The Diagnostic Yield and Complications ofPercutaneous Needle Aspiration Biopsy for the Intrathoracic Lesions.
10.4046/trd.1996.43.6.916
- Author:
Seung Hun JANG
1
;
Cheol Hyeon KIM
;
Won Jung KOH
;
Chul Gyu YOO
;
Young Whan KIM
;
Sung Koo HAN
;
Young soo SHIM
Author Information
1. Department of Internal Medicine and Tuberculosis Research Institute, Seoul National University College of Medicine, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Percutaneous needle aspiration biopsy;
Intrathoracic lesion;
Diagnostic yield;
Complication
- MeSH:
Biopsy;
Biopsy, Needle*;
Catheters;
Chest Tubes;
Diagnosis;
Fever;
Hemoptysis;
Humans;
Lung Neoplasms;
Mediastinum;
Needles*;
Pneumothorax;
Proliferating Cell Nuclear Antigen;
Retrospective Studies;
Sputum;
Thoracotomy;
Tolnaftate;
Tuberculosis, Pulmonary
- From:Tuberculosis and Respiratory Diseases
1996;43(6):916-924
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Bacground: Percutaneous needle aspiration biopsy (PCNA) is one of the most frequently used diagnostic methods for intrathoracic lesions. Previous studies have reported wide range of diagnostic yield from 28 to 98%. However, diagnostic yield has been increased by accumulation of experience, improvement of needle and the image guiding systems. We analysed the results of PCNA performed for one year to evaluate the diagnostic yield, the rate and severity of complications and factors affecting the diagnostic yield. Method: 287 PCNAs undergone in 236 patients from January, 1994 to December, 1994 were analysed retrospectively. The intrathoracic lesions was targeted and aspirated with 21-23 G Chiba needle under fluoroscopic guiding system. Occasionally, 19-20 G Biopsy gun was used for core tissue specimen. The specimen was requested for microbiologic, cytologic and histopathologic examination in the case of obtained core tissue. Diagnostic yields and complication rate of benign and malignant lesions were calculated based on patients' charts. The comparison for the diagnostic yields according to size and shape of the lesions was analysed with chi square test (p<0.05). Results: There are 19.9% of consolidative lesion and 80.1% of nodular or mass lesion, and the lesion is located at the right upper lobe in 26.3% of cases, the right middle lobe in 6.4%, the right lower lobe 21.2%, the left upper lobe in 16.8%, the left lower lobe in 10.6%, and mediastinum in 1.3%. The lesion distributed over 2 lobes is as many as 17.4% of cases. There are 74 patients with benign lesions, 142 patients with malignant lesions in final diagnosis and confirmative diagnosis was not made in 22 patients despite of all available diagnostic methods. 2 patients have lung cancer and pulmonary tuberculosis concomittantly. Experience with 236 patients showed that PCNA can diagnose benign lesions in 62.2% (42 patients) of patients with such lesions and malignant lesions in 82.4% (117 patients) of patients. For the patients in whom the first PCNA failed to make diagnosis, the procedure was repeated and the cumulative diagnostic yield was increased as 44.6%, 60.8%, 62.2% in benign lesions and as 73.4%, 81.7%, 82.4% in malignant lesions through serial PCNA. Thoracotomy was performed in 9 patients with benign lesions and in 43 patients with malignant lesions. PCNA and thoracotomy showed the same pathologic result in 44.4% (4 patients) of benign lesions and 58.1% (25 patients) of malignant lesions. Thoracotomy confirmed 4 patients with malignat lesions against benign result of PCNA and 2 patients with benign lesions against malignant result of PCNA. There are 1.0% (3 cases) of hemoptysis, 19.2% (55 cases) of blood tinged sputum, 12.5% (36 cases) of pneumothorax and 1.0% (3 cases) of fever through 287 times of PCNA. Hemoptysis and blood tinged sputum didn't need therapy. 8 cases of pneumothorax needed insertion of classical chest tube or pig-tail catheter. Fever subsided within 48 hours in all cases. There was no difference between size and shape of lesion with diagnostic yield. Conclusion: PCNA shows relatively high diagnostic yield and mild degree complications but the accuracy of histologic diagnosis has to be improved.
