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From: Ed Uthman <[email protected]>
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Subject: Biopsy Report Guide (monthly posting, 38K, v. 1.2)
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Summary: Explanation of the pathologist's report on biopsies,
aimed at the educated layperson.
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Version: 1.2
Last-modified: November 12, 1997
Archive-name: pathology/biopsy-report-guide
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Maintainer: Ed Uthman <[email protected]>

             The Biopsy Report: A Patient's Guide

              Ed Uthman, MD ([email protected])
            Diplomate, American Board of Pathology

INTRODUCTION

Many medical conditions, including all cases of cancer, must be
diagnosed by removing a sample of tissue from the patient and
sending it to a pathologist for examination. This procedure is
called a biopsy, a Greek-derived word that may be loosely translated
as "view of the living." Any organ in the body can be biopsied using
a variety of techniques, some of which require major surgery (e.g.,
staging splenectomy for Hodgkin's disease), while others do not even
require local anesthesia (e.g., fine needle aspiration biopsy of
thyroid, breast, lung, liver, etc). After the biopsy specimen is
obtained by the doctor, it is sent for examination to another
doctor, the anatomical pathologist, who prepares a written report
with information designed to help the primary doctor manage the
patient's condition properly.

The pathologist is a physician specializing in rendering medical
diagnoses by examination of tissues and fluids removed from the
body. To be a pathologist, a medical graduate (M.D. or D.O.)
undertakes a five-year residency training program, after which he or
she is eligible to take the examination given by the American Board
of Pathology. On successful completion of this exam, the pathologist
is "Board-certified." Almost all American pathologists practicing in
JCAHO-accredited hospitals and in reputable commercial labs are
either Board-certified or Board-eligible (a term that designates
those who have recently completed residency but have not yet passed
the exam). There is no qualitative difference between
M.D.-pathologists and D.O.- pathologists, as both study in the same
residency programs and take the same Board examinations.

TYPES OF BIOPSIES

   1. Excisional biopsy. A whole organ or a whole lump is
      removed (excised). These are less common now, since the
      development of fine needle aspiration (see below). Some types
      of tumors (such as lymphoma, a cancer of the lymphocyte blood
      cells) have to be examined whole to allow an accurate
      diagnosis, so enlarged lymph nodes are good candidates for
      excisional biopsies. Some surgeons prefer excisional biopsies
      of most breast lumps to ensure the greatest diagnostic
      accuracy. Some organs, such as the spleen, are dangerous to
      cut into without removing the whole organ, so excisional
      biopsies are preferred for these.

      A special type of excisional biopsy of the breast is the
      needle localization biopsy, also called the "wire-guided
      biopsy." This is used when the patient presents with an
      abnormal mammogram, but no lump can be felt in the breast.
      Since the surgeon cannot feel anything, it is necessary for
      the radiologist, who can see the abnormality on the x-ray, to
      provide some sort of guide. While the patient is positioned
      in the mammography machine, the radiologist (a physician who
      specializes in diagnostic imaging) uses the mammogram and a
      special grid to insert a needle directly into the abnormal
      area. When a follow-up mammogram determines the needle is in
      the right place, a wire with a barb on the end is inserted
      through the hollow needle into the abnormal area. The needle
      is withdrawn from around the wire, leaving the wire fixed in
      place (because of the barb, it cannot fall out). The surgeon
      then cuts into the breast and follows the wire to the area in
      question, removes this area, and sends it to the pathologist.
      The pathologist then determines if the appropriate tissue has
      been removed and advises the surgeon appropriately. In some
      cases, it is necessary to x-ray the actual biopsy specimen to
      determine if the suspicious area has been removed.

   2. Incisional biopsy. Only a portion of the lump is removed
      surgically. This type of biopsy is most commonly used for
      tumors of the soft tissues (muscle, fat, connective tissue)
      to distinguish benign conditions from malignant soft tissue
      tumors, called sarcomas.

