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Youssef, Molly J.

https://orcid.org/0000-0002-9646-6053

Mayo Clinic

Mayo Clinic

Citations 26

Lumbosacral Nevus Simplex in a Newborn Girl with an Asymmetrical Y-Shaped Gluteal Cleft
Leopold, Kaitlin N., Ahn, Edward S. , Youssef, Molly J. , Gregory, Seth W. , Leopold, Kaitlin

Pediatrics In Review | October 1, 2021 | Volume: 42 | Issue: 10 | Pages: e41-e44

10.1542/pir.2020-002162 Get It

Acral localized acquired cutis laxa as presenting sign of underlying systemic amyloidosis
Vork, Diana L. , Shah, Kabeer , Youssef, Molly J. , Wieland, Carilyn N. , Shah, Kabeer K

Journal of Cutaneous Pathology | June 28, 2020 | Volume: 47 | Issue: 11 | Pages: 1050-1053

10.1111/cup.13791 Get It

AbstractAcral localized acquired cutis laxa (ALACL) is a rare variant of acquired cutis laxa, and the clinical appearance is characterized by loose, redundant and wrinkled skin of the distal extremities. By definition, histopathology of affected tissue reveals sparse or fragmented elastic fibers. However, this can be difficult to assess on routine staining, and sometimes requires electron microscopy. The condition has been associated with plasma cell dyscrasias or recurrent inflammatory states. We present a case of a 65‐year‐old man who presented with enlarged and doughy finger pads. Skin biopsy showed diffuse dermal amyloid deposition displacing dermal stroma and reduction of elastic fibers, although these changes were subtle on routine hematoxylin and eosin staining. Mass spectrometry of laser capture microdissected tissue showed AL kappa‐type amyloid and further workup revealed a diagnosis of primary systemic AL‐kappa amyloidosis requiring bone marrow transplantation. This case represents an unusual presentation of acquired cutis laxa and highlights the need for a high index of suspicion when reviewing histopathology of this entity. In addition, the case highlights the importance of investigation into possible systemic associations, such as plasma cell dyscrasias.
Chilblains‐like dermatologic manifestation of COVID‐19 diagnosed by serology via multidisciplinary virtual care
Kerber, Alyssa , Soma, David , Youssef, Molly J. , Kerber, Alyssa A, Soma, David B

International Journal of Dermatology | June 4, 2020 | Volume: 59 | Issue: 8 | Pages: 1024-1025

10.1111/ijd.14974 Get It

Dental root abnormalities in four children with PHACE syndrome
Youssef, Molly J. , Siegel, Dawn H. , Chiu, Yvonne E. , Drolet, Beth A. , Hodgson, Brian D. , Chiu, Yvonne E

Pediatric Dermatology | April 1, 2019 | Volume: 36 | Issue: 4 | Pages: 505-508

10.1111/pde.13818 Get It

AbstractPHACE(S) syndrome is a condition characterized by posterior fossa malformations, hemangiomas, arterial anomalies, cardiac defects, eye abnormalities, sternal cleft, and supraumbilical raphe. We present four children with PHACE(S) syndrome who have absence of or severe malformation of the roots of their permanent first molars (PFMs). Root abnormalities in the children's molars were bilateral and not restricted to the segments affected by cutaneous hemangioma. The reason for root abnormalities is unknown, but given the rarity of these findings in healthy children, it is likely an additional dental manifestation of PHACE syndrome. The absence of functional roots in the PFMs can result in significant consequences. Therefore, we recommend a panoramic dental radiograph during transitional dentition for children with PHACE syndrome to screen for dental root abnormalities.
Online education improves pediatric residents’ understanding of atopic dermatitis
Craddock, Megan , Blondin, Heather M., Youssef, Molly J. , Tollefson, Megha M. , Hill, Lauren , Hanson, Janice L. , Bruckner, Anna L. , Craddock, Megan F

Pediatric Dermatology | November 29, 2017 | Volume: 35 | Issue: 1 | Pages: 64-69

10.1111/pde.13323 Get It

AbstractBackground/ObjectivesPediatricians manage skin conditions such as atopic dermatitis (AD) but report that their dermatologic training is inadequate. Online modules may enhance medical education when sufficient didactic or clinical teaching experiences are lacking. We assessed whether an online module about AD improved pediatric residents’ knowledge and changed their clinical management of AD.MethodsTarget and control cohorts of pediatric residents from two institutions were recruited. Target subjects took a 30‐question test about AD early in their residency, reviewed the online module, and repeated the test 6 months and 1 year later. The control subjects, who had 1 year of clinical experience but had not reviewed the online module, also took the test. The mean percentage of correct answers was calculated and compared using two‐sided, two‐sample independent t tests and repeated‐measures analysis of variance. For a subset of participants, clinical documentation from AD encounters was reviewed and 13 practice behaviors were compared using the Fisher exact test.ResultsTwenty‐five subjects in the target cohort and 29 subjects in the control cohort completed the study. The target cohort improved from 18.0 ± 3.2 to 23.4 ± 3.4 correctly answered questions over 1 year (P < .001). This final value was greater than that of the control cohort (20.7 ± 4.5; P = .01). Meaningful differences in practice behaviors were not seen.ConclusionPediatric residents who reviewed an online module about AD demonstrated statistically significant improvement in disease‐specific knowledge over time and had statistically significantly higher scores than controls. Online dermatology education may effectively supplement traditional clinical teaching.
Ichthyosis prematurity syndrome mimics keratitis–ichthyosis–deafness syndrome at birth: Use of electron microscopy and genetic testing
Youssef, Molly J. , Wolz, Michael , Harris, Malinda N. , Richard, Gabrielle , Bridges, Alina G. , Wieland, Carilyn N. , Hand, Jennifer L. , Wolz, Michael M

International Journal of Dermatology | October 13, 2015 | Volume: 55 | Issue: 8 | Pages: No page available

10.1111/ijd.13099 Get It