Cervical cancer natural history, complications and prognosis: Difference between revisions
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*Cervical cancer arises from squamous-columnar junction. | *Cervical cancer arises from squamous-columnar junction. | ||
*The earliest microscopic change corresponding to [[cervical intraepithelial neoplasia]](CIN) is [[dysplasia]] of the epithelial or surface lining of the cervix,are associated with HPV infection, such as koilocytes, are also commonly seen in Cervical intraepithelial neoplasia (CIN). | *The earliest microscopic change corresponding to [[cervical intraepithelial neoplasia]](CIN) is [[dysplasia]] of the epithelial or surface lining of the cervix,are associated with HPV infection, such as koilocytes, are also commonly seen in Cervical intraepithelial neoplasia (CIN). | ||
*However most CIN spontaneously regress. Left untreated, about 70% of CIN-1 will regress within one year, and 90% will regress within two years. About 50% of CIN 2 will regress within 2 years without treatment. | *However most CIN spontaneously regress. Left untreated, about 70% of CIN-1 will regress within one year, and 90% will regress within two years. About 50% of CIN 2 will regress within 2 years without treatment. | ||
*Progression to cervical cancer in situ (CIS) occurs in approximately 11% of [[cervical intraepithelial neoplasia]](CIN1) and 22% of [[cervical intraepithelial neoplasia]](CIN2). Progression to invasive cancer occurs in approximately 1% of [[cervical intraepithelial neoplasia]] (CIN1), 5% in [[cervical intraepithelial neoplasia]] (CIN2) and at least 12% in [[cervical intraepithelial neoplasia]] (CIN3). | *Progression to cervical cancer in situ (CIS) occurs in approximately 11% of [[cervical intraepithelial neoplasia]](CIN1) and 22% of [[cervical intraepithelial neoplasia]](CIN2). Progression to invasive cancer occurs in approximately 1% of [[cervical intraepithelial neoplasia]] (CIN1), 5% in [[cervical intraepithelial neoplasia]] (CIN2) and at least 12% in [[cervical intraepithelial neoplasia]] (CIN3). | ||
* This process can be quite slow. Longitudinal studies have shown that in patients with untreated in situ cervical cancer, 30% to 70% will develop invasive carcinoma over a period of 10 to 12 years. However, in about 10% of patients, lesions can progress from in situ to invasive in a period of less than 1 year. As it becomes invasive, the tumor breaks through the basement membrane and invades the cervical stroma. | * This process can be quite slow. Longitudinal studies have shown that in patients with untreated in situ cervical cancer, 30% to 70% will develop invasive carcinoma over a period of 10 to 12 years. However, in about 10% of patients, lesions can progress from in situ to invasive in a period of less than 1 year. As it becomes invasive, the tumor breaks through the basement membrane and invades the cervical stroma. | ||
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==Complications== | ==Complications== | ||
Advanced stage of cervical cancer can cause varieties of complications, some of these are include:<ref name="SchmitzIsaacs1957">{{cite journal|last1=Schmitz|first1=Herbert E.|last2=Isaacs|first2=John H.|title=Complications of Advanced Cervical Cancer and Their Management|journal=Radiology|volume=69|issue=3|year=1957|pages=324–329|issn=0033-8419|doi=10.1148/69.3.324}}</ref> | |||
* Pain | |||
* Vaginal hemorrhage | |||
* Enterovaginal, rectovaginal, and vesico- or ureterovaginal fistulas | |||
* Renal failure and/or uremia | |||
* Malnutrition | |||
* Anemia | |||
* Mental depression | |||
* | * | ||
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Average [[years of potential life lost]] from cervical cancer are | Average [[years of potential life lost]] from cervical cancer are | ||
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Revision as of 21:27, 11 February 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
If left untreated, 30-70% of patients with in situ cervical cancer may progress to develop cervical cancer. Common complications of cervical cancer include vaginal bleeding, fistula and renal failure. Prognosis is generally good, and the 5 year survival rate of patients with cervical cancer is approximately 67.9%.
Natural history
- Cervical cancer arises from squamous-columnar junction.
- The earliest microscopic change corresponding to cervical intraepithelial neoplasia(CIN) is dysplasia of the epithelial or surface lining of the cervix,are associated with HPV infection, such as koilocytes, are also commonly seen in Cervical intraepithelial neoplasia (CIN).
- However most CIN spontaneously regress. Left untreated, about 70% of CIN-1 will regress within one year, and 90% will regress within two years. About 50% of CIN 2 will regress within 2 years without treatment.
- Progression to cervical cancer in situ (CIS) occurs in approximately 11% of cervical intraepithelial neoplasia(CIN1) and 22% of cervical intraepithelial neoplasia(CIN2). Progression to invasive cancer occurs in approximately 1% of cervical intraepithelial neoplasia (CIN1), 5% in cervical intraepithelial neoplasia (CIN2) and at least 12% in cervical intraepithelial neoplasia (CIN3).
- This process can be quite slow. Longitudinal studies have shown that in patients with untreated in situ cervical cancer, 30% to 70% will develop invasive carcinoma over a period of 10 to 12 years. However, in about 10% of patients, lesions can progress from in situ to invasive in a period of less than 1 year. As it becomes invasive, the tumor breaks through the basement membrane and invades the cervical stroma.
- In advanced disease, metastases may be present in the abdomen, lungs.
- The patient may present with dyspnea, cough with blood-stained sputum, persistent pain or discomfort in the chest, edema hands/feet.
- Once the cancer spreads to the other organs, it is most likely fatal.
Complications
Advanced stage of cervical cancer can cause varieties of complications, some of these are include:[1]
- Pain
- Vaginal hemorrhage
- Enterovaginal, rectovaginal, and vesico- or ureterovaginal fistulas
- Renal failure and/or uremia
- Malnutrition
- Anemia
- Mental depression
Prognosis
The prognosis for patients with cervical cancer is markedly affected by the extent of disease at the time of diagnosis. More than 90% of cervical cancer cases can be detected early through the use of the Pap test and HPV testing.
- Prognostic Factors
- Clinical stage
- Clinical stage as a prognostic factor is supplemented by several gross and microscopic pathologic findings in surgically treated patients.
- Gynecologic Oncology Group identified the following variables that were significant for progression-free interval and survival:
- Periaortic and pelvic lymph node status.
- Tumor size
- Patient age
- Performance status
- Bilateral disease
- Clinical stage
- Other prognostic factors
- Other prognostic factors that may affect outcome include the following:
- Human immunodeficiency virus (HIV) status: Women with HIV have more aggressive and advanced disease and a poorer prognosis.
- C-myc overexpression: A study of patients with known invasive squamous carcinoma of the cervix found that overexpression of the C-myc oncogene was associated with a poorer prognosis.
- Number of cells in S phase: The number of cells in S phase may also have prognostic significance in early cervical carcinoma.
- HPV-18 DNA: HPV-18 DNA has been found to be an independent adverse molecular prognostic factor. Two studies have shown a worse outcome when HPV-18 was identified in cervical cancers of patients undergoing radical hysterectomy and pelvic lymphadenectomy.
- A polymorphism in the Gamma-glutamyl hydrolase enzyme, which is related to folate metabolism, has been shown to decrease response to cisplatin, and as a result is associated with poorer outcomes.
Average years of potential life lost from cervical cancer are
- ↑ Schmitz, Herbert E.; Isaacs, John H. (1957). "Complications of Advanced Cervical Cancer and Their Management". Radiology. 69 (3): 324–329. doi:10.1148/69.3.324. ISSN 0033-8419.