Case Report No-Needle Jet Intradermal Aminolevulinic Acid Photodynamic Therapy for Recurrent Nodular Basal Cell Carcinoma of the Nose: A Case Report

Similar documents
Dual Wavelength Phototherapy System

Clinical Study Treatment of Mesh Skin Grafted Scars Using a Plasma Skin Regeneration System

Photodynamic Therapy for the Treatment of Actinic Keratoses and Other Skin Lesions

Periocular skin cancer

Skin disorders. Basal cell carcinoma December 2009 Anthony Ormerod, Sanjay Rajpara, and Fiona Craig ...

Corporate Medical Policy

Allergic contact dermatitis to topical prodrugs used in photodynamic therapy Cordey, Helen; Ibbotson, Sally

Living Beyond Cancer Skin Cancer Detection and Prevention

Photodynamic Photorejuvenation: An 18- month Experience on Combination of ALA-IPL and a 630nm LED Continuous Light Source

1) Photodynamic therapy with topical 5 aminolevulinic acid is considered medically necessary and is covered for the treatment of:

A Retrospective Study of Treatment of Squamous Cell Carcinoma In situ. Övermark, Meri.

I have a skin lump doc! What s next? 12 th August 2017 Dr. Sue-Ann Ho Ju Ee

Photodynamic Therapy for the Treatment of Actinic Keratoses and Other Skin Lesions

Case Report A Rare Cutaneous Adnexal Tumor: Malignant Proliferating Trichilemmal Tumor

Photodynamic Therapy (PDT) Basics and clinical applications

Cutaneous Malignancies: A Primer COPYRIGHT. Marissa Heller, M.D.

Case Report A Case of Cystic Basal Cell Carcinoma Which Shows a Homogenous Blue/Black Area under Dermatoscopy

Periocular Malignancies

A Comparison of the Efficacy of Ablative Fractional Laser-assisted Photodynamic Therapy according to the Density of Ablative Laser Channel

Scottish Medicines Consortium

Interesting Case Series. Aggressive Tumor of the Midface

Photodynamic Therapy with Ablative Carbon Dioxide Fractional Laser for Treating Bowen Disease

PRODUCT INFORMATION METVIX

Case Report Metastatic Malignant Melanoma of Parotid Gland with a Regressed Primary Tumor

STUDY. Laser-Mediated Photodynamic Therapy of Actinic Keratoses

Skin Malignancies Non - Melanoma & Melanoma Marilyn Ng, MD Dept. of Surgery M&M Conference Downstate Medical Center July 19, 2012

MOHS MICROGRAPHIC SURGERY: AN OVERVIEW

Skin NCG (Anglia East & Anglia West)

Skin Cancer. 5 Warning Signs. American Osteopathic College of Occupational and Preventive Medicine OMED 2012, San Diego, Monday, October 8, 2012 C-1

Intraoperative Dermoscopy for Identification of Early Basal Cell Carcinomas in Basal Cell Nevus Syndrome

Development of Low-Cost Photodynamic Therapy Device

MULTIDIODE PDT 630 TM

STUDY. Photodynamic Therapy Using Topical Methyl Aminolevulinate vs Surgery for Nodular Basal Cell Carcinoma

General information about skin cancer

Clinical characteristics

Nonmelanoma skin cancers

Photodynamic Therapy with Ablative Carbon Dioxide Fractional Laser in Treatment of Actinic Keratosis

CASE REPORT Superficial Spreading Basal Cell Carcinoma of the Face: A Surgical Challenge

Kentaro Tanaka, 1 Hiroki Mori, 1 Mutsumi Okazaki, 1 Aya Nishizawa, 2 and Hiroo Yokozeki Introduction. 2. Case Presentation

Topical Photodynamic Therapy Using Intense Pulsed Light for Treatment of Actinic Keratosis: Clinical and Histopathologic Evaluation

Mandana Moosavi 1 and Stuart Kreisman Background

Benign versus Cancerous Lesions How to tell the difference FMF 2014 Christie Freeman MD, CCFP, DipPDerm, MSc

Alireza Bakhshaeekia and Sina Ghiasi-hafezi. 1. Introduction. 2. Patients and Methods

PDT in Medical and Aesthetic Dermatology: An European Perspective. Rolf-Markus Szeimies Recklinghausen, Germany

