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4.
Pediatr Dermatol ; 38(1): 45-49, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32767593

ABSTRACT

BACKGROUND/OBJECTIVE: Papular scars are a recently described clinical phenotype of acne scarring characterized by papules occurring on the nose and chin. We have observed a similar presentation of nasal papules among patients seen in our clinic for acne and sought to further characterize the clinical and histopathological characteristics of this entity. METHODS: In this single-site case series, a retrospective review of electronic medical records of patients with nasal papules in association with acne vulgaris between April 2018 and April 2019 was performed. Clinical and histopathologic findings were recorded. RESULTS: We identified 20 patients who presented with a similar clinical phenotype of predominantly skin-colored, dome-shaped papules concentrated on the nose and chin in association with a history of more classic facial acne vulgaris. Papular lesions were seen predominately in adolescent Hispanic males. Concomitant acne on other areas of the face was identified in 18 patients at presentation while two patients had a history of adolescent acne. Biopsies were performed for five patients. Histopathologic examination demonstrated features of fibrosis and dilated thin-walled blood vessels, typical of angiofibromas. CONCLUSION: We present a series of adolescent patients with large, flesh-colored to erythematous papules seen predominantly on the nose. These lesions are histologically indistinguishable from angiofibromas and may represent an under-recognized yet disfiguring sequela of acne that may disproportionately affect adolescents with skin of color.


Subject(s)
Acne Vulgaris , Angiofibroma , Acne Vulgaris/diagnosis , Adolescent , Angiofibroma/diagnosis , Humans , Male , Nose , Retrospective Studies , Skin
5.
Pediatr Dermatol ; 37(6): 1185-1186, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32869334

ABSTRACT

BRAF inhibitor-induced neutrophilic panniculitis is a rare event that is well-characterized in adults undergoing therapy for metastatic melanoma. To date, there are very few reports of this event in children undergoing BRAF inhibitor therapy for low-grade gliomas, all of which were seen with vemurafenib. We report a case of dabrafenib-induced neutrophilic panniculitis in a 9-year-old girl that manifested within several weeks of initiating dual BRAF-MEK inhibitor therapy for glioblastoma multiforme. This case highlights neutrophilic panniculitis as a side effect of dabrafenib in children and serves as a reminder to consider cutaneous side effects of BRAF inhibitors as they are increasingly used to treat children with primary brain tumors.


Subject(s)
Glioblastoma , Panniculitis , Skin Neoplasms , Antineoplastic Combined Chemotherapy Protocols , Child , Female , Glioblastoma/drug therapy , Humans , Imidazoles , Mitogen-Activated Protein Kinase Kinases/therapeutic use , Oximes/adverse effects , Panniculitis/chemically induced , Panniculitis/diagnosis , Protein Kinase Inhibitors/adverse effects , Proto-Oncogene Proteins B-raf/genetics , Pyridones/therapeutic use , Skin Neoplasms/drug therapy
6.
JAMA Dermatol ; 156(2): 196-200, 2020 02 01.
Article in English | MEDLINE | ID: mdl-31895414

ABSTRACT

Importance: Olmsted syndrome is a rare and disabling genodermatosis for which no successful treatment is currently available. Objective: To evaluate the clinical response to the mammalian target of rapamycin (mTOR) inhibitor sirolimus and/or the epidermal growth factor receptor (EGFR) inhibitor erlotinib among patients with Olmsted syndrome. Design, Setting, and Participants: This case series focused on 4 children with treatment-refractory Olmsted syndrome. These children received treatments (initiated in 2017 and 2018) at the outpatient dermatology clinic at the Children's Hospital of Wisconsin in Milwaukee, Wisconsin; Children's National Hospital in Washington, DC; and Hospital Infantil Pequeno Príncipe, Curitiba in Paraná, Brazil. Exposures: Immunohistochemical analyses for mTOR and EGFR activation were performed on skin biopsy specimens from 2 patients. Oral sirolimus was administered to these 2 patients at a dosage of 0.8 mg/m2 twice daily, titrated to a goal trough whole-blood concentration of 10 to 15 ng/mL. Erlotinib was administered to all 4 patients at a dosage of 2 mg/kg/d. Main Outcomes and Measures: Clinical responses were assessed with visual analog scales for pruritus and pain and/or the Children's Dermatology Life Quality Index. Adverse effects were monitored throughout treatment. Results: Four patients (mean [SD] age, 7 [6] years; 2 boys and 2 girls) were analyzed. Lesional skin immunostaining showed increased phosphorylated ribosomal protein S6 (RPS6) and phosphorylated EGFR staining in the epidermis, indicating enhanced mTOR and EGFR signaling activation. Patients 1 and 2 were initially treated with sirolimus, displaying substantial clinical improvement in erythema and periorificial hyperkeratosis afterward. When switched to erlotinib, these patients showed substantial palmoplantar keratoderma (PPK) improvement. Patients 3 and 4 were treated with erlotinib only and later showed rapid and near complete resolution of PPK and substantial improvement in Children's Dermatology Life Quality Index scores. All 4 patients had sustained improvements in pruritus and pain. No severe adverse effects were reported. Conclusions and Relevance: This study's findings suggest that the EGFR-mTOR cascade may play a substantial role in the pathophysiological process of Olmsted syndrome and may serve as a major therapeutic target. Oral sirolimus and erlotinib may be a promising, life-altering treatment for pediatric patients with Olmsted syndrome.


Subject(s)
Erlotinib Hydrochloride/administration & dosage , Keratoderma, Palmoplantar/drug therapy , Protein Kinase Inhibitors/administration & dosage , Sirolimus/administration & dosage , Adolescent , Brazil , Child , Child, Preschool , ErbB Receptors/antagonists & inhibitors , Female , Humans , Immunosuppressive Agents/administration & dosage , Infant , Keratoderma, Palmoplantar/genetics , Male , Signal Transduction/drug effects , Syndrome , TOR Serine-Threonine Kinases/antagonists & inhibitors , Treatment Outcome
7.
Pediatr Dermatol ; 35(5): 683-684, 2018 Sep.
Article in English | MEDLINE | ID: mdl-30211459
8.
J Am Acad Dermatol ; 78(1): 70-80, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29102053

ABSTRACT

BACKGROUND: Patients with psoriasis are at an increased risk for depression. However, the impact of treatment on this risk is unclear. OBJECTIVE: Evaluate the incidence and impact of treatment on depression among patients with moderate-to-severe psoriasis. METHODS: We defined a study population within the Psoriasis Longitudinal Assessment and Registry and measured the incidence of depressive symptoms (Hospital Anxiety and Depression Scale-Depression score ≥8) and adverse events (AEs) of depression within cohorts receiving biologics, conventional systemic therapies, or phototherapy. Patients were evaluated at approximately 6-month intervals. Multivariate modeling determined the impact of treatment on risk. RESULTS: The incidence rates of depressive symptoms were 3.01 per 100 patient-years (PYs) (95% confidence interval [CI], 2.73-3.32), 5.85 per 100 PYs (95% CI, 4.29-7.97), and 5.70 per 100 PYs (95% CI, 4.58-7.10) for biologics, phototherapy, and conventional therapy, respectively. Compared with conventional therapy, biologics reduced the risk for depressive symptoms (hazard ratio, 0.76; 95% CI, 0.59-0.98), whereas phototherapy did not (hazard ratio, 1.05; 95% CI, 0.71-1.54). The incidence rates for AEs of depression were 0.21 per 100 PYs (95% CI, 0.15-0.31) for biologics, 0.55 per 100 PYs (95% CI, 0.21-1.47) for phototherapy, and 0.14 per 100 PYs (95% CI, 0.03-0.55) for conventional therapy; the fact that there were too few events (37 AEs) precluded modeling. LIMITATIONS: Incomplete capture of depression and confounders in the patients on registry. CONCLUSION: Compared with conventional therapy, biologics appear to be associated with a lower incidence of depressive symptoms among patients with psoriasis.


Subject(s)
Biological Products/therapeutic use , Depression/epidemiology , Psoriasis/psychology , Psoriasis/therapy , Quality of Life , Registries , Adult , Age Factors , Biological Products/pharmacology , Comorbidity , Depression/diagnosis , Depressive Disorder/diagnosis , Depressive Disorder/epidemiology , Female , Humans , Incidence , Longitudinal Studies , Male , Middle Aged , Phototherapy/methods , Prognosis , Proportional Hazards Models , Psoriasis/diagnosis , Risk Assessment , Severity of Illness Index , Sex Factors , United States/epidemiology
9.
Clin Dermatol ; 35(6): 530-540, 2017.
Article in English | MEDLINE | ID: mdl-29191345

ABSTRACT

Cutaneous vasculitis, inflammatory destruction of blood vessels, can present with a wide range of clinical and pathologic findings across a number of heterogeneous conditions. Although some vasculitides are present in both children and adults, some important differences exist in clinical presentation, etiology, management, and prognosis in childhood vasculitis versus adult vasculitis. Cutaneous vasculitis is rare in children, and most childhood vasculitides, of which Henoch-Schönlein purpura is the most common, histologically are small vessel leukocytoclastic vasculitis. In children, infectious etiologies are more common than in adults. Childhood cutaneous vasculitis is most often self-limited with a good prognosis, and treatment is mainly supportive. © 2017 Elsevier Inc. All rights reserved.


