Continually Updated Clinical Reference
 
 
  All Sources     eMedicine     Medscape     Drug Reference     MEDLINE
 
eMedicine - Skin Malignancies, Basal Cell Carcinoma : Article by

Quick Find
Authors & Editors
Basal Cell Carcinoma: Evaluation, Diagnosis, and Management
Histopathology
Presentation
Diagnosis
Treatment
Recurrence
Medical Legal Considerations
Multimedia
References




Patient Education
Cancer and Tumors Center

Skin Cancer Overview

Skin Cancer Causes

Skin Cancer Symptoms

Skin Cancer Treatment

Skin Biopsy Introduction

Skin Biopsy Preparation




Author: Maurice Y Nahabedian, MD, FACS, Associate Professor of Plastic Surgery, Department of Plastic and Reconstructive Surgery, Georgetown University

Maurice Y Nahabedian is a member of the following medical societies: American College of Surgeons, American Society of Plastic Surgeons, and Plastic Surgery Research Council

Editors: Shahin Javaheri, MD, Chief, Department of Plastic Surgery, Martinez Veterans Affairs Outpatient Clinic; Consulting Staff, Advanced Aesthetic Plastic & Reconstructive Surgery; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Wayne Stadelmann, MD, Stadelmann Plastic Surgery, PC; Nicolas (Nick) G Slenkovich, MD, Practice Director, Colorado Plastic Surgery Center at Swedish Medical Center; Jorge I de la Torre, MD, FACS, Professor of Surgery and Physical Medicine and Rehabilitation, Residency Program Director, Division of Plastic Surgery, University of Alabama at Birmingham; Director, Center for Advanced Surgical Aesthetics

Author and Editor Disclosure

Synonyms and related keywords: BCC, malignancy, skin cancer, malignant lesions, melanoma, squamous cell carcinoma, SCC, skin lesions

Basal cell carcinoma is the most common human malignancy. Although this lesion can be significantly invasive and locally destructive, distant metastases are uncommon. Most of these lesions are located on the face and scalp, with the nose, cheek, and periorbital regions the most common sites. Basal cell carcinoma rarely is found on the lip or hand.

The increasing incidence of skin cancer has raised concerns about congenital and acquired skin lesions. These lesions range from benign conditions such as a freckle or keratosis to malignant lesions such as basal or squamous cell carcinoma. The incidence of these lesions varies, ranging from 500-1000 cases per 100,000 people. Annually, more than 400,000 people find out they have skin cancer. Etiology is related to a variety of factors that includes skin type, age, and sun exposure.

Predisposing factors include individuals with a fair or light complexion, a history of severe sunburns, and poor tanning capability. It is prudent for all physicians to possess a basic understanding and knowledge of the types and characteristics of common skin lesions, because they are frequently asked to evaluate them. This article provides a framework for the surgeon to facilitate the evaluation, diagnosis, and management of cutaneous basal cell carcinoma.

For excellent patient education resources, visit eMedicine's Cancer and Tumors Center. Also, see eMedicine's patient education articles Skin Cancer and Skin Biopsy.



The natural history of basal cell carcinoma is that of a slowly growing lesion increasing in size and depth over months and years. Histologically, basal cell carcinomas arise from the basal layer of the epidermis and the pilosebaceous adnexa. The 5 subtypes of basal cell carcinoma include nodular, superficial, micronodular, infiltrating, and morpheaform (ie, sclerosing). The classification into subtypes, first described by Lang and Maize, has strong implications for clinical management. The basosquamous variant is relatively uncommon but more aggressive and does have significant metastatic potential.

The morpheaform and infiltrative subtypes are more aggressive in nature with higher recurrence rates. They comprise approximately 10% of basal cell cancers. The infiltrating and morpheaform basal cell carcinomas exhibit islands of tumor extending into the tissue and may exhibit perineural invasion in 3% of patients. This finding helps classify these two histotypes as the most aggressive, with the highest rates of recurrence and positive margins after excision. Nodular and superficial histotypes exhibit the least aggressive growth. Micronodular patterns are intermediate between most and least aggressive. For histological subtypes, the location of occurrence is most often the face, followed by the neck.