   3. Endoscopic biopsy.This is probably the most commonly
      performed type of biopsy. It is done through a fiberoptic
      endoscope the doctor inserts into the gastrointestinal tract
      (alimentary tract endoscopy), urinary bladder (cystoscopy),
      abdominal cavity (laparoscopy), joint cavity (arthroscopy),
      mid-portion of the chest (mediastinoscopy), or trachea and
      bronchial system (laryngoscopy and bronchoscopy), either
      through a natural body orifice or a small surgical incision.
      The endoscopist can directly visualize an abnormal area on
      the lining of the organ in question and pinch off tiny bits
      of tissue with forceps attached to a long cable that runs
      inside the endoscope.

   4. Colposcopic biopsy.This is a gynecologic procedure that
      typically is used to evaluate a patient who has had an
      abnormal Pap smear. The colposcope is actually a close-
      focusing telescope that allows the physician to see in detail
      abnormal areas on the cervix of the uterus, so that a good
      representation of the abnormal area can be removed and sent
      to the pathologist.

   5. Fine needle aspiration (FNA) biopsy.This is an
      extremely simple technique that has been used in Sweden for
      decades but has only been developed widely in the US over the
      last ten years. A needle no wider than that typically used to
      give routine injections (22 to 25 gauge) is inserted into a
      lump (tumor), and a few tens to thousands of cells are drawn
      up (aspirated) into a syringe. These are smeared on a slide,
      stained, and examined under a microscope by the pathologist.
      A diagnosis can often be rendered in a few minutes. Tumors of
      deep, hard-to-get-to structures (pancreas, lung, and liver,
      for instance) are especially good candidates for FNA, as the
      only other way to sample them is with major surgery. Such FNA
      procedures are typically done by a radiologist under guidance
      by ultrasound or computed tomography (CT scan) and require no
      anesthesia, not even local anesthesia. Thyroid lumps are also
      excellent candidates for FNA.

      Because of recent interest in cost containment, FNA is now
      widely applied in diagnosing breast lumps. While the
      technique is excellent in experienced hands, false negatives
      and false positives do occur. A false negative causes delay
      in diagnosis of breast cancer allowing the tumor to grow and
      spread, and a false positive is likely to result in an
      unnecessary mastectomy. I would therefore offer the following
      recommendations to any patient who has been encouraged to
      have a breast FNA:

             Studies have clearly shown that the diagnostic accuracy
             of breast FNA is optimal when the same person who
             interprets the smears also performs the biopsy itself.
             Accordingly, I recommend that patients have the actual
             procedure performed by a pathologist who does a good
             number of these cases as a part of his or her practice.

             FNAs that are positive for cancer should be confirmed
             by frozen section at the time of surgery, before the
             mastectomy is performed.

             An FNA that shows no cancer cells is no assurance that
             the patient does not have cancer. A negative FNA means
             that either 1) the patient does not have cancer, or 2)
             the patient does have cancer, but the needle missed the
             diagnostic cells.

   6. Stereotactic needle biopsy. This relatively new technique
      for evaluating breast lesions attempts to combine the
      advantages of FNA (no scar, no anesthesia, inexpensive),
      excisional biopsy (acquisition of solid pieces of tissue
      rather than smears) and needle localization (precise guidance
      by x-ray or ultrasound imaging). The patient lies on her
      abdomen, so that the breast hangs down into a space that can
      be x-rayed by a computerized imaging device. The computer
      displays the mammographic image on a screen. The radiologist
      identifies the abnormality and marks it electronically on the
      screen. The computer then positions a movable arm directly
      over the abnormal area. A biopsy device is attached to the
      arm, and the spring-loaded gun quickly inserts a hollow
      biopsy needle into the breast. The needle is removed, and the
      tissue it contains is sent to the pathologist for diagnosis.

