Dispnea After Appendectomy Operation: Case Report


Arslan Z., Biyikli M., Yildiz K., Cetinarslan B. , Ilgazli A.

TRAKYA UNIVERSITESI TIP FAKULTESI DERGISI, vol.27, no.2, pp.205-208, 2010 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 27 Issue: 2
  • Publication Date: 2010
  • Doi Number: 10.5174/tutfd.2008.00622.1
  • Title of Journal : TRAKYA UNIVERSITESI TIP FAKULTESI DERGISI
  • Page Numbers: pp.205-208

Abstract

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial lung disease. Its estimated prevalence is two to five cases per million. Young male adults develop the disease most frequently. Greater than 90% of cases of PLCH occur in smokers. Diabetes insipidus (DI) occurs in about 11% to 40% of patients and pneumothoraces occur in 10% to 30% of patients. The diagnosis of PLCH can be confirmed by BAL, transbronchial biopsy, or surgical lung biopsy. We present a case referred to us with dispnea developed after appendectomy operation, coexisting with DI, and diagnosed to have PLCH using transbronchial lung biopsy.