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Hart, Melissa

Mayo Clinic

Mayo Clinic Health System

Citations 3

S1550 Multi-Focal Pancreatic Solid Lesions: Not Always a Solid Malignancy
Adenote, Abimbola, Quingalahua, Elit C., Niendorf, Eric, Hart, Melissa, Quingalahua, Elit C., Hart, Melissa, Machicado, Jorge D.

American Journal of Gastroenterology | October 24, 2021 | Volume: 116 | Issue: 1 | Pages: S702-S702

10.14309/01.ajg.0000779732.42851.c7 Get It

S3094 An Uncommon Urologic Cause of Gastric Outlet Obstruction
Adenote, Abimbola, Quingalahua, Elit C., Niendorf, Eric, Hart, Melissa, Quingalahua, Elit C., Hart, Melissa, Machicado, Jorge D.

American Journal of Gastroenterology | October 24, 2021 | Volume: 116 | Issue: 1 | Pages: S1277-S1277

10.14309/01.ajg.0000785908.57172.90 Get It

UBA1 and DNMT3A mutations in VEXAS syndrome. A case report and literature review
Shaukat, Farah, Hart, Melissa, Bansal, Pankaj , Burns, Timothy, Bansal, Pankaj , Hart, Melissa, Burns, Timothy Francis

Modern Rheumatology Case Reports | September 4, 2021 | Volume: 6 | Issue: 1 | Pages: 134-139

10.1093/mrcr/rxab021 Get It

ABSTRACT Vacuoles, E1 enzyme, X linked, autoinflammatory, somatic (VEXAS) syndrome is a recently described X-linked autoinflammatory condition associated with somatic mutation of the ubiquitin-like modifier activating enzyme 1 (UBA1) gene. It often coexists with myelodysplastic syndrome, which can occur due to DNA (cytosine-5)-methyltransferase 3A (DNMT3A) mutation. These patients, predominantly males, present after the fifth decade of life with unique systemic inflammatory clinical features and have haematological abnormalities and vacuolated precursor cells on bone marrow pathology. Here we describe a unique case of VEXAS syndrome in a patient harbouring DNMT3A gene mutation with coexisting UBA1 mutation with a review of literature.