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2.
Clin Exp Dermatol ; 47(10): 1857-1858, 2022 Oct.
Article in English | MEDLINE | ID: mdl-35633107

ABSTRACT

Encorafenib is a BRAF inhibitor increasingly used as a second-line treatment for metastatic melanoma and colorectal cancer. BRAF inhibitors have been reported to be associated with new and changing melanocytic lesions, including eruptive naevi. We describe two cases of eruptive naevi secondary to encorafenib used for the treatment of BRAF-mutant metastatic colorectal cancer.


Subject(s)
Colonic Neoplasms , Exanthema , Nevus, Pigmented , Rectal Neoplasms , Skin Neoplasms , Antineoplastic Combined Chemotherapy Protocols , Carbamates , Humans , Mutation , Nevus, Pigmented/pathology , Protein Kinase Inhibitors/therapeutic use , Proto-Oncogene Proteins B-raf/genetics , Skin Neoplasms/chemically induced , Skin Neoplasms/drug therapy , Skin Neoplasms/pathology , Sulfonamides
3.
Oxf Med Case Reports ; 2021(11-12): omab120, 2021.
Article in English | MEDLINE | ID: mdl-34987850

ABSTRACT

We report a case of membranous conjunctivitis and erythema multiforme major (EMM) after a coronavirus disease 2019 (COVID-19) diagnosis. A previously well 18-year-old man presented with increasingly erythematous eyes and oral and genital ulceration 2 weeks after confirmation of COVID-19 infection. Clinical examination showed sloughy membranous conjunctivitis with normal visual acuity. He was reviewed by dermatology and diagnosed with EMM secondary to severe acute respiratory syndrome coronavirus 2 infection. The symptoms resolved with oral and topical steroids, lubricants and chloramphenicol eye drops. Erythema multiforme has been reported in association with COVID-19, although the major form is rare. Ophthalmologists should consider current or previous COVID-19 infection in patients presenting with conjunctivitis or pseudomembrane formation. Prompt initiation of steroids aids resolution.

4.
Expert Opin Biol Ther ; 18(3): 237-249, 2018 03.
Article in English | MEDLINE | ID: mdl-29202595

ABSTRACT

INTRODUCTION: Arrhythmias can cause symptoms ranging from simple dizziness to life-threatening circulatory collapse. Current management includes medical therapy and procedures such as catheter ablation or device implantation. However, these strategies still pose a risk of serious side effects, and some patients remain symptomatic. Advancement in our understanding of how arrhythmias develop on the cellular level has made more targeted approaches possible. In addition, contemporary studies have found that several genes are involved in the pathogenesis of arrhythmias. AREAS COVERED: In the present review, the authors explore the cellular and genetic mechanisms leading to arrhythmias as well as the progress that has been made in using both gene and cell therapy to treat tachy- and bradyarrhythmias. They also consider why gene and cell therapy has resulted into a few clinical trials with promising results, however still not applicable in routine clinical practice. EXPERT OPINION: The question currently is whether such biological therapies could replace current established approaches. The contemporary evidence suggests that despite recent advances in this field, it will need more work in experimental models before this is applied into clinical practice. Gene and cell studies targeting conduction and repolarization are promising, but still not ready for use in the clinical setting.


Subject(s)
Arrhythmias, Cardiac/therapy , Animals , Arrhythmias, Cardiac/metabolism , Arrhythmias, Cardiac/pathology , Bradycardia/metabolism , Bradycardia/pathology , Bradycardia/therapy , Cell- and Tissue-Based Therapy , Genetic Therapy , Humans , Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels/genetics , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Stem Cells/cytology , Stem Cells/metabolism , Tachycardia/metabolism , Tachycardia/pathology , Tachycardia/therapy
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