Opinion 6 March 2013

Comparison of PpIX accumulation and destruction during. methyl-aminolevulinate photodynamic therapy (MAL-PDT) of

INTENSE PULSED LIGHT VERSUS ADVANCED FLUORESCENT TECHNOLOGY PULSED LIGHT FOR PHOTODAMAGED SKIN: A SPLIT-FACE PILOT COMPARISON

ORE Open Research Exeter

Skin Cancer 101: Diagnosis and Management of the Most Common Cancer

Patient Guide. The precise answer for tackling skin cancer. Brachytherapy: Because life is for living

5-ALA Photopreparation Using Pulsed NIR Enhances Skin Fluorescence via Temperature-Independent Cell Signaling Pathways

Dermatologic Applications of Photodynamic Therapy

R. F. Falkenstern-Ge, 1 S. Bode-Erdmann, 2 G. Ott, 2 M. Wohlleber, 1 and M. Kohlhäufl Introduction. 2. Histology

Presentation Product & clinics

Medical Policy. MP Dermatologic Applications of Photodynamic Therapy

Case Report Clear Cell Basal Cell Carcinoma

Know who is at risk: LOOK! for ABCDs, rapidly changing lesions, do a biopsy when indicated

New and Emerging Therapies: Non-Melanoma Skin Cancers. David J. Goldberg, MD, JD Skin Laser and Surgery Specialists of NY/NJ

Diagnosis and Management of Actinic Keratosis (AKs)

Case Report Multiple Giant Cell Tumors of Tendon Sheath Found within a Single Digit of a 9-Year-Old

UWMC Roosevelt Clinic Rotation Goals 2011 Procedural Dermatology Fellowship Program 1

Skin Cancer in Organ Transplant Recipients Challenges and Opportunities

Learning Objectives. Tanning. The Skin. Classic Features. Sun Reactive Skin Type Classification. Skin Cancers: Preventing, Screening and Treating

Technicians & Nurses Program

Needle-free injection of 5-aminolevulinic acid in photodynamic therapy for the treatment of condylomata acuminata

Fluorescence Diagnosis For Follow- Up Of Mycosis Fungoides Therapy

Skin lesions The Good and the Bad. Dr Virginia Hubbard Ipswich Hospital NHS Trust Barts and the London School of Medicine and Dentistry

Case Report Five-Year Survival after Surgery for Invasive Micropapillary Carcinoma of the Stomach

Know who is at risk: LOOK! for ABCDs, rapidly changing lesions, do a biopsy when indicated

Large majority caused by sun exposure Often sun exposure before age 20 Persons who burn easily and tan poorly are at greatest risk.

Conference Paper Programmed Cell Death Induced by Modulated Electrohyperthermia

Identifying Skin Cancer. Mary S. Stone MD Professor of Dermatology and Pathology University of Iowa Carver College of Medicine March, 2018

Single Technology Appraisal (STA) Vismodegib for treating basal cell carcinoma [ID1043]

Photodynamic Therapy for the Treatment of Actinic Keratoses and Other Skin Lesions

Case Study: The Surgical Management of Angiokeratoma Resulting from Radiotherapy for Penile Cancer

Have a Voice in Your Choice!

Case Report Primary Neuroendocrine Carcinoma of Ocular Adnexa

Case Report Denosumab Chemotherapy for Recurrent Giant-Cell Tumor of Bone: A Case Report of Neoadjuvant Use Enabling Complete Surgical Resection

Fractional CO 2 Laser Skin Resurfacing for the Treatment of Sun-Damaged Skin and Actinic Keratoses COS DERM

Synchronous Hepatic Cryotherapy and Resection

Clinical Study Basal Cell Carcinoma: 10 Years of Experience

Case Report A Case of Primary Submandibular Gland Oncocytic Carcinoma

Photodynamic therapy in the treatment of basal cell carcinoma

Case Report Internal Jugular Vein Thrombosis in Isolated Tuberculous Cervical Lymphadenopathy

Skin Cancers Emerging Trends and Treatment Approaches

Treatment of Leg Telangiectasia (Spider Veins) with Magma Long Pulse ND - Laser 1064 nm Case Study

Case Report Two Cases of Small Cell Cancer of the Maxillary Sinus Treated with Cisplatin plus Irinotecan and Radiotherapy

What is the ideal wavelength?

