Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
1.
J Clin Aesthet Dermatol ; 7(11): 35-7, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25489381

ABSTRACT

OBJECTIVE: To determine the efficacy of treating patients with a recent onset, biopsy-proven keratoacanthoma with short-contact topical 5% 5-fluorouracil cream twice daily until resolution. DESIGN: Chart review of 10 patients who applied 5% 5-fluorouracil for the treatment of biopsy-proven keratoacanthoma. SETTING: Outpatient clinic of a board-certified dermatologist. PARTICIPANTS: The study population was 90-percent women (9/10), 10-percent men (1/10) and ranged in ages from 52 to 92 years old with a mean age of 74.4. MEASUREMENTS: Patients were followed for weekly visits for the duration of their treatment and at varying, less-frequent intervals after resolution of the lesion clinically. Photographs were taken at each visit. RESULTS: The authors performed a retrospective analysis of 10 patients with biopsy-confirmed keratoacanthomas treated with topical 5-fluorouracil. One patient elected to have Mohs surgery after one week of topical 5-fluorouracil due to personal concern and cosmetic appearance and did not complain of any side effects due to the drug. Of the nine patients that remained on topical 5-fluorouracil, all patients had complete resolution of the lesion within six weeks. The range in the number of weeks to resolution was four to six weeks. Two patients required a one- to two-week drug holiday secondary to erythema, which resolved without any further complication or patient discomfort. All nine patients who continued therapy reported satisfaction with the results and showed excellent compliance with treatment. CONCLUSION: Short-contact topical 5% 5-fluorouracil appears to provide excellent cosmetic results and is well-tolerated by patients. This should be an initial consideration for the treatment of keratoacanthomas and does not preclude future surgical intervention if deemed necessary.

3.
JAMA Dermatol ; 150(5): 542-5, 2014 May.
Article in English | MEDLINE | ID: mdl-24623282

ABSTRACT

IMPORTANCE: Keratocystic odontogenic tumors (KCOTs) of the jaw affect more than 65% of patients with basal cell nevus syndrome (BCNS). Surgery frequently causes facial disfigurement and is not always curative. Most BCNS-related and some sporadic KCOTs have malignant activation of the Hedgehog signaling pathway. OBSERVATIONS: We examined the effect of vismodegib (an oral Hedgehog pathway inhibitor) on KCOT size in patients with BCNS enrolled in a clinical trial testing vismodegib for basal cell carcinoma prevention (NCT00957229), using pretreatment and posttreatment magnetic resonance imaging. Four men and 2 women had pretreatment KCOTs (mean longest diameter, 2.0 cm; range, 0.7-3.3 cm), occurring primarily in the mandible. Patients were treated with vismodegib, 150 mg/d, for a mean (SD) of 18.0 (4.8) months (range, 11-24 months). Four patients experienced a size reduction and 2 had no change. Vismodegib reduced the mean longest diameter of KCOTs in all patients by 1.0 cm (95% CI, 0.03-1.94; P = .02) or 50% from baseline. We observed no enlargement of existing KCOTs or new KCOT development. CONCLUSIONS AND RELEVANCE: Vismodegib shrinks some KCOTs in patients with BCNS and may offer an alternative to surgical therapy. These effects were maintained for at least 9 months after drug cessation in 1 patient. Further studies assessing long-term efficacy and optimal maintenance regimens should be performed.


Subject(s)
Anilides/administration & dosage , Basal Cell Nevus Syndrome/drug therapy , Jaw Neoplasms/drug therapy , Odontogenic Tumors/drug therapy , Pyridines/administration & dosage , Skin Neoplasms/drug therapy , Adult , Basal Cell Nevus Syndrome/mortality , Basal Cell Nevus Syndrome/pathology , Biopsy, Needle , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Humans , Immunohistochemistry , Jaw Neoplasms/complications , Jaw Neoplasms/pathology , Magnetic Resonance Imaging/methods , Male , Middle Aged , Neoplasm Invasiveness/pathology , Neoplasm Staging , Odontogenic Tumors/mortality , Odontogenic Tumors/pathology , Patient Selection , Prognosis , Prospective Studies , Risk Assessment , Skin Neoplasms/mortality , Skin Neoplasms/pathology , Survival Analysis , Treatment Outcome
4.
Cancer Prev Res (Phila) ; 7(3): 292-9, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24441673

ABSTRACT

Sporadic human basal cell carcinomas (BCC) are generally well managed with current surgical modalities. However, in the subset of high-risk patients predisposed to developing large numbers of BCCs, there is an unmet need for effective, low-morbidity chemoprevention. This population includes fair-skinned patients with extensive sun exposure and those with genodermatoses such as the basal cell nevus (Gorlin) syndrome (BCNS). Tazarotene (Tazorac, Allergan) is a topical retinoid with relative specificity for RAR-ß and RAR-γ receptors. We previously demonstrated tazarotene's robust anti-BCC efficacy in Ptch1(+/-) mice, a murine equivalent of BCNS, and others have found it to have some efficacy against sporadic human BCCs. We report here results of a randomized, double-blind, vehicle-controlled study in patients with BCNS evaluating the efficacy of topically applied tazarotene for BCC chemoprevention (N = 34 subjects), along with an open-label trial evaluating tazarotene's efficacy for chemotherapy of BCC lesions (N = 36 subjects) for a maximum follow-up period of 3 years. We found that only 6% of patients had a chemopreventive response and that only 6% of treated BCC target lesions were clinically cured. Our studies provide no evidence for either chemopreventive or chemotherapeutic effect of tazarotene against BCCs in patients with BCNS.


