Merkel cell cancer overview: Difference between revisions
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{{Merkel cell cancer}} | {{Merkel cell cancer}} | ||
{{CMG}} | {{CMG}}; {{AE}} {{VKG}} {{AAM}} | ||
==Overview== | ==Overview== | ||
Merkel cell carcinoma is a very rare and highly aggressive [[cutaneous]] [[cancer]]. This cancer is a type of [[neuroendocrine tumor]], like [[small cell lung cancer]]. Merkel cell carcinoma is the most serious form of [[skin cancer]]. when merkel cell carcinoma metastasized to the [[lymph nodes]], the average 5-year survival rate for a patient with merkel cell carcinoma is less than 50 percent. Recurrence may occur in up to half of all the patients with merkel cell carcinoma. Merkel cell cancer usually occurs on either the face, head, or neck. Patients with merkel cell carcinoma usually present with a rapid growing, firm, painless, red/violaceous skin [[lesion]]. Merkel cell carcinoma usually [[metastasize]]s first to regional [[lymph nodes]] and then to other organs, and spreads to other parts of the body, especially the [[liver]], [[lungs]], [[brain]] and [[bone]]s. The predominant therapy for merkel cell carcinoma is surgical resection, but chemoradiation may also be required in more advanced disease. | |||
==Historical Perspective== | |||
[[Merkel cell]] was first discovered by Freidrich Sigmund Merkel and also mentioned by Cyril Toker, in 1972.Merkel cell polyomavirus, the pathogen responsible for Merkel cell cancer, was first discovered in 2008. | |||
==Classification== | |||
Merkel cell carcinoma is classified into 3 subgroups: Trabecular, intermediate, and small cell. | |||
==Pathophysiology== | |||
It is understood that merkel cell cancer is the result caused by either [[merkel cell]] [[polyomavirus]], [[ultraviolet]] (UV), [[radiation exposure]] and [[immunosuppression]]. | |||
==Causes== | |||
Common causes of merkel cell carcinoma include [[merkel cell]] [[polyomavirus]], age, skin tone, exposure to [[sunlight]] and history of [[immunosuppression]]. | |||
==Differential Diagnosis== | |||
Merkel cell cancer must be differentiated from other skin lesions, such as [[basal cell carcinoma]], [[squamous cell carcinoma]], [[malignant melanoma]], [[lymphoma]], vascular tumors, and other benign skin tumors. | |||
==Epidemiology and Demographics== | |||
The [[incidence]] of merkel cell carcinoma ranges from 0.15 to 0.44 per 100,000 individuals. The [[median]] age at diagnosis is approximately 65 years. Merkel cell carcinoma is more common among males and individuals of Caucasian race. | |||
==Risk Factors== | |||
Risk factors for the development of [[merkel cell cancer]] include old age, male gender, caucasian race, chronic exposure to [[sunlight]], [[immunodeficiency]], and personal history of [[cancer]]. | |||
==Screening== | |||
According to the [[USPSTF|U.S. Preventive Service Task Force (USPSTF)]], there is insufficient evidence to recommend routine screening for [[skin cancers]], including merkel cell cancer. | |||
==Natural History, Complications and Prognosis== | |||
Merkel cell cancer is an aggressive [[cutaneous]] cancer that grows very rapidly. Merkel cell cancer usually [[Metastasis|metastasizes]] first to regional [[Lymph node|lymph nodes]]. Merkel cell cancer is a highly aggressive [[tumor]] with a [[mortality]] rate that approaches 30% to 40% within 3 years of diagnosis. | |||
==Diagnosis== | |||
===Staging=== | |||
The staging of merkel cell cancer is based on the [[TNM staging system]]. | |||
===History and Symptoms=== | |||
Patients with merkel cell carcinoma usually present with a rapid growing, painless, small [[mass]] that is typically located on sun exposed area of the body. | |||
===Physical Examination=== | |||
Physical exam findings of merkel cell cancer include red/violaceous skin [[mass]] that appear in [[Sun exposure|sun]] exposed areas. | |||
===Laboratory Findings=== | |||
Laboratory findings consistent with the diagnosis of merkel cell cancer include [[immunohistochemistry]], [[Cytogenetics|cytogenetic]] and [[molecular]] analysis, and [[Lymph node biopsy|lymph node biopsy.]] . | |||
===CT=== | |||
[[Computed tomography|CT scan]] is useful in detecting [[metastasis]] to organs and regional lymph nodes in merkel cell carcinoma. | |||
===Other Imaging Findings=== | |||
[[Positron emission tomography]] ([[Positron emission tomography|PET]]) imaging may be used for the staging of merkel cell cancer. | |||
===Other Diagnostic Studies=== | |||
Other diagnostic studies for merkel cell cancer include [[skin biopsy]], which demonstrates positive [[Keratin 20|cytokeratin-20]] , and [[electron microscopy]], which demonstrates [[granules]], and [[cytoplasmic]] extensions. | |||
==Treatment== | |||
===Medical Therapy=== | |||
The predominant therapy for Merkel cell cancer is surgical resection. Adjunctive chemoradiation and adjuvant [[immunotherapy]] may also be required in more advanced disease. | |||
===Surgery=== | |||
The majority of cases of Merkel cell cancer are treated with [[Cancer#Surgery|surgery]]. | |||
===Primary Prevention=== | |||