Dermatopathology: The tumor is composed of keratinocytes which show atypia, increase mitoses and abnormal mitoses.

Regeneron and Sanofi are financial supporters of The Skin Cancer Foundation and collaborated in the development of this article. US-ONC /2018

fluorouracil 0.5% / salicylic acid 10% cutaneous solution (Actikerall ) SMC No. (728/11) Almirall S.A.

1. Written information to patient /GP: fax ASAP to GP & offer copy of consultation letter.

INVESTIGATIVE REPORT. (Accepted November 18, 2010.) Acta Derm Venereol 2011; 91:

Research Article Clinical Outcome of a Novel Anti-CD6 Biologic Itolizumab in Patients of Psoriasis with Comorbid Conditions

Case Report Overlap of Acute Cholecystitis with Gallstones and Squamous Cell Carcinoma of the Gallbladder in an Elderly Patient

Vision Health: Conditions, Disorders & Treatments EYELID DISORDERS

Review Article Treatment of Facial Basal Cell Carcinoma: A Review

Non-melanoma Skin Cancer

Case Report Medial Radial Head Dislocation Associated with a Proximal Olecranon Fracture: A Bado Type V?

Transcription:

Skin Cancer Volume 0, Article ID 790509, 5 pages doi:0.55/0/790509 Case Report No-Needle Jet Intradermal Aminolevulinic Acid Photodynamic Therapy for Recurrent Nodular Basal Cell Carcinoma of the Nose: A Case Report Daniel Barolet, and Annie Boucher RoseLab Skin Optics Laboratory, Graham Boulevard, Suite 06, Montreal, Quebec, Canada HR L5 Dermatology Division, Department of Medicine, McGill University, Montreal, Quebec, Canada HG Y6 Correspondence should be addressed to Daniel Barolet, daniel.barolet@mcgill.ca Received 7 July 00; Revised 7 September 00; Accepted September 00 Academic Editor: Robert Dellavalle Copyright 0 D. Barolet and A. Boucher. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Photodynamic therapy (PDT) with aminolevulinic acid (ALA) to treat nodular basal cell carcinoma (BCC) has been shown to be beneficial. The success rate of ALA-PDT in the treatment of nodular BCC is dependent on optimal penetration of the photosensitizing agent and subsequent PpIX production. To enhance topical delivery of drugs intradermally, a needleless jet injection (NLJI), which employs a high-speed jet to puncture the skin without the side effects of needles, was used in one patient with recurrent BCC of the nose. Photoactivation was then performed using red light emitting diode [CW @ λ 60 nm, irradiance 50 mw/cm, total fluence 5 J/cm ] for 7 minutes. Excellent cosmesis was obtained. Aside from mild crusting present for six days, no other adverse signs were noted. Clinically, there was no recurrent lesion up two years postintervention. Additional studies in larger samples of subjects are needed to further evaluate this promising technique.. Introduction Basal cell carcinoma (BCC) is the most frequent type of skin cancer in humans [, ]. Nodular variant is the most common form and usually presents as a round, pearly, fleshcolored papule with overlying small blood vessels. As it expands, it often ulcerates centrally, leaving a raised, pearly border with telangiectases. They are often seen in sunlightexposed areas and on actinic damaged skin. Although it is rarely life-threatening, if left untreated, it can produce local destruction, cause bleeding, and be disfiguring. Moreover, large and longstanding tumours may metastasize into regional lymph nodes and surrounding tissues and bones. Hence, these lesions must be treated readily. A wide range of treatment options exist to treat nodular BCCs (e.g., cryotherapy, Imiquimod 5% cream, laser, and radio therapies), yet, surgical excision and Mohs micrographic surgery remain the gold standard treatments for this condition. Unfortunately, postoperative scars are often visible and undesirable on areas such as the face. Photodynamic therapy (PDT) is a treatment modality that is increasingly used in dermato-oncology as an alternative to surgery to treat nodular BCC. PDT is based on photochemical reactions mediated through the interaction of light, oxygen, and a photosensitizing molecule (e.g., aminolevulinic acid [ALA]) induced protoporphyrin IX (PpIX) production, during which cytotoxic reactive oxygen species are formed causing damage (necrosis, apoptosis) to the target structures. Results from clinical research suggest that topical PDT is efficacious in nodular BCC [ 6] and conveys the advantage over surgery of better cosmesis [7 ]. The comparative outcome of excision surgery versus topical-pdt (ALA or methyl aminolevulinate [MAL]) was documented in three randomized clinical trials in primary nodular BCC [8 ]. In all studies, the lesions were prepared with superficial curettage or debridement. The photosensitizing agent (0% ALA cream or 60 mg/g of MAL cream) was then applied to the lesion area and predefined margin, with a light-occlusive dressing for an incubation period that lasted between and 6 hours. Across the studies, different

