L
Luke Y.C. Chen
Researcher at University of British Columbia
Publications - 73
Citations - 1909
Luke Y.C. Chen is an academic researcher from University of British Columbia. The author has contributed to research in topics: Medicine & Eosinophilia. The author has an hindex of 17, co-authored 63 publications receiving 1099 citations. Previous affiliations of Luke Y.C. Chen include Vancouver General Hospital & Halifax.
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Lymphocyte-variant hypereosinophilic syndrome presenting as chronic dermatitis and responding to mycophenolic acid.
TL;DR: A case of L-HES showing skin presentation, chronicity of clinical course, and successful treatment with mycophenolic acid (MFA) is presented, which represents the first case in which cutaneous manifestations and eosinophilia have been successfully managed with MFA.
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Grappling with troublesome knowledge.
Luke Y.C. Chen,Gary Poole +1 more
TL;DR: Mending such gaps includes determining the role of all the members of the community of clinical practice and moving beyond the traditional student– supervisor dyad focus.
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Etoposide‐based treatment of adult HLH is associated with high biochemical response but poor survival outcomes
TL;DR: Biochemical response to treatment was high, with 21/23 adults achieving >75% reduction in serum ferritin, but one year survival was only 7/21 compared to 7/10 in pediatric cases.
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Treatment of lymphocyte-variant hypereosinophilic syndrome (L-HES): what to consider after confirming the elusive diagnosis
TL;DR: In this article, the authors searched the literature for clinical trials and observational studies, including case reports, of patients treated for lymphocyte-variant hypereosinophilic syndrome (L-HES).
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IgG4-related prostatitis manifesting as urinary obstruction in a 28-year-old male
Aria Jazdarehee,Azin Ahrari,Drew Bowie,Silvia D. Chang,Henry Tran,Shahin Jamal,Luke Y.C. Chen,Karen C. Tran +7 more
TL;DR: A 28-year-old man of Asian descent with a history of sinusitis and priapism presented to hospital with rigors and voiding symptoms, and he was diagnosed with IgG4-RD one month prior to presentation, following pathological analysis of a submandibular mass that demonstrated chronic sclerosing sialadenitis as mentioned in this paper .