Bio

Clinical Focus


  • Dermatology

Academic Appointments


Professional Education


  • Fellowship:University of California San Francisco (2012) CA
  • Residency:University of California San Francisco (2011) CA
  • Internship:University of California San Francisco (2007) CA
  • Medical Education:University of California San Francisco (2006) CA
  • Board Certification: Pediatric Dermatology, American Board of Dermatology (2012)
  • Board Certification: Dermatology, American Board of Dermatology (2011)
  • Board Certification: Pediatrics, American Board of Pediatrics (2011)
  • Fellowship, University of California San Francisco, Pediatric Dermatology (2012)
  • Residency, University of California San Francisco, Dermatology; Pediatrics (2011)
  • Internship, University of California, Pediatrics (2007)
  • M.D., University of California San Francisco, School of Medicine (2006)
  • B.A., Princeton University, Chemistry (2001)

Publications

Journal Articles


  • Plaque-Like Myofibroblastic Tumor: Report of Three Cases PEDIATRIC DERMATOLOGY Marqueling, A. L., Dasher, D., Friedlander, S. F., McCalmont, T. H., Frieden, I. J. 2013; 30 (5): 600-607

    Abstract

    Plaque-like myofibroblastic tumor of infancy (PMTI) was first reported in 2007. The first two cases described large, plaque-like tumors presenting in infancy with microscopic features consistent with dermatofibroma but with immunohistochemical features of myofibrocytic lineage. We present three additional cases of PMTI, the first cases reported since the initial two cases, and describe additional clinical features of this condition, including presentation in early childhood as opposed to infancy, development of ulceration, and aggressive growth. We propose shortening the name of this condition to plaque-like myofibroblastic tumor because presentation can occur in infancy or in early childhood.

    View details for DOI 10.1111/pde.12185

    View details for Web of Science ID 000324092500032

    View details for PubMedID 23848365

  • Systemic treatments for severe pediatric psoriasis: a practical approach. Dermatologic clinics Marqueling, A. L., Cordoro, K. M. 2013; 31 (2): 267-288

    Abstract

    Severe psoriasis is uncommon in children, but when it occurs, can be physically, emotionally and socially disabling. Systemic treatments such as phototherapy, acitretin, methotrexate and cyclosporine have been used to manage severe pediatric psoriasis for decades. Newer biologic agents have demonstrated their effectiveness in adult psoriasis and are accumulating promising data in children. This article discusses the use of these treatments including their indications, efficacy, adverse effects, and monitoring requirements. The aim is to provide practical, clinically relevant information regarding the use of these medications alone and in various combinations based on available evidence and cumulative experience.

    View details for DOI 10.1016/j.det.2012.12.005

    View details for PubMedID 23557655

  • Propranolol and Infantile Hemangiomas Four Years Later: A Systematic Review PEDIATRIC DERMATOLOGY Marqueling, A. L., Oza, V., Frieden, I. J., Puttgen, K. B. 2013; 30 (2): 182-191

    Abstract

    To systematically review the literature evaluating efficacy and adverse events of propranolol treatment for infantile hemangiomas, we searched the MEDLINE and Cochrane databases for all studies examining the response of infantile hemangiomas (IHs) to propranolol published between June 12, 2008, and June 15, 2012. Forty-one studies with 1,264 patients were included; 74% of patients were female and approximately 30% had received other treatments before propranolol. Propranolol was initiated at a mean age of 6.6 months at a mean dose of 2.1 mg/kg/day and for a mean treatment duration of 6.4 months. The response rate for patients with IHs treated with propranolol was 98% (range 82%-100%), with response rate defined as any improvement with propranolol. Treatment response rates were comparable for studies evaluating IHs at specific sites, such as periorbital IHs. Studies that followed patients after treatment completion reported IH rebound growth in 17% of patients. There were 371 adverse events reported in 1,189 patients. The most common adverse events were changes in sleep (n = 136) and acrocyanosis (n = 61). Serious adverse events were rare, with reports of symptomatic hypotension in five patients, hypoglycemia in four, and symptomatic bradycardia in one. This systematic review of 1,264 patients treated with propranolol for IHs showed a high rate of efficacy and a low rate of serious adverse events.

