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13


Assessing the use of methotrexate as an alternate therapy for pemphigus vulgaris and pemphigus foliaceus

Kolla, Avani; Shah, Payal; Cymerman, Rachel; Fruchter, Renee; Adotama, Prince; Soter, Nicholas A
Methotrexate is historically recognized as an effective treatment of pemphigus but its utility as a single or alternate steroid-sparing agent was not recognized in recent consensus recommendations in pemphigus management. We aimed to evaluate the efficacy and safety of a treatment course for pemphigus that involves methotrexate as a single or steroid-sparing agent. In a retrospective cohort study, we examined patients with pemphigus vulgaris or pemphigus foliaceus who were on ≥3 months of methotrexate therapy. Efficacy and safety were evaluated by established pemphigus disease endpoints. Of the 34 patients who met inclusion criteria, 25 (73.5%) were on glucocorticoids at time of methotrexate initiation (median follow-up: 5.4 years; median time on methotrexate: 3.7 years). An appreciable proportion achieved disease control (91.2%), with some achieving clinical remission off all systemic therapies (23.5%). For patients on glucocorticoids, median time to control was 42 days, median time to minimal steroid dose tapering (5 mg prednisone) was 161 days, and median time to complete steroid tapering was 308 days. For patients on methotrexate as a single agent, median time to control was 119 days. Among all patients, relapse commonly occurred (88.2%). At last follow-up, 26.5% were managed on topical therapies alone and 11.8% required systemic steroid therapy. Methotrexate was largely tolerated with a low incidence of adverse events leading to treatment discontinuation (2.9%). Methotrexate has the potential to be an effective and well-tolerated option for patients and may be considered for use as an alternate single or steroid-sparing agent for pemphigus.
PMID: 35734997
ISSN: 1529-8019
CID: 5282032

Telogen effluvium: a sequela of COVID-19

Mieczkowska, Karolina; Deutsch, Alana; Borok, Jenna; Guzman, Anthony K; Fruchter, Renee; Patel, Parth; Wind, Olivia; McLellan, Beth N; Mann, Ranon E; Halverstam, Caroline P
PMID: 33226117
ISSN: 1365-4632
CID: 4680282

Teaching Targeted Drug Discovery and Development to Healthcare Professionals

Fruchter, Renee; Ahmad, Meleha; Pillinger, Michael; Galeano, Claudia; Cronstein, Bruce N; Gold-von Simson, Gabrielle
Drug discovery and development (DDD) is an interdisciplinary enterprise that spans the translational continuum. Despite DDD's importance, formal training within medical and biomedical schools is lacking. In this tutorial, we outline the current educational landscape in DDD and the growing educational need in this area. Lastly, we describe the Health Innovations and Therapeutics concentration as an example of how to design and implement an educational program in DDD.
PMCID:5944588
PMID: 29110398
ISSN: 1752-8062
CID: 2773132

Characteristics and Alternative Treatment Outcomes of Antimalarial-Refractory Cutaneous Lupus Erythematosus

Fruchter, Renee; Kurtzman, Drew J B; Patel, Mital; Merola, Joseph; Franks, Andrew G Jr; Vleugels, Ruth Ann; Femia, Alisa N
PMCID:5817470
PMID: 28636714
ISSN: 2168-6084
CID: 2604392

Lichenoid vulvar disease: A review

Fruchter, R; Melnick, L; Pomeranz, M K
Vulvar dermatoses are common, potentially debilitating conditions that can be seen by a variety of medical specialists. Lichenoid vulvar diseases, namely lichen sclerosus (LS), lichen planus (LP), and lichen simplex chronicus (LSC), can all negatively impact patients' quality of life and LS and LP also have an association with squamous cell carcinoma. It is essential that dermatologists are familiar with the unique features of each of these conditions to ensure the appropriate management and follow up. Herein, we provide an update on the epidemiology, clinical presentation, histopathology, and treatment of patients with vulvar LS, LP, and LSC.
PMCID:5419035
PMID: 28492056
ISSN: 2352-6475
CID: 2549112

Erythema Nodosum in Association with Idiopathic Granulomatous Mastitis: A Case Series and Review of the Literature

Fruchter, R; Castilla, C; Ng, E; Pomeranz, M K; Femia, A N
Idiopathic granulomatous mastitis (IGM) is a chronic inflammatory disease characterized by tender, erythematous, indurated breast plaques with associated edema, drainage, and scar formation.1 IGM is often mistaken for breast carcinoma or infectious mastitis.1,2 Histopathology readily distinguishes IGM from breast carcinoma, as the primary finding in IGM is granulomas centered around mammary lobules.3 Nevertheless, differentiating IGM from bacterial mastitis and other mimickers, such as atypical mycobacterial infections or sarcoidosis, can be more difficult.4 Herein, we report the largest case series of concurrent IGM and erythema nodosum (EN)
PMID: 28271562
ISSN: 1468-3083
CID: 2477092

Groove Sign of Eosinophilic Fasciitis

Fruchter, Renee; Mazori, Daniel R; Femia, Alisa N
PMID: 28277348
ISSN: 1536-7355
CID: 2477242

Characteristics and treatment of postirradiation morphea: A retrospective multicenter analysis

Fruchter, Renee; Kurtzman, Drew J B; Mazori, Daniel R; Wright, Natalie A; Patel, Mital; Vleugels, Ruth Ann; Femia, Alisa N
PMID: 27692734
ISSN: 1097-6787
CID: 2273862

Epidemiology and treatment of refractory cutaneous lupus erythematosus [Meeting Abstract]

Fruchter, R; Kurtzman, D; Lin, J; Femia, AN; Vleugels, R
ISI:000380028800176
ISSN: 1523-1747
CID: 2216112

Focal full-thickness epidermal necrosis in association with adalimumab in a patient with ulcerative colitis [Meeting Abstract]

Fruchter, R; Lopatin, S; Malter, LB; Femia, AN
ISI:000380028800142
ISSN: 1523-1747
CID: 2216182