      The downside of stereotactic needle biopsy is that, because
      only a tiny amount of tissue is removed, a negative result is
      no guarantee the patient does not have cancer. Another
      problem is that occasionally the biopsy will remove the
      portions of the lesion that were responsible for its being
      identified as abnormal in the first place. This leaves the
      surgeon with no "signpost" to follow in trying to remove by
      lumpectomy a cancer that was diagnosed by stereotactic needle
      biopsy.

   7. Punch biopsy. This technique is typically used by
      dermatologists to sample skin rashes and small masses. After
      a local anesthetic is injected, a biopsy punch, which is
      basically a small (3 or 4 mm in diameter) version of a cookie
      cutter, is used to cut out a cylindrical piece of skin. The
      hole is typically closed with a suture and heals with minimal
      scarring.

   8. Bone marrow biopsy. In cases of abnormal blood counts,
      such as unexplained anemia, high white cell count, and low
      platelet count, it is necessary to examine the cells of the
      bone marrow. In adults, the sample is usually taken from the
      pelvic bone, typically from the posterior superior iliac
      spine. This is the prominence of bone on either side of the
      pelvis underlying the "bikini dimples" on the lower
      back/upper buttocks. Hematologists do bone marrow biopsies
      all the time, but most internists and pathologists and many
      family practitioners are also trained to perform this
      procedure.

      With the patient lying on his/her stomach, the skin over the
      biopsy site is deadened with a local anesthetic. The needle
      is then inserted deeper to deaden the surface membrane
      covering the bone (the periosteum). A larger rigid needle
      with a very sharp point is then introduced into the marrow
      space. A syringe is attached to the needle and suction is
      applied. The marrow cells are then drawn into the syringe.
      This suction step is occasionally uncomfortable, since it is
      impossible to deaden the inside of the bone. The contents of
      the syringe, which to the naked eye looks like blood with
      tiny chunks of fat floating around in it, is dropped onto a
      glass slide and smeared out. After staining, the cells are
      visible to the examining pathologist or hematologist.

      This part of procedure, the aspiration, is usually followed
      by the core biopsy, in which a slightly larger needle is used
      to extract core of bone. The calcium is removed from the bone
      to make it soft, the tissue is processed (see "Specimen
      Processing," below) and tissue sections are made. Even though
      the core biopsy procedure involves a bigger needle, it is
      usually less painful than the aspiration.

SPECIMEN PROCESSING

After the specimen is removed from the patient, it is processed in
one or both of two major ways:

   1. Histologic sections. This involves preparation of stained,
      thin (less than 5 micrometers, or 0.005 millimeters) slices
      mounted on a glass slide, under a very thin pane of glass
      called a coverslip. There are two major techniques for
      preparation of histologic sections:

             a. Permanent sections. This technique gives the
             best quality of specimen for examination, at the
             expense of time. The fresh specimen is immersed in a
             fluid called a fixative for several hours (the
             necessary time dependent on the size of the specimen).
             The fixative, typically formalin (a 10% solution of
             formaldehyde gas in buffered water), causes the
             proteins in the cells to denature and become hard and
             "fixed." Adequate fixation is probably the most
             important technical aspect of biopsy processing.

             The fixed specimen is then placed in a machine that
             automatically goes through an elaborate overnight cycle
             that removes all the water from the specimen and
             replaces it with paraffin wax. The next morning, a
             technical professional, called a histologic technician,
             or "histotech," removes the paraffin-impregnated
             specimen and "embeds" it in a larger bloc of molten
             paraffin. This is allowed to solidify by chilling and
             is set in a cutting machine, called a microtome. The
             histotech uses the microtome to cut thin sections of
             the paraffin block containing the biopsy specimen.
             These delicate sections are floated out on a water bath
             and picked up on a glass slide.