    View details for DOI 10.1111/pde.12089

    View details for Web of Science ID 000315961500003

    View details for PubMedID 23405852

  • Keratosis pilaris rubra - A common but underrecognized condition ARCHIVES OF DERMATOLOGY Marqueling, A. L., Gilliam, A. E., Prendiville, J., Zvulunov, A., Antaya, R. J., Sugarman, J., Pang, M., Lee, P., Eichenfield, L., Metz, B., Goldberg, G. N., Phillips, R. J., Frieden, I. J. 2006; 142 (12): 1611-1616

    Abstract

    Keratosis pilaris is a common skin disorder of childhood that often improves with age. Less common variants of keratosis pilaris include keratosis pilaris atrophicans and atrophodermia vermiculata.In this case series from dermatology practices in the United States, Canada, Israel, and Australia, the clinical characteristics of 27 patients with keratosis pilaris rubra are described. Marked erythema with follicular prominence was noted in all patients, most commonly affecting the lateral aspects of the cheeks and the proximal arms and legs, with both more marked erythema and widespread extent of disease than in keratosis pilaris. The mean age at onset was 5 years (range, birth to 12 years). Sixty-three percent of patients were male. No patients had atrophy or scarring from their lesions. Various treatments were used, with minimal or no improvement in most cases.Keratosis pilaris rubra is a variant of keratosis pilaris, with more prominent erythema and with more widespread areas of skin involvement in some cases, but without the atrophy or hyperpigmentation noted in certain keratosis pilaris variants. It seems to be a relatively common but uncommonly reported condition.

    View details for Web of Science ID 000242803400012

    View details for PubMedID 17178988

  • A population-based analysis of laboratory abnormalities during isotretinoin therapy for acne vulgaris ARCHIVES OF DERMATOLOGY Zane, L. T., Leyden, W. A., Marqueling, A. L., Manos, M. 2006; 142 (8): 1016-1022

    Abstract

    To determine the incidence of abnormal laboratory test results among isotretinoin users.Retrospective cohort.Comprehensive managed care health plan in Northern California.The study population comprised 13 772 patients aged 13 to 50 years with acne, undergoing oral isotretinoin therapy between March 1995 and September 2002.Laboratory values for serum triglyceride, total cholesterol, and liver transaminase levels; white blood cell count, hemoglobin level, and platelet count; and frequency of abnormal laboratory results by severity grade as defined by the National Cancer Institute Common Terminology Criteria for Adverse Events v3.0.Substantial increases in the cumulative incidence of abnormalities were seen in serum lipid and transaminase levels, but not in hematologic parameters, during isotretinoin treatment compared with the baseline period. The cumulative incidence of new abnormalities in patients with normal values at baseline was 44% for triglyceride level, 31% for total cholesterol level, and 11% for transaminase level. Moderate to severe abnormalities in lipid and transaminase levels were generally transient and reversible. New abnormalities in hematological test results were uncommon.The incidence of abnormally high serum lipid levels during isotretinoin treatment may be greater than previously estimated. Elevations in transaminase level are generally mild. Normal baseline values of serum lipid and transaminase levels do not preclude the development of new abnormalities during isotretinoin treatment. Routine monitoring of white blood cell count, hemoglobin level, and platelet count during isotretinoin therapy may be of little utility without clinical suspicion of an abnormality. The clinical significance of laboratory abnormalities during isotretinoin therapy remains to be determined.

    View details for Web of Science ID 000239762700009

    View details for PubMedID 16924051

  • Depression and suicidal behavior in acne patients treated with isotretinoin: A systematic review SEMINARS IN CUTANEOUS MEDICINE AND SURGERY Marqueling, A. L., Zane, L. T. 2005; 24 (2): 92-102

    Abstract

    Isotretinoin (13-cis retinoic acid) is an effective treatment for severe cystic or recalcitrant acne vulgaris; however, concerns have been raised regarding its potential association with depression and suicidal behavior. We sought to explore the proposed relationship between isotretinoin use and the risk of depression and attempted and completed suicide in patients with acne vulgaris by performing a systematic literature search for studies reporting primary data on depression and suicidal behavior in patients treated with isotretinoin for acne vulgaris. Nine studies met the qualifying criteria for our analysis. Rates of depression among isotretinoin users ranged from 1% to 11% across studies, with similar rates in oral antibiotic control groups. Overall, studies comparing depression before and after treatment did not show a statistically significant increase in depression diagnoses or depressive symptoms. Some, in fact, demonstrated a trend toward fewer or less severe depressive symptoms after isotretinoin therapy. This decrease was particularly evident in patients with pretreatment scores in the moderate or clinical depression range. No correlation between isotretinoin use and suicidal behavior was reported, although only one retrospective study presented data on this topic. Although the current literature does not support a causative association between isotretinoin use and depression, there are important limitations to many of the studies. The available data on suicidal behavior during isotretinoin treatment are insufficient to establish a meaningful causative association.

    View details for DOI 10.1016/j.sder.2005.04.003

    View details for Web of Science ID 000235864500006

    View details for PubMedID 16092797

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