The impact of coaxial core biopsy guided by FDG PET/CT in oncological patients
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作者:
Cerci, Juliano Julio
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Quanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, BrazilQuanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Cerci, Juliano Julio
[1
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Pereira Neto, Carlos Cunha
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Quanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, BrazilQuanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Pereira Neto, Carlos Cunha
[1
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Krauzer, Cassiano
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Quanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Univ Tecnol Fed Parana, Curitiba, Parana, BrazilQuanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Krauzer, Cassiano
[1
,2
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Sakamoto, Danielle Giacometti
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Byori Lab Patol, Curitiba, Parana, BrazilQuanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Sakamoto, Danielle Giacometti
[3
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Vitola, Joao Vicente
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Quanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, BrazilQuanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
Vitola, Joao Vicente
[1
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机构:
[1] Quanta Diagnost & Terapia, Div PET CT, BR-80045170 Curitiba, Parana, Brazil
[2] Univ Tecnol Fed Parana, Curitiba, Parana, Brazil
When deciding on therapy, FDG PET/CT-positive results should be confirmed by histology if possible. We evaluated the impact of percutaneous PET/CT-guided biopsies on histological confirmation of PET/CT-positive lesions. We prospectively evaluated 126 patients who had undergone a PET/CT scan with positive results with an indication for histological evaluation of lesions. Imaging was performed in a PET/CT scanner with a fluoroscopic imaging system. A total of 130 lesions were accessed by PET/CT-guided biopsy. The technical feasibility, clinical success and complication rates of PET/CT-guided biopsies were evaluated. Of 130 PET/CT-positive lesions, 128 (98.5 %) were successfully accessed and representative tissue samples obtained. Two lesions were reaccessed due to inconclusive histological results. Histology showed that 99 of the 130 lesions (76.2 %) were malignant, and 31 lesions (23.8 %) were benign (inflammatory cells or necrotic tissue); these patients had no recurrence of disease after a minimum follow-up of 6 months. Also, in 23 of the 130 lesions (17.7 %), the patient was referred for the PET/CT-guided biopsy due to a previous nontumoral biopsy result, and of these 23 lesions, 21 were found to be malignant. The complication rates were: pneumothorax in 15/130 (11.5 %; resolved spontaneously), haemoptysis in 2/130 (1.5 %) and severe haemothorax in 1/130 (0.8 %); there was no procedure-related mortality. PET/CT-guided biopsy is feasible and may optimize the diagnostic yield of image-guided interventions. Also, PET/CT-positive lesions with no morphological correlation may now be accessible to percutaneous interventions.
机构:
Azienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Azienda Osped Univ Policlin Modena, Dipartimento Oncol & Ematol, SC Med Nucl, Modena, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Rossetti, V.
Cappelli, A.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Malattie Apparato Digerente & Med In, UO Radiol, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Cappelli, A.
Balbi, T.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Ematol Oncol & Med Lab, UO Anat & Istol Patol, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Balbi, T.
Gasbarrini, A.
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Ist Ortoped Rizzoli, Dipartimento Patol Ortoped Traumatol Specialist, SC Chirurg Vertebrale Indirizzo Oncol & Degenerat, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Gasbarrini, A.
Mangiacotti, F.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Mangiacotti, F.
Brocchi, S.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Malattie Apparato Digerente & Med In, UO Radiol, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Brocchi, S.
Zanoni, L.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Zanoni, L.
Golfieri, R.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Malattie Apparato Digerente & Med In, UO Radiol, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Golfieri, R.
Fanti, S.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy
Fanti, S.
Nanni, C.
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Azienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, ItalyAzienda Osped Univ S Orsola Malpighi, Dipartimento Med Specialist Diagnost & Sperimenta, UO Med Nucl, Bologna, Italy