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$Unique_ID{BRK03557}
$Pretitle{}
$Title{Cancers, Skin, General}
$Subject{Cancers Skin General Melanoma Non-Melanoma Melanoma Malignant Basal
Cell Carcinoma Squamous Cell Carcinomas Acral Lentiginious Melanoma Juvenile
Melanoma Kaposi's Sarcoma Malignant Lentico Melanoma Dysplastic Nevus Syndrome
Xeroderma Pigmentosum}
$Volume{}
$Log{}
Copyright (C) 1990, 1991, 1992 National Organization for Rare Disorders,
Inc.
786:
Cancers, Skin, General
** IMPORTANT **
It is possible that the main title of the article (Skin Cancers, General)
is not the name you expected. Please check the SYNONYM listing to find the
alternate names and disorder subdivisions covered by this article.
Synonyms
Melanoma
Non-Melanoma
Disorder Subdivisions:
Melanoma, Malignant
Basal Cell Carcinoma
Squamous Cell Carcinomas
Acral Lentiginious Melanoma
Juvenile Melanoma
Kaposi's Sarcoma
Malignant Lentico Melanoma
Information on the following diseases can be found in the Related
Disorders section of this report:
Dysplastic Nevus Syndrome
Xeroderma Pigmentosum
General Discussion
** REMINDER **
The information contained in the Rare Disease Database is provided for
educational purposes only. It should not be used for diagnostic or treatment
purposes. If you wish to obtain more information about this disorder, please
contact your personal physician and/or the agencies listed in the "Resources"
section of this report.
There are many different types of Skin Cancer. Combined together all
types of Skin Cancer represent the most prevalent type of cancer. Most skin
cancers are characterized by changes in the color or texture of the skin, but
some types begin under the skin where they can spread to other parts of the
body. Malignant melanoma is the most dangerous of this type of skin cancer.
Symptoms
Skin Cancer is the most common of all cancers. The incidence of Skin Cancer
is rising faster than any other type of cancer, increasing more than 30%
percent in recent years. The most dangerous form of skin cancer is malignant
melanoma. It occurs below the surface of the skin and spreads easily to
other locations in the body. Malignant Melanoma may appear as a lesion that
does not heal, or an existing mole that shows changes in size and color. Non-
melanoma type skin cancers are mainly basal cell and squamous cell carcinomas
that occur on the skins surface and are easier to locate and treat. They may
appear as small, shiny nodules or ulcerated crusted lesions. They may also
appear as flat, scar-like hardened patches which bleed, or patchy and scaly
elevations on the skin. If left untreated both types of skin cancer can
spread (metastasize) to other parts of the body causing further disease.
Causes
Most types of skin cancer are caused by over-exposure to the sun's harmful
ultra violet rays. B type ultraviolet rays are related to onset of
malignant melanoma. However, the direct relationship is not fully
understood. Life style and skin coloring also contribute to the development
of skin cancer. Some scientists believe that there may be a genetic
predisposition for some forms of skin cancer but more study is necessary to
determine exactly why this happens. A genetic predisposition means that a
person may carry a gene for a disease but it may not be expressed unless
something in the environment triggers the disease.
Affected Population
Skin Cancers affect males and females in equal numbers. However, persons
with fair skin and hair, and persons living closer to the equator and/or at
higher elevations, have a higher risk of developing skin cancer than others.
The various types of skin cancers, when combined, represent the most
prevalent type of cancer.
The following disorders are the most common types of Skin Cancers.
Malignant Melanoma is a common skin cancer that arises from the melanin
cells of the upper layer of the skin (epidermis) or from similar cells that
can be found in moles (nevi). This type of skin cancer may send down roots
into deeper layers of the skin. Some of these microscopic roots can spread
(metastasize) causing new tumor growths in vital organs of the body. A
physician should be consulted when any lesions, pigmented or not, becomes
itchy, burns, softens or hardens, forms a scab, bleeds, becomes surrounded by
a reddened or inflamed area, changes color, size or shape. (For more
information on this disorder, choose "Malignant Melanoma" as your search term
in the Rare Disease Database).
