Derek Chu, M.D., is Clinical Associate Professor of Dermatology and Pediatrics at Lucile Packard Children's Hospital. He completed his medical school and residency training at the University of Pennsylvania, followed by a pediatric dermatology fellowship at UCSF. Dr. Chu's clinical interests encompass a wide array of topics within pediatric dermatology, including vascular tumors and malformations, inflammatory skin diseases, dermato-oncology, neonatal dermatology, and procedural dermatology.
Clinical Associate Professor, Dermatology
Boards, Advisory Committees, Professional Organizations
Member, American Academy of Dermatology (2012 - Present)
Member, Society for Pediatric Dermatology (2010 - Present)
Fellowship: UCSF Dept of Dermatology (2016) CA
Medical Education: Perelman School of Medicine University of Pennsylvania (2011) PA
Board Certification: American Board of Dermatology, Pediatric Dermatology (2016)
Board Certification, American Board of Dermatology, Pediatric Dermatology (2016)
Board Certification, American Board of Dermatology (2015)
Fellowship, University of California San Francisco, Pediatric Dermatology (2016)
Residency, Hospital of the University of Pennsylvania, Dermatology (2015)
Internship, Children's Hospital of Philadelphia, Pediatrics (2012)
MD, University of Pennsylvania School of Medicine (2011)
BS, Massachusetts Institute of Technology (2007)
Cutaneous signs of nutritional disorders.
International journal of women's dermatology
1800; 7 (5Part A): 647-652
This review article focuses on the dermatologic manifestations of selected nutrient deficiencies, including protein-energy and micronutrient-related malnutrition. The various nutrient deficiencies presented may share common features. However, distinctive cutaneous signs may prompt clinicians to consider a nutritional cause and help distinguish a nutrient deficiency from other common dermatologic conditions. The recent reemergence of forgotten nutritional deficiencies, such as scurvy and pellagra, in the context of predisposing risk factors that may uniquely affect women more than men makes this topic timely. Recognition of nutritional disorders is important because appropriate treatment may reverse cutaneous signs and prevent irreversible sequelae.
View details for DOI 10.1016/j.ijwd.2021.09.003
View details for PubMedID 35024418
Characteristics of melanoma in white and nonwhite children, adolescents, and young adults: Analysis of a pediatric melanoma institutional registry, 1995-2018
2019; 36 (4): 448–54
View details for DOI 10.1111/pde.13836
View details for Web of Science ID 000474933900017
Characteristics of melanoma in white and nonwhite children, adolescents, and young adults: Analysis of a pediatric melanoma institutional registry, 1995-2018.
OBJECTIVES: To characterize clinical differences among nonwhite/multiethnic vs white children, adolescents, and young adults with melanoma or atypical melanocytic neoplasms, including atypical Spitz tumors.PATIENTS AND METHODS: A cohort of 55 patients (< 25years of age) prospectively followed from 1995 to 2018 in the Stanford Pigmented Lesion and Melanoma Program was analyzed for differences in clinical presentation, including skin phototype, race/ethnicity, age, sex, tumor/melanoma characteristics, and outcome.RESULTS: Seventeen patients (9 males and 8 females) were classified as nonwhite (predominantly skin phototype IV) and of Hispanic, Asian, or Black/African American ethnicity, and 38 patients (21 males and 17 females) were classified as white (predominantly phototypes I/II). Ages ranged from 6months to 24years, and median follow-up was 36months (range 1-180months). Melanomas were diagnosed in 87% of whites in our cohort, compared to 65% of nonwhites, with the remainder representing mainly atypical Spitz tumors. Lesions were usually brought to the attention of a health care provider by the patient or family (P<0.05). Compared with whites, nonwhites were more likely to present at a younger mean age (10.9years vs 15.4years, P<0.05) and with pink/clinically amelanotic tumors (59% vs 24%, P=0.02).CONCLUSIONS: This long-term prospective institutional study showed clinically relevant differences between nonwhite vs white children, adolescents, and young adults diagnosed with melanoma and atypical melanocytic neoplasms. Nonwhite patients presented at a younger age and had more clinically amelanotic melanocytic tumors. Increased recognition of clinical factors and risk of these tumors in nonwhites could result in earlier diagnosis.
View details for PubMedID 30993772