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Japanese Journal of Clinical Oncology 30:450-452 (2000)
© 2000 Foundation for Promotion of Cancer Research

Lung Cancer Implantation in the Chest Wall Following Percutaneous Fine Needle Aspiration Biopsy

Takeshi Yoshikawa1, Junji Yoshida1, Mitsuyo Nishimura1, Tomoyuki Yokose2, Yutaka Nishiwaki1 and Kanji Nagai1,+

1Department of Thoracic Oncology, National Cancer Center Hospital East and 2Pathology Division, National Cancer Center Research Institute East, Kashiwa, Chiba, Japan


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
We describe a 70-year-old man with lung cancer implantation in the chest wall following percutaneous fine needle aspiration biopsy. He underwent lobectomy after percutaneous transthoracic fine needle aspiration biopsy using a 19-gauge needle. Twenty-six months after the biopsy, he noticed a hard subcutaneous tumor at the biopsy site in the chest wall. Ribs and intercostal muscles were resected. The primary lung tumor and the chest wall tumor were histologically identical, but were not contiguous to each other. We concluded that the subcutan­eous tumor was due to needle biopsy implantation. This complication is extremely rare, but open biopsy should always be considered as a possible alternative. During the procedure, care must be taken with the least chance of implantation and patients should be observed carefully after needle biopsy.


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
Fine needle aspiration biopsy (FNAB) in patients with a pulmonary nodule is a reliable and simple diagnostic procedure (1,2). Malignant cell implantation is a potential, but extremely uncommon complication (1,3,4). We describe a case of lung cancer with cancer implantation in the FNAB needle tract.


    CASE REPORT
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
A 70-year-old man underwent left lower lobectomy and lymph node dissection for lung cancer in January 1997. Preoperative transbronchial lung biopsy had failed to show evidence of malignancy, but percutaneous transthoracic FNAB of the lung lesion through the left posterior chest wall using a 19-gauge needle in November 1996 yielded a diagnosis of moderately differentiated adenocarcinoma. The postoperative pathological diagnosis was moderately differentiated adenocarcinoma (Fig. 1), T3N0M0, stage IIB (5). The cancer had invaded the elastic layer of the parietal pleura, which was resected together with the lower lobe, but had not invaded either the ribs or intercostal muscles.



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Figure 1. Microscopic examination of the primary lung cancer with hematoxylin–eosin stain.

 
In January 1999, 26 months after the FNAB, he noticed a hard subcutaneous tumor in the left posterior chest wall. The tumor was located at the FNAB site and distant from the thoracotomy incision. It was 3 cm in diameter, fixed to the eighth and ninth ribs, firm and painless. CT scan of the chest indicated that the mass was in the subcutaneous layer and in the previous FNAB needle tract (Fig. 2a and b). FNAB of the tumor had demonstrated adenocarcinoma. There was no evidence of distant metastasis. We speculated that the mass was lung cancer implantation resulting from the previous FNAB.



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Figure 2. (a) Chest CT scan before the first operation, showing the primary lung tumor (arrow) in the left lower lobe. (b) Chest CT scan before the second operation, showing the subcutaneous tumor (arrow) at the FNAB site.

 
The tumor, overlying skin, eighth and ninth ribs and intercostal muscles were surgically resected 29 months after the first surgical intervention. The chest wall defect was restored with a sheet of Marlex mesh (Davol, Cranston, RI, USA). The postoperative course was uneventful and he was discharged 9 days after the operation. The patient is doing well with no signs of recurrence 6 months after resection. Pathologically, the tumor was diagnosed as moderately differentiated adenocarcinoma without periosteal invasion (Figs 3 and 4). As the primary lung tumor and the chest wall tumor were histologically identical but not contiguous and the chest wall tumor was located precisely at the FNAB site, we concluded that the chest wall tumor was FNAB implantation.



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Figure 3. Microscopic examination of the chest wall tumor with hematoxylin–eosin stain (low magnification view).

 


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Figure 4. Microscopic examination of the chest wall tumor with hematoxylin–eosin stain (high magnification view). The specimens from the primary lung cancer (Fig. 1) and chest wall tumor (Fig. 4) were histologically identical.

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
FNAB is a well-established technique for definitive diagnosis of tumor because of its high diagnostic yield, simplicity and low morbidity (1,2). FNAB in the lung may be complicated by pneumothorax, hemorrhage, infection and air emboli. Tumor cell implantation along the needle tract is an extremely rare but potential complication of this technique (1,3,4).