             The the paraffin is dissolved from the tissue on the
             slide. With a series of solvents, water is restored to
             the sections, and they are stained in a mixture of
             dyes. The most common dyes used are hematoxylin, a
             natural product of the heartwood of the logwood tree,
             Haematoxylon campechianum, which is native to Central
             America, and eosin, an artifcial aniline dye. The stain
             combination, casually referred to by pathologists as "H
             and E" yields pink, orange, and blue sections that make
             it easier for us to distinguish different parts of
             cells. Typically, the nucleus of cells stains dark
             blue, while the cytoplasm stains pink or orange.

             b. Frozen sections. This technique allows one to
             examine histologic sections within a few minutes of
             removing the specimen from the patient, but the price
             paid is that the quality of the sections is not nearly
             as good as those of the permanent section. Still, a
             skilled pathologist and a knowledgeable surgeon can
             work together to use the frozen section's rapid
             availability to the patient's great benefit.

   2. Smears. The specimen is a liquid, or small solid chunks
      suspended in liquid. This material is smeared on a microscope
      slide and is either allowed to dry in air or is "fixed" by
      spraying or immersion in a liquid. The fixed smears are then
      stained, coverslipped, and examined under the microscope.

Like the frozen section, smear preparations can be examined within a
few minutes of the time the biopsy was obtained. This is especially
useful in FNA procedures (see above), in which a radiologist is
using ultrasound or CT scan to find the area to be biopsied. He or
she can make one "pass" with the needle and immediately give the
specimen to the pathologist, who can within a few minutes determine
if a diagnostic specimen was obtained. The procedure can be
terminated at that point, sparing the patient the discomfort and
inconvenience of repeated sticks.

PATHOLOGIC EXAMINATION

A. THE GROSS DESCRIPTION

The pathologist begins the examination of the specimen by dictating
a description of the specimen as it looks to the naked eye. This is
the "gross exam" or the "gross." Some pathologists may refer to the
gross exam as the "macroscopic." Most biopsies are small,
nondescript bits of tissue, so the gross description is brief and
serves mostly as a way to code which biopsy came from what area and
to use for troubleshooting if there is a question of specimen
mislabeling. A typical gross description of an endoscopic colon
biopsy follows:

      "Polyp of sigmoid colon." An ovoid, smooth- surfaced,
      firm, pale tan nodule, measuring 0.6 x 0.4 x 0.3 cm.
      Cassette 'A', all, bisected.

In the above example, the first item (in quotes) is an exact
recitation of how the specimen was labeled by the doctor who took
the biopsy. After that is a textual description of what the specimen
looked like, followed by measurements indicating its size. The
"Cassette 'A', all, bisected" phrase indicates that the specimen was
cut in half ("bisected"), submitted for tissue processing in its
entirety ("all") in a small container (cassette) labeled "A," which
will eventually be placed in the tissue processor.

Larger organs removed as biopsies have correspondingly longer and
more detailed gross descriptions. The following is the gross
description of a spleen removed to assess whether Hodgkin's disease
(a cancer of lymph tissues) has spread into it:

      "Spleen". An entire spleen, weighing 127 grams, and
      measuring 13.0 x 4.1 x 9.2 cm. The external surface is
      smooth, leathery, homogeneous, and dark purplish-brown.
      There are no defects in the capsule. The blood vessels
      of the hilum of the spleen are patent, with no thrombi
      or other abnormalities. The hilar soft tissues contain
      a single, ovoid, 1.2-cm lymph node with a dark grey cut
      surface and no focal lesions

      On section of the spleen at 2 to 3 mm intervals, there
      are three well-defined pale-grey nodules on the cut
      surface, ranging from 0.5 to 1.1 cm in greatest
      dimension. The remainder of the cut surface is
      homogeneous, dark purple, and firm.

      Summary of cassettes: 1, hilar blood vessels; 2, hilar
      lymph node, entirely submitted; 3 - 6 spleen nodules,
      entirely submitted; 7 - 8, spleen, away from nodules.

In the spleen described above, the pathologist found a few lumps
(nodules), representing the most important data in this gross
examination. These possibly represent the tumors of Hodgkin's
disease, subject to confirmation by the microscopic examination.
Much of the remainder of the verbage relates to "pertinent
negatives," or things that were routinely looked for but not found,
such as a rupture of the spleen capsule (suggesting an
intraoperative accident), blood clots ("thrombi") in the vessels
supplying the spleen, and evidence of an infection (in which case
the cut surface of the spleen would be soft instead of firm). In
addition, a lymph node was serendipitously found adherent to the
spleen, and this was briefly described as having a normal
appearance.

