ICD-10-PCS 0?D???X (without force),
0?B???X (with force)
MeSH D001706
OPS-301 code 1-40...1-49 (without incision)
1-50...1-58 (with incision)
MedlinePlus 003416

A biopsy is a medical test commonly performed by a surgeon, interventional radiologist, or an interventional cardiologist involving extraction of sample cells or tissues for examination to determine the presence or extent of a disease. The tissue is generally examined under a microscope by a pathologist, and can also be analyzed chemically. When an entire lump or suspicious area is removed, the procedure is called an excisional biopsy. When only a sample of tissue is removed with preservation of the histological architecture of the tissue’s cells, the procedure is called an incisional biopsy or core biopsy. When a sample of tissue or fluid is removed with a needle in such a way that cells are removed without preserving the histological architecture of the tissue cells, the procedure is called a needle aspiration biopsy. Biopsies are most commonly performed for insight into possible cancerous and inflammatory conditions.

Medical use


Lung biopsy in a case of suspected lung cancer under control of computed tomography.

When cancer is suspected, a variety of biopsy techniques can be applied. An excisional biopsy is an attempt to remove an entire lesion. When the specimen is evaluated, in addition to diagnosis, the amount of uninvolved tissue around the lesion, the surgical margin of the specimen is examined to see if the disease has spread beyond the area biopsied. "Clear margins" or "negative margins" means that no disease was found at the edges of the biopsy specimen. "Positive margins" means that disease was found, and a wider excision may be needed, depending on the diagnosis.

When intact removal is not indicated for a variety of reasons, a wedge of tissue may be taken in an incisional biopsy. In some cases, a sample can be collected by devices that "bite" a sample. A variety of sizes of needle can collect tissue in the lumen (core biopsy). Smaller diameter needles collect cells and cell clusters, fine needle aspiration biopsy.[1]

Pathologic examination of a biopsy can determine whether a lesion is benign or malignant, and can help differentiate between different types of cancer. In contrast to a biopsy that merely samples a lesion, a larger excisional specimen called a resection may come to a pathologist, typically from a surgeon attempting to eradicate a known lesion from a patient. For example, a pathologist would examine a mastectomy specimen, even if a previous nonexcisional breast biopsy had already established the diagnosis of breast cancer. Examination of the full mastectomy specimen would confirm the exact nature of the cancer (subclassification of tumor and histologic "grading") and reveal the extent of its spread (pathologic "staging").

Liquid biopsy

There are two types of liquid biopsy (which is not really a biopsy as they are blood tests that do not require a biopsy of tissue): circulating tumor cell assays or cell-free circulating tumor DNA tests.[2] These methods provide a non-invasive alternative to repeat invasive biopsies to evaluate the mutations in cancer and plan individualized treatments. In addition, because cancer is a heterogeneous genetic disease, and excisional biopsies provide only a snapshot in time of some of the rapid, dynamic genetic changes occurring in tumors, liquid biopsies provide some advantages over tissue biopsy-based genomic testing.[3] In addition, excisional biopsies are invasive, can’t be used repeatedly, and are ineffective in understanding the dynamics of tumor progression and metastasis.[4][5] By detecting and quantifying genomic alterations in CTCs and cell-free DNA in blood, liquid biopsy can provide real-time information on the stage of tumor progression, treatment effectiveness, and cancer metastasis risk.[6] This technological development could make it possible to diagnose and manage cancer from repeated blood tests rather than from a traditional biopsy.[6][7][8][9]

Circulating tumor cell tests are under development by Epic Sciences.[10] The tests analyze circulating tumor cells (CTCs)[7][11] Analysis of individual CTCs demonstrated a high level of heterogeneity seen at the single cell level for both protein expression and protein localization and the CTCs reflected both the primary biopsy and the changes seen in the metastatic sites.

Analysis of cell-free circulating tumor DNA (cfDNA) has an advantage over circulating tumor cells assays in that there is approximately 100 times more cell-free DNA than there is DNA in circulating tumor cells.[2] These tests analyze fragments of tumor-cell DNA that are continuously shed by tumors into the bloodstream. Companies offering cfDNA next generation sequencing testing include Personal Genome Diagnostics and Guardant Health.[3] These tests are moving into widespread use when a tissue biopsy has insufficient material for DNA testing or when it is not safe to do an invasive biopsy procedure, according to a recent report of results on over 15,000 advanced cancer patients sequenced with the Guardant Health test.[12]

A 2014 study of the blood of 846 patients with 15 different types of cancer in 24 institutions was able to detect the presence of cancer DNA in the body. They found tumor DNA in the blood of more than 80 percent of patients with metastatic cancers and about 47 percent of those with localized tumors. The test does not indicate the tumor site(s) or other information about the tumor. The test did not produce false positives.[10]

Such tests may also be useful to assess whether malignant cells remain in patients whose tumors have been surgically removed. Up to 30 percent are expected to relapse because some tumor cells remain. Initial studies identified about half the patients who later relapsed, again without false positives.[10]

Another potential use is to track the specific DNA mutations driving a tumor. Many new cancer medications block specific molecular processes. Such tests could allow easier targeting of therapy to tumor.[10]

Precancerous conditions

For easily detected and accessed sites, any suspicious lesions may be assessed. Originally, this was skin or superficial masses. X-ray, then later CT, MRI, and ultrasound along with endoscopy extended the range.

