Basal Cell Carcinoma Mark H. Tseng MD SUNY Downstate University Hospital June 17, 2005
History
Discrete, raised, circular ulceration.
History Pt was admitted to xx Hospital in 2005 for bleeding. He was transfused 5 units of blood.
History Pt arrived at SUNY Downstate on xx 2005. He was evaluated and biopsies of the margins was taken. Path came back negative and surgery was scheduled.
History PMH: None PSH: Tonsillectomy Family Hx: None Social Hx: -Habits: ------Allergies: NKDA MEDS: Multivitamins
Vitals Temperature: 98.8F Blood Pressure: 120/73 Heart Rate: 90 Respiratory Rate: 14 Saturation: 99% on room air
Physical Exam General: Appears age appropriate HEENT: large ulcer extending to left neck, friable, no active bleeding. Chest: large left mass/ulcer approx. 3 feet x 3 feet extending from: Anterior: chest Lateral: shoulder Medial: neck Posterior: Back Lung: CTA bilaterally, no wheezing, no rales Heart: S1S2 Abdomen: soft, nt, nd, +bs
LABS 5/3/05 pre-op: Wbc: 9 H/H: 10/33 Plt: 408 Na: 136 K: 4.6 Cl: 101 HCO3: 23 BUN: 21 Crea: 1.1 Glucose: 69 Alb: 3.1 PT: 14.5 INR: 1.2 PTT: 26
Shoulder X- RAY
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Aggressive osteolytic lesions @ distal clavicle and acromion
History Because of the large area of ulceration, the depth of invasion, and the vital structures involved. A team of surgeon from various surgical specialties were involved. - General Surgery - Plastic Surgery - Orthopedics Surgery - Vascular Surgery
Operating Team
Dr. Bakshandeh
Dr. Schwartzman
Dr. Deitch
Intra-op
Taken to OR and intubated.
Intra-op: resection
Incision through skin, subQ, fat, to level of fascia.
Intra-op: resection
Dissection carried deep to the pectoralis major.
Intra-op: resection
Dissection carried up to clavicle superiorly, medially into the neck, and posterior back along latissimus. Deepest part of incision was @ level of the shoulder. Tumor invading the supraclavicular space.
Intra-op: resection
Resection of lateral clavicular head and acromion
Intra-op: reconstruction
Transverse incision made 1 cm below the nipple. Pectoralis major was dissected off the pectoralis minor.
Intra-op: reconstruction
Once pectoralis major was freed Muscle flap was adv. superiorly covering the defect
Intra-op: reconstruction
STSG at 13,000 of inch harvest from left thigh
Intra-op: reconstruction
1000 sq. cm of STSG used to cover the open area.
Hospital course Immediate post-op: extubated and hemodynamically stable. POD #1 Transfer to floor POD #9 Rehab was started POD #14 Discharge
Pathology
Ulcerating basal cell carcinoma with squamous and adenoid foci Margins are free of tumor
Basal Cell Carcinoma: Overview and Management Mark H. Tseng MD SUNY Downstate University Hospital June 17, 2005
Overview
Introduction Epidemiology
Incidence Risk factors
Anatomy/Histology Clinical presentation Diagnosis Treatment Prognosis Conclusion References
Introduction
Most common skin cancer arising from the basal layer of epidermis and its ppendages Low metastatic potiential Locally invasive, aggressive, and destructive to skin and bone
Epidemiology
Skin cancer: approx. 1.5 million cases per year BCC is most common skin cancer 80% is BCC White >> Black Men >> women BCC increase with age
Aged 55-70 has 100 fold higher incidence of BCC than age 20 and younger
15% 4% 1% 80%
Basal Cell Squamous Cell Melanoma Etc.
Striking geographic variation Higher incidence closer to the equator *Australia is 40X that of Finland
* Marks, R, Staples, M, Giles, GG. Trends in nonnon-melanocytic skin cancer treated in Australia: the second national survey. Int J Cancer 1993; 53:585.
Risk Factors: Environmental Sun exposure is the most important environmental cause of BCC. Ultraviolet light – Sun Exposure Ionizing radiation causes mutation of tumor suppressor genes UV B light: 280-320nm, UV A light 320400nm But, UVA rays pass deeper into the skin. UVB radiation is thought to be the cause of melanoma and other types of skin cancer. UVA radiation may cause skin damage that can lead to skin cancer and cause premature aging of the skin.
