Case 94 (14 Aug 1999)



Diagnosis: Inflammatory Pseudotumor


Radiologic Findings

  • Chest PA shows an about 2-cm-sized well-defined round nodule in right lower lung zone.
     
  • On CT scan, the lesion is located just posterior to the right major fissure and shows slightly lobulated margin anteriorly.

  • On enhanced scan, the attenuation value of the nodule is similar to that of chest wall muscle.

  • On pathology (below), the nodule was composed of fibroblasts, collagen and inflammatory cells, mainly of lymphocyte and plasma cells.
     

 

 

Brief Review

  • Pulmonary inflammatory pseudotumor is an uncommon, non-neoplastic, occasionally aggressive proliferative process that may begin as an organizing pneumonia.
     
  • It has many synonyms, including plasma cell granuloma, inflammatory myofibroblastic tumor, histiocytoma, xanthoma, fibroxanthoma, xanthogranuloma, plasma cell tumor, fibrous xanthoma, xanthomatous pseudotumor, and plasma cell-histiocytoma complex.
    And the term inflammatory pseudotumor has been widely accepted.
     
  • Gross pathology demonstrates that pulmonary inflammatory pseudotumors are typically well-defined, firm, lobulated parenchymal nodule or mass with a whorled and often heterogeneous appearance on cut section.
     
  • The histologic findings are proliferation of spindle-shaped fibroblasts and permeation of collagen with lymphocytes, fibrosis, granulomatous inflammation, lymphoid hyperplasia, and intraalveolar fibrosis at the edge of the tumor.
     
  • Pulmonary inflammatory pseudotumor is typically a solitary, peripheral, sharply circumscribed, lobulated mass with an anatomic bias for the lower lobes.
     
  • CT most commonly shows a well-marginated, lobulated mass of heterogeneous attenuation with variable patterns of contrast enhancement and calcification.
     
  • T1-weighted MR images typically show a heterogeneous mass of intermediate signal intensity that displays a nonspecific increase in signal intensity on T2-weighted images.
     
  • Extraparenchymal extension and primary involvement of mediastinal and hilar structures are unusual.
     
  • Calcification within the lesion is uncommon, but not rare.
     
  • The tumor occurs more frequently in children than in adults.
     
  • Atelectasis and pleural effusion may occur.
     
  • Cavitation and lymphadenopathy are rare.
     
  • The radiologic differential diagnosis for pulmonary inflammatory pseudotumor is extensive because the typical lesion may be characterized as a solitary pulmonary nodule or mass.

  • A primary or metastatic neoplasm should be considered, but in children without an underlying malignancy, a solitary peripheral pulmonary nodule or mass is more likely to represent an inflammatory pseudotumor than a neoplasm.
     


 

References

  1. Agrons GA, Rosado-de-Christenson ML, Kirejczyk WM, et al. Pulmonary inflammatory pseudotumor : radiologic features. Radiology 1998;206:511-518
     
  2. Kim HS, Jung GS, Baek KH, et al. Inflammatory pseudotumor of the lung : CT findings and pathologic correlation. J Korean Radiol Soc 1998;38:75-82
     
  3. Shapiro MP, Gale E, CarterBL. Variable CT appearance of plasma cell granuloma of the lung. J Comput Assist Tomogr 1987;11(1):49-51
     




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