The last paragraph of the gross description gives the identifying
"codes" of the slices of the specimen submitted for microscopic
examination in cassettes. The microscope slides prepared from the
processed samples will be labeled with the same numbers as the
cassettes, and the pathologist doing the microscopic examination
can, by referring to the typed gross description, know from what
part of the specimen the tissue on the slide came.

B. THE MICROSCOPIC EXAMINATION

The microscopic description, or the "micro" is a narrative
description of the findings gained from examination of the glass
slides under the microscope. The micro is considered somewhat
"optional" in a written report. In such a case, the diagnosis (see
below) is considered to speak for itself. Here is a the microscopic
description on the report of the colon biopsy given above:

      Specimen A: The sections show a polypoid structure
      consisting of a central fibrovascular core, surrounded
      by a mantle of mucosa showing an adenomatous
      architecture with a predominantly tubular pattern. The
      tubules are lined by tall columnar epithelium showing
      nuclear pseudostratification, hyperchromasia, increased
      mitotic activity, and loss of cytoplasmic mucin. There
      in no evidence of stromal invasion.

It can be readily seen that the language of microscopy is much more
arcane than that used for gross descriptions. It is way beyond the
scope of this monograph to cover the nuances of descriptive
microscopic pathology. In general, microscopic descriptions are
communications between pathologists for referral and quality
assurances purposes.

C. THE DIAGNOSIS

This is analogous to the "bottom line" of a financial report. The
purpose of the gross examination, the processing of the tissue, and
the microscopic examination is to build a logical argument toward a
terse assessment of what significance the biopsy has in regard to
the patient's health. Here is the diagnosis for the colon biopsy,
above:

      Colon, sigmoid, endoscopic biopsy: tubular adenoma
      (adenomatous polyp)

This format is widely used, but variations occur. The first term is
the organ or tissue involved ("colon"). The second term ("sigmoid")
specifies the site in the colon from which the biopsy was obtained.
The next term ("endoscopic biopsy") denotes the type of surgical
procedure used in obtaining the biopsy. Then follows the diagnosis
proper, in this case "tubular adenoma," a common benign tumor of the
large intestine and rectum, which increases the risk for developing
colorectal cancer in the future. In this particular case, an older
synonym for tubular adenoma, "adenomatous polyp," follows in
parentheses.

GLOSSARY OF IMPORTANT DIAGNOSTIC TERMS

Finally, it may be useful to present a brief glossary of important
terms used in pathologic diagnoses. Terms in the definition that are
in ALL CAPS have their own entry.

ABSCESS

      A closed pocket containing pus. Some abscesses are easily
      diagnosed clinically, as they are painful and may "point out"
      such that pus becomes visible, but deep and chronic abscesses
      may just look like a TUMOR clinically and require biopsy to
      distinguish them from neoplasm.

ATYPICAL

      The simple, straightforward definition would be "unusual,"
      but "atypical" means much more than that. In a diagnosis, the
      use of the term atypical is a vague warning to the physician
      that the pathologist is worried about something, but not
      worried enough to say that the patient has cancer. For
      instance, lymphomas (cancers of the lymph nodes) are
      notoriously difficult to diagnose. Some lymph node biopsies
      are very disturbing but do not quite fulfil the criteria for
      cancer. Such a case may be diagnosed as "atypical lymphoid
      HYPERPLASIA." Other important atypical hyperplasias are those
      of the breast (atypical ductal hyperplasia and atypical
      lobular hyperplasia) and the lining of the uterus (atypical
      endometrial hyperplasia). Both of these conditions are
      thought to be precursor warning signs that the patient is at
      high risk of developing cancer of the respective organ
      (breast and uterus).

