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Erythema Ab Igne: Decoding Skin Presentations of Vasculitis Mimickers in Autoimmunity
Buontempo, Michael G; Ramachandran, Vignesh; Mazori, Daniel R; Femia, Alisa; Sikora, Michelle; Sicco, Kristen Lo; Caplan, Avrom S
PMID: 37871732
ISSN: 1555-7162
CID: 5614292
Clinical Characteristics of Erythema Nodosum and Associations With Chronicity and Recurrence
Shah, Jill T; Richardson, William Mark; Caplan, Avrom S; Mazori, Daniel R; Femia, Alisa N
PMCID:10765308
PMID: 38170490
ISSN: 2168-6084
CID: 5628332
A fatal case of hemophagocytic lymphohistiocytosis due to neonatal lupus erythematosus [Case Report]
Mazori, Daniel R; Kleitsch, Julianne; Kabir, Soodeh; Uwakwe, Laura N; Glick, Sharon A
Neonatal lupus erythematosus (NLE) is an autoimmune disease caused by the passive transfer of autoantibodies from mother to child during pregnancy. A rare complication of NLE is hemophagocytic lymphohistiocytosis (HLH), a potentially life-threatening hyperinflammatory state more commonly associated with other rheumatologic disorders. Herein, we describe a fatal case of NLE-associated HLH.
PMID: 37666795
ISSN: 1525-1470
CID: 5627982
Hyaluronidase Injections for Oral Microstomia in Systemic Sclerosis and Mixed Connective Tissue Disease
Min, Michelle S; Goldman, Nathaniel; Mazori, Daniel R; Guo, Lisa N; Vleugels, Ruth Ann; LaChance, Avery H
PMCID:10585489
PMID: 37851438
ISSN: 2168-6084
CID: 5612912
Utility of magnetic resonance imaging in the diagnosis of eosinophilic fasciitis: A multicenter retrospective cohort study
Shahriari, Neda; Mazori, Daniel R; Shahriari, Mona; Taylor, Dustin; Shaw, Katharina; LaChance, Avery H; Femia, Alisa N; Vleugels, Ruth Ann
PMID: 37659455
ISSN: 1097-6787
CID: 5609322
Cutaneous neonatal lupus in patients with skin of color: A retrospective cohort study from a national registry
Kleitsch, Julianne; Mazori, Daniel R; Masson, Mala; Izmirly, Peter M; Saxena, Amit; Buyon, Jill P; Glick, Sharon A
PMID: 36997071
ISSN: 1097-6787
CID: 5463392
Mepolizumab for refractory eosinophilic fasciitis: a retrospective analysis from two tertiary care centres [Letter]
Sanchez-Melendez, Stephanie N; Shaw, Katharina S; Pan, Catherina X; Taylor, Dustin L; Shahriari, Neda; Mazori, Daniel R; Vleugels, Ruth Ann
PMID: 37246772
ISSN: 0392-856x
CID: 5543142
Efficacy of a dermatology interest group-sponsored biopsy and suturing workshop for medical students
Flagg, Elizabeth E; Kearney, Caitlin A; Needle, Carli D; Himeles, Jaclyn R; Marji, Jackleen S; Zampella, John G; Mazori, Daniel R
PMCID:10149358
PMID: 37138829
ISSN: 2666-3287
CID: 5544912
Intravenous immunoglobulin"“refractory necrobiotic xanthogranuloma successfully treated with tofacitinib 2% cream
Shahriari, Neda; Mazori, Daniel R.; Merola, Joseph F.
SCOPUS:85146042488
ISSN: 2352-5126
CID: 5408322
Dermatomyositis Diagnosis and Treatment in the Inpatient Setting
Hejazi, Emily Z.; Mittal, Lavanya; Sicco, Kristen Lo; Mazori, Daniel R.; Femia, Alisa N.; Caplan, Avrom S.
Purpose of Review: Dermatomyositis can present with a range of manifestations and severity that may necessitate hospital admission. Dermatologists are frequently consulted for patients with dermatomyositis inpatient. Herein we describe clinical features and management of multisystem complications of dermatomyositis with a focus on the inpatient setting. Recent Findings: Patients with dermatomyositis are at risk for hospitalization due to disease flares, infections, and systemic complications. Furthermore, patients may seek care for symptoms including shortness of breath, fever, or cutaneous eruptions which can lead to a new diagnosis of dermatomyositis. Patients with dermatomyositis have increased healthcare utilization and necessitate multidisciplinary and collaborative care. Cutaneous findings may be subtle yet provide important prognostic information. Symptoms arising from skin disease may also be chronic and refractory. Summary: Dermatologists are essential in both diagnosing and managing dermatomyositis and must be attuned to the multiple systemic manifestations and complications that impact inpatient care.
SCOPUS:85154591754
ISSN: 2162-4933
CID: 5499992