Retronychia

Abstract: Retronychia is a recently described disorder caused by ingrowth of the proximal nail plate into the proximal nail fold. It is suspected when there is persistent paronychia, particularly in the setting of trauma. This disease is probably underdiagnosed due to limited knowledge among dermatologists and the presence of incomplete clinical forms. Nail plate avulsion is the diagnostic and curative procedure of choice, despite reports of relapse.

Osteocondromas: presentación del osteocondroma subungueal / Osteochondromas: introducing the subungual osteochondroma

Resumen: Introducción: Los osteocondromas subungueales son tumoraciones benignas de la región sub- o periungueal que ocasionan elevación, ulceración y deformidad a dicho nivel. Objetivos: Investigar la incidencia de osteocondroma subungueal en un segmento de población pediátrica. Material y métodos: Estudio retrospectivo, transversal, descriptivo y observacional, basado en la revisión de expedientes con resultado histopatológico de osteocondroma de 2001 a 2014. Resultados: Cuatro de los osteocondromas correspondieron a la presentación subungueal, con una distribución por sexos de 1:1 y un promedio de edad de 9.5 años, relación 3:1, derecho:izquierdo; el cuarto dedo fue el más afectado. Discusión: El osteocondroma sunbungueal presenta una incidencia de 8.5% de todos los osteocondromas.

Abstract: Introduction: Subungual osteochondromas are benign tumors of the sub- or periungual region, causing lifting, ulceration and deformity at that level. Objective: To research the incidence of subungual osteochondromas in a specific pediatric population. Material and methods: Retrospective, transversal, descriptive and observational study based on the review of records with a histopathological result of osteochondroma from 2001 to 2014. Results: The pathological assessment featured four osteochondromas that corresponded to the subungual presentation, with an equal gender distribution of 1:1, an average age of 9.5 years, right: left ratio of 3:1; the 4th finger was the most affected. Discussion: Subungual osteochondroma has an incidence of 8.5% of all osteochondromas.

Do you know this syndrome? Clouston syndrome

Abstract Ectodermal dysplasias are conditions that present primary defects in two or more tissues of ectodermal origin and can be classified as hypohidrotic and hidrotic. Hidrotic ectodermal dysplasia or Clouston syndrome is an autosomal dominant genodermatosis and appears as a triad of clinical findings: palmoplantar keratoderma, nail dystrophy, and hypotrichosis. The hair is sparse and brittle. The nails become thickened and dystrophic, which is an essential characteristic of the syndrome. The diagnosis is made based on clinical findings. This study reports a case of a patient who began with changes in hair, nails and palmoplantar keratoderma in early childhood.

Posible asociación autoinmune entre síndrome de Laugier-Hunziker y síndrome de Sjögren: reporte de un caso y revisión de la literatura / Laugier-Hunziker syndrome in a patient with Sjögren’s syndrome: report of one case

Laugier-Hunziker syndrome is a rare benign idiopathic condition characterized by acquired macular pigmentation of lips and buccal mucosa, often accompanied with melanonychia. The main concern with this condition is to rule out other differential diagnosis with systemic repercussions and similar hyperpigmentation patterns, such as Peutz-Jeghers syndrome, adrenal insufficiency and melanoma. We report a 58-year-old female with a 20-year history of Sjögren’s syndrome, presenting with melanonychia and hyperpigmentation in the buccal mucosa. She had no relevant medication history and is a non-smoker. The patient denied any other symptoms. The histopathology confirmed the diagnosis of Laugier-Hunziker syndrome.

Qué debe saber el reumatólogo del compromiso de piel para el manejo de la artritis psoriática / Which must be known by the rheumatologist of the skin commitment for the management of psoriatic arthritis

La artritis psoriática es una patología inflamatoria crónica que puede afectar a articulaciones periféricas y/o axiales, las que pertenecen al “espectro psoriático”. Es una enfermedad subdiagnosticada y subtratada, que puede traer consecuencias funcionales, laborales y de calidad de vida en los individuos que la padecen. Se estima que el 30 por ciento de los pacientes con psoriasis presentan compromiso articular. Entre los factores de riesgo para desarrollarla se encuentran; psoriasis cutáneas severas, evolución prolongada de más de 10 años, obesidad y psoriasis ungueal. Esta última puede presentar alteraciones de la matriz y/o del lecho ungueal, las que se pueden manifestar aisladamente o en conjunto. El diagnóstico de la artritis psoriática y de la psoriasis ungueal puede representar un verdadero desafío. Es de gran relevancia el diagnóstico temprano y el tratamiento correcto, ya que permiten preservar una mejor funcionalidad y calidad de vida de los pacientes.