[[Primary prevention]] of merkel cell cancer includes avoidance of excessive [[sun exposure]] and use of [[sunscreen]]. | |||
===Secondary Prevention=== | |||
There are no established measures for the [[secondary prevention]] of merkel cell cancer. | |||
==References== | ==References== | ||
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[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Types of cancer]] | [[Category:Types of cancer]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Up-To-Date]] | |||
[[Category:Oncology]] | |||
[[Category:Medicine]] | |||
[[Category:Dermatology]] | |||
[[Category:Surgery]] | |||
Latest revision as of 13:20, 25 March 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2] Ahmad Al Maradni, M.D. [3]
Overview
Merkel cell carcinoma is a very rare and highly aggressive cutaneous cancer. This cancer is a type of neuroendocrine tumor, like small cell lung cancer. Merkel cell carcinoma is the most serious form of skin cancer. when merkel cell carcinoma metastasized to the lymph nodes, the average 5-year survival rate for a patient with merkel cell carcinoma is less than 50 percent. Recurrence may occur in up to half of all the patients with merkel cell carcinoma. Merkel cell cancer usually occurs on either the face, head, or neck. Patients with merkel cell carcinoma usually present with a rapid growing, firm, painless, red/violaceous skin lesion. Merkel cell carcinoma usually metastasizes first to regional lymph nodes and then to other organs, and spreads to other parts of the body, especially the liver, lungs, brain and bones. The predominant therapy for merkel cell carcinoma is surgical resection, but chemoradiation may also be required in more advanced disease.
Historical Perspective
Merkel cell was first discovered by Freidrich Sigmund Merkel and also mentioned by Cyril Toker, in 1972.Merkel cell polyomavirus, the pathogen responsible for Merkel cell cancer, was first discovered in 2008.
Classification
Merkel cell carcinoma is classified into 3 subgroups: Trabecular, intermediate, and small cell.
Pathophysiology
It is understood that merkel cell cancer is the result caused by either merkel cell polyomavirus, ultraviolet (UV), radiation exposure and immunosuppression.
Causes
Common causes of merkel cell carcinoma include merkel cell polyomavirus, age, skin tone, exposure to sunlight and history of immunosuppression.
Differential Diagnosis
Merkel cell cancer must be differentiated from other skin lesions, such as basal cell carcinoma, squamous cell carcinoma, malignant melanoma, lymphoma, vascular tumors, and other benign skin tumors.
Epidemiology and Demographics
The incidence of merkel cell carcinoma ranges from 0.15 to 0.44 per 100,000 individuals. The median age at diagnosis is approximately 65 years. Merkel cell carcinoma is more common among males and individuals of Caucasian race.
Risk Factors
Risk factors for the development of merkel cell cancer include old age, male gender, caucasian race, chronic exposure to sunlight, immunodeficiency, and personal history of cancer.
Screening
According to the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend routine screening for skin cancers, including merkel cell cancer.
Natural History, Complications and Prognosis
Merkel cell cancer is an aggressive cutaneous cancer that grows very rapidly. Merkel cell cancer usually metastasizes first to regional lymph nodes. Merkel cell cancer is a highly aggressive tumor with a mortality rate that approaches 30% to 40% within 3 years of diagnosis.
Diagnosis
Staging
The staging of merkel cell cancer is based on the TNM staging system.
History and Symptoms
Patients with merkel cell carcinoma usually present with a rapid growing, painless, small mass that is typically located on sun exposed area of the body.
Physical Examination
Physical exam findings of merkel cell cancer include red/violaceous skin mass that appear in sun exposed areas.
Laboratory Findings
Laboratory findings consistent with the diagnosis of merkel cell cancer include immunohistochemistry, cytogenetic and molecular analysis, and lymph node biopsy. .
CT
CT scan is useful in detecting metastasis to organs and regional lymph nodes in merkel cell carcinoma.
Other Imaging Findings
Positron emission tomography (PET) imaging may be used for the staging of merkel cell cancer.
Other Diagnostic Studies
Other diagnostic studies for merkel cell cancer include skin biopsy, which demonstrates positive cytokeratin-20 , and electron microscopy, which demonstrates granules, and cytoplasmic extensions.
Treatment
Medical Therapy
The predominant therapy for Merkel cell cancer is surgical resection. Adjunctive chemoradiation and adjuvant immunotherapy may also be required in more advanced disease.
Surgery
The majority of cases of Merkel cell cancer are treated with surgery.
Primary Prevention
Primary prevention of merkel cell cancer includes avoidance of excessive sun exposure and use of sunscreen.
Secondary Prevention
There are no established measures for the secondary prevention of merkel cell cancer.