Involvement of 2p23 in pulmonary inflammatory pseudotumors

Hum Pathol. 2001 Apr;32(4):428-33. doi: 10.1053/hupa.2001.23523.

Abstract

Pulmonary inflammatory pseudotumors (IP) are rare mesenchymal proliferations that have a polymorphic histology and an unpredictable biologic behavior. The histologic spectrum of IP has led to uncertainty as to whether this tumor has a reactive or neoplastic pathogenesis. Reports of extrapulmonary IP have identified clonal chromosomal aberrations involving 2p23 in the region of the ALK gene. Using fluorescence in situ hybridization with a probe flanking the ALK gene at 2p23 and immunostaining for the ALK gene product, we studied formalin-fixed, paraffin-embedded tissues of pulmonary IP and found a subset (33%) with 2p23 aberrations. We suggest that chromosomal rearrangements and ALK immunostaining may be helpful in the diagnosis of a group of pulmonary IP and should be investigated as a potential tool for predicting their future biologic behavior. An association with anaplastic large-cell lymphoma was also observed. HUM PATHOL 32:428-433.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anaplastic Lymphoma Kinase
  • Child
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 2*
  • Female
  • Humans
  • Male
  • Plasma Cell Granuloma, Pulmonary / genetics*
  • Plasma Cell Granuloma, Pulmonary / pathology
  • Protein-Tyrosine Kinases / genetics*
  • Receptor Protein-Tyrosine Kinases

Substances

  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases