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Institut für Pathologie - Klinikum Fürth  

6th edition 2002 UICC (01.01.2003)

(Aids & Proposals)


CONTENT

1. The TNM Formula

2. Number of Lymph Nodes for pN Classification

3. Lymph Node Preparation






THE TNM FORMULA


y r c p Tis,1-4 (m)(4) X; N0-3(mi)(sn)(i)(mol)(3/17)X; M0-1(mi)(i)(mol)X; V0-2; L0-1; G1-4; R0-2

Assessement of TNM categories may be performed by conventional or sophisticated methods
which should be mentioned because of different prognostic significance.



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yrcp
  • y Classification during or after multimodality therapy
  • r Classification for recurrent tumor
  • c Pretreatment clinical classification
  • p Classification by the pathologist
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T

Extent of Primary Tumor
  • is = in situ carcinoma
  • 1-4= extent only of the invasive component with invasion of a named anatomical structure and/or measured in metric units
  • (m) and/or (4)= multiple primary tumors and/or the number of different primary tumors.
    (In the liver and thyroid gland the multiplicity is considered in the pT1-4 categories!)
  • X= extent of primary tumor cannot be assessed
Further explanations: pT assessement should be able to evaluate the highest pT
(if there is any doubt the lower pT should be chosen); tumor on lymphatic vessels should not be
considered as local spread (except kidney and liver); direct infiltration in an adjacent organ is
the highest pT category and no metastasis
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N

Regional Lymph Node Metastasis
  • 0= no regional lymph node metastasis (minimal number of nodes for pN0 see table)
  • 1-3=presence of lymph node metastasis with description of number, localization, size, and perinodal invasion
  • mi= only micrometastasis present (2 mmor less)
  • sn= sentinel lymph node = first lymph node that takes up lymph from primary tumor.
    - x(sn) sentinel LN cannot be assessed.
    - 0 = no LN metastasis
    - 1 = LN metastasis
  • i, mol= isolated tumor cells. ( ITC ) = tumor cells < 2 mm found by specific histochemical methods.
    - N0= no metastasis, no examination for proof of ITC
    - N0(i-)= no metastasis, no morphological proof of ITC
    - N0(i+)= no metastasis, morphological proof of ITC
    - N0(mol-)= no metastasis, no not-morphological proof of ITC
    - N0(mol+)= no metastasis, not-morphological proof of ITC
  • (3/17)= number of lymph nodes involved/number of lymph nodes examined (optional)
  • X= presence or absence of lymph node metastases cannot be assessed
Further explanations: pN assessment should be able to exclude pN0; (s Table)
per definitionem: direct infiltration of a lymph node or a tumor nodule > 3 mm formed or contoured like a lymph node ( whithout lymphatic tissue) in a tumor draining region are classified as lymph node metastases

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M

Distant Metastasis
  • 0= no distant metastasis
  • 1= distant metastasis present
  • (mi)= microscopical metastasis; 2 mm or less
  • i, mol= isolated tumor cells. ( ITC ) = tumor cells < 2 mm found by specific histochemical methods.
    - M0= no metastasis, no examination for proof of ITC
    - M0(i-)= no metastasis, no morphological proof of ITC
    - M0(i+)= no metastasis, morphological proof of ITC
    - M0(mol-)= no metastasis, no not-morphological proof of ITC
    - M0(mol+)= no metastasis, not-morphological proof of ITC
  • X= distant metastases cannot be assessed
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V

Venous Invasion
  • 0= no venous invasion
  • 1= microscopic venous invasion present
  • 2=macroscopic venous invasion
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L

Lymph vessel invasion
  • 0=no lymph vessel invasion
  • 1= lymph vessel invasion present. Consider only proven lymphatic vessels lined with endothelium
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G

Grade of Malignancy (not applicable for: carcinoma of the thyroid gland,
pleural mesothelioma, malignant melanoma of the skin and eyelid,
retinoblastoma, malignant testicular tumors, Wilms tumor, neuroblastoma)

Histological grade of malignancy according to WHO:

  • 1= well differentiated
  • 2= moderately differentiated
  • 3= poorly differentiated
  • 4= undifferentiated (small cell carcinoma of any site,
    undifferentiated carcinoma where provided, large cell carcinoma of the lung,
    Ewing sarcoma, rhabdomyosarcoma of soft tissue)
G 1-2 can be summarized as low grade and G 3-4 as high grade. Same prognostic significance.
- bone/sarcoma of soft tissue: highgrade/lowgrade.
- special grades for liver, breast and corpus uteri.