Inflammatory conditions

A biopsy of the temporal arteries is often performed for suspected vasculitis. In inflammatory bowel disease (Crohn's disease and ulcerative colitis), frequent biopsies are taken to assess the activity of disease and to assess changes that precede malignancy.[13]

Biopsy specimens are often taken from part of a lesion when the cause of a disease is uncertain or its extent or exact character is in doubt. Vasculitis, for instance, is usually diagnosed on biopsy.

Biopsied sites

Location Description
Bone marrow Since blood cells are formed in the bone marrow, a bone marrow biopsy is employed in the diagnosis of abnormalities of blood cells when the diagnosis cannot be made from the peripheral blood alone. In malignancies of blood cells (leukemia and lymphoma) a bone marrow biopsy is used in staging the disease. The procedure involves taking a core of trabecular bone using a trephine, and then aspirating material.
Gastrointestinal tract Flexible endoscopy enables access to the upper and lower gastrointestinal tract, such that biopsy of the esophagus, stomach and duodenum via the mouth and the rectum, colon and terminal ileum are commonplace. A variety of biopsy instruments may be introduced through the endoscope and the visualized site biopsied. Until recently, the majority of the small intestine could not be visualized for biopsy. The double-balloon “push-pull” technique allows visualization and biopsy of the entire gastrointestinal tract.[15]

Needle core biopsies or aspirates of the pancreas may be made through the duodenum or stomach.[16]

Lung Biopsies of the lung can be performed in a variety of ways depending on the location.
Liver In hepatitis, most biopsies are not used for diagnosis, which can be made by other means. Rather, it is used to determine response to therapy which can be assessed by reduction of inflammation and progression of disease by the degree of fibrosis or, ultimately, cirrhosis.

In Wilson's disease, the biopsy is used to determine the quantitative copper level.

Prostate Forms of prostate biopsy include transrectal biopsy and transurethral biopsy
Nervous system Forms include brain biopsy, nerve biopsy, and meningeal biopsy
Urogenital system Forms include renal biopsy, endometrial biopsy and cervical conization
Other Other sites include breast biopsy, lymph node biopsy, muscle biopsy, and skin biopsy

Analysis of biopsied material

After the biopsy is performed, the sample of tissue that was removed from the patient is sent to the pathology laboratory. A pathologist who specializes in diagnosing diseases (such as cancer) by examining tissue under a microscope. When the laboratory (see Histology) receives the biopsy sample, the tissue is processed and an extremely thin slice of tissue is removed from the sample and attached to a glass slide. Any remaining tissue is saved for use in later studies, if required. The slide with the tissue attached is treated with dyes that stain the tissue, which allows the individual cells in the tissue to be seen more clearly. The slide is then given to the pathologist, who examines the tissue under a microscope, looking for any abnormal findings. The pathologist then prepares a report that lists any abnormal or important findings from the biopsy. This report is sent to the physician who originally performed the biopsy on the patient.


One of the earliest diagnostic biopsies was developed by the Arab physician Abulcasis (1013–1107). A needle was used to puncture a goiter, and the material was characterized.[17]


Biopsy is of Greek origin, coming from the words βίος bios, "life," and ὄψις opsis, "a sight."[18]

French dermatologist Ernest Besnier introduced the word biopsie to the medical community in 1879.[19]

