J Pathol Transl Med.  2017 May;51(3):320-324. 10.4132/jptm.2016.09.07.

Unusual Histology of Eosinophilic Myenteric Ganglionitis: A Case Report

Affiliations
  • 1Department of Pathology, Eulji University School of Medicine, Daejeon, Korea.
  • 2Department of Radiology, Eulji University School of Medicine, Daejeon, Korea.
  • 3Department of Surgery, Eulji University School of Medicine, Daejeon, Korea. jhjang@eulji.ac.kr

Abstract

Eosinophilic myenteric ganglionitis is a disorder characterized by infiltration of the Auerbach myenteric plexus by eosinophils. As a cause of chronic intestinal pseudo-obstruction (CIPO), eosinophilic myenteric ganglionitis has been rarely reported and the majority of the reported cases in the literature were children. We experienced a case of eosinophilic myenteric ganglionitis associated with CIPO in a 53-year-old female patient. Histologic examination of the resected descending colon showed moderate eosinophilic infiltrates with hypogangliosis in the myenteric plexus. Immunohistochemical study revealed increased number of CD4-positive lymphocytes and stronger but scantier glial fibillary acid protein expression in the inflamed myenteric plexus.

Keyword

Eosinophils; Ganglionitis; Pseudo-obstruction

MeSH Terms

CD4-Positive T-Lymphocytes
Child
Colon, Descending
Eosinophils*
Female
Ganglion Cysts*
Humans
Intestinal Pseudo-Obstruction
Middle Aged
Myenteric Plexus

Figure

  • Fig. 1. Abdominopelvic computed tomography shows markedly dilated colon filled with feces (A). Transition point between the dilated proximal and collapsed distal colon is noted (B, arrow).

  • Fig. 2. Approximately half of the resected segment of the descending colon was dilated.

  • Fig. 3. Summary of histologic findings: thickened muscularis mucosa in the dilated colon (A), many eosinophils in Auerbach’s myenteric plexus (B), hypogangliosis in synaptophysin immunostain (C), scattered CD4-positive lymphocytes in the affected myenteric plexus (D) and stonger but scantier glial fibrillary acidic protein positivity in our patient (E) in contrast to the control patient (in box).


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