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R

Residual Tumor Classification
  • 0 = no residual tumor
  • 1 = residual tumor demonstrated microscopically (also positive cytology on lavage before the beginning of the surgical procedure on the tumor)
  • 2 = macroscopic residual tumor (local or distant! e.g. non resectable liver metatasis of a locally completely
    resectable primary tumor), if possible microscopic confirmation
Further explanations: R classification is one of the most important prognostic factor; R1 may be used for the quality control of surgery (surgeon supposed curative, R0 resection)

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Minimal number of lymph nodes that should be found by the pathologists in a surgical specimen of different cancer sites


The UICC (UICC TNM Supplement 1993. Hermanek P, Henson DE, Hutter RVP, Sobin LH (eds) Springer 1993) recommend a minimal number of lymph nodes for the determination of pN0 category of the TNM system.
The number of nodes and nodes involved must be indicated after the pN category in parenthesis e.g. pN0 (0/21) or pN1 (2/21). These data can be also used for quality control.

Head and neck (excl. thyroid gland)10
Thyroid gland6
Esophagus6
Stomach15
Small bowel6
Colorectum12
Anal canal6
Liver, gall bladder, extrahepatic bile ducts3
Pancreas, ampulla10
Lung, pleura6
Soft tissue, bones6
Skin6
Breast (level I nodes)6
Vulva, vagina (lower third)6
Vagina (upper part), cervix, corpus uteri, ovary 10
Penis6
Prostate gland, testis, kidney, kidney pelvis,
ureter, urinary bladder, urethra
8
Ophtalmic tumors6
Pediatric tumors3

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Preparation of Lymph Nodes for pN Classification

General Considerations

  1. A minimal number of regional lymph nodes should be found to state the pN0 category (s table)
  2. The highest possible pN category can be sometimes diagnosed by examination of one or
    a limited number of lymph nodes. In this situation the examination of further lymph nodes is not needed.

Methodical considerations

  1. In our experience the most simple and best method is the preparation of lymph
    nodes after overnight or longer fixation in formaldehyde. A careful palpation of the fatty
    tissue and slicing will result an appropiate number of nodes. All suspected nodules
    must be embedded and cut (10-30% of these nodules will be than small vessel convolutes).

    "Evidence of a good nodal dissection is the finding of nodules
    of lymphoid tissue in the 1- to 3-mm range, with a sprinkling
    of pieces of fibrofatty tissue and small vessels in cross section.
    Conversely, inadequate sampling is characterized by the finding of
    only a few nodes measuring 1 cm or more." KJ Lewin, RH Riddell
    WM Weinstein Gastrointestinal Pathology and its Clinical
    Implications. Igaku-Shoin, New York Tokyo 1992

  2. We embed lymph node groups (max. 5-6 nodes/capsula). Large nodes may be embedded in several capsulas.

  3. Step sections are a very useful method to find small nodes in the embedded tissue.

  4. In large bowel and stomach specimens the lymph nodes are localized around the blood vessels. The slicing up of the vessels will help to find and localize the nodes

    Rectum specimen with opened a. mesenterica inf.
    and a. rectalis sup.

  5. In several lymph nodes regions the preparation is difficult because lymph nodes contain fibrous or fatty tissue. Inflammations may lead to fixation of the nodes and the preparation of a single node is difficult or impossible.
    This applies to the following regions:
    inguinal,iliacal, obturator, all retroperitoneal nodes, nodes around the genitourinary tract,mediastinal, hilus of the lung.

  6. The so called clearing techniques are time consuming and hazardous; we find an equivalent number of nodes (e.g. ca 30 nodes/gastrectomy; 20 nodes/Whipple specimen; 25 nodes/rectum specimen) after formaldehyde fixation and careful preparation.

  7. The preparation of nodes needs some time and patience (25-40 min/large gastrointestinal specimen) Consider: the surgeon needs more time for preparation and a useful pathological diagnosis!

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