See also


  1. Sausville, Edward A. and Longo, Dan L. "Principles of Cancer Treatment: Surgery, Chemotherapy, and Biologic Therapy", Harrison's Principles of Internal Medicine, 16th Ed. Kaspar, Dennis L. et al., eds. p.446 (2005).
  2. 1 2 Dawson SJ, Tsui DW, Murtaza M, Biggs H, Rueda OM, Chin SF, Dunning MJ, Gale D, Forshew T, Mahler-Araujo B, Rajan S, Humphray S, Becq J, Halsall, Wallis M, Bentley D, Caldas C, Rosenfeld N (2013). "Analysis of Circulating Tumor DNA to Monitor Metastatic Breast Cancer". The New England Journal of Medicine. 368 (13): 1199–1209. doi:10.1056/NEJMoa1213261. Retrieved October 7, 2016.
  3. 1 2 Oxnard GR, Paweletz CP, Sholl LM (October 7, 2016). "Genomic Analysis of Plasma Cell-Free DNA in Patients With Cancer". JAMA Oncolology. doi:10.1001/jamaoncol.2016.2835.
  4. Marrinucci D, Bethel K, Luttgen M, Bruce RH, Nieva J, Kuhn P (Sep 2009). "Circulating tumor cells from well-differentiated lung adenocarcinoma retain cytomorphologic features of primary tumor type". Archives of Pathology & Laboratory Medicine. 133 (9): 1468–71. doi:10.1043/1543-2165-133.9.1468 (inactive 2015-01-10). PMC 4422331Freely accessible. PMID 19722757.
  5. Lebofsky R, Decraene C, Bernard V, Kamal M, Blin A, Leroy Q, Rio Frio T, Pierron G, Callens C, Bieche I, Saliou A, Madic J, Rouleau E, Bidard FC, Lantz O, Stern MH, Le Tourneau C, Pierga JY (Apr 2015). "Circulating tumor DNA as a non-invasive substitute to metastasis biopsy for tumor genotyping and personalized medicine in a prospective trial across all tumor types". Molecular Oncology: 783–90. doi:10.1016/j.molonc.2014.12.003. Retrieved October 7, 2016.
  6. 1 2 Nieva JJ, Kuhn P (Aug 8, 2012). "Fluid biopsy for solid tumors: a patient's companion for lifelong characterization of their disease.". Future Oncology. 9 (8): 989–998. doi:10.2217/fon.12.91. PMC 3658625Freely accessible. PMID 22894671.
  7. 1 2 Nieva J, Wendel M, Luttgen MS, Marrinucci D, Bazhenova L, Kolatkar A, Santala R, Whittenberger B, Burke J, Torrey M, Bethel K, Kuhn P (Feb 2012). "High-definition imaging of circulating tumor cells and associated cellular events in non-small cell lung cancer patients: a longitudinal analysis". Physical Biology. 9 (1): 016004. Bibcode:2012PhBio...9a6004N. doi:10.1088/1478-3975/9/1/016004. PMC 3388002Freely accessible. PMID 22306961.
  8. Hekimian K, Meisezahl S, Trompelt K, Rabenstein C, Pachmann K (2012). "Epithelial Cell Dissemination and Readhesion: Analysis of Factors Contributing to Metastasis Formation in Breast Cancer". ISRN Oncology. 2012: 601810. doi:10.5402/2012/601810. PMC 3317055Freely accessible. PMID 22530147.
  9. Rolle A, Günzel R, Pachmann U, Willen B, Höffken K, Pachmann K (2005). "Increase in number of circulating disseminated epithelial cells after surgery for non-small cell lung cancer monitored by MAINTRAC(R) is a predictor for relapse: A preliminary report". World J Surg Oncol. 3 (1): 18. doi:10.1186/1477-7819-3-18. PMC 1087511Freely accessible. PMID 15801980.
  10. 1 2 3 4 Regalado, Antonio (August 11, 2014). "Spotting Cancer in a Vial of Blood". MIT Technology Review. Retrieved 2016-04-23.
  11. Crowley E, Di Nicolantonio F, Loupakis F, Bardelli A (Aug 2013). "Liquid biopsy: monitoring cancer-genetics in the blood". Nature Reviews Clinical Oncology. 10 (8): 472–484. doi:10.1038/nrclinonc.2013.110. PMID 23836314.
  12. "Tracking Tumor Resistance: The Early Promise of "Liquid" Cancer Tests" (PDF). Journal of the National Cancer Institute. 108 (9). Sep 2016. doi:10.1093/jnci/djw220. Retrieved October 7, 2016.
  13. Friedman, S. and Blumberg, R.S. "Inflammatory Bowel Disease", Harrison's Principles of Internal Medicine, 16th Ed. Kaspar, Dennis L. et al., eds. pp.1176-1789, 2005.
  14. Mens health - Testicular Biopsy
  15. Saibeni S, Rondonotti E, Iozzelli A, Spina L, Tontini GE, Cavallaro F, Ciscato C, de Franchis R, Sardanelli F, Vecchi M (2007). "Imaging of the small bowel in Crohn's disease: a review of old and new techniques". World J. Gastroenterol. 13 (24): 3279–87. PMC 4172707Freely accessible. PMID 17659666.
  16. Iglesias-Garcia J, Dominguez-Munoz E, Lozano-Leon A, Abdulkader I, Larino-Noia J, Antunez J, Forteza J (2007). "Impact of endoscopic ultrasound-guided fine needle biopsy for diagnosis of pancreatic masses". World J. Gastroenterol. 13 (2): 289–93. PMC 4065960Freely accessible. PMID 17226911.
  17. Anderson JB, Webb AJ (1987). "Fine-needle aspiration biopsy and the diagnosis of thyroid cancer". The British journal of surgery. 74 (4): 292–296. doi:10.1002/bjs.1800740422. PMID 3580805.
  18. "biopsy". Online Etymology Dictionary.
  19. Zerbino DD (1994). "Biopsy: Its history, current and future outlook". Likars'ka sprava / Ministerstvo okhorony zdorov'ia Ukrainy (3–4): 1–9. PMID 7975522.

External links

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