CARCINOMA

      A malignant NEOPLASM whose cells appear to be derived from
      EPITHELIUM. This word can be used by itself or as a suffix.
      Cancers composed of columnar epithelial cells are often
      called adenocarcinomas. Those of squamous cells are called
      squamous cell carcinomas. The type of cancer typically
      recapitulates the type of epithelium that normally lines the
      affected organ. For instance, almost all cancers of the colon
      are adenocarcinomas, and columnar epithelium is the normal
      lining of the colon. There are exceptions, however.

DYSPLASIA

      An ATYPICAL proliferation of cells. This may be loosely
      thought of as an intermediate category between HYPERPLASIA
      and NEOPLASIA. It finds its best use as a term to describe
      the phenomenon in which EPITHELIUM proliferates and develops
      the microscopic appearance of neoplastic tissue, but
      otherwise tends to "behave itself" and continues to line body
      surfaces without actually invading them, as a true malignant
      neoplasm would do. It may be convenient (but not totally
      accurate) to consider dysplasia as a "pre-cancer" or an
      incipient cancer. Probably the most commonly occurring type
      of dysplasia is that of the cervix of the uterus, where a
      progression from dysplasia to neoplasia can be clearly
      demonstrated. Other dysplasias, such as those of the breast
      and prostate, are more difficult to clearly relate to
      neoplasia at this time.

EPITHELIUM

      A specialized type of tissue that normally lines the surfaces
      and cavities of the body. There are three main types: 1)
      columnar epithelium, which lines the stomach, intestines,
      trachea and bronchi, salivary and other glands, pancreas,
      gallbladder, nasal cavity and sinuses, uterus (including
      inner cervix), Fallopian tubes, kidneys, testes, vasa
      deferentia, and other ductal structures, 2) stratified
      squamous epithelium, which lines the skin, oral cavity,
      throat, esophagus, anus, outer urethra, vagina, and outer
      cervix, and 3) transitional epithelium (urothelium), which
      lines the urine-collecting part of the kidneys, the ureters,
      bladder, and inside part of the urethra.

GRANULOMA

      A special type of INFLAMMATION characterized by accumulations
      of macrophages, some of which coalesce into "giant cells."
      Granulomatous inflammation is especially characteristic of
      tuberculosis, some deep fungal infections (like
      histoplasmosis and coccidioidomycosis), sarcoidosis (a
      disease of unknown cause), and reaction to foreign bodies.

HYPERPLASIA

      A proliferation of cells which is not NEOPLASTIC. In some
      cases, this may be a result of the body's normal reaction to
      an imbalance or other stimulus, while in other cases the
      physiologic cause of the proliferation is not apparent. An
      example of the former process is the enlargement of lymph
      nodes in the neck as a result of reaction to a bacterial
      throat infection. The lymphocytes which make up the node
      divide and proliferate, taking up more volume in the node and
      causing it to expand. An example of hyperplasia in which the
      stimulus is not known is benign prostatic hyperplasia (BPH),
      in which the prostate gland enlarges in older men for no
      known reason. While hyperplasias do not invade other organs
      or METASTASIZE to other parts of the body, they can still
      cause problems because of their local physical expansion. For
      instance, in BPH, the enlarged prostate pinches off the
      urethra and interferes with the flow of urine. If untreated,
      permanent kidney damage can result.

INFLAMMATION

      A reaction, usually mediated by the immune system, to noxious
      stimuli, manifested clinically by swelling, pain, tenderness,
      redness, heat, and/or loss of function of the affected part.
      To a pathologist, however, inflammation means the
      infiltration of certain immune system cells into the tissue
      or organ being examined. These inflammatory cells include 1)
      neutrophils, which are the white blood cells that make up pus
      and are seen in acute or early inflammations, 2) lymphocytes,
      which are typically seen in more chronic or longstanding
      inflammations, and 3) macrophages (histiocytes), which are
      also seen in chronic inflammation. Some types of inflammation
      are readily diagnosable by the primary care physician, such
      as an infected skin wound that is tender, hot, and draining
      pus. Other types of inflammation are not so readily apparent
      clinically and require biopsy to distinguish them from
      neoplasms. The suffix "-itis" is appended to a root word to
      indicate "inflammation of _____." For example, cervicitis,
      pharyngitis, gastritis, and thyroiditis are inflammations of
      the cervix, pharynx (throat), stomach, and thyroid gland,
      respectively.

