Publications by authors named "Senhong Lee"
Article Synopsis
- Immunoglobulin type gamma 4-related disease (IgG4-RD) is a fibroinflammatory disease that can affect the whole body or just the skin, with common symptoms being red bumps or plaques, especially on the head and neck.
- A new case is reported where IgG4-RD displayed an unusual skin symptom of eruptive cherry angiomas.
- This highlights the diverse ways IgG4-RD can present, expanding our understanding of its cutaneous manifestations.
Background: Left ventricular thrombus (LVT) has a 5% incidence after anterior ST-elevation myocardial infarction (STEMI). Multiple risk factors predispose to LVT formation, including left ventricular systolic dysfunction and infarct size, however measurable predictors during index left heart catheterization (LHC) have not been determined.
Methods: We performed a retrospective analysis of patients presenting between January 2010 and September 2017 with anterior STEMI who had in-hospital transthoracic echocardiography (TTE).
Rapid-onset diabetic ketoacidosis secondary to nivolumab therapy.
Endocrinol Diabetes Metab Case Rep
April 2018
Unlabelled: We report a case of a 67-year-old man with type 2 diabetes presented with diabetic ketoacidosis, two weeks after his first dose of nivolumab therapy for non-small-cell lung carcinoma. He was started on empagliflozin two days prior in the setting of hyperglycaemia after the initiation of nivolumab therapy. Laboratory evaluation revealed an undetectable C-peptide and a positive anti-glutamic acid decarboxylase (GAD) antibody.
View Article and Find Full Text PDFBackground: Melasma is a common acquired disorder of hyperpigmentation that commonly affects those with skin of color. Tranexamic acid (TXA) is a novel treatment for melasma that has a multimodal mechanism of action.
Objective: To provide a comprehensive review of the literature regarding the evidence on the mode of action, safety profile, and efficacy of TXA in the treatment of melasma.
Keratoacanthoma formation after skin grafting is rare. We report the third case in the literature of multiple keratoacanthomas developed at both split-thickness skin graft donor and recipient sites. We provide possible explanations for this poorly understood phenomenon and highlight its implications on treatment options.
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