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Differentiation of desquamative interstitial pneumonia (DIP) from pulmonary adenocarcinoma by immunocytochemistry.

AbstractAIM:
After a misdiagnosis of pulmonary adenocarcinoma as desquamative interstitial pneumonia (DIP), we investigated whether immunohistochemical markers could differentiate these conditions.
METHODS AND RESULTS:
Three cases of DIP and one pulmonary adenocarcinoma masquerading as DIP were studied by light and electron microscopy. All cases were mucin-negative. The cases of DIP were CD68 positive but cytokeratin-negative. The adenocarcinoma was cytokeratin-positive (AE1/3 and CAM5.2), as well as showing some CD68-positive cells. Markers for carcinoma (CEA, Ber-EP4, and Leu M1) were negative in all cases. Ultrastructurally the adenocarcinoma appeared to be derived from Type II pneumocytes.
CONCLUSION:
Before a diagnosis of DIP is made, cytokeratin markers should be used.
AuthorsA E Mutton, P S Hasleton, A Curry, P W Bishop, J Egan, K B Carroll, S Hanley
JournalHistopathology (Histopathology) Vol. 33 Issue 2 Pg. 129-35 (Aug 1998) ISSN: 0309-0167 [Print] England
PMID9762545 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Biomarkers
Topics
  • Adenocarcinoma (chemistry, pathology, ultrastructure)
  • Adult
  • Biomarkers (analysis)
  • Diagnosis, Differential
  • Fatal Outcome
  • Female
  • Humans
  • Immunohistochemistry
  • Lung (chemistry, ultrastructure)
  • Lung Diseases, Interstitial (pathology)
  • Lung Neoplasms (chemistry, pathology, ultrastructure)
  • Male
  • Microscopy, Electron
  • Middle Aged

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