Skin Cancer light sources were used to activate the photosensitizer in the red spectrum (570 to 70 nm), in order to improve tissue penetration, for a total dose of 75 J/cm or 5 J/cm. Patients received either one or two cycles of PDT, and in some trials, PDT was repeated after months if there was evidence of residual lesions. Short-term ( months) results for clearance rate revealed no significant difference between topical- PDT and surgery. Long-term followups (up to five years), however, indicated superior lesional response of surgery over PDT overall, although PDT was also deemed efficacious and exhibited a more favourable cosmetic outcome. Differential efficacy of MAL-PDT versus ALA-PDT was not assessed in these trials but one further study conducted by Kuijpers et al. (006) [] did not observe any differences in short-term efficacy (8 weeks) between these agents, suggesting that both ALA and MAL can be equally used as topical photosensitizers in PDT for nodular BCC. Overall, the use of topical-pdt with red light appears to be a reasonable treatment option for nodular BCC, and in particular, in situations where surgery may be a suboptimal treatment choice [, 4]. One possible limitation of PDT in nodular BCC is the penetration depth of the photosensitizer into the thick tumour volume, which can impact subsequent PpIX production levels and treatment efficacy [5, 6]. The application of ALA intralesionally, as opposed to topically, has been suggested as a mean to increase the penetration of photosensitizers. Recent research has reported higher fluorescence and PpIX levels after the intracutaneous administration of ALA in contrast to conventional topical application [7, 8]. The use of traditional needles, however, may lead to profound vascular compromise with possible vasoconstriction, deep purpura, necrosis, and infection and cause pain [9]. An alternative technique to enhance delivery of drugs intradermally is the needleless jet injection (NLJI) which employs a high-speed jet to puncture the skin and distribute the photosensitizer more evenly without the side effects of needles [0]. The potential of NLJI for the field of ALA- PDT has recently been highlighted by a preliminary in vitro investigation using a cross-linked hydrogel as a transparent skin model []. This case study aimed at assessing the in vivo human efficacy of NLJI ALA-PDT with red light (60 nm) in the treatment of a patient with recurrent nodular BCC of the nose.. Materials and Methods.. Case Description. The patient was a 5-year old female type I Caucasian with recurrent nodular BCC of the nose after two unsuccessful excisional surgeries done by a qualified plastic surgeon with 5 mm margins. The diagnosis of nodular BCC was confirmed by histopathological examination. Her past medical history indicated varicose veins and face-lift surgery. She was not taking any medication prior to and after the procedure. The patient presented a fibrotic translucent lesion of 5,5 mm diameter with telangiectasia and central atrophy on the left ala of her nose. Given the recurrences after surgery, the size and location of the lesion, PDT with intradermal administration of ALA was considered for this patient. Data was collected in accordance with the Declaration of Helsinki and the Principles of Good Clinical Practice... Procedure. An alcohol swab was used to clean the injection site before injection. A MadaJet Medical Injector (MADA Inc, Carlstadt, NJ) was used to deliver a high pressure spray of 0.4 cc, 0% ALA solution intradermally into the lesion (Figure ). After an incubation period of one hour, the area was illuminated with red light emitting diode [CW @ λ 60 nm, irradiance 50 mw/cm,totalfluence 5 J/cm ] for 7 minutes. Before returning home, the patient was instructed on posttreatment skin care, which included applying topical fusidic acid cream twice a day, a plain moisturiser, sun avoidance, and the use of a sunscreen (SPF 0)... Clinical Assessments. Assessments of the lesion by means of visual analysis of digital photographs were carried out by two blinded physicians. Digital photographs (Canon Dual Flash EOS 0D, Canon, Tokyo, Japan with EX SIGMA 50 mm :.8 macrolens, Sigma, Aizu, Japan) were taken at each visit maintaining as much as possible identical ambient lighting, pose, and camera angles. The lesion was assessed for clinical and morphological aspects. Raters assessed the lesion for degree of improvement from baseline to Month 6,, and 4 using a 5-point scale (0= none; = mild; = moderate; = good; 4= excellent). Raters also assessed cosmetic outcome at Month 6,, and 4 using a 4-point scale as follows: () excellent: no scarring, atrophy, or induration and slight or no redness or change in pigmentation compared with adjacent skin; () good: no scarring, atrophy, or induration and moderate redness or increase in pigmentation compared with adjacent skin; () fair: slight to moderate occurrence of scarring, atrophy, or induration; (4) poor: extensive occurrence of scarring, atrophy, or induration []. In addition, raters were asked to assess the overall cosmetic outcome using a 4-point scale (= poor; = fair; = good; 4= excellent) at Month 6,, and 4..4. Adverse Effects Monitoring. Adverse reactions were assessed at each visit, including signs of erythema, oedema, hematoma, ulcer scaling/crusting, bronzing, textural changes, hyperpigmentation, and hypopigmentation..5. Patient Satisfaction. At the last followup visit, the patient was asked to rate her satisfaction level with the treatment results.. Results and Discussion Lesion evaluations by two blinded clinicians revealed significant improvement for clinical and morphological aspects over time. The degree of improvement from baseline was rated as being moderate to good (scoresofand)atmonth6, good (scoresof)atmonth,andexcellent (scores of 4) at Month 4 (Figure (a)). Cosmetic outcome was deemed

