RESUMO
Down syndrome (DS) is associated with many dermatological conditions, including hidradenitis suppurativa, folliculitis, and alopecia areata. Despite the high incidence of skin conditions in this population, there are no quality of life (QoL) studies in the dermatology literature focused on patients with DS or their caregivers. The frequently used QoL assessment tool, the Dermatology Life Quality Index (DLQI), has yet to be studied in this population. This study addresses these disparities by capturing how various skin conditions affect the QoL of people with DS and their caregivers and assessing the utility of the DLQI.
Assuntos
Cuidadores , Síndrome de Down , Qualidade de Vida , Dermatopatias , Humanos , Cuidadores/psicologia , Masculino , Feminino , Criança , Adolescente , Adulto , Dermatopatias/psicologia , Inquéritos e Questionários , Adulto Jovem , Pré-Escolar , Pessoa de Meia-IdadeRESUMO
Metopic ridge (MeR) is a midline osseous forehead prominence resulting from physiologic closure of the underlying metopic suture. This mass-like ridge can be mistaken for serious conditions such as a craniosynostosis or vascular anomaly, prompting concern and workup. We reviewed patients presenting for a forehead mass to Vascular Anomalies and Dermatology clinics and diagnosed with MeR to increase familiarity with this finding and to encourage MeR in the differential diagnosis of pediatric midline forehead masses.
Assuntos
Craniossinostoses , Dermatologia , Malformações Vasculares , Humanos , Criança , Lactente , Craniossinostoses/diagnóstico , Craniossinostoses/cirurgia , Suturas Cranianas , Malformações Vasculares/diagnóstico , Diagnóstico DiferencialAssuntos
Alopecia em Áreas , Síndrome de Down , Doenças da Glândula Tireoide , Humanos , Alopecia em Áreas/diagnóstico , Alopecia em Áreas/epidemiologia , Síndrome de Down/diagnóstico , Síndrome de Down/epidemiologia , Doenças da Glândula Tireoide/diagnóstico , Doenças da Glândula Tireoide/epidemiologiaRESUMO
Down syndrome (DS) is the most common chromosomal condition and affects many organs including the skin. Dermatologists are an integral part of the DS care team. This is a review of both common and rare dermatologic conditions in DS. We provide practical strategies for a successful dermatology interview and examination. We explore the downstream effects of trisomy of chromosome 21, in particular on the immune system, and how these insights may enhance our pathophysiologic understanding of their cutaneous conditions.
Assuntos
Síndrome de Down , Dermatopatias , Síndrome de Down/complicações , Humanos , Pele , Dermatopatias/diagnósticoRESUMO
BACKGROUND/OBJECTIVES: Neonatal abstinence syndrome (NAS) incidence continues to rise in the United States due to increasing opioid use disorder in pregnancy. While cutaneous excoriations have been noted in NAS, there is a paucity of literature regarding abnormal nail findings in NAS. METHODS: A retrospective, observational case series was conducted of twelve patients with NAS and abnormal nail findings who were admitted to the neonatal intensive care unit between January 1, 2018, and May 1, 2020. RESULTS: Twelve neonates (10 male, 2 female, mean gestational age at birth 38.1 weeks) with NAS diagnosis and abnormal nail findings were identified between January 1, 2018, and May 1, 2020. NAS was diagnosed by elevated Modified Finnegan Neonatal Abstinence Syndrome Tool (M-FNAST) scores. All patients required pharmacologic treatment for NAS with seven (58.3%) requiring phenobarbital in addition to first-line morphine. Common nail findings included periungual erythema, yellow crusting, desquamation of the proximal and/or distal lateral nail folds and sheared distal nail edges. Two patients (16.7%) required antibiotic treatment for paronychia. Peak M-FNAST scores were positively correlated with number of abnormal nail findings (r = .58, P = .047). CONCLUSIONS: Twelve neonates with severe NAS demonstrated similar nail abnormalities, likely secondary to NAS agitation and motor hyperactivity. Nail exams, therefore, are important in the setting of suspected or confirmed NAS to limit continued nail trauma and infection. Our findings also introduce an association between NAS severity and abnormal nail findings, which will require larger studies for further confirmation.
Assuntos
Doenças da Unha , Síndrome de Abstinência Neonatal , Transtornos Relacionados ao Uso de Opioides , Complicações na Gravidez , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Metadona , Síndrome de Abstinência Neonatal/diagnóstico , Síndrome de Abstinência Neonatal/tratamento farmacológico , Síndrome de Abstinência Neonatal/epidemiologia , Gravidez , Estudos RetrospectivosRESUMO
BACKGROUND: Current literature addressing dermatologic conditions associated with Down syndrome is limited, with emphasis on rare skin conditions and lack of consensus on the incidence of more common disorders. OBJECTIVE: We sought to evaluate dermatologic conditions in patients with Down syndrome diagnosed and managed by dermatologists. METHODS: This was a retrospective analysis of 101 pediatric and adult patients with Down syndrome seen by the University of Massachusetts Dermatology Department between 2008 and 2018. RESULTS: Folliculitis was the most common diagnosis overall (30.7%), followed by seborrheic dermatitis (26.7%) and hidradenitis suppurativa (22.8%). Eczematous dermatitis, alopecia areata, and xerosis were the most common diagnoses observed in children aged 0-12 years; hidradenitis suppurativa, folliculitis, and seborrheic dermatitis in adolescents aged 13-17 years; and folliculitis, seborrheic dermatitis, and xerosis in adults 18 years and older. Other notable diagnoses present overall included onychomycosis (9.9%) and psoriasis (8.9%). Malignant cutaneous tumors were present in two patients, specifically basal cell carcinoma and malignant melanoma in situ. LIMITATIONS: This was a retrospective, single-institution study. CONCLUSION: Dermatologic conditions in patients with Down syndrome vary by age but are most often adnexal and eczematous disorders. Trisomy of chromosome 21 and the resulting downstream effects, specifically on the immune system, may account for these findings.
Assuntos
Síndrome de Down , Hidradenite Supurativa , Psoríase , Dermatopatias , Neoplasias Cutâneas , Adolescente , Adulto , Criança , Pré-Escolar , Síndrome de Down/complicações , Síndrome de Down/epidemiologia , Humanos , Lactente , Recém-Nascido , Psoríase/complicações , Psoríase/diagnóstico , Psoríase/epidemiologia , Estudos Retrospectivos , Dermatopatias/diagnóstico , Dermatopatias/epidemiologia , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/epidemiologiaRESUMO
Verruciform xanthoma is a benign, wart-like lesion that can clinically mimic squamous cell carcinoma. We describe two teenage patients with severe genodermatoses, recessive dystrophic epidermolysis bullosa (RDEB), and keratitis-ichthyosis-deafness (KID) syndrome, respectively, each found to have plaques suspicious for malignancy, later demonstrated on histopathologic examination to be verruciform xanthoma. We discuss the connection between these severe genodermatoses and the suspected pathophysiology of verruciform xanthoma. In addition, we highlight the importance of recognizing verruciform xanthoma as a clinical mimicker of squamous cell carcinoma, for which patients with RDEB and KID syndrome are at increased risk.
Assuntos
Xantomatose/diagnóstico , Adolescente , Carcinoma de Células Escamosas/diagnóstico , Diagnóstico Diferencial , Epidermólise Bolhosa Distrófica/complicações , Epidermólise Bolhosa Distrófica/genética , Feminino , Humanos , Ceratite/complicações , Ceratite/genética , Masculino , Neoplasias Cutâneas/diagnóstico , Verrugas/diagnóstico , Verrugas/etiologia , Verrugas/genética , Xantomatose/etiologia , Xantomatose/genética , Xantomatose/patologiaRESUMO
Althouygh Menkes disease has well-recognized neurologic, developmental, and cutaneous features, the initial presentation may resemble child abuse. We describe a 5-month-old boy with multiple fractures indicative of nonaccidental trauma who was ultimately diagnosed with Menkes disease. Copper deficiency leads to connective tissue abnormalities and may result in subdural hematomas, wormian bones, cervical spine defects, rib fractures, and spurring of the long bone metaphyses. Several of these findings, including fractures and subdural hematomas, may be misinterpreted as child abuse.
Assuntos
Maus-Tratos Infantis/diagnóstico , Fraturas Múltiplas/diagnóstico por imagem , Recém-Nascido Prematuro , Síndrome dos Cabelos Torcidos/diagnóstico , Diagnóstico Diferencial , Serviço Hospitalar de Emergência , Seguimentos , Fraturas Múltiplas/diagnóstico , Humanos , Lactente , Masculino , Síndrome dos Cabelos Torcidos/diagnóstico por imagem , Radiografia/métodos , Medição de RiscoRESUMO
A 61-year-old immunosuppressed renal transplant patient with inflammatory bowel disease presented with tender pink nodules on the trunk and extremities. An initial biopsy was suggestive of metastatic Crohn disease, but after disease persistence, a second biopsy revealed disseminated Mycobacterium haemophilum. Atypical mycobacterial infections should be considered in immunosuppressed patients. This case highlights the complexities of diagnosing such infections in patients with an underlying granulomatous condition and the particular growth requirements of M. haemophilum.
Assuntos
Doença de Crohn/diagnóstico , Hospedeiro Imunocomprometido , Infecções por Mycobacterium/diagnóstico , Mycobacterium haemophilum , Infecções Oportunistas/diagnóstico , Doença de Crohn/complicações , Diagnóstico Diferencial , Feminino , Humanos , Imunossupressores/efeitos adversos , Falência Renal Crônica/cirurgia , Transplante de Rim/efeitos adversos , Pessoa de Meia-Idade , Infecções por Mycobacterium/microbiologia , Infecções por Mycobacterium/patologia , Infecções Oportunistas/microbiologia , Infecções Oportunistas/patologiaRESUMO
Phototherapy can be a safe and effective treatment for various skin diseases in children. Special considerations governing the use of this treatment modality in pediatric populations include patient, family, and facility-based factors that are oriented around heightened concerns with regard to safety and tolerability of treatment. Although phototherapy has been found to be effective in a wide range of dermatologic conditions affecting pediatric populations, including psoriasis, atopic dermatitis, pityriasis lichenoides, cutaneous T-cell lymphoma, and vitiligo, there is need for additional research on other conditions in which phototherapy has shown promise.
Assuntos
Seleção de Pacientes , Dermatopatias/radioterapia , Terapia Ultravioleta , Adolescente , Criança , Pré-Escolar , Dermatite Atópica/radioterapia , Humanos , Lactente , Recém-Nascido , Linfoma Cutâneo de Células T/radioterapia , Pitiríase Liquenoide/radioterapia , Psoríase/radioterapia , Terapia Ultravioleta/efeitos adversos , Terapia Ultravioleta/métodos , Vitiligo/radioterapiaRESUMO
PURPOSE OF REVIEW: Vitiligo and alopecia areata are common, disfiguring skin diseases. Treatment options are limited and include nontargeted approaches, such as corticosteroids, topical calcineurin inhibitors, narrow band ultraviolet B phototherapy, and other immune-modifying agents. The purpose of this article is to review shared, novel mechanisms between vitiligo and alopecia areata, as well as discuss how they inform the development of future targeted treatments. RECENT FINDINGS: Vitiligo and alopecia areata are both autoimmune diseases, and striking similarities in pathogenesis have been identified at the level of both the innate and adaptive immune system. Increased reactive oxygen species and high cellular stress level have been suggested as the initiating trigger of the innate immune system in both diseases, and genome-wide association studies have implicated risk alleles that influence both innate and adaptive immunity. Most importantly, mechanistic studies in mouse models of vitiligo and alopecia areata have specifically implicated an interferon (IFN)γ-driven immune response, including IFNγ, IFNγ-induced chemokines, and cytotoxic CD8 T cells as the main drivers of disease pathogenesis. These recent discoveries may reveal an effective strategy to develop new treatments, and several proof-of-concept clinical studies support this hypothesis. SUMMARY: The identification of IFNγ-driven immune signaling pathways has enabled discoveries of potential new treatments for vitiligo and alopecia areata, and supports initiation of larger clinical trials.
