Poorly differentiated adenocarcinoma manifesting as multifocal obstructive disease -a rare occurrence

Authors

  • Pragati Aditya Sathe Department of Pathology, Seth G. S. Medical College & KEM Hospital, Mumbai, India
  • Jayashri Popat Chaudhari Department of Pathology, Seth G. S. Medical College & KEM Hospital, Mumbai, India
  • Manjusha Milind Karegar Department of Pathology, Seth G. S. Medical College & KEM Hospital, Mumbai, India
  • Amit Suresh Mirjolkar Department of Pathology, Seth G. S. Medical College & KEM Hospital, Mumbai, India

Keywords:

Visceral carcinomatosis, multifocal obstruction, adenocarcinoma

Abstract

We describe an autopsy of a very unusual case of an adult female presenting with multifocal obstructive symptoms  like  achalasia, obstructive jaundice and bilateral hydronephrosis . Primary clinical diagnosis was tuberculosis and malignancy.  Although the patient was extensively worked up in the hospital with multiple biopsies, the diagnosis could not be made. Autopsy revealed contiguous involvement of entire gastrointestinal tract from esophagus till colon by a poorly differentiated adenocarcinoma with diffuse thickening, firmness and rigidity of the wall. The tumor cells were focally expressing CK 20 favouring a colonic primary.  Colonic   adenocarcinoma usually spread by either lymphatic or hematogenous way to lymph nodes, liver and lung. This unusual way of spread of this tumor contiguously from colon till esophagus, with Urinary bladder and distal CBD infiltration make it very unique.

DOI:10.21276/APALM.1757

Author Biography

Pragati Aditya Sathe, Department of Pathology, Seth G. S. Medical College & KEM Hospital, Mumbai, India

Pathology, Assistant Professor

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Published

28-04-2018

How to Cite

1.
Sathe PA, Chaudhari JP, Karegar MM, Mirjolkar AS. Poorly differentiated adenocarcinoma manifesting as multifocal obstructive disease -a rare occurrence. Ann of Pathol and Lab Med [Internet]. 2018 Apr. 28 [cited 2024 Dec. 27];5(4):C68-71. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/1757

Issue

Section

Case Report