Basal Cell Carcinoma is a common skin cancer. It may appear as small,
shiny, firm nodules; ulcerated, crusted lesions; or flat, scar-like hardened
patches which may bleed. This type of skin cancer is difficult to
differentiate from psoriasis or localized dermatitis without a biopsy.
Squamous Cell Carcinoma usually appears on sun-exposed areas of the skin,
but may occur anywhere on the body. The lesions begin as a small red
elevation or patch with a scaly or crusted surface. They may become nodular,
sometimes with a warty surface. In some, the bulk of the cancer may lie
below the level of the surrounding tissue. A biopsy is essential to diagnose
this disorder.
Acral Lentiginious Melanoma is a malignant skin cancer that usually
occurs in areas or the body that are not excessively exposed to sunlight and
where hair follicles are absent.
Juvenile Melanoma is a benign, elevated, pink to purplish-red papule,
with a slightly scaly surface. It usually appears on the face, especially
the cheeks. This type of melanoma most often occurs before puberty and has
been mistaken for malignant melanoma.
Malignant Lentigo Melanoma is a precancerous area on the skin that
resembles a freckle. It can be brown or black in color, irregular in shape,
and it usually occurs on the face. This type of melanoma occurs most often
in older persons.
Kaposi's Sarcoma is a type of skin cancer usually found in people whose
immune system is dysfunctional. It appears as small pigmented (tan to
purple) papules, plaques, nodules, tumors or ulcers on the skin. This type
of skin cancer can infiltrate the body, involving the throat and
gastrointestinal tract, disseminating to other organs such as the liver,
lungs and bone. Chemotherapy has been helpful in treating Kaposi's Sarcoma.
Until the last 10 years it was seen mostly in older men of Ashkenazi Jewish
or Mediterranean descent, and in those with a compromised immune system. The
more recent increased incidence of Kaposi's Sarcoma is due to AIDS; about 30%
of those with AIDS will get Kaposi's Sarcoma. (For more information on this
disorder, choose "Kaposi's Sarcoma" or "AIDS" as your search term in the Rare
Disease Database).
Related Disorders
Symptoms of the following disorders can be similar to those of Skin Cancer.
Comparisons may be useful for a differential diagnosis:
Dysplastic Nevus Syndrome is a rare disorder that usually starts during
adulthood. The disorder is characterized by large moles which are reddish-
brown to pink in color. The moles have an irregular border. The presence of
dust-like melanin, which gives the moles their color, and abnormally large
nuclei of skin cells called melanocytes (all visible under the microscope),
are characteristic of Dysplastic Nevus Syndrome. The mole-like tumors may
spread to adjacent parts of the skin, or through the blood and lymph
circulation to other organs. Certain changes in the melanocyte nuclei
indicate when Dysplastic Nevus Syndrome may be changing to Malignant
Melanoma. (For more information on this disorder, choose "Dysplastic Nevus
Syndrome" as your search term in the Rare Disease Database).
Xeroderma Pigmentosum is a rare autosomal recessive hereditary skin
disorder which begins during early childhood. It is characterized by a
defect in the ability of certain connective tissue cells to repair skin
damaged by the ultraviolet rays of the sun. The skin of people with
Xeroderma Pigmentosum is markedly hypersensitive to sunlight. Plaques and
blisters develop when exposed to the sun. Many persons with XP go on to
develop skin cancer. (For more information on this disorder, choose
"Xeroderma" as your search term in the Rare Disease Database).
Therapies: Standard
Treatment of Skin Cancer depends on the depth, level, type, stage and
location of the lesion at the time of diagnosis. Surgery to remove the
affected area is usually the first step in treatment. If the cancer has
progressed beyond the skin and is affecting other organs then the physician
must make the determination as to further treatment. Chemotherapy (drugs)
are used in some courses of treatment, as is radiation. Preventative
measures are the most helpful. Many dermatologists recommend that parents
begin the protection of their children against the suns harmful rays as soon
as they are old enough to be playing out of doors. A sun blocking lotion is
the most useful protection in keeping the harmful ultra violet rays of the
sun off of a person's skin.
