Allison Therese Vidimos

Dr. Allison Therese Vidimos

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Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
Open access
PDF file
XHXingpei Hao
Xingpei Hao
SBSteven D. Billings
Steven D. Billings
FWFangbai Wu
Fangbai Wu
TSTodd W. Stultz
Todd W. Stultz
GPGary W. Procop
Gary W. Procop
AVAllison Therese Vidimos
Allison Therese Vidimos
Dermatofibrosarcoma protuberans (DFSP) is a slow growing, low- to intermediate-grade dermal soft-tissue tumor. It has a high local recurrence rate but low metastatic potential. It is characterized by a uniform spindle cell arrangement, classically with a storiform pattern and CD34 immunoreactivity. The histomorphology and immunophenotype overlap with a broad range of other neoplasms. The standard treatment is complete surgical excision. The surgical procedures include wide local excision (WLE) with tumor free margins, Mohs micrographic surgery (MMS) and amputation. Unresectable DFSPs are treated with radiation therapy and/or targeted therapy. DFSP has characteristic t(17; 22) (q22; q13), resulting in a COL1A1- PDGFB fusion transcripts in more than 90% of DFSPs. Molecular detection of the gene rearrangement or fusion transcripts is helpful for the diagnosis of patients with atypical morphology and for screening candidates for targeted therapy with tyrosine kinase inhibitors. The aims of the present review are to update the clinical presentation, tumorigenesis and histopathology of DFSP and its variants for diagnosis and differential diagnosis from other benign and malignant tumors, to compare the advantages and drawbacks of WLE and MMS, to propose the baseline for selecting surgical procedure based on tumor’s location, size, stage and relationship with surrounding soft tissue and bone structures, and to provide a biologic rationale for the systemic therapy. We further propose a modified clinical staging system of DFSP and a surveillance program for the patients after surgical excision.

1 May 2004 in Dermatologic Surgery
Verified
Journal Article
Closed access
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PSParrish Sadeghi
Parrish Sadeghi
FPFrancis A. Papay
Francis A. Papay
AVAllison Therese Vidimos
Allison Therese Vidimos
Trigeminal trophic syndrome is a unilateral, frequently crescent-shaped neurotrophic ulceration of the face occurring after injury to the trigeminal nerve. The appearance of the ulcers resembles other disease entities such as granulomatous disease, neoplasm, vasculitis, infection, and factitial dermatitis. The objectives of this study are to increase awareness of this disorder and to emphasize the importance of eliciting a thorough neurologic history when evaluating facial ulcerations. Four cases are reported and, using MEDLINE, the English and non-English literature from 1982 to 2002 is reviewed. Including this report, there have been 60 cases of trigeminal trophic syndrome reported from 1982 to 2002. The age at presentation ranged from 14 months to 93 years. Time of onset from injury to the trigeminal ganglion or its branches and the development of the ulcers ranged from 2 weeks to 30 years. One-third of the patients had undergone trigeminal nerve ablation for the treatment of trigeminal neuralgia and another third had a history of stroke. Other causes included craniotomy, head trauma, herpes infection. The majority of cases of trigeminal trophic syndrome are associated with a history of stroke or trigeminal nerve ablation. Successful surgical outcome can be achieved if the underlying neurologic pathology is addressed before the reconstructive procedure.

1 March 2021 in Journal of the American Academy of Dermatology
Verified
Journal Article
Closed access
MRMarla Rodriguez
Marla Rodriguez
BBBrandon T. Beal
Brandon T. Beal
MMManisha Manmohan
Manisha Manmohan
ESElanee Simmons
Elanee Simmons
VVVamsi Varra
Vamsi Varra
AVAllison Therese Vidimos
Allison Therese Vidimos

1 April 2011 in Dermatologic Clinics
Verified
Journal Article
Closed access
AVAllison Therese Vidimos
Allison Therese Vidimos
TSTodd W. Stultz
Todd W. Stultz

5 April 2024 in Dermatologic Surgery
Verified
Journal Article
Open access
CDChen Mhs Dun
Chen Mhs Dun
CWChristi M. Msn Walsh
Christi M. Msn Walsh
CHCaitlin W. Hicks
Caitlin W. Hicks
TSThomas Stasko
Thomas Stasko
AVAllison Therese Vidimos
Allison Therese Vidimos
MMMartin A. Makary
Martin A. Makary
BACKGROUND: Mohs micrographic surgery efficiently treats skin cancer through staged resection, but surgeons' varying resection rates may lead to higher medical costs. OBJECTIVE: To evaluate the cost savings associated with a quality improvement. MATERIALS AND METHODS: The authors conducted a retrospective cohort study using 100% Medicare fee-for-service claims data to identify the change of mean stages per case for head/neck (HN) and trunk/extremity (TE) lesions before and after the quality improvement intervention from 2016 to 2021. They evaluated surgeon-level change in mean stages per case between the intervention and control groups, as well as the cost savings to Medicare over the same time period. RESULTS: A total of 2,014 surgeons performed Mohs procedures on HN lesions. Among outlier surgeons who were notified, 31 surgeons (94%) for HN and 24 surgeons (89%) for TE reduced their mean stages per case with a median reduction of 0.16 and 0.21 stages, respectively. Reductions were also observed among outlier surgeons who were not notified, reducing their mean stages per case by 0.1 and 0.15 stages, respectively. The associated total 5-year savings after the intervention was 92 million USD. CONCLUSION: The implementation of this physician-led benchmarking model was associated with broad reductions of physician utilization and significant cost savings.

9 December 2011 in Pediatric Dermatology
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Journal Article
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EFEsteban Fernández‐Faith
Esteban Fernández‐Faith
DKDouglas Kress
Douglas Kress
MPMelissa Piliang
Melissa Piliang
MSMandi Sachdeva
Mandi Sachdeva
AVAllison Therese Vidimos
Allison Therese Vidimos