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4.
Pediatr Dermatol ; 41(3): 465-467, 2024.
Article in English | MEDLINE | ID: mdl-38409816

ABSTRACT

Pediatric dermatofibromas are considered rare in young children and have not been well characterized, often misdiagnosed clinically. We performed a retrospective case series of children younger than 18 years with histopathologically diagnosed dermatofibromas at our institutions and evaluated age at onset and diagnosis, sex, lesion location, and size, associated symptoms, change over time, and pre-biopsy diagnosis. Overall, dermatofibromas were most common on the back and chest (20/53; 38%), followed by the legs (15/53; 28%) and arms (12/53; 23%) with the most common pre-biopsy diagnosis of "cyst" (23/53; 43%), followed by dermatofibroma (16/53; 30%), and pilomatricoma (12/53; 23%). Our study reinforces previous findings of truncal predominance of pediatric dermatofibromas, different from adults.


Subject(s)
Histiocytoma, Benign Fibrous , Skin Neoplasms , Humans , Retrospective Studies , Female , Male , Child , Skin Neoplasms/pathology , Histiocytoma, Benign Fibrous/pathology , Child, Preschool , Adolescent , Infant , Torso/pathology
5.
J Am Acad Dermatol ; 90(1): 111-121, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37271455

ABSTRACT

Since the initial identification of vaccine-derived rubella virus (RuV) in the cutaneous granulomas of pediatric patients with inborn errors of immunity in 2014, more than 80 cases of RuV granulomas have been reported implicating both vaccine-derived and wild type RuV. Previously thought to arise exclusively in patients with significant immunocompromise, the identification of RuV granulomas in clinically immunocompetent patients adds nuance to our understanding of the interplay between host environment, immune dysregulation, and RuV granuloma formation. This review summarizes the literature on RuV granulomas including clinical and histopathologic features, proposed pathomechanisms supporting granuloma development, and potential therapeutic options. There is no standardized algorithm to guide the workup and diagnosis of suspected RuV granulomas. We highlight the importance of contributing RuV granuloma cases to ongoing Centers for Disease Control and Prevention surveillance efforts to monitor wild type and vaccine-derived RuV transmission. Studies advancing our understanding of RuV granulomas may provide insights into the role of viral infectious agents in granulomatous disease pathogenesis and guide the development of improved therapeutic options.


Subject(s)
Rubella , Vaccines , Humans , Child , Rubella virus/physiology , Rubella/complications , Rubella/diagnosis , Granuloma , Vaccination
6.
JAMA Dermatol ; 159(12): 1387-1388, 2023 12 01.
Article in English | MEDLINE | ID: mdl-37878273

ABSTRACT

A man in his 30s with AIDS presented with acute onset painful scattered umbilicated papulopustules and ovoid ulcerated plaques with elevated, pink borders on the face, trunk, and extremities. What is your diagnosis?


Subject(s)
Staining and Labeling , Humans
9.
Ophthalmic Plast Reconstr Surg ; 39(5): e148-e150, 2023.
Article in English | MEDLINE | ID: mdl-37279015

ABSTRACT

Necrobiotic xanthogranuloma (NXG) is a progressive non-Langerhans cell histiocytosis with a predilection for the periorbital area. NXG is most commonly associated with monoclonal gammopathy and ophthalmic complications. The authors present a 69-year-old man who was evaluated for a left upper eyelid nodule and plaques on the lower extremities, trunk, abdomen, and right upper extremity. Biopsy of the eyelid was supportive for NXG. Serum protein electrophoresis was positive for a monoclonal gammopathy, IgG light chain kappa. MRI showed preseptal involvement. The periocular nodules cleared with a high dose of prednisone; however, the other skin lesions persisted. Bone marrow biopsy showed kappa-restricted 6% plasma cells and he was treated with intravenous immunoglobulin. This case illustrates the importance of clinicopathologic correlations to render an NXG diagnosis.


Subject(s)
Necrobiotic Xanthogranuloma , Paraproteinemias , Male , Humans , Aged , Necrobiotic Xanthogranuloma/complications , Necrobiotic Xanthogranuloma/diagnosis , Necrobiotic Xanthogranuloma/drug therapy , Paraproteinemias/complications , Paraproteinemias/diagnosis , Eyelids/pathology , Plasma Cells/pathology , Face
10.
Arch Dermatol Res ; 315(8): 2449-2451, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37184600

ABSTRACT

Use of inpatient teledermatology increased during the COVID-19 pandemic. We surveyed the Society for Dermatology Hospitalists to better characterize the impact of COVID-19 on teledermatology use by inpatient dermatology providers, particularly on provider perceptions of teledermatology. Prior to the COVID-19 pandemic, 40% (8/20) of surveyed providers had used telehealth at their institution to help perform inpatient consults, while 90% (18/20) adapted use of teledermatology during the pandemic. 80% (16/20) reported that their opinion of teledermatology changed as a result of the COVID-19 pandemic, with the vast majority (87.5%, 14/16) reporting having a more positive opinion. Benefits of teledermatology included efficiency, ability to increase access safely, and ability for clinicians to focus on complex cases. Some providers expressed concerns over the potential implications regarding the perception of dermatology within medicine, limitations of inadequate photos, and breakdowns in communication with consulting teams and patients. Robust algorithms and or utilization criteria of teledermatology may help to mitigate risk, while increasing access to inpatient dermatologic evaluation.


Subject(s)
COVID-19 , Dermatology , Skin Diseases , Telemedicine , Humans , Skin Diseases/diagnosis , Skin Diseases/therapy , Inpatients , Pandemics , COVID-19/epidemiology
14.
JAMA Dermatol ; 159(4): 365-366, 2023 04 01.
Article in English | MEDLINE | ID: mdl-36790788

ABSTRACT

This Viewpoint discusses actionable approaches in providing dermatologic care for displaced persons.


Subject(s)
Delivery of Health Care , Dermatology , Refugees , Humans
15.
JAMA Dermatol ; 159(3): 299-307, 2023 03 01.
Article in English | MEDLINE | ID: mdl-36753150

ABSTRACT

Importance: Morphea is an insidious inflammatory disorder of the skin and deeper tissues. Determining disease activity is challenging yet important to medical decision-making and patient outcomes. Objective: To develop and validate a scoring tool, the Morphea Activity Measure (MAM), to evaluate morphea disease activity of any type or severity that is easy to use in clinical and research settings. Design, Setting, and Participants: This pilot diagnostic study was conducted from September 9, 2019, to March 6, 2020, in 2 phases: development and validation. During the development phase, 14 morphea experts (dermatologists and pediatric dermatologists) used a Delphi consensus method to determine items that would be included in the MAM. The validation phase included 8 investigators who evaluated the tool in collaboration with 14 patients with pediatric morphea (recruited from a referral center [Medical College of Wisconsin]) during a 1-day in-person meeting on March 6, 2020. Main Outcomes and Measures: During the development phase, online survey items were evaluated by experts in morphea using a Likert scale (score range, 0-10, with 0 indicating not important and 10 indicating very important); agreement was defined as a median score of 7.0 or higher, disagreement as a median score of 3.9 or lower, and no consensus as a median score of 4.0 to 6.9. During the validation phase, reliability (interrater and intrarater agreement using intraclass correlation coefficients), validity (using the content validity index and κ statistics as well as correlations with the modified Localized Scleroderma Severity Index and the Physician Global Assessment of Activity using Spearman ρ coefficients), and viability (using qualitative interviews of investigators who used the MAM tool) were evaluated. Descriptive statistics were used for quantitative variables. Data on race and ethnicity categories were collected but not analyzed because skin color was more relevant for the purposes of this study. Results: Among 14 survey respondents during the development phase, 9 (64.3%) were pediatric dermatologists and 5 (35.7%) were dermatologists. After 2 rounds, a final tool was developed comprising 10 items that experts agreed were indicative of morphea activity (new lesion in the past 3 months, enlarging lesion in the past 3 months, linear lesion developing progressive atrophy in the past 3 months, erythema, violaceous rim or color, warmth to the touch, induration, white-yellow or waxy appearance, shiny white wrinkling, and body surface area). The validation phase was conducted with 14 patients (median age, 14.5 years [range, 8.0-18.0 years]; 8 [57.1%] female), 2 dermatologists, and 6 pediatric dermatologists. Interrater and intrarater agreement for MAM total scores was good, with intraclass correlation coefficients of 0.844 (95% CI, 0.681-0.942) for interrater agreement and 0.856 (95% CI, 0.791-0.901) for intrarater agreement. Correlations between the MAM and the modified Localized Scleroderma Severity Index (Spearman ρ = 0.747; P < .001) and the MAM and the Physician Global Assessment of Activity (Spearman ρ = 0.729; P < .001) were moderately strong. In qualitative interviews, evaluators agreed that the tool was easy to use, measured morphea disease activity at a single time point, and should be responsive to changes in morphea disease activity over multiple time points. Conclusions and Relevance: In this study, the MAM was found to be a reliable, valid, and viable tool to measure pediatric morphea activity. Further testing to assess validity in adults and responsiveness to change is needed.


Subject(s)
Physicians , Scleroderma, Localized , Adult , Humans , Child , Female , Adolescent , Male , Scleroderma, Localized/diagnosis , Scleroderma, Localized/pathology , Reproducibility of Results , Severity of Illness Index , Skin/pathology
16.
IDCases ; 31: e01694, 2023.
Article in English | MEDLINE | ID: mdl-36687371
17.
18.
JAMA Dermatol ; 158(10): 1216-1218, 2022 Oct 01.
Article in English | MEDLINE | ID: mdl-35921087

ABSTRACT

This case report describes a woman in her 40s with a 2-week history of abrupt painful ulcerations of the perineum.


Subject(s)
Perineum , Skin Ulcer , Humans , Skin Ulcer/diagnosis , Skin Ulcer/etiology
19.
Pediatr Dermatol ; 39(4): 616-618, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35560434

ABSTRACT

A 6-year-old girl presented with nightly fever, persistent joint pain of the knees, ankles, lower back, and hip. Her skin lesions were evanescent salmon-colored patches along with persistent pruritic light to dark pink papules and plaques on her face, post-auricular scalp, trunk, thigh, and bilateral upper extremities. Skin biopsy supported the diagnosis of fixed papules and plaques of systemic juvenile idiopathic arthritis (sJIA). We report this case to highlight diagnostic features of this exceedingly rare cutaneous presentation of sJIA presenting with typical cutaneous salmon-colored evanescent eruptions.


Subject(s)
Arthritis, Juvenile , Exanthema , Still's Disease, Adult-Onset , Arthritis, Juvenile/complications , Arthritis, Juvenile/diagnosis , Arthritis, Juvenile/drug therapy , Biopsy , Child , Exanthema/pathology , Female , Humans , Skin/pathology , Still's Disease, Adult-Onset/diagnosis , Still's Disease, Adult-Onset/pathology
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