LESION

      This is a vague term meaning "the thing that is wrong with
      the patient." A lesion may be a TUMOR, an area of
      INFLAMMATION, or an invisible biochemical abnormality (like
      the abnormality of the sensitivity of the body's cells to
      insulin in adult-onset diabetes).

METAPLASIA

      The phenomenon by which one type of tissue is replaced by
      another type. This often results from chronic irritation of
      an EPITHELIAL lining. A good example is the cervix, in which
      chronic irritation and INFLAMMATION causes the relatively
      delicate normal columnar epithelium to be replaced by tougher
      squamous epithelium (similar to that which normally lines the
      vagina, which is naturally "built tougher" for obvious
      reasons). This phenomenon is called "squamous metaplasia." In
      it's pure state, metaplasia is not harmful, but some
      metaplasias are markers for increased risk of more serious
      diseases. For instance, a type of intestinal metaplasia of
      the stomach (in which columnar epithelium of the intestinal
      type replaces that of the gastric type) is considered a risk
      factor for the subsequent development of cancer of the
      stomach.

METASTATIC

      Of or pertaining to METASTASIS, or the process by which
      malignant NEOPLASMS can shed individual cells, which can
      travel through the lymph vessels or blood vessels, lodge in
      some distant organ, and grow into tumors in their own right.
      There are two major routes of metastasis, 1) hematogenous, in
      which the cells travel through the blood vessels, and 2)
      lymphogenous, in which the lymphatic vessels conduct the
      cancer cells. In the case of lymphogenous metastasis, the
      metastatic tumors can grow from cancers cells entrapped in
      the lymph nodes that collect the lymph draining from the
      organ where the original cancer has developed, causing the
      nodes to enlarge. In the case of breast cancer, the axillary
      (underarm) nodes are the first to become involved. In the
      case of cancer of the larynx (voice box), the nodes on either
      side of the neck (cervical nodes) are first. Hematogenous
      metastases tend to deposit in the lungs, liver, and brain.
      Many cancers metastasize both lymphogenously and
      hematogenously. Most cancer operations attempt to remove not
      only the cancerous organ, but also the lymph nodes that drain
      that organ. Some types of cancer, especially the most common
      ones (lung, breast, colon, and prostate cancers) tend to
      metastasize to lymph nodes first. Pathologic examination of
      these nodes is important in "staging" the cancer, which gives
      the patient and the doctor some idea as to the odds of curing
      the cancer and how to best treat it. A typical diagnosis of a
      specimen of a "radical" removal of a cancer may read like,

             Breast, left, mastectomy: infiltrating ductal
             cancinoma; three of fifteen axillary nodes
             contain metastatic carcinoma.

NECROSIS

      Death of tissue. Necrosis may be seen in inflammatory
      conditions, as well as in NEOPLASMS.

NEOPLASM, or NEOPLASIA

      A "new growth" of the body's own cells, a proliferation of
      cells no longer under normal physiologic control. These may
      be "benign" or "malignant." Benign neoplasms are typically
      tumors (lumps or masses) that, if removed, never bother the
      patient again. Even if they are not removed, they are not
      capable of destroying adjacent organs or "seeding" out to
      other parts of the body. Malignant neoplasms, or "cancers,"
      are those whose natural history (i.e., behavior if untreated)
      is to cause the death of the patient. Malignancy is expressed
      by 1) local invasion, in which the neoplasm extends into
      vital organs and interferes with their function, 2)
      METASTASIS, in which cells from the tumor seed out to other
      parts of the body and then grow into tumors themselves,
      and/or 3) paraneoplastic syndromes, in which the neoplasm
      secretes metabolic poisons or inappropriately large amounts
      of hormones that cause problems with functions of various
      body systems.