Psoriatic arthritis is a chronic inflammatory pathology that can affect both axial and peripheral joints, belonging to the “psoriatic spectrum”. It is an underdiagnosed and undertreated condition, which can bring functional, labor and quality of life consequences in individuals suffering from it. About 30 percent of patients with psoriasis also have joint involvement. Risk factors for developing the disease include severe cutaneous psoriasis of more than 10 years, obese patients and nail psoriasis. Within the nail psoriasis, there are manifestations of the nail matrix and the nail bed, which can be manifested in isolation or in conjunction. However, the differential diagnosis of these lesions and psoriatic arthritis itself can be a real challenge. Early diagnosis and correct treatment depend to a large extent on our patients having better functionality and quality of life.

Laugier-Hunziker syndrome - Case report

Laugier-Hunziker syndrome is a rare, acquired disorder characterized by lenticular hyperpigmentation of the oral mucosa and longitudinal melanonychia. We present the case of a 63-year-old female with progressive, asymptomatic hyperpigmentation of buccal mucosa and a 7-year history of hyperpigmentation in several fingernails. Laugier-Hunziker syndrome was diagnosed based on the clinical features presented, dermoscopic findings and exclusion of underlying systemic diseases. Laugier-Hunziker syndrome is regarded as a diagnosis of exclusion. By identifying Laugier-Hunziker syndrome, other, more severe syndromes associated with hyperpigmentations can be excluded, namely Addison’s disease and Peutz-Jeghers syndrome.

Síndrome de Laugier-Hunziker / Laugier-Hunziker syndrome

A Síndrome de Laugier-Hunziker é uma doença adquirida, caracterizada por hiperpigmentação macular da mucosa oral e lábios, frequentemente associada à melanoníquia longitudinal. Não está associada a manifestações sistêmicas ou a malignidades, e o seu conhecimento é importante no diagnóstico diferencial das hiperpigmentações mucocutâneas, achado frequente na prática clínica. Relatamos um caso de uma paciente de 56 anos, cujo diagnóstico foi feito com base nos achados clínicos e histopatológicos e pela ausência de pólipos à colonoscopia (AU)

The Laugier-Hunziker syndrome is an acquired disorder characterized by macular hyperpigmentation of the oral mucosa and lips, often associated with longitudinal melanonychia. It is not associated with systemic manifestations or malignancies and knowledge of it is important in the differential diagnosis of mucocutaneous hyperpigmentation, a common finding in clinical practice. We report a case of a 56 year-old patient, whose diagnosis was based on clinical and histopathological findings and the absence of polyps at colonoscopy (AU)

Nail psoriasis: a review of the literature

Nails are considered epidermal appendages, and as such, are commonly affected in patients with psoriasis, 80% of whom are likely to develop nail psoriasis as a result of their condition. Two patterns of nail disorders have been shown to be caused by psoriasis. Nail matrix involvement can result in features such as leukonychia, pitting (punctures or cupuliform depressions), red spots in the lunula and crumbling. Nail bed involvement, on the other hand, can cause onycholysis, salmon or oil-drop patches, subungual hyperkeratosis and splinter hemorrhages. Nail disease causes aesthetic and functional impairment, and is indicative of more severe forms of psoriasis as well as of joint involvement. The treatment for nail psoriasis involves behavioral interventions, topical medications, or systemic therapy in case of extensive skin or joint involvement. This article presents a review of the main features of nail psoriasis, its clinical presentation, diagnostic and assessment methods, clinical repercussions, and of its available treatment options.

Idiopathic acquired leukonychia

A rare case of 29 years old healthy male patient with persistent progressive total whitening of all the finger and toe nails [Idiopathic acquired leukonychia] since the age of 20 years is being presented here. The nail changes were of great concern in terms of social embarrassment to the patient. Idiopathic acquiredleukonychia is a rare chromatic disorder of the nails not associated with other abnormalities and discernible etiology. To the best of our knowledge, probably it is the second case report from India after the first one reported from Mumbai earlier. Hence it is presented here for its rarity

Onicomatricoma: tumor raro do aparelho ungueal: relato de três casos / Onychomatricoma: a rare tumor of the nail apparatus: report of three cases

Os onicomatricomas são tumores benignos raros que se originam a partir da matriz ungueal e do estroma subjacente. São geralmente assintomáticos e de crescimento lento. Acometem igualmente homens e mulheres de meia idade, comprometendo com maior frequência os dígitos das mãos. As características clínicas fundamentais para o diagnóstico são: faixa longitudinal amarelada de espessura variável, estilhaços hemorrágicos, estrias longitudinais associadas à hipercurvatura transversal e projeções digitiformes emergentes da matriz ungueal. Os autores relatam três casos desse tumor acometendo pododáctilos, enfatizando seus principais aspectos clínicos, achados dermatoscópicos e tratamento cirúrgico.