The most common presentation of basal cell carcinoma is in a Caucasian male older than 60 years. Patients commonly present with multiple coexisting tumors. There is a well-documented association of basal cell carcinoma with previous ionizing radiation and immunosuppression, as observed in patients with organ transplantation.

Basal cell carcinoma often is described as a pearly or translucent mass with raised borders and telangiectasias coursing throughout. The lesion may ulcerate, giving rise to the term "rodent ulcer." This classic presentation often is observed in nodular histotypes. Superficial basal cell carcinoma often presents as an erythematous patch or plaque. The lesion may be scaly, with areas of atrophy or scarring, and can be mistaken for eczema or psoriasis. Infiltrating and morpheaform tumors often do not have distinctive characteristics. They may present like scars with indistinct borders. As previously mentioned, the tumor often extends beyond the apparent borders of the lesion, with islands of tumor extending into the tissue.



Accurate diagnosis of suspicious lesions requires biopsy. Biopsy techniques include shave, punch, incision, and excision. Ensuring that the full thickness of the lesion is incorporated into the specimen is important. Shave biopsy is a safe and simple technique for skin lesions of unknown histotype; it does not require suturing. This technique is recommended for superficial lesions with a low suspicion of malignancy. Incisional, punch, and excisional biopsy allow removal of the full thickness of the specimen, which permits accurate diagnosis. These techniques are recommended if a higher possibility of malignancy exists.



Electrodesiccation and curettage

Electrodesiccation and curettage is the most common treatment method used by dermatologists. Separate the well-circumscribed tumor from surrounding normal skin and remove any extension of disease with electrodesiccation. Use this method for primary treatment of nodular basal cell carcinoma smaller than 2 cm and superficial basal cell carcinoma of any size. The cure rates for this treatment modality reportedly are 90-98%. Recurrence rates of 50% are reported for tumors wider than 3 cm.

Cryotherapy

This modality is indicated in the management of primary lesions smaller than 2 cm. Overall cure rates of more than 95% are reported using cryosurgery. Significant scarring, hypopigmentation, and potential injury to adjacent nerves are associated with this treatment. Most significantly, there is no microscopic confirmation of tumor eradication by this method. Cryosurgery is contraindicated in patients with cryoglobulinemia and the more aggressive basal cell carcinomas such as the infiltrating and morpheaform subtypes. It is also contraindicated when scar contracture may cause problems such as periorbital or perioral lesions.

Surgical excision

Cure rates for surgical excision of basal cell carcinoma are higher than 90%. The size, histotype, and anatomic location of the lesion help determine cure rates. Margins of 2-5 mm are recommended to achieve cure. "The larger the lesion, the wider the margin" is a good general rule. The reconstruction of the defect most often can be achieved by undermining the skin edges and by primary closure. Smaller lesions can be safely excised by general practitioners; patients with larger or more complex lesions are best referred to a plastic surgeon.

Mohs micrographic surgery may prove advantageous in certain critical areas, such as the medial and lateral canthal area, perioral area, and in the area of the nasal ala. Cure rates for this technique, which uses horizontal frozen sections of the entire undersurface of the excised tissue, are reportedly 99% for primary lesions and 96% for recurrent lesions. Examine the sections microscopically and plan the extent of the resection accordingly.



Recurrence rates are higher in tumors wider than 3 cm or in areas where maximum tissue preservation is required, such as those mentioned above. Basal cell carcinomas with positive margins after primary resection must be re-excised for cure. Histologic features associated with higher recurrence rates include cellular palisading, ulceration, and lymphatic infiltration. Recurrent tumors require larger surgical margins than those used in primary resections. Mohs micrographic technique also is indicated in the management of recurrent lesions.