-OMA

      This suffix means "tumor" or "lump." It typically, but not
      invariably, refers to a NEOPLASM ("GRANULOMA" is an
      exception). In referring to neoplasms, benign ones are
      typically referred to by a word, the prefix of which refers
      to the organ or tissue of origin, followed by the suffix
      "-oma." For example, leiomyoma, osteoma, chondroma, adenoma,
      and hemangioma, refer to benign neoplasms of smooth muscle,
      bone, cartilage, glandular tissue, and blood vessel tissue,
      respectively. The analogous terms for malignant versions of
      these neoplasms are, leiomyoSARCOMA, osteosarcoma,
      chondrosarcoma, adenoCARCINOMA, and angiosarcoma.There are
      exceptions to these vocabulary rules. For instance, hepatomas
      and melanomas are all malignant. Other tumors, such as those
      of the adrenal glands, cannot be classified into benign or
      malignant categories based on pathologic appearance. Only
      their behavior in time shows their true colors. An example is
      pheochromocytoma (a tumor of the adrenal medulla), ten per
      cent of which are malignant, but we don't know just by
      looking at the tumor if a given case will fall into that ten
      per cent.

POLYP

      A structure consisting of a rounded head attached to a
      surface by a stalk (also called a "pedicle" or "peduncle"). A
      mushroom growing from the soil is an excellent example of
      what a polyp looks like. Polyps my be HYPERPLASTIC,
      METAPLASTIC, NEOPLASTIC, INFLAMMATORY, or none of the above.
      The typical polyps removed from the colon of adults during
      colonoscopy are benign neoplasms called tubular adenomas or
      adenomatous polyps. The typical nasal polyps that develop in
      people with allergies are inflammatory. The common benign
      polyps removed from the cervix are of uncertain origin.

SARCOMA

      A malignant NEOPLASM whose cells appear to be derived from
      those other than EPITHELIUM. The connective tissues of the
      body (fibrous tissue, muscle, bone, cartilage, fat, and
      lining of joints) tend to give rise to sarcomas. In adults,
      CARCINOMAS are much more common than sarcomas. This makes
      sense, because as we age, our body linings are assaulted by
      one noxious substance after the other. So it is no surprise
      that those epithelial cells on the forefront of our battle
      with the environment are the first to lose control of their
      growth and development. In children, sarcomas make up a
      greater proportion of cancers. While the connective tissues
      of adults are rather stable and protected from environmental
      assault, those of children are still growing and developing,
      the cells dividing, raising the likelihood that something
      will go haywire and cause a cell to lose control over its
      growth.

SUPPURATION, SUPPURATIVE INFLAMMATION

      A type of acute INFLAMMATION characterized by infiltration of
      neutrophils at the microscopic level and formation of pus at
      the gross level. ABSCESS is special type of suppurative
      inflammation.

TUMOR

      A mass or lump that can be felt with the hand or seen with
      the naked eye. This may be a NEOPLASM, HYPERPLASIA,
      distention, swelling, or anything that causes a local
      increase in volume. The thing to remember is that not all
      tumors are cancers, and not all cancers are tumors.

Note: Please send all constructive comments regarding this FAQ to Ed
Uthman, MD ([email protected]).

This article is provided as is without any express or implied
warranties. While every effort has been taken to ensure the accuracy
of the information, the author assumes no responsibility for errors
or omissions, or for damages resulting from use of the information
herein.

Copyright (c) 1994-96, Edward O. Uthman. This material may be
reformatted and/or freely distributed via online services or other
media, as long as it is not substantively altered. Authors,
educators, and others are welcome to use any ideas presented herein,
but I would ask for acknowledgment in any published work derived
therefrom.

version 1.2U, 11/12/97