Peer-reviewed veterinary case report
Ultrasound-guided needle biopsy for thyroid cancer diagnosis in dogs
By Scheemaeker, Stephanie et al.·Published in Veterinary and comparative oncology·2023·Small Animal Department·View original on PubMed →
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Original publication title: Ultrasound-guided core needle biopsy in dogs with thyroid carcinoma.
- Species:
- dog
Plain-English summary
A group of dogs with suspected thyroid cancer underwent a new type of biopsy called ultrasound-guided core needle biopsy (UGCNB) to see if it could safely provide a diagnosis without needing surgery. In this study, 9 dogs had both UGCNB and traditional excisional biopsy (EB) performed. The UGCNB was successful in identifying cancerous thyroid tissue in 7 out of 9 dogs, while the EB confirmed cancer in 8 out of 9 dogs. The results suggest that UGCNB is a reliable method for diagnosing thyroid cancer in dogs that cannot undergo surgery, allowing for better treatment planning.
People also search for: dog thyroid cancer diagnosis · ultrasound-guided biopsy in dogs · thyroid cancer treatment for dogs
Abstract
Currently, a histological diagnosis of highly vascularized canine (c) thyroid carcinoma (TC) is primarily obtained following excisional biopsy (EB) through thyroidectomy. Non-EBs are contraindicated in unresectable invasive cTCs due to their highly vascularized nature, which subsequently, lack histological diagnosis. We hypothesised ultrasound-guided core needle biopsy (UGCNB) to be a safe biopsy technique to obtain an accurate histological diagnosis in unresectable TCs. Nine client-owned dogs with suspected naturally occurring TC, presented for surgical excision, were included. First, a UGCNB was taken from the cervical tumour, followed by EB. Haemorrhage following UGCNB was evaluated preoperatively and once the tumour was surgically exposed by visual inspection and ultrasonography. Histological analysis, including cell organisation, tumour capsular and vascular invasion, and immunohistochemistry were performed and compared between both biopsy specimens (i.e., UGCNB and EB) of the same dog. Pre- and peroperative visual inspection revealed minor, localised haemorrhage, subsequent to the UGCNB, in 7/9 dogs. Histology of the EBs confirmed TC in 8/9 dogs and was inconclusive in 1/9 dogs. Histology of the UGCNBs revealed neoplastic thyroid tissue in 7/9 UGCNBs and was inconclