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A Systematic Review of Follicular Psoriasis: A Unique but Under-Recognized Entity.
J Psoriasis Psoriatic Arthritis
October 2023
Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Background: Follicular psoriasis (FP) is a rare and under-recognized subtype of psoriasis that affects hair follicles and can be frequently misdiagnosed due to its unique presentation.
Objective: We aimed to analyze the frequently reported clinical, histological, and dermatoscopic features of FP, as well as their treatment options.
Methods: We conducted a systematic review of the PubMed/MEDLINE database using the search terms "follicular" and "psoriasis.
Grading Acanthosis Nigricans Using a Smartphone and Color Analysis: A Novel Noninvasive Method to Screen for Impaired Glucose Tolerance and Type 2 Diabetes.
Diabetes Spectr
February 2024
Department of Life Sciences, University of the West Indies, St. Augustine, St. Augustine, Trinidad and Tobago.
Article Synopsis
- The study aimed to create ANcam, a smartphone-based method for noninvasive screening of acanthosis nigricans (AN) in people with impaired glucose tolerance (IGT).
- Participants included both adults and juveniles in Trinidad and Tobago, with data collected on their health history and A1C levels; images were analyzed using the ANcam app.
- Results showed ANcam effectively identified hyperpigmentation related to IGT with high accuracy, revealing strong correlations between specific color channels and health metrics like BMI and blood pressure.
Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis.
Cureus
October 2022
Dermatology Department, King Abdulaziz Hospital, Makkah, SAU.
Article Synopsis
- - Pityriasis rubra pilaris (PRP) is a rare skin condition with six types; Type 5 is known as atypical juvenile PRP, which affects younger individuals.
- - A 17-year-old boy, experiencing itchy skin lesions since age seven, was diagnosed with Type 5 PRP after skin examination and a biopsy showed specific patterns in the skin.
- - The patient was treated with isotretinoin (20 mg twice daily) and scheduled for regular follow-ups to monitor his condition.
The clinical features of juvenile dermatomyositis: A single-centre inception cohort.
Semin Arthritis Rheum
December 2022
Child Health Evaluative Sciences, Hospital for Sick Children Research Institute, Toronto, Canada; Division of Rheumatology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada; Department of Pediatrics, Faculty of Medicine, University of Toronto, Toronto, ON, Canada; Institute of Health Policy, Management & Evaluation, The Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada. Electronic address:
Introduction: Juvenile Dermatomyositis (JDM), a severe and rare autoimmune disease, is the most common idiopathic inflammatory myopathy in children. We describe the clinical features of a large single-centre cohort.
Methods: We studied an inception cohort (0-18 years old) referred for diagnosis to the JDM clinic at The Hospital for Sick Children (SickKids), between January 1989 and September 2017.
Juvenile Granulosa Cell Tumor Mimicking HAIR-AN in a 4-year-old: A Case Report.
J Clin Res Pediatr Endocrinol
May 2024
Stony Brook University, Renaissance Faculty of Medicine, Department of Surgery, Division of Pediatric Surgery, New York, USA
Predominantly androgen secreting juvenile granulosa cell tumors (JGCT) are uncommon and few reports have been published. We present a case of a JGCT that presented with signs of prepubertal hyperandrogenism and insulin resistance to highlight the possible interaction between hyperandrogenemia and hyperinsulinism. A 4-year-old girl presented with acanthosis nigricans and hyperinsulinism, mimicking the hyperandrogenism, insulin resistance and acanthosis nigricans syndrome at an age much younger than is typical for this diagnosis.
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