Amount of UV B exposure during childhood and adolescence is directly proportional to risk for BCC
Risk Factors: Sunburns The Behavior Risk Factor Surveillance System provided data showing nearly 32% of all adults in the US report having had a sunburn in 1999. More than 57% of adults age 18 to 29 reported having had a sunburn. Over 40% of children are reported to have had sunburns over the preceding year.
Risk Factor: Sun exposure
Childhood sun exposure is more important than exposure during adult life.
*Canadian case control study 226 men with BCC and 406 age-match controls
Aggressive sun protection before age 18 reduce nonmelanoma skin cancer by 78%. The type, quantity and timing of sun exposure necessary to increase the risk of BCC are not clearly defined.
*Gallagher, Bajdik, Bajdik, CD, et al. Sunlight exposure, Basal cell carcinoma. Arch Dermatol 1995; 131:157.
How can it be PREVENTED?
For most of us, it’s too late !! But we can keep our kids from getting sunburns. USE SUNSCREEN
*Large randomized trial evaluating sunscreen and betacarotene (oral antioxidant) on prevention of BCC and SCC followed over 4 years. Users of sunscreen has 40% reduction in skin cancer over non-users Beta carotene failed to decrease incidence over placebo.
*Green, A, Williams, G, Neale, R, et al. Daily sunscreen application and betacarotene supplementation in prevention of basal-cell and squamous-cell carcinomas of the skin: a randomised controlled trial. Lancet 1999; 354:723.
Risk Factors
The following groups have the least melanin and are at greatest risk for BCC: fair complexion, light hair, blue/green eyes, inability to tan, history of multiple or severe sunburns, frequent use of tanning beds, ladies! Celtic ancestry
Risk Factors
Smoking Arsenic Radiation Therapy Burns, Scars, Ulcers Chronic immunosuppression
*Transplant patients Incidence is increased 10 fold in transplant patients compare to nontransplant patients
Albinism Mutation of PTCH gene (tumor suppressor gene) on chromosome 9 in patients with familial basal cell nevus syndrome. Bazex's syndrome (basal cell carcinomas, follicular atrophoderma, hypotrichosis, and hypohidrosis or hyperhidrosis) Gorlin's syndrome (multiple basal cell carcinomas, pitting of the palms and the soles of the feet, mandibular cysts, spine and rib anomalies, calcification of the falx cerebri, and cataracts )
*Hartevelt, MM, Bavinck, JN, Kootte, AM, et al. Incidence of skin cancer after renal transplantation in the Netherlands. Transplantation 1990; 49:506.
Skin Structure
Epidermis Dermis Hypodermis Epidermal appendages
Skin Histology
Stratum corneum stratum lucidum stratum granulosum stratum spinosum stratum basale
Clinical Presentation
Slowly growing malignancy of the epidermis Rarely metastasizes (.028-.55%) Cells appear histologically similar to basal cells of epidermis
Clinical Presentation
Distribution of BCC: 70% on face 25% on trunk 5% on penis, vulva, or perianal skin
Clinical subtypes (4) Nodular Superficial Pigmented Morpheaform
Clinical Presentation
Nodular
Discrete, raised, circular Central ulceration Pink, waxy rolled borders Relatively non-aggressive
Clinical Presentation
Superficial
Threadlike, waxy border Red, scaling patches Spread by radial extension Uncommon in Head and Neck
Clinical Presentation
Pigmented
Resemble nevus or melanoma Behave the same as nodular variant
Clinical Presentation
Morpheaform
Macular, whitish, or yellowish plaque Indistinct clinical margins Aggressive behavior Worst prognosis
Clinical Presentation
Histologic Subtypes (4) Solid Cystic Adenoid Keratotic (Basosquamous)
Clinical Presentation
Solid – no cellular differentiation
Clinical Presentation
Cystic
Differentiation towards sebaceous glands Cystic spaces within tumor lobules
Clinical Presentation
Adenoid
Glandular pattern Lacelike pattern
Clinical Presentation
Keratotic (Basosquamous)
Basal cell CA with differentiation towards hair structures Shows feature of both basal cell and squamous cell carcinomas More aggressive clinically Undifferentiated cells in combination with parakeratotic cells and horn cysts
Diagnosis