Subject(s)
Skin Diseases, Vascular , Vasculitis , Adolescent , Adult , Child , Child, Preschool , Humans , IgA Vasculitis/diagnosis , IgA Vasculitis/epidemiology , IgA Vasculitis/etiology , IgA Vasculitis/therapy , Infant , Infant, Newborn , Mucocutaneous Lymph Node Syndrome/diagnosis , Mucocutaneous Lymph Node Syndrome/drug therapy , Mucocutaneous Lymph Node Syndrome/epidemiology , Mucocutaneous Lymph Node Syndrome/etiology , Polyarteritis Nodosa/diagnosis , Polyarteritis Nodosa/drug therapy , Polyarteritis Nodosa/epidemiology , Polyarteritis Nodosa/etiology , Skin Diseases, Vascular/diagnosis , Skin Diseases, Vascular/epidemiology , Skin Diseases, Vascular/etiology , Skin Diseases, Vascular/therapy , Vasculitis/diagnosis , Vasculitis/epidemiology , Vasculitis/etiology , Vasculitis/therapy , Vasculitis, Leukocytoclastic, Cutaneous/diagnosis , Vasculitis, Leukocytoclastic, Cutaneous/drug therapy , Vasculitis, Leukocytoclastic, Cutaneous/etiology
10.
Clin Dermatol ; 35(6): 555-565, 2017.
Article in English | MEDLINE | ID: mdl-29191347

ABSTRACT

Granulomatous diseases represent a heterogeneous group of conditions characterized by histiocytic inflammation that affect patients of any age. These diseases differ widely in their pathogenesis and include infectious and noninfectious conditions. This review focuses on noninfectious granulomatous conditions, with particular emphasis on age-related differences in the onset, epidemiology, clinical manifestations, prognosis, and age-specific management of specific granulomatous disorders. Knowledge of age-specific aspects of granulomatous conditions in adults and children improves both the extent of the diagnostic workup and the management of these patients.


Subject(s)
Granuloma/diagnosis , Granuloma/therapy , Sarcoidosis/diagnosis , Skin Diseases/diagnosis , Skin Diseases/therapy , Adolescent , Adult , Child, Preschool , Erdheim-Chester Disease/diagnosis , Erdheim-Chester Disease/epidemiology , Erdheim-Chester Disease/therapy , Granuloma/epidemiology , Granuloma Annulare/diagnosis , Granuloma Annulare/epidemiology , Granuloma Annulare/therapy , Humans , Infant , Infant, Newborn , Melkersson-Rosenthal Syndrome/drug therapy , Necrobiotic Xanthogranuloma/diagnosis , Necrobiotic Xanthogranuloma/epidemiology , Necrobiotic Xanthogranuloma/therapy , Sarcoidosis/drug therapy , Sarcoidosis/epidemiology , Sarcoidosis/etiology , Skin Diseases/epidemiology , Skin Diseases/etiology , Xanthogranuloma, Juvenile/diagnosis , Xanthogranuloma, Juvenile/epidemiology , Xanthogranuloma, Juvenile/therapy
11.
Clin Dermatol ; 35(1): 64-67, 2017.
Article in English | MEDLINE | ID: mdl-27938814

ABSTRACT

Both the metabolism and dietary intake of vitamins and minerals are essential to homeostatic function in the body. Dietary excess or deficiency, as well as genetic and acquired disorders in metabolism, can present dermatologically and systemically. More specifically, disorders in metabolism of zinc, biotin, essential fatty acids, and vitamin B, can appear with acrally distributed dermatoses. Recognition of the dermatologic manifestations associated with nutritional disorders is important for early diagnosis and management.