Skin Cancer (a) (b) (c) Figure : Experimental procedure. (a) Intradermal administration of ALA with a MadaJet medical injector; (b) lesion immediately postmadajet and prior to the PDT procedure; (c) lesion after the PDT procedure. Rater score Degree of improvement 4 0 Rater Rater Rater Rater Rater Month Month 6 Rater Month 4 0 = none; = mild; = moderate; = good; 4 = excellent (a) Rater score Cosmetic outcome 4 0 Rater Rater Rater Month 6 Rater Rater Rater Month 4 Month = excellent; = good; = fair; 4 = poor Rater score (b) Overall cosmetic outcome 4 0 Rater Rater Rater Month 6 Rater Rater Rater Month 4 Month = poor; = fair; = good; 4 = excellent (c) Figure : Results from the clinical assessments by two blinded physicians for (a) the degree of improvement from baseline, (b) the cosmetic outcome, and (c) overall cosmetic outcome at Month 6,, and 4. Pre M6 D (a) (b) M (c) M4 (d) (e) Figure : Treatment area pre-treatment (Pre), at day (D) and month 6 (M6), Month (M), and Month 4 (M4) post-pdt.

4 Skin Cancer progressively better between Month 6 and Month 4, at which timepoint it was appraised as excellent (scores of ), defined as no scarring, atrophy, or induration and slight or no redness or change in pigmentation compared with adjacent skin (Figure (b)). Moreover, the overall cosmetic outcome was judged to be good (scores of ) at Month 6 and excellent (scoresof4)atmonthand4(figure (c)). Finally, clinical appraisal revealed that there was no recurrent lesion up two years postintervention. Figure depicts digital photographs of the treatment area pretreatment and up to Month 4 post-pdt. The procedure was generally well tolerated by the patient, aside from a slight but bearable sensation of heat during photoactivation. With the exception of mild crusting present for six days, no other adverse signs, such hematoma or ulcer, were noted. Clinically, there was no recurrent lesion up to Month 4. Histological confirmation of BCC clearance was not obtained as the patient did not give consent to the skin biopsy procedure. The patient s satisfaction level with the treatment was extremely high. 4. Conclusion Nodular BCC is a common form of skin cancer and must be treated readily as it can invade surrounding areas and cause significant destruction and disfigurement. In the present case, ALA-PDT with NLJI was used to directly deliver the photosensitizer into the lesion, to enhance PDT effects. This approach proved to be remarkably effective and well tolerated with no unusual adverse reactions and no recurrence two years postintervention in this patient with a large and high risk lesion. The selection of this technique had several advantages over more conventional methods for this particular patient. For one, this method did not necessitate mechanical impairment of the skin or removing the stratum corneum which can create discomfort for patients and complicate future outpatient treatments. In addition, unlike previously reported data with intracutaneous administration of ALA with traditional needles, no perceptible vascular compromise leading to necrosis was observed in the present case [9]. Moreover, the patient was able to avoid Mohs micrographic and extensive reconstructive surgery of the nose. Such a delivery method may be considered for recurrent lesions confined to surgically tricky or complex anatomical areas in selected patients. This technique may not be suitable, however, to treat large areas with multiple lesions at once, where