Therapies: Investigational
Scientists are studying many new drugs to treat various types of skin
cancers. Melaccine, antimelanoma antibody and Technetium Tc 99m are being
studied for the treatment of melanoma. For the treatment of Kaposi's Sarcoma
interferon alfa, nl, interferon alfa 2a and interferon alfa 2b are being
studied. Autologous bone marrow transplants are being done experimentally
for treatment of Malignant Melanoma but this procedure carries a very high
risk. Scientists are searching for ways to enhance the immune system which
may be helpful for many types of cancer. More research is necessary to
determine the long-term safety and effectiveness of these and other new drugs
and procedures being tested for skin cancers.
Another orphan biologic being tested for use in treating Malignant
Melanoma patients is Interferon Beta (Recombinant) (r-IFN)-beta). The
manufacturer is Biogen, Inc.
Clinical trials are underway to study Interleukin-2 and Tumor-
Infiltrating Lymphocytes in patients with Melanoma. Interested persons may
wish to contact:
Timothy J. Eberlein, M.D.
Brigham and Women's Hospital
75 Francis St.
Boston, MA 02115
(617) 732-6799
to see if further patients are needed for this research.
The orphan product Melphalan, trade name Alkeran for injection, is being
tested as a treatment for Metastic Melanoma. The product is being sponsored
by Burrough Wellcome Co., 3030 Cornwallis Rd., Research Triangle Park, NC,
27709.
This disease entry is based upon medical information available through
April 1992. Since NORD's resources are limited, it is not possible to keep
every entry in the Rare Disease Database completely current and accurate.
Please check with the agencies listed in the Resources section for the most
current information about this disorder.
Resources
For more on General Skin Cancer, please contact:
National Organization for Rare Disorders
P.O. Box 8923
New Fairfield, CT 06812-1783
(203) 746-6518
The Skin Cancer Foundation
475 Park Avenue, South
New York, NY 10016
212-725-5176
Melanoma Foundation
750 Menlo Avenue, Suite 250
Menlo Park, CA 94025
American Cancer Society
1599 Clifton Rd., NE
Atlanta, GA 30329
(404) 320-3333
NIH/National Cancer Institute
9000 Rockville Pike, Bldg. 31, Rm. 1A2A
Bethesda, MD 20892
1-800-4-CANCER
The National Cancer Institute has developed PDQ (Physician Data Query), a
computerized database designed to give the public, cancer patients and
families, and health professionals quick and easy access to many types of
information vital to patients with this and many other types of cancer. To
gain access to this service, call:
Cancer Information Service (CIS)
1-800-4-CANCER
In Washington, DC and suburbs in MD and VA, 636-5700
In Alaska, 1-800-638-6070
In Oahu, Hawaii, (808) 524-1234 (Neighbor islands call collect).
References
CECIL TEXTBOOK OF MEDICINE, 18th Ed.: James B. Wyngaarden, and Lloyd H.
Smith, Jr., Editors; W.B. Saunders Co., 1988. Pp. 1094, 2336-2340.
MELANOMA METASTATIC TO THE GASTROINTESTINAL TRACT. J. Kruse, et al.; Am
Fam Physician, (January, 1990, issue 41 (1)). Pp. 165-168.
PROGNOSIS OF THICK CUTANEOUS MELANOMA OF THE TRUNK AND EXTREMITY. D.
Coit, et al.; Arch Surg, (March, 1990, issue 125 (3)). Pp. 322-326.
CLINICAL CHARACTERISTICS OF MALIGNANT MELANOMAS DEVELOPING IN PERSONS
WITH DYSPLASTIC NEVI. J.K. River, Cancer, (March 1, 1990, issue 65 (5)). Pp.
1232-1236.
MALIGNANT MELANOMA OF SOFT PARTS (CLEAR CELL SARCOMA). A STUDY OF 17
CASES, WITH EMPHASIS ON PROGNOSTIC FACTORS. A.S. Sara, et al,; Cancer
(January 15, 1990, issue 65 (2)). Pp. 367-374.