Assuntos
Alopecia em Áreas/imunologia , Autoimunidade , Imunossupressores/uso terapêutico , Imunoterapia/métodos , Vitiligo/imunologia , Imunidade Adaptativa/genética , Imunidade Adaptativa/imunologia , Alopecia em Áreas/tratamento farmacológico , Alopecia em Áreas/genética , Estudo de Associação Genômica Ampla , Humanos , Imunidade Inata/genética , Imunidade Inata/imunologia , Interferon gama/imunologia , Espécies Reativas de Oxigênio/imunologia , Transdução de Sinais/efeitos dos fármacos , Vitiligo/tratamento farmacológico , Vitiligo/genéticaRESUMO
We report two girls, ages 9 and 17 years, with a clinical diagnosis of neurofibromatosis 1 (NF-1) who presented with ill-defined, blanchable, erythematous patches on the dorsal feet and ankles. We hypothesized that these patches were a rare cutaneous finding in NF-1 that exist on a clinical and histopathologic spectrum with previously described NF-1 vascular lesions including blue-red macules and skin ulceration due to NF-1 vasculopathy. We suggest that these lesions be called neurovascular stains (NVSs) to unify their clinical and histopathologic features.
Assuntos
Neurofibromatose 1/patologia , Adolescente , Vasos Sanguíneos/patologia , Criança , Feminino , HumanosRESUMO
Capillary malformation (CM) can be a "red flag" for several syndromic vascular anomalies. We identified a subset of patients with diffuse CM and fetal pleural effusion and documented the type of CM, the etiology of the pleural effusion, the potential syndromic diagnosis, and outcome. Patients with a history of CM and fetal pleural effusion were identified by searching the database of patients evaluated at the Vascular Anomalies Center at Boston Children's Hospital. Standardized patient interviews and a retrospective review of records, photographs, and imaging studies were conducted. Five patients had diffuse CM and fetal pleural effusion. Two patients had macrocephaly-CM (M-CM), one had features of M-CM and CLOVES (congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and spinal/skeletal anomalies and/or scoliosis), and one had diffuse CM with overgrowth. The pleural fluid was chylous in four patients. One patient had thoracic lymphatic malformation. Recurrent effusion occurred in one patient coincident with pneumonia at age 11 years. Four patients had a history of reactive airway disease and episodic pulmonary infections. The diagnosis of vascular anomaly-overgrowth syndromes, particularly M-CM, should be considered in neonates with fetal pleural effusion.
