| 词条 | Invasive carcinoma of no special type | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| 释义 |
|name = Invasive carcinoma of no special type |synonym = Invasive ductal carcinoma |image = |image_size = |alt = |caption = |pronounce = |specialty = Oncology, Dermatology, Breast surgery |symptoms = |complications = |onset = |duration = |types = |causes = |risks = |diagnosis = |differential = |prevention = |treatment = |medication = |prognosis = |frequency = |deaths = }}Invasive carcinoma of no special type (NST) also known as invasive ductal carcinoma or ductal NOS and previously known as invasive ductal carcinoma, not otherwise specified (NOS) is a group of breast cancers that do not have the "specific differentiating features".[1] Those that have these features belong to other types.[1] In this group are: pleomorphic carcinoma, carcinoma with osteoclast-like stromal giant cells, carcinoma with choriocarcinomatous features, and carcinoma with melanotic features.[1] It is a diagnosis of exclusion, which means that for the diagnosis to be made all the other specific types must be ruled out.[1] ClassificationInvasive carcinoma of no special type (NST) is the most common form of invasive breast cancer. It accounts for 55% of breast cancer incidence upon diagnosis, according to statistics from the United States in 2004.[2] On a mammogram, it is usually visualized as a mass with fine spikes radiating from the edges. On physical examination, this lump usually feels much harder or firmer than benign breast lesions such as fibroadenoma. On microscopic examination, the cancerous cells invade and replace the surrounding normal tissues. IDC is divided in several histological subtypes. Signs and symptomsIn many cases, ductal carcinoma is asymptomatic, and detected as abnormal results on mammography. When symptoms occur, a painless, enlarging mass that does not fluctuate with the menstrual period may be felt.[3] {{rp|274–275}} Pinching of the overlying skin may also be seen. Certain subtypes, such as inflammatory carcinomas, may result in a swollen, enlarged and tender breast. All variants of cancer, if there is metastatic spread, may cause enlarged lymph nodes and affect other organs.[4] {{rp|746–747}} CausesThe cancer may form from the precancerous lesion called ductal carcinoma in situ.[1] DiagnosisTumor sizeTumors under 1 cm in diameter are unlikely to spread systemically. Tumors are staged by size.[5]
Lymph node involvementAbsence of cancer cells in the lymph nodes is a good indication that the cancer has not spread systemically. Presence of cancer in the lymph nodes indicates the cancer may have spread. In studies, some women have had presence of cancer in the lymph nodes, were not treated with chemotherapy, and still did not have a systemic spread. Therefore, lymph node involvement is not a positive predictor of spread.[5]
Clinical stagingTumor size staging and node involvement staging can be combined into a single clinical staging number.
Histologic appearance{{Main|Bloom-Richardson grading system}}The appearance of cancer cells under a microscope is another predictor of systemic spread. The more different the cancer cells look compared to normal duct cells, the greater the risk of systemic spread. There are three characteristics that differentiate cancer cells from normal cells.
The histologic appearance of cancer cells can be scored on these three parameters on a scale from one to three. The sum of these grades is a number between 3 and 9. The score is called a Bloom Richardson Grade (BR) and is expressed [sum of the grades]/9. For example, cells that were graded 2 on all three parameters would result in a BR score of 6/9. A score of 5 and under is considered Low. 6 to 7 is considered Intermediate. 8 to 9 is considered High.[5] Vascular invasion{{Main|Lymphovascular invasion}}The presence of cancer cell in small blood vessels is called vascular invasion. The presence of vascular invasion increases the probability of systemic spread.[5] DNA analysisDNA analysis indicates the amount of DNA in cancer cells and how fast the cancer is growing. Cells with the normal amount of DNA are called diploid. Cells with too much or too little DNA are called aneuploid. Aneuploid cells are more likely to spread than diploid cells. DNA testings indicates the rate of growth by determining the number of cells in the synthetic phase (S Phase). An S Phase > 10% means a higher chance of spreading. The results of DNA testing are considered less reliable predictors of spread than size, histology, and lymph node involvement.[5] PrognosisAccording to the NIH Consensus Conference {{where|date=December 2013}}, if DCIS is allowed to go untreated, the natural course or natural history varies according to the grade of the DCIS. Unless treated, approximately 60 percent of low-grade DCIS lesions will have become invasive at 40 years follow-up.