Esophageal Adenocarcinoma Methods and Protocols

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  1. Barrett mucosa is considered a precursor to esophageal adeno-
    carcinoma [ 13 ]. Barrett mucosa may be identified macro-
    scopically as a velvety texture at the distal esophagus mucosa
    distinct from the smooth squamous mucosa that extends
    proximally. Its presence or absence and relation to the tumor
    are useful for the distinction between adenocarcinoma of the
    distal esophagus and proximal stomach, which are etiologi-
    cally distinct. It may involve the distal esophagus circumfer-
    entially or partially and the new squamocolumnar junction is
    often irregular. Occasionally, Barrett mucosa may appear as
    islands, separated from the gastro-esophageal junction by
    normal squamous mucosa. Barrett mucosa should be con-
    firmed by microscopy.

  2. Lymph nodes may be more difficult to locate following che-
    motherapy and radiotherapy. However, all lymph nodes should
    be harvested and examined histologically. The lymph nodes
    must be embedded in such a way to ensure that the numbers
    of involved and uninvolved lymph nodes can be quantified. In
    completely resected carcinomas, lymph node status is the most
    important independent prognostic factor [ 5 , 7 , 14 ].

  3. An example of a typical block key for this kind of specimen is
    given below:
    Block key:
    1A Proximal margin.
    1B Distal margin.
    1C–D Tumor to circumferential margin.
    1E–F Proximal and distal tumor to mucosa.
    1G–H Gastro-esophageal junction.
    1I–K 4 whole lymph nodes per block.
    1 L–N 1 bisected lymph node per block.

  4. A typical microscopic report includes following features:


MICROSCOPIC
Tumor location.
Histologic type.
Histological grade.
Maximum tumor dimension.
Depth of invasion.
Peritoneal involvement.
Pleural involvement.
Lymphatic and capillary space invasion.
Vein and artery space invasion.
Perineural invasion.

Cut Up of Resected Specimen of Esophageal Adenocarcinoma
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