Publications by authors named "Starling Tolliver"

Article Synopsis
  • Recent studies show dermatology residents are satisfied treating skin conditions in people of color, but their comfort levels with hair-related issues specific to these populations are unclear.
  • The study surveyed dermatology residents in the U.S. to assess their comfort level and knowledge regarding common hair conditions, especially those affecting individuals with skin of color.
  • Results indicated residents felt confident about common conditions but struggled with topics like natural hair care and creating hair regimens, emphasizing the need for better training and diversity in dermatology programs.
View Article and Find Full Text PDF

Neurofibromatosis (NF) and tuberous sclerosis complex (TSC) are the two most common neurocutaneous disorders, both transmitted as autosomal dominant or, in the case of NF, also as a mosaic condition. The causative genetic mutations in these neurocutaneous disorders can lead to benign skin changes or uninhibited growth and proliferation in multiple organ systems due to the loss of tumor suppression in mitogen-activated protein kinase and mammalian target of rapamycin signaling pathways. Common clinical features in NF include pigmented lesions, known as café au lait patches, neurofibromas, intertriginous freckles (Crowe's sign), and benign fibrous growths, such as hamartomas in multiple organ systems.

View Article and Find Full Text PDF

Introduction: African American (AA) women have reported hair maintenance as a barrier to regular exercise; however, to our knowledge, this study is the first to identify primary care provider thoughts, attitudes, beliefs, and knowledge regarding hair as a barrier to increased physical activity among AA females.

Methods: A 13-question electronic survey was sent via email to 151 clinicians working within a department of family medicine's 8 ambulatory clinics within a large urban academic medical center.

Results: A total of 62 primary care clinicians completed the survey, which is a response rate of 41%.

View Article and Find Full Text PDF

Necrolytic migratory erythema (NME) is a rare skin disorder that is a cutaneous manifestation of the glucagonoma syndrome. It presents with annular eruptions of migrating erythematous papules and plaques with superficial epidermal necrosis, central flaccid bullae, and crusted erosions located primarily in the intertriginous areas. Treatment with the long-acting somatostatin analog Octreotide is a potential therapy to help ameliorate skin symptoms.

View Article and Find Full Text PDF