Assuntos
Capilares/anormalidades , Derrame Pleural/complicações , Malformações Vasculares/etiologia , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Megalencefalia/diagnóstico , Derrame Pleural/diagnóstico , Malformações Vasculares/diagnósticoRESUMO
Hutchinson-Gilford progeria syndrome (HGPS) is a rare, uniformly fatal, premature aging disease with distinct dermatologic features. We sought to identify and describe the initial skin and hair findings as potential diagnostic signs of the disease. We performed a chart review of the structured initial intake histories of 39 individuals with HGPS enrolled in clinical trials from 2007 to 2010 at Boston Children's Hospital, limited to cutaneous history from birth to 24 months. Medical photographs were provided through the clinical trials and the Progeria Research Foundation Medical and Research Database at Brown University Center for Gerontology and Healthcare Research. All 39 patients reported skin and hair abnormalities within the first 24 months of life. Pathologies included sclerodermoid change, prominent superficial veins, dyspigmentation, and alopecia. The mean age of presentation for each finding was <12 months. The most frequently reported skin feature was sclerodermoid change, which commonly involved the abdomen and bilateral lower extremities. Prominent superficial vasculature manifested as circumoral cyanosis and pronounced veins on the scalp and body. Hypo- and hyperpigmentation were observed over areas of sclerodermoid change. Scalp alopecia progressed in a distinct pattern, with preservation of the hair over the midscalp and vertex areas for the longest period of time. HGPS has distinct cutaneous manifestations during the first 2 years of life that may be the first signs of disease. Awareness of these findings could expedite diagnosis.
Assuntos
Progéria/patologia , Pele/patologia , Boston , Criança , Pré-Escolar , Progressão da Doença , Feminino , Humanos , Lactente , MasculinoRESUMO
Although it is known that hematopoietic stem cell transplantation (HSCT) survivors are at risk of nonmelanoma skin cancer (NMSC), there is limited literature on the incidence of NMSC during childhood in this population. We present 4 HSCT patients ages 13 to 20 years diagnosed with NMSC in our clinic over a 1-year period. Each patient had multiple risk factors associated with NMSC including chronic graft-versus-host disease, prolonged immunosuppression, total-body irradiation, and voriconazole therapy. We conclude that the incidence of NMSC in children after HSCT may be underestimated and should be further investigated. Appropriate skin cancer screening, including annual skin examinations, are advised for pediatric patients with identifiable risk factors.
Assuntos
Carcinoma de Células Escamosas/epidemiologia , Transplante de Células-Tronco Hematopoéticas , Neoplasias Cutâneas/epidemiologia , Adolescente , Adulto , Antifúngicos/administração & dosagem , Boston/epidemiologia , Seguimentos , Doença Enxerto-Hospedeiro/complicações , Humanos , Hospedeiro Imunocomprometido , Incidência , Masculino , Estadiamento de Neoplasias , Prognóstico , Pirimidinas/administração & dosagem , Fatores de Risco , Neoplasias Cutâneas/diagnóstico , Taxa de Sobrevida , Sobreviventes , Triazóis/administração & dosagem , Voriconazol , Irradiação Corporal Total , Adulto JovemRESUMO
CONTEXT: Although systemic analgesic therapies are the mainstay of pain treatment in pediatric palliative care, there are cases where they fail to adequately relieve symptoms or produce side effects that undermine effectiveness. Regional anesthesia may be considered as a potential therapy for these patients. OBJECTIVES: To review the literature on regional techniques in pediatric patients with life-limiting and chronic conditions, including pain from tumor infiltration, chest pain in advanced pulmonary disease, chronic abdominal pain, phantom limb pain, and spasticity and dystonia. Where relevant, the authors' clinical experiences are included. METHODS: References were identified by searches of PubMed from 1980 until June 2012 with related terms. RESULTS: Case reports and case series were identified for each condition. Regional anesthesia techniques performed included central neuraxial infusions, peripheral nerve and plexus blocks or infusions, neurolytic blocks, and implanted intrathecal ports and pumps for baclofen, opioids, local anesthetics, and other adjuvants. The reports described positive contributions to the management of moderate-to-severe pain. Clinical context for these techniques frequently included the failure of systemic treatments and/or intolerable medication side effects. Complications varied according to the procedure and the underlying patient pathology; however, these risks were often acceptable when the potential benefits were consistent with the overall goals of care. CONCLUSION: The present medical literature on regional anesthesia techniques in children receiving palliative care is limited to case reports and case series. Based on this evidence, recommendations must be provisional. Careful thought and discussion with pain management specialists are encouraged when pain symptoms are inadequately managed or the treatments produce deleterious side effects.