standard PDT and other approaches or their combination would be more appropriate. The choice of the best possible procedure for a given patient is dependent on the type, size, and location of the lesion. It should be noted that, in general and for the nodular subtype in particular, surgical excision remains the treatment of choice to treat BCCs []. Whatever the chosen approach, biopsies are recommended to confirm the diagnosis and determine the histologicalsubtype,aswellastodocumentlesionclearance post-intervention. The post-pdt histological confirmation was unfortunately not possible for this patient. While BCCs are well recognised clinically, and results from clinical trials generally show agreement between clinical and histological assessments of tumours [], the need for cautious long-term followups in this patient is warranted. The results obtained in this case are encouraging; however, supplementary studies in larger samples of patients and in the long-term are needed to further evaluate this promising technique. Future controlled studies are also necessary in order to determine if other photosensitizers, light sources, and wavelengths would procure added benefits to patients with an optimal clinical efficacy/side effectsratio. Other types of lesions, such as superficial BCC, Bowen s, and squamous cell carcinoma, could also potentially benefit from the use of this novel method and could be the object of additional trials. Acknowledgment The authors acknowledge Isabelle Lussier, PhD from Med- Strategis, for the paper preparation. References [] D. J. Hauben, H. Zirkin, D. Mahler, and M. Sacks, The biologic behavior of basal cell carcinoma part I, Plastic and Reconstructive Surgery, vol. 69, no., pp. 0 09, 98. [] M. M. Bagheri and B. Safai, Cutaneous malignancies of keratinocytic origin, Clinics in Dermatology,vol.9,no.,pp. 44 5, 00. [] M.R.T.M.Thissen,C.A.Schroeter,andH.A.M.Neumann, Photodynamic therapy with delta-aminolaevulinic acid for nodular basal cell carcinomas using a prior debulking technique, British Dermatology, vol. 4, no., pp. 8 9, 000. [4]A.M.Soler,T.Warloe,A.Berner,andK.E.Giercksky, A follow-upstudyofrecurrenceandcosmesisincompletely responding superficial and nodular basal cell carcinomas treated with methyl 5-aminolaevulinate-based photodynamic therapy alone and with prior curettage, British Dermatology, vol. 45, no., pp. 467 47, 00. [5] P. Lehmann, Methyl aminolaevulinate-photodynamic therapy: a review of clinical trials in the treatment of actinic keratoses and nonmelanoma skin cancer, British Dermatology, vol. 56, no. 5, pp. 79 80, 007. [6] P. Foley, M. Freeman, A. Menter et al., Photodynamic therapy with methyl aminolevulinate for primary nodular basal cell carcinoma: results of two randomized studies, International Dermatology, vol. 48, no., pp. 6 45, 009. [7] D. Fayter, M. Corbett, M. Heirs, D. Fox, and A. Eastwood, A systematic review of photodynamic therapy in the treatment of precancerous skin conditions, Barrett s oesophagus and cancers of the biliary tract, brain, head and neck, lung, oesophagus and skin, Health Technology Assessment, vol. 4, no. 7, pp. 9, 00. [8] L. E. Rhodes, M. De Rie, Y. Enström et al., Photodynamic therapy using topical methyl aminolevulinate vs surgery for nodular basal cell carcinoma, Archives of Dermatology, vol. 40, no., pp. 7, 004. [9] L. E. Rhodes, M. A. De Rie, R. Leifsdottir et al., Five-year follow-up of a randomized, prospective trial of topical methyl

