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1.
Epilepsia ; 65(4): 1147-1148, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38441298

Subject(s)
Ring Chromosomes , Humans
2.
Int J Womens Dermatol ; 9(3): e100, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37502778

ABSTRACT

There are a growing number of patients with acute and recurrent pustular reactive dermatitis reported without clear parameters to define the entities. Consolidation of cases under the term acute and recurrent pustulosis (ARP) will aid dermatologists in diagnosing such patients in the future. Objective: Describe the parameters which define acute and recurrent pustulosis and communicate the high predominance for onset in young women based on reported cases. Methods: PubMed literature search for reports of recurrent follicularly centered neutrophilic eruptions. Results: According to the clinical characteristics of ARP, 23 patients were identified from prior reports. Interestingly, 20 out of 23 patients were women with a high predominance in early adulthood. Limitations: This is an understudied and underreported clinical entity. Therefore, limitations include availability of case reports and lack of prior research available on PubMed. Conclusion: ARP is defined as follicular pustules that occur and remit without treatment and within a week of an identifiable trigger, predominantly affecting women. Consolidating reports of ARP under clear criteria will aid clinical dermatologists in diagnosing this unreported dermatitis.

4.
JAMA Dermatol ; 159(2): 136-138, 2023 Feb 01.
Article in English | MEDLINE | ID: mdl-36542399
5.
J Clin Invest ; 133(1)2023 01 03.
Article in English | MEDLINE | ID: mdl-36355435

ABSTRACT

BackgroundAcute febrile neutrophilic dermatosis (Sweet syndrome) is a potentially fatal multiorgan inflammatory disease characterized by fever, leukocytosis, and a rash with a neutrophilic infiltrate. The disease pathophysiology remains elusive, and current dogma suggests that Sweet syndrome is a process of reactivity to an unknown antigen. Corticosteroids and steroid-sparing agents remain frontline therapies, but refractory cases pose a clinical challenge.MethodsA 51-year-old woman with multiorgan Sweet syndrome developed serious corticosteroid-related side effects and was refractory to steroid-sparing agents. Blood counts, liver enzymes, and skin histopathology supported the diagnosis. Whole-genome sequencing, transcriptomic profiling, and cellular assays of the patient's skin and neutrophils were performed.ResultsWe identified elevated IL-1 signaling in lesional Sweet syndrome skin caused by a PIK3R1 gain-of-function mutation specifically found in neutrophils. This mutation increased neutrophil migration toward IL-1ß and neutrophil respiratory burst. Targeted treatment of the patient with an IL-1 receptor 1 antagonist resulted in a dramatic therapeutic response and enabled a tapering off of corticosteroids.ConclusionDysregulated PI3K/AKT signaling is the first signaling pathway linked to Sweet syndrome and suggests that this syndrome may be caused by acquired mutations that modulate neutrophil function. Moreover, integration of molecular data across multiple levels identified a distinct subtype within a heterogeneous disease that resulted in a rational and successful clinical intervention. Future patients will benefit from efforts to identify potential mutations. The ability to directly interrogate the diseased skin allows this method to be generalizable to other inflammatory diseases and demonstrates a potential personalized medicine approach for patients with clinically challenging disease.Funding SourcesBerstein Foundation, NIH, Veterans Affairs (VA) Administration, Moseley Foundation, and H.T. Leung Foundation.


Subject(s)
Sweet Syndrome , Female , Humans , Middle Aged , Sweet Syndrome/drug therapy , Sweet Syndrome/genetics , Neutrophils/pathology , Phosphatidylinositol 3-Kinases/genetics , Adrenal Cortex Hormones , Mutation , Class Ia Phosphatidylinositol 3-Kinase
7.
Cutis ; 110(4): 175-176, 2022 10.
Article in English | MEDLINE | ID: mdl-36446090

Subject(s)
Petrolatum , Humans
11.
JAMA Dermatol ; 158(8): 865-866, 2022 08 01.
Article in English | MEDLINE | ID: mdl-35704294
12.
Int J Womens Dermatol ; 8(1): e006, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35620033

ABSTRACT

Allergic contact dermatitis represents a T cell-mediated, delayed-type hypersensitivity response to exogenous agents. While allergic contact dermatitis is one of the most common causes of skin disease encountered by dermatologists, emerging trends within the field are in constant flux, as influenced by ever-changing industry practices and evolving consumer behaviors. Although certain allergens continue to predominate, new chemicals are frequently being introduced, thus shifting the pattern of allergen exposure and sensitization. This review examines the impact of trends in new and emerging contact allergens, with particular attention to clinical contexts in which these agents may be encountered. In addition, we offer a working knowledge of these allergens' characteristics, sources, and relevance, while outlining recommendations to accurately evaluate, diagnose, and provide appropriate counseling for these diseases.

14.
JAMA Dermatol ; 157(3): 326-329, 2021 03 01.
Article in English | MEDLINE | ID: mdl-33566057

ABSTRACT

In 1981, the HIV/AIDS epidemic was first recognized in young gay men presenting with opportunistic infections and Kaposi sarcoma. Over the past 40 years, there has been an unparalleled and hugely successful effort on the part of physicians, scientists, public health experts, community activists, and grassroots organizations to study, treat, and prevent HIV/AIDS. Yet the role of dermatologists in the investigation of HIV/AIDS and in the treatment of infected patients has largely been neglected in the historical literature. It is important to revisit dermatologists' historic contributions and problematic biases during this epidemic and honor the legacy of the dermatologists who were instrumental in treating and advocating for patients affected by HIV/AIDS.


Subject(s)
Acquired Immunodeficiency Syndrome/history , Dermatologists/history , HIV Infections/history , Acquired Immunodeficiency Syndrome/epidemiology , Anniversaries and Special Events , Dermatologists/organization & administration , Dermatology/history , HIV Infections/epidemiology , History, 20th Century , Humans , Physician's Role/history
15.
J Am Acad Dermatol ; 84(5): 1348-1355, 2021 May.
Article in English | MEDLINE | ID: mdl-33434594

ABSTRACT

BACKGROUND: There are limited data regarding the long-term outcomes of spironolactone use for women with acne and its effect on truncal acne. OBJECTIVE: To comprehensively describe outcomes of patients treated with spironolactone in routine clinical practice, including long-term outcomes. METHODS: We performed a retrospective case series of 403 adult women treated for acne with spironolactone at an academic medical center between 2008 and 2019. Rates of objective, as assessed by Comprehensive Acne Severity Scale scores, and subjective acne clearance were evaluated, as well as rates of treatment discontinuation, dosage changes, and drug survival. Logistic regression was used to assess for association between incidence of menstrual adverse effects and combined oral contraceptive use. RESULTS: As evaluated by Comprehensive Acne Severity Scale scores, at the first follow-up, 75.5%, 84.0%, and 80.2% of patients with available data had reduction or complete clearance of acne on the face, chest, and back, respectively. The mean drug survival was 470.7 days. Menstrual adverse effects were less common among those using combined oral contraception (odds ratio, 0.23; 95% confidence interval, 0.11-0.50). LIMITATIONS: This study was conducted at a single academic medical center. CONCLUSIONS: Spironolactone improves clinical outcomes and is well tolerated for many adult women with acne using it for an extended duration.


Subject(s)
Acne Vulgaris/drug therapy , Menstruation Disturbances/epidemiology , Mineralocorticoid Receptor Antagonists/administration & dosage , Spironolactone/administration & dosage , Administration, Oral , Adult , Contraceptives, Oral, Combined/administration & dosage , Contraceptives, Oral, Combined/adverse effects , Drug Therapy, Combination/adverse effects , Drug Therapy, Combination/methods , Female , Humans , Incidence , Menstruation Disturbances/chemically induced , Mineralocorticoid Receptor Antagonists/adverse effects , Retrospective Studies , Spironolactone/adverse effects , Time Factors , Torso , Treatment Outcome , Young Adult
17.
Int J Dermatol ; 59(11): 1401-1408, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32966597

ABSTRACT

Today, parents are warned to protect their children from the sun's ultraviolet (UV) rays, the most preventable and leading cause of skin cancer. Yet, during the first half of the 20th century, the medical community widely extolled the health benefits of daily sunbaths for babies and children. What initially had begun as evidence-based medical therapies to prevent pediatric diseases, specifically tuberculosis and rickets, soon took on a life of its own as physicians, public health experts, and the general public embraced sunbathing and tanning as a means to ensure health and wellbeing for children and families. Here, we trace how specific medical therapies entered mainstream pediatric medicine and, converging with societal and cultural forces, shaped attitudes and behaviors towards sunbathing that still exist today. Understanding our complex history with the sun may shed light on the current peak of skin cancer incidence and future disease development. Moreover, it may help improve how we educate parents and children about sun safety by taking into account the current social and cultural context of medical practice and health communication.


Subject(s)
Skin Neoplasms , Sunbathing , Child , Health Knowledge, Attitudes, Practice , Humans , Phototherapy , Skin Neoplasms/drug therapy , Skin Neoplasms/prevention & control , Sunscreening Agents/therapeutic use , Ultraviolet Rays
18.
Int J Womens Dermatol ; 6(1): 70-71, 2020 Jan.
Article in English | MEDLINE | ID: mdl-32025564
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