These complications are more likely to follow the use of cutting needles or large-bore needles (4), because such needles yield larger stromal fragments, resulting in a more severe visceral injury. Tumor spread along the needle tract following FNAB has rarely been reported (1,6,7). Sinner reported only one case of FNAB-related tumor seeding in a total of 1264 patients (0.08%) (1). Lalli et al. reported more than 1500 procedures without a single incidence of needle tract implantation (3). Harrison et al. reported that two patients (3%) suffered from needle tract implantation after FNAB, although they had only 66 patients in their series (8). Our case is the only one in our institution in approximately 900 needle biopsy cases during the 7-year period from January 1993 to January 2000.

Totally effective prevention and management of tumor cell implantation following FNAB remains undetermined. Wolinsky and Lischner (9) performed immediate radiotherapy after needle biopsy to prevent tumor implantation, but nevertheless one patient in their series developed tumor implantation in the chest wall. Seyfer et al. (7) reported a case of chest wall implantation of pulmonary adenocarcinoma after FNAB, successfully managed by aggressive chest wall resection and immediate reconstruction with a rectus abdominis musculocutaneous flap. In our case, we performed tumor resection including the skin, ribs and intercostal muscles, as no other lesions were detected, with no recurrence so far.

Because of its rare incidence (1), this complication should not affect the use of FNAB in lung cancer patients. Wolinsky and Lischner concluded that FNAB should not be performed to lesions likely to be malignant and operable (9). Even if FNAB does not reveal malignancy, this cannot deny the possibility of a malignant lesion and the procedure may make an operable lesion incurable. One should avoid invasive examinations and perform open biopsy when CT scan indicates malignancy or the patient wants to undergo tumor resection. However, if the diagnosis remains indeterminate and the patient’s tolerance for surgery is uncertain, FNAB may be justified (9). One should take special care, such as using a smaller bore needle and avoiding multiple punctures with a single needle, because it is likely that contamination by more cancer cells will provide a better opportunity for tumor cells to grow along the needle tract.

Since the reported interval between FNAB and implantation tumor development ranged from 6 days to 30 months (8,10), careful examination for implantation should be performed for about 3 years.


    Acknowledgments
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
The authors thank Professor J. Patrick Barron of the International Medical Communications Center of Tokyo Medical University for reviewing the manuscript. This work was supported in part by a Grant-in-Aid for Cancer Research from the Japan Ministry of Health and Welfare.


    FOOTNOTES
 
+ For reprints and all correspondence: Takeshi Yoshikawa, Department of Thoracic Oncology, National Cancer Center Hospital, 5–1, Kashiwanoha 6-chome, Kashiwa, Chiba 277–8577, Japan Back


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 Acknowledgments
 REFERENCES
 
1 Sinner WN. Complication of percutaneous transthoracic needle aspiration biopsy. Acta Radiol Diagn 1976;17:813–28.

2 Kline TS, Neal HS. Needle aspiration biopsy: a critical appraisal: eight years and 3267 specimens later. J Am Med Assoc 1978;239:36–9.[Abstract/Free Full Text]

3 Lalli AF, McCormack LJ, Zelch M, Reich NE, Belovich D. Aspiration biopsies of chest lesions. Radiology 1978;127:35–40.[Abstract]

4 Sinner WN, Zajicek J. Implantation metastasis after percutaneous trans­thoracic needle aspiration biopsy. Acta Radiol Diagn 1976;17:473–80.

5 Sobin LH, Wittekind CH. TNM classification of Malignant Tumours, 5th edn. New York: Wiley 1997;93–100.

6 Müller NL, Bergin CJ, Miller RR, Ostrow DN. Seeding of the malignant cells into the needle track after lung and pleural biopsy. J Can Assoc Radiol 1986;37:192–4.

7 Seyfer AE, Walsh DS, Graeber GM, Nuno IN, Eliasson AH. Chest wall implantation of lung cancer after thin-needle aspiration biopsy. Ann Thorac Surg 1989;48:284–6.[Abstract]

8 Harrison BDW, Thorpe RS, Kitchener PG, McCann BG, Pilling JR. Percutaneous trucut lung biopsy in the diagnosis of localized pulmonary lesions. Thorax 1984;39:493–499.[Abstract/Free Full Text]

9 Wolinsky H, Lischner MW. Needle track implantation of tumor after percutaneous lung biopsy. Ann Intern Med 1969;71:359–62.

10 Berger RL, Dargan EL, Huang BL. Dissemination of cancer cells by needle biopsy of the lung. J Thorac Cardiovasc Surg 1972;63:430–2.[Web of Science][Medline]

Received April 6, 2000; accepted August 15, 2000.


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