  • Failure to document the appearance and behavior of all suspicious lesions and explain to the patient the recommendations for observation or biopsy
  • Failure to refrain from labeling or coding a skin lesion of uncertain behavior as a carcinoma until after it is biopsied and the final pathology is determined
  • Failure to obtain informed consent (which is mandatory) prior to any operative procedure
  • Failure to be absolutely sure that specimens are labeled correctly and sent in separate containers when more than one lesion is removed
  • Failure to ensure that the correct lesion or lesions are being removed (photographs and mirrors are useful)
  • Failure to inform patients that biopsies will leave scars and additional procedures may be necessary depending on the final pathology
  • Failure to notify the patient of the results once they are available, rather than waiting for the patient to call, once the final pathology is available



Media file 1:  This translucent pink papule has telangiectases and a crusted erosion characteristic of nodular basal cell carcinoma (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 2:  Nodular basal cell carcinoma presenting as a waxy translucent papule with central depression and a few small erosions (Image courtesy of Michael L Ramsey, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 3:  Nodular basal cell carcinoma. Nodular aggregates of basalioma cells are present in the dermis and exhibit peripheral palisading (PP) and retraction artifact (RA). Melanin also is present within the tumor and in the surrounding stroma, as seen in pigmented basal cell carcinoma (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Image

Media file 4:  Scale, erythema, and a threadlike raised border are present in this superficial basal cell carcinoma on the trunk (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 5:  Larger superficial basal cell carcinoma (Image courtesy of Michael L Ramsey, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 6:  Histology of superficial basal cell carcinoma. Nests of basaloid cells are seen budding from the undersurface of the epidermis (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 7:  Pigmented basal cell carcinoma has features of nodular basal cell carcinoma with the addition of darker pigmentation from melanin deposition. The pigmentation often has the appearance of dark droplets within the lesion, as seen in this picture (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 8:  This infiltrating basal cell cancer has ill-defined borders and telangiectases (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 9:  Postoperative wound after Mohs micrographic surgery demonstrates extensive subclinical involvement typical of many infiltrating and morpheaform basal cell carcinomas (Image courtesy of Michael L Ramsey, MD).
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 10:  Large scarlike morpheaform basal cell cancer (Image courtesy of Michael L Ramsey, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 11:  Basal cell carcinoma (Image courtesy of Hon Pak, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 12:  A 68-year-old patient presenting with an advanced basal cell carcinoma (BCC) of the right periorbital region, frontal view (Images courtesy of M Abraham Kuriakose, DDS, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 13:  Lateral view of face showing extent of tumor (Images courtesy of M Abraham Kuriakose, DDS, MD)
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo



  • Brown CI, Perry AE. Incidence of perineural invasion in histologically aggressive types of basal cell carcinoma. Am J Dermatopathol. Apr 2000;22(2):123-5. [Medline].
  • Constantino D, Lowe L, Brown DL. Basosquamous carcinoma: An under recognized, high risk cutaneous neoplasm - case study and review of literature. J. Plast Reconstr Aesthet Surg. 2006;59 (4):424-8. [Medline].
  • Dixon AY, Lee SH, McGregor DH. Factors predictive of recurrence of basal cell carcinoma. Am J Dermatopathol. Jun 1989;11(3):222-32. [Medline].
  • Gorney M, Martello J. The genesis of plastic surgeon claims. A review of recurring problems. Clin Plast Surg. Jan 1999;26(1):123-31, ix. [Medline].
  • Lang PG Jr, Maize JC. Histologic evolution of recurrent basal cell carcinoma and treatment implications. J Am Acad Dermatol. Feb 1986;14(2 Pt 1):186-96. [Medline].
  • Miller SJ, Malden MA, eds. Cutaneous oncology: Pathophysiology, Diagnosis, and Management. Blackwell Science Inc;1998.
  • Raasch B, Wooley T. Management of primary superficial basal cell carcinoma. Aust Fam Physician. 2006;35:455-8. [Medline].
  • Raasch BA, Buettner PG, Garbe C. Basal cell carcinoma: histological classification and body site distribution. Br J Dermatol. 2006;155(2):401-7. [Medline].
  • Sexton M, Jones DB, Maloney ME. Histologic pattern analysis of basal cell carcinoma. Study of a series of 1039 consecutive neoplasms. J Am Acad Dermatol. Dec 1990;23(6 Pt 1):1118-26. [Medline].

Skin Malignancies, Basal Cell Carcinoma excerpt

Article Last Updated: Sep 29, 2006