Onychomatricomas are rare benign tumors originating from the nail matrix and underlying stroma. They are usually asymptomatic and slow growing, affecting both middle-aged men and women, and more frequently involve the digits of the hands. Key clinical features for diagnosis are: yellowish longitudinal band of variable width, splinter hemorrhages, longitudinal grooves associated with the transverse overcurvature and fingerlike projections emerging from the nail matrix. The authors report three cases of this tumor affecting toes, emphasizing main clinical aspects, dermoscopic findings, and surgical treatment.

Patología ungueal no micótica en pediatría / Non mycotic ungueal pathology in pediatrics

Nail alterations in children are a very frequent cause for consultation in primary care, pediatrics and dermatology. Its exact prevalence is unknown. Some of them are identical to those in adults, but there are some whose frequency is much higher in children, because they arise or develop exclusively in that period of life. Although some ungueal changes are considered isolated anomalies that have only cosmetic relevance, others might be diagnostic clues of associated diseases; they may be disabling and have a prognostic value for adult life. For that reason, good knowledge and proper management of them by specialists is fundamental. This report describes main alterations that may be observed in the ungueal apparatus during childhood, due to physiological alterations and congenital or acquired disease.

Las alteraciones ungueales en los niños representan un motivo de consulta frecuente en atención primaria, pediatría y dermatología. Su prevalencia exacta se desconoce. Algunas alteraciones son idénticas a las de los adultos, pero existen otras que se observan con mayor frecuencia en niños ya que se presentan o desarrollan exclusivamente en esta etapa de la vida. Aunque algunos cambios ungueales sean considerados como anomalías aisladas de importancia sólo cosmética, otros pueden ser claves diagnósticas para enfermedades asociadas, pueden ser discapacitantes y pueden tener importancia pronostica en la vida adulta. Por esto un adecuado reconocimiento y manejo por parte del especialista es fundamental. En este artículo se describen las principales alteraciones fisiológicas y enfermedades congénitas o adquiridas que se pueden observar en el aparato ungueal durante la infancia.

Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis

Alopecia totalis (AT) and alopecia universalis (AU), severe forms of alopecia areata (AA), show distinguishable clinical characteristics from those of patch AA. In this study, we investigated the clinical characteristics of AT/AU according to the onset age. Based on the onset age around adolescence ( or = 13 yr), 108 patients were classified in an early-onset group and the other 179 patients in a late-onset group. We found that more patients in the early-onset group had a family history of AA, nail dystrophy, and history of atopic dermatitis than those in the late-onset group. These clinical differences were more prominent in patients with AU than in those with AT. In addition, significantly more patients with concomitant medical disorders, especially allergic diseases were found in the early-onset group (45.8%) than in the late-onset group (31.2%). All treatment modalities failed to show any association with the present hair condition of patients. In the early-onset group, patients with AU or a family history of AA showed worse prognosis, whereas this trend was not observed in the late-onset group. Systemic evaluations might be needed in early-onset patients due to the higher incidence of comorbid diseases. It is suggested that patients with AU or family history of AA make worse progress in the early-onset group than in the late-onset group.

Síndrome da unha amarela: relato de caso / Yellow nail syndrome: case report

A síndrome da unha amarela é uma doença rara, caracterizada pela tríade de linfedema, derrame pleural e unhas Distróficas de crescimento lento e coloração amarelada. Várias associações já foram descritas, entre elas, afecções crônicas do aparelho respiratório, doenças autoimunes, malignidades e estados de imunodeficiência. Entre os casos citados na literatura, apenas cerca de um terço se apresenta com todos os achados e o caso relatado a seguir é um exemplo da tríade clássica.

The yellow nail syndrome is a rare disease, in which there is a triad of lymphedema, pleural effusion and slow-growing dystrophic yellow nails. Many associations have already been described; among them, chronic respiratory tract diseases, autoimmune disorders, malignancies and immunodeficiency conditions. Only one third of cases in the literature show all findings. The case reported next is an example of the classical triad.

Tumores comuns e raros do aparelho ungueal / Rare and common tumors of the nail unit

O aparelho ungueal pode ser acometido por tumores benignos e malignos, estes podem ser comuns ou raros. Tumores ungueais podem ser tardiamente diagnosticados, provavelmente, porque a unha pode esconder lesões tumorais ou mimetizar dermatoses inflamatórias.

Tratamento de disfunções ungueais com órteses / Treatment of nail disorders using orthesis

Neste artigo abordaremos causas comuns de afecções ungueais que causam dor: a hipercurvatura transversa da unha (HT) e a onicocriptose.A primeira tem como etiologia principal o fator hereditário e deformidades dos artelhos, enquanto a segunda também pode estar associada à má poda das unhas e uso inadequado de calçados.Tanto a HT quanto a onicocriptose podem advir de disfunções na biomecânica da marcha. Uma HT pode evoluir para onicocriptose e por isso seus tratamentos muitas vezes são semelhantes, tanto cirúrgica quanto conservadoramente.Dentre os tratamentos, este artigo enfoca o conservador, particularmente a aplicação de órteses ungueais, suas indicações e eficácia.