Subject(s)
Biotin/deficiency , Deficiency Diseases/complications , Fatty Acids, Essential/deficiency , Foot Dermatoses/etiology , Hand Dermatoses/etiology , Metabolic Diseases/complications , Zinc/deficiency , Biotin/metabolism , Deficiency Diseases/diagnosis , Deficiency Diseases/drug therapy , Dietary Supplements , Humans , Metabolic Diseases/diagnosis , Metabolic Diseases/drug therapy , Zinc/metabolism
13.
Clin Dermatol ; 33(4): 414-9, 2015.
Article in English | MEDLINE | ID: mdl-26051055

ABSTRACT

The appropriate intake and metabolism of vitamins and minerals are critical to maintaining homeostasis. Imbalance in essential nutrients, either through dietary excess or deficiency or disorders in metabolism, can result in a spectrum of dermatologic and systemic manifestations. Certain nutrient deficiencies produce a characteristic pattern of cutaneous eruption. Recognition of these patterns is important, as they can alert the physician to an underlying nutritional disease. We review nutritional diseases involving zinc, biotin, essential fatty acids, vitamin B6 (pyridoxine), and riboflavin that present specifically with intertriginous eruptions.


Subject(s)
Acrodermatitis/epidemiology , Avitaminosis/diagnosis , Avitaminosis/epidemiology , Deficiency Diseases/epidemiology , Intertrigo/epidemiology , Zinc/deficiency , Acrodermatitis/diagnosis , Comorbidity , Deficiency Diseases/diagnosis , Fatty Acids, Essential/deficiency , Female , Humans , Intertrigo/diagnosis , Male , Prevalence , Prognosis
15.
Clin Dermatol ; 31(6): 677-700, 2013.
Article in English | MEDLINE | ID: mdl-24160272

ABSTRACT

Many dermatologic diseases are chronic with no definitive cure. For some diseases, the etiology is not completely understood, with treatment being difficult and associated with side effects. In such cases, patients may try alternative treatments to prevent onset, reduce symptom severity, or prevent reoccurrence of a disease. Dietary modification, through supplementation and exclusion, is an extremely popular treatment modality for patients with dermatologic conditions. It is, therefore, important for dermatologists to be aware of the growing body of literature pertaining to nutrition and skin disease to appropriately inform patients on benefits and harms of specific dietary interventions. We address the role of nutrition in psoriasis, atopic dermatitis, urticaria, and bullous diseases and specific dietary modifications as an adjunct or alternative to conventional therapy.


Subject(s)
Diet , Dietary Supplements , Skin Diseases/diet therapy , Skin Diseases/drug therapy , Trace Elements/therapeutic use , Vitamins/therapeutic use , Acrodermatitis/drug therapy , Acrodermatitis/etiology , Dermatitis, Atopic/diet therapy , Dermatitis, Atopic/drug therapy , Dermatitis, Atopic/etiology , Food Hypersensitivity/complications , Humans , Necrolytic Migratory Erythema/etiology , Pellagra/drug therapy , Porphyrias, Hepatic/diet therapy , Porphyrias, Hepatic/drug therapy , Porphyrias, Hepatic/etiology , Psoriasis/diet therapy , Psoriasis/drug therapy , Psoriasis/etiology , Skin Diseases/etiology , Skin Diseases, Vesiculobullous/diet therapy , Skin Diseases, Vesiculobullous/drug therapy , Skin Diseases, Vesiculobullous/etiology , Urticaria/diet therapy , Urticaria/drug therapy , Urticaria/etiology , Zinc/deficiency
18.
Clin Dermatol ; 30(5): 486-91, 2012.
Article in English | MEDLINE | ID: mdl-22902218

ABSTRACT

In dermatology, clinical photographs are an essential component of patient care, enabling clinicians to document changes in skin pathology over time. Recent advances in digital technology and the electronic medical record have revolutionized clinical photography; however, these advances bring with them new ethical, legal, and social concerns. Photographs, more than other forms of documentation, have the potential to make patients uncomfortable. The act of photography, especially for those images requiring exposure of the genital area or the entire body, can be an uncomfortable experience for patients, necessitating the clinician and photographer to take an empathic stance in this setting. The Internet has elicited an increasing, and a very real, concern for patients about possible distribution and use of images outside of their individual care. The clinician and staff can allay these fears by professionally and empathetically addressing their concerns. In addition, it is important that patients receive appropriate informed consent about clinical photographs and the potential use of the images in their care, education, and research. Given the multitude of methods for recording clinical photographs, combined with the increasing complexity of image storage, standardization becomes a critical tool in providing consistency among images and achieving more equitable and efficacious care. To achieve this goal and improve the baseline standard of continuity of care for dermatological practices, we review the role of photographs, develop a model for patient consent, and establish standards for photography so as to provide the most ethical care for the patient.


Subject(s)
Bioethical Issues , Nevus, Pigmented/pathology , Photography/ethics , Skin Neoplasms/pathology , Child, Preschool , Confidentiality , Dermatology/ethics , Genitalia, Male , Humans , Informed Consent , Male
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