Subject(s)
Basal Cell Nevus Syndrome/drug therapy , Carcinoma, Basal Cell/drug therapy , Carcinoma, Basal Cell/prevention & control , Dermatologic Agents/therapeutic use , Nicotinic Acids/therapeutic use , Skin Neoplasms/drug therapy , Skin Neoplasms/prevention & control , Adult , Cross-Over Studies , Double-Blind Method , Female , Humans , Male , Middle Aged , Pharmaceutical Vehicles , Treatment Outcome
5.
World Neurosurg ; 80(5): 655.e15-21, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23207734

ABSTRACT

OBJECTIVE: Conventionally, neuroendoscopic excision of intraventricular tumors has been difficult and time consuming because of lack of an effective decompression system that can be used through the working channel of the endoscope. METHODS: The authors report their initial experience in purely endoscopic excision of large intraventricular tumors with the minimally invasive NICO Myriad system. The NICO Myriad is a side cutting soft tissue aspiration system that uses an inner reciprocating cannula and an outer stationary sheath with a side port. During decompression, applied suction approximates the tumor into the lumen of the outer sheath, with the inner cannula excising the tissue by oscillation of the cutting edge. The tumor is then removed by aspiration through the inner sheath. RESULTS: Three patients with large intraventricular tumors were operated by a purely endoscopic approach using a GAAB rigid endoscope and the NICO Myriad system. Of these, two had intraventricular craniopharyngiomas and one had a lateral ventricular subependymoma. The tumor size varied between 1.9 and 4.5 cm in the largest diameter. A relatively firm and solid tumor was encountered in two and a multicystic tumor with thick adherent walls in one. The tumor could be subtotally removed in one and near totally in two. There were no long-term complications. CONCLUSION: The NICO Myriad is a highly effective tumor decompression system that can be effectively used in a purely endoscopic approach to intraventricular lesions.


Subject(s)
Cerebral Ventricle Neoplasms/surgery , Craniopharyngioma/surgery , Decompression, Surgical/methods , Glioma, Subependymal/surgery , Neuroendoscopy/methods , Adolescent , Cerebral Ventricle Neoplasms/diagnosis , Craniopharyngioma/diagnosis , Decompression, Surgical/instrumentation , Glioma, Subependymal/diagnosis , Humans , Male , Middle Aged , Neuroendoscopy/instrumentation , Suction/instrumentation , Suction/methods , Tumor Burden
6.
Childs Nerv Syst ; 28(10): 1785-90, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22885708

ABSTRACT

PURPOSE: The authors assess the role of flexible hollow core CO2 laser system (Omniguide system) in resection of intraspinal lipomas. METHODS: Eight patients with intraspinal lipomas were operated using an Omniguide laser system over a 22-month period. The age range varied between 6 months and 16 years. All of them had lipoma of the conus medullaris associated with lumbar subcutaneous lipoma. Two of these had previous surgery with resection of the subcutaneous part of the lipoma; in one of them, a partial resection of the conus medullaris lipoma had also been performed. In six, there were no obvious motor or sensory deficits whereas two had gross neurologic deficits, with the deficits occurring in one after the previous decompression. Resection of the conus lipoma, untethering of the spinal cord, and reconstruction of the decompressed conus was performed in all aided with Omniguide laser system. The power settings of the laser system ranged from 4 to 8 W. RESULTS: Subtotal to near-total resection was achieved in all. None of the patients developed any new motor or sensory deficits. Three had postoperative CSF leaks which initially required reoperation with graft resuturing and subsequently placement of lumboperitoneal shunt. One child with preexisting neurologic deficits improved in power over the next 12 months. CONCLUSION: Flexible CO2 laser system was precise and convenient in decompressing the conus lipomas and untethering of the cord in lumbar spinal lipomas.


Subject(s)
Lasers, Gas/therapeutic use , Lipoma/surgery , Neurosurgical Procedures/instrumentation , Neurosurgical Procedures/methods , Spinal Cord Neoplasms/surgery , Adolescent , Child , Female , Humans , Infant , Lumbosacral Region/surgery , Magnetic Resonance Imaging , Male , Radiography , Plastic Surgery Procedures , Spinal Cord/diagnostic imaging , Spinal Cord/surgery , Treatment Outcome
SELECTION OF CITATIONS
SEARCH DETAIL
...