Initial evaluation involves
Assessment of location Punch or excisional biopsy Staging
Diagnosis - Staging
Treatment: Techniques
Electrodessication and curettage Cryosurgery Radiation therapy Photodynamic therapy Excisional surgery Mohs surgery
Treatment
Treatment: Electrodessication and Curettage
Used to remove tumor by feel with small margin of normal tissue Reserved for histologically and clinically favorable basal cell carcinomas. Not used for squamous cell lesions
Treatment: Cryosurgery
Uses liquid Nitrogen to kill tumor cells Typical temperature of -50°C . Tissue-sparing, but leave open wound Hypopigmentation and scarring may result Limited to favorable small lesions with welldefined borders
Treatment: Radiation Therapy
Used extensively in the past, now sparingly High cure rate (95%) Does not allow surgical staging Currently reserved for poor operative candidates, adjuvant in high risk malignancy Protracted treatment course, and expensive Radiodermatitis, delayed carcinogenesis
Treatment: Photodynamic Therapy
Photosensitizing drug (porphyrin, 5-ALA) applied topically, orally or parenterally and localizes into tumor cells Drug is activated by exposure to light (laser) Efficacy is low (45%) Side effects include local edema, erythema, blistering, ulceration Used as palliation
Treatment: Excisional Surgery
Most often used by surgeons, especially for larger lesions Can be with cold steel or laser Can allow reconstruction in the same sitting Frozen sections decrease recurrence rate Can be time consuming and inconvenient If more than 1/3 of a cosmetic facial unit is excised, better cosmesis with removal of entire unit
Mohs Surgery
First described by Frederic E. Mohs in 1941 Mohs micrographic surgery (MMS) Gold standard for treating high-risk skin cancers Series of precise excision and microscopic evaluation 99% 5 year cure rate for BCC Lowest recurrence rate Advantages: precision, excellent cure rate, better cosmesis because it spares normal tissue Disadvantages: time consuming and expensive
Mohs Surgery: Indications
Treatment: Recurrence Rate
All of the non-Mohs' modalities have roughly equal and excellent cure rates for BCC without high-risk prognostic factors Recurrence rates for tumors treated by Moh’s Micrographic Surgery appear to be lower at all points in time and averages between 1-2%. The key predictors of tumor recurrence are size and site of the lesion, histology of tumor, and skill of the operator There is an increased risk of BCC recurrence regardless of treatment modality with increasing time.
Prognosis
Excellent Significant morbidity and disfigurement Pt with BCC are susceptible to other skin cancer
*40% over 3 years
Slow-growing tumor Metastasis is rare: 0.1%
Usually deeply invasive or large ( 10 x 10 cm or greater ) Fatal within eight months Routine metastatic workup is not recommend unless symptoms supervene
*Marcil, Marcil, I, Stern, RS. Risk of developing a subsequent nonmelanoma skin cancer in patients with a history of nonmelanoma skin cancer: a critical review of the literature and metameta-analysis. Arch Dermatol 2000; 136:1524.
Conclusion
BCC is the most common malignancy Risk factors: sunlight Use sunscreen Moh’s surgery is gold standard High risk of developing a second BCC
References Marks, R, Staples, M, Giles, GG. Trends in non-melanocytic skin cancer treated in Australia: the second national survey. Int J Cancer 1993; 53:585. Gallagher, Bajdik, CD, et al. Sunlight exposure, Basal cell carcinoma. Arch Dermatol 1995; 131:157 Green, A, Williams, G, Neale, R, et al. Daily sunscreen application and betacarotene supplementation in prevention of basal-cell and squamous-cell carcinomas of the skin: a randomised controlled trial. Lancet 1999; 354:723. Hartevelt, MM, Bavinck, JN, Kootte, AM, et al. Incidence of skin cancer after renal transplantation in the Netherlands. Transplantation 1990; 49:506. Marcil, I, Stern, RS. Risk of developing a subsequent nonmelanoma skin cancer in patients with a history of nonmelanoma skin cancer: a critical review of the literature and meta-analysis. Arch Dermatol 2000; 136:1524.
The End