica dominante, que se manifesta em crianças e se torna mais evidente na vida adulta. Seu modo de herança é autossômica dominante com mutação na loricrina e no gen da Conexina 26. Os pacientes com esta mutação apresentam hiperqueratose das palmas das mãos e plantas dos pés, com bandas constritivas dos dígitos, normalmente no quinto dedo e hiperqueratose em forma de estrela do mar nas regiões dorsais das mãos e dos pés. A doença ocorre principalmente em mulheres brancas, onde as bandas constritivas fibrosas aparecerem nos dígitos e podem levar ao estrangulamento progressivo e auto-amputação (pseudo-ainhum).Os autores relatam o caso de uma variante ictiosiforme da síndrome de Vohwinkel.


Subject(s)
Female , Humans , Middle Aged , Abnormalities, Multiple/pathology , Hand Deformities, Congenital/pathology , Hearing Loss, Sensorineural/pathology , Ichthyosis/pathology , Keratoderma, Palmoplantar/pathology , Abnormalities, Multiple/genetics , Hand Deformities, Congenital/genetics , Hearing Loss, Sensorineural/genetics , Ichthyosis/genetics , Keratoderma, Palmoplantar/genetics , Mutation
11.
An. bras. dermatol ; 88(5): 850-852, out. 2013. graf
Article in English | LILACS | ID: lil-689727

ABSTRACT

Crack cocaine addiction is a public health problem in Brazil. It is an endemic disease that affects rural and urban areas. The Ministry of Health has launched emergency programs for the treatment of dependents and to combat drug trafficking. Recognition of dermatological signs of this disease is important because through them the diagnosis can be suspected and early treatment of patients with crack cocaine addiction be provided.


A dependência química do crack é um problema de saúde pública no Brasil. Trata-se de uma endemia que afeta a zona rural e a zona urbana. O Ministério da Saúde lançou programas emergenciais para o tratamento dos dependentes e o combate ao tráfico de drogas. Reconhecer os sinais dermatológicos iniciais desta doença é importante, pois através deles, pode-se suspeitar do diagnóstico e então proporcionar ao paciente o tratamento precoce.


Subject(s)
Adult , Humans , Male , Burns/etiology , Crack Cocaine/adverse effects , Finger Injuries/etiology , Nose/injuries , Atrophy , Cocaine-Related Disorders/etiology , Drug Users
12.
An. bras. dermatol ; 86(6): 1222-1223, nov.-dez. 2011. ilus
Article in Portuguese | LILACS | ID: lil-610436

ABSTRACT

A acroceratoelastoidose é um tipo de ceratodermia palmoplantar, originalmente descrita pelo dermatologista mineiro Oswaldo Gonçalves Costa. É uma rara genodermatose autossômica dominante, embora possa ocorrer de forma esporádica. A doença não é congênita, com as primeiras manifestações na infância e adolescência. O quadro clínico é caracterizado por múltiplas pápulas amareladas, por vezes translúcidas e ceratóticas, medindo aproximadamente 2-4 mm de diâmetro, ocasionalmente umbilicadas, localizadas na margem lateral das mãos e pés, simetricamente, o que é sua expressão clínica mais típica. Os achados histopatológicos mais comuns são: hiperceratose, acantose discreta e elastorrexe, que é observada pela coloração com orceína.


Acrokeratoelastoidosis is a type of palmoplantar keratoderma first described by Oswaldo Gonçalves Costa, a Brazilian Dermatologist from the state of Minas Gerais. It is a rare autosomal-dominant genodermatosis; however it may occur sporadically. The disease is not congenital; rather, its onset occurs in childhood or adolescence. Clinically, the condition is characterized by multiple yellowish papules, sometimes glossy and keratotic, measuring approximately 2-4 mm in diameter, sometimes umbilicated, and located symmetrically on the sides of the hands and feet, symmetry being the most typical sign. The most common histopathological findings are hyperkeratosis, mild acanthosis and elastorrhexis, as revealed by orcein staining.


Subject(s)
Adult , Humans , Male , Carcinoma, Squamous Cell/pathology , Leg Ulcer/pathology , Skin Neoplasms/pathology
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