Skin Cancer 5 aminolevulinate photodynamic therapy vs surgery for nodular basal cell carcinoma, Archives of Dermatology, vol. 4, no. 9, pp. 6, 007. [0]L.Berroeta,C.Clark,R.S.Dawe,S.H.Ibbotson,andC.J. Fleming, A randomized study of minimal curettage followed by topical photodynamic therapy compared with surgical excision for low-risk nodular basal cell carcinoma, British Dermatology, vol. 57, no., pp. 40 40, 007. [] K. Mosterd, M. R. T. M. Thissen, P. Nelemans et al., Fractionated 5-aminolaevulinic acid-photodynamic therapy vs. surgical excision in the treatment of nodular basal cell carcinoma: results of a randomized controlled trial, British Dermatology, vol. 59, no. 4, pp. 864 870, 008. [] D.I.Kuijpers,M.R.Thissen,C.A.Thissen,andM.H.Neumann, Similar effectiveness ofmethylaminolevulinate and5- aminolevulinate in topical photodynamic therapy for nodular basal cell carcinoma, Drugs in Dermatology, vol. 5, no. 7, pp. 64 645, 006. [] N. R. Telfer, G. B. Colver, and C. A. Morton, Guidelines for the management of basal cell carcinoma, British Dermatology, vol. 59, no., pp. 5 48, 008. [4] C. A. Morton, K. E. McKenna, and L. E. Rhodes, British Association of Dermatologists Therapy Guidelines and Audit Subcommittee and the British Photodermatology Group, Guidelines for topical photodynamic therapy: update, British Dermatology, vol. 59, no. 6, pp. 45 66, 008. [5]Q.Peng,A.M.Soler,T.Warloe,J.M.Nesland,andK.-E. Giercksky, Selective distribution of porphyrins in skin thick basal cell carcinoma after topical application of methyl 5- aminolevulinate, Photochemistry and Photobiology B, vol. 6, no., pp. 40 45, 00. [6] Q. Peng, T. Warloe, K. Berg et al., 5-Aminolevulinic acidbased photodynamic therapy. Clinical research and future challenges, Cancer, vol. 79, no., pp. 8 08, 997. [7] A. W. De Blois, R. J. E. Grouls, E. W. Ackerman, and W. J. A. Wijdeven, Development of a stable solution of 5- aminolaevulinic acid for intracutaneous injection in photodynamic therapy, Lasers in Medical Science, vol. 7, no., pp. 08 5, 00. [8] P. Cappugi, L. Mavilia, P. Campolmi, E. F. Reali, M. Mori, and R. Rossi, New proposal for the treatment of nodular basal cell carcinoma with intralesional 5-aminolevulinic acid, Journal of Chemotherapy, vol. 6, no. 5, pp. 49 49, 004. [9] F. H. Sakamoto, A. Doukas, W. Farinelli, Z. Tannous, and R. R. Anderson, Intradermal aminolevulinic acid photodynamic therapy (ALA-PDT), Lasers in Surgery and Medicine, 007, abstract S9:5. [0] J. Baxter and S. Mitragotri, Jet-induced skin puncture and its impact on needle-free jet injections: experimental studies and a predictive model, Controlled Release, vol. 06, no., pp. 6 7, 005. [] M.Garland,D.I.J.Morrow,R.F.Donnelly,andP.A.McCarron, A preliminary investigation into the topical delivery of pre-formed photosensitisers by jet injection, Pharmacy and Pharmacology, vol. 58, no. S, 006, abstract A6. [] L. E. Rhodes, M. A. De Rie, R. Leifsdottir et al., Five-year follow-up of a randomized, prospective trial of topical methyl aminolevulinate photodynamic therapy vs surgery for nodular basal cell carcinoma, Archives of Dermatology, vol. 4, no. 9, pp. 6, 007. [] F. I. Ezughah, A. G. Affleck, A. Evans, S. H. Ibbotson, and C. J. Fleming, Confirmation of histological clearance of superficial basal cell carcinoma with multiple serial sectioning and Mohs micrographic surgery following treatment with imiquimod 5% cream, Dermatological Treatment, vol. 9, no., pp. 56 58, 008.

MEDIATORS of INFLAMMATION The Scientific World Journal Volume 04 Gastroenterology Research and Practice Volume 04 Diabetes Research Volume 04 Volume 04 Volume 04 International Endocrinology Immunology Research Disease Markers Volume 04 Volume 04 Submit your manuscripts at BioMed Research International PPAR Research Volume 04 Volume 04 Obesity Ophthalmology Volume 04 Evidence-Based Complementary and Alternative Medicine Stem Cells International Volume 04 Volume 04 Oncology Volume 04 Volume 04 Parkinson s Disease Computational and Mathematical Methods in Medicine Volume 04 AIDS Behavioural Neurology Research and Treatment Volume 04 Volume 04 Volume 04 Oxidative Medicine and Cellular Longevity Volume 04