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1.
Dermatol Surg ; 46(3): 319-326, 2020 03.
Article in English | MEDLINE | ID: mdl-31356441

ABSTRACT

BACKGROUND: The treatment of nonmelanoma skin cancer (NMSC) in the elderly population is a source of significant debate. Mohs micrographic surgery (MMS) is a highly effective treatment option yet not every patient with a cutaneous malignancy that meets appropriate use criteria (AUC) should be treated with surgery. OBJECTIVE: The purpose of this study was to use the Karnofsky Performance Status (KPS) scale to categorize the functional status of patients aged 75 years and older who required treatment of NMSC. The authors wanted to see whether functionality played a role on the treatment selection. METHODS: Patients aged 75 years and older presenting for biopsy of a suspected NMSC that met AUC for MMS were included in the study. Trained medical assistants used the KPS scale to assess patient functionality. Treatment modality was recorded once the biopsy confirmed the NMSC. RESULTS: A cohort of 203 subjects met inclusion criteria for the study. There was a statistically significant difference in utilization of surgical treatments between high and low functionality patients (p = .03). CONCLUSION: Dermatologists consider patient functionality when selecting a treatment for NMSC and use less invasive modalities for patients with poor functional status, even when the tumor meets AUC.


Subject(s)
Karnofsky Performance Status , Skin Neoplasms/therapy , Aged , Aged, 80 and over , Biopsy , Carcinoma, Basal Cell/therapy , Carcinoma, Squamous Cell/therapy , Female , Geriatric Assessment , Humans , Male , Mohs Surgery , Patient Selection , Prospective Studies , United States
2.
Cutis ; 88(4): 178-81, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22106725

ABSTRACT

An 85-year-old man sought treatment of multiple nontender bluish papules of 3 years' duration on the forearms, forehead, and temples. On physical examination, blue-tinged, semitranslucent, dome-shaped papules were noted. Workup revealed multiple hidrocystomas. We discuss the findings in our patient and review the literature.


Subject(s)
Hidrocystoma/pathology , Sweat Gland Neoplasms/pathology , Aged, 80 and over , Face , Forearm , Forehead , Hidrocystoma/diagnosis , Humans , Male , Sweat Gland Neoplasms/diagnosis
3.
Lasers Surg Med ; 42(5): 408-11, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20583246

ABSTRACT

BACKGROUND/OBJECTIVE: The purpose of this study was to assess the effects of fluence, pulse stacking, and multiple passes on the depth of injury caused by a fractionated Er:YAG laser in an in vivo farm pig model. DESIGN/MATERIAL/METHODS: A fractionated 2,940 nm Er:YAG laser (Pixel, Alma Lasers, Caesarea, Israel) was applied to the flank skin of a Yorkshire cross pig. The 11 mmx11 mm handpiece was comprised of either 49 or 81 microbeams (200 microm diameter), depending on the tip configuration. There were six different parameter sets divided according to total energy per pulse (150, 285, and 500 mJ) and tip type (81 or 49 microbeams per 11 mmx11 mm macrospot). Each of these six groups was subdivided according to number of stacked pulses (1, 3, and 6) and number of passes (1, 3, and 6). This resulted in a total of 36 treatment parameters. RESULTS: With the 49 microbeam configuration, a single pulse resulted in partial epidermal ablation at 150 mJ, complete epidermal ablation at 285 mJ and partial dermal ablation at 500 mJ to a depth of 90 microm. Stacking the pulses resulted in a significant increase in ablation with each fluence with the maximal depth of ablation measured at 140 microm after six stacked pulses at 500 mJ. Increasing the number of passes did not result in a significant increase in ablative depth, but did create a larger surface area of ablation. Residual thermal damage (RTD) was minimal and remained between 10 and 20 microm. CONCLUSIONS: The fractionated Er:YAG laser exhibited some of the same tissue interactions as its fully ablative counterparts. An increase in fluence resulted in an increase in ablative depth with minimal RTD. Additionally, RTD was unaffected by pulse stacking or by additional passes. Differences were that pulse stacking appeared to yield a more rapid decrease in ablation efficiency and additional passes did not seem to increase the depth of ablation.