[6] High-grade DCIS lesions that have been inadequately resected and not given radiotherapy have a 50 percent risk of becoming invasive breast cancer within seven years. Approximately half of low-grade DCIS detected at screening will represent overdiagnosis, but overdiagnosis of high-grade DCIS is rare. The natural history of intermediate-grade DCIS is difficult to predict. Approximately one-third of malignant calcification clusters detected at screening mammography already have an invasive focus. The prognosis of IDC depends, in part, on its histological subtype. Mucinous, papillary, cribriform, and tubular carcinomas have longer survival, and lower recurrence rates. The prognosis of the most common form of IDC, called "IDC Not Otherwise Specified", is intermediate. Finally, some rare forms of breast cancer (e.g., sarcomatoid carcinoma, inflammatory carcinoma) have a poor prognosis. Regardless of the histological subtype, the prognosis of IDC depends also on tumor size, presence of cancer in the lymph nodes, histological grade, presence of cancer in small vessels (vascular invasion), expression of hormone receptors and of oncogenes like HER2/neu. These parameters can be entered into models that provide a statistical probability of systemic spread. The probability of systemic spread is a key factor in determining whether radiation and chemotherapy are worthwhile. The individual parameters are important also because they can predict how well a cancer will respond to specific chemotherapy agents. Overall, the 5-year survival rate of invasive ductal carcinoma was approximately 85% in 2003.[7] TreatmentTreatment of invasive carcinoma of no special type (NST) depends on the size of the mass (size of the tumor measured in its longest direction):
The treatment options offered to an individual patient are determined by the form, stage and location of the cancer, and also by the age, history of prior disease and general health of the patient. Not all patients are treated the same way. See also
References1. ^1 2 3 4 {{cite journal|last1=Sinn|first1=HP|last2=Kreipe|first2=H|title=A Brief Overview of the WHO Classification of Breast Tumors, 4th Edition, Focusing on Issues and Updates from the 3rd Edition.|journal=Breast care (Basel, Switzerland)|date=May 2013|volume=8|issue=2|pages=149–154|pmid=24415964|doi=10.1159/000350774|pmc=3683948}} 2. ^Percentage values are from United States statistics 2004. Subtype specific incidences are taken from [https://archive.is/20130223233954/http://cebp.aacrjournals.org/content/18/6/1763/T6.expansion.html Table 6] (invasive) and [https://archive.is/20130223054758/http://cebp.aacrjournals.org/content/18/6/1763/T3.expansion.html Table 3] (in situ) from {{cite journal |vauthors=Eheman CR, Shaw KM, Ryerson AB, Miller JW, Ajani UA, White MC |title=The changing incidence of in situ and invasive ductal and lobular breast carcinomas: United States, 1999-2004 |journal=Cancer Epidemiol. Biomarkers Prev. |volume=18 |issue=6 |pages=1763–9 |date=June 2009 |pmid=19454615 |doi=10.1158/1055-9965.EPI-08-1082 |url=}}. These are divided by total breast cancer incidence (211,300 invasive and 55,700 in situ cases) as reported from Breast Cancer Facts & Figures 2003-2004 {{cite web|url=http://www.cancer.org/docroot/stt/content/stt_1x_breast_cancer_facts__figures_2003-2004.asp |title=Archived copy |accessdate=2010-06-15 |deadurl=yes |archiveurl=https://web.archive.org/web/20090415173047/http://www.cancer.org/docroot/STT/content/STT_1x_Breast_Cancer_Facts__Figures_2003-2004.asp |archivedate=2009-04-15 |df= }} 3. ^{{cite book|editor=Nicki R. Colledge|editor2=Brian R. Walker|editor3=Stuart H. Ralston|others=Illustrated by Robert Britton|title=Davidson's principles and practice of medicine.|year=2010|publisher=Churchill Livingstone/Elsevier|location=Edinburgh|isbn=978-0-7020-3084-0|edition=21st}} 4. ^{{cite book|title= Robbins basic pathology|publisher= Saunders/Elsevier|date=2007|isbn=978-0-8089-2366-4}} 5. ^1 2 3 4 Link, John; The Breast Cancer Survival Manual, 4th Edition 6. ^{{Cite journal| last1 = Evans | first1 = A.| journal = Breast Cancer Research| volume = 6|title=Ductal carcinoma in situ (DCIS): are we overdetecting it?| pages = P23| year = 2004| doi = 10.1186/bcr842| pmc = 3300383}} 7. ^NOTE: Number really refers to invasive ductal carcinoma, despite title. {{cite journal |vauthors=Arpino G, Bardou VJ, Clark GM, Elledge RM |title=Infiltrating lobular carcinoma of the breast: tumor characteristics and clinical outcome |journal=Breast Cancer Res. |volume=6 |issue=3 |pages=R149–56 |year=2004 |pmid=15084238 |pmc=400666 |doi=10.1186/bcr767 |url=}} External links{{Medical resources| ICD10 = {{ICD10|C50}} | ICD9 = {{ICD9|174}}, {{ICD9|175}} | ICDO = {{ICDO|8500|3}} | OMIM = | DiseasesDB = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D018270 | GeneReviewsNBK = | GeneReviewsName = | NORD = | GARDNum = | GARDName = | Orphanet = | AO = | RP = | WO = | OrthoInfo = | NCI = | Scholia = | SNOMED CT = }}
1 : Breast cancer |
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