Subject(s)
Burns/etiology , Burns/pathology , Lasers, Solid-State/adverse effects , Skin/injuries , Skin/pathology , Animals , Swine
4.
J Drugs Dermatol ; 5(9): 835-7, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17039647

ABSTRACT

OBJECTIVE: Although numerous taste studies have compared the palatability of antibiotic suspensions, few have compared the palatability of corticosteroid suspensions. Therefore, we compared the taste of 8 commonly prescribed liquid corticosteroid suspensions with the intent to help guide prescribing practices and improve patient compliance. METHODS: We conducted a randomized, double-blind study using 31 adult volunteers ages 24 to 57. All volunteers were asked to sample 8 different pediatric corticosteroid suspensions and to rate the palatability of their taste and aftertaste. The mean scores for each sample were then compared. RESULTS: The 8 suspensions fell into 2 groups based on their taste scores: one group with relatively high scores or more acceptable tastes (Orapred, Pediapred, and a dexamethasone suspension) and a second group with relatively low scores or less acceptable tastes (a prednisone suspension and 4 cherry-flavored prednisolone suspensions). CONCLUSIONS: The results demonstrate a significant difference in palatability between corticosteroid suspensions. Not only will this new information help clinicians choose between otherwise equivalent corticosteroid suspensions but, given the importance children place on taste, may improve compliance as well.


Subject(s)
Adrenal Cortex Hormones/administration & dosage , Skin Diseases/drug therapy , Taste , Administration, Oral , Adrenal Cortex Hormones/adverse effects , Adult , Chemistry, Pharmaceutical , Decision Support Techniques , Dexamethasone/administration & dosage , Dexamethasone/adverse effects , Double-Blind Method , Female , Humans , Male , Patient Compliance , Prednisolone/administration & dosage , Prednisolone/adverse effects , Prednisone/administration & dosage , Prednisone/adverse effects , Suspensions , Treatment Outcome
5.
J Am Acad Dermatol ; 50(4): 591-4, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15034509

ABSTRACT

BACKGROUND: Smallpox is notorious for leaving its survivors with disfiguring scars, but it is unclear how these scars are produced. Modern dermatopathology textbooks report that smallpox produced epidermal lesions, yet the process of scarring requires dermal involvement. OBJECTIVES: Our goal was to uncover past theories on the mechanism of smallpox scarring. METHODS: We conducted a comprehensive review of English-language textbooks and English-translations of textbooks in general medicine, dermatology, pathology, and dermatopathology from the past 150 years as well as relevant journal publications for the same time period. RESULTS: We identified five different theories to explain the scarring of smallpox. The five proposals are that scarring resulted from: the extension of suppuration into the dermis; the extension of suppuration into the dermis along with inappropriate treatment and scratching; secondary bacterial ecthyma; the destruction of elastic fibers; or the destruction of sebaceous glands. CONCLUSION: The theory that best fits clinical and histological observations is that smallpox caused scars through the destruction of sebaceous glands, first proposed by Gerrit Bras in 1952. Although this explanation is not found in any dermatopathology text, it is supported by today's leading authorities on smallpox. However, since variola virions have never actually been identified in sebaceous glands, or even in the dermis, further study of preserved tissue is warranted. Until then, the mechanism of scar formation remains speculative.


Subject(s)
Cicatrix/physiopathology , Smallpox/physiopathology , Cicatrix/pathology , Dermis/pathology , Dermis/physiopathology , Humans , Sebaceous Glands/pathology , Sebaceous Glands/physiopathology , Skin/pathology , Skin/physiopathology , Smallpox/pathology
6.
N Engl J Med ; 347(9): 690-1, 2002 Aug 29.
Article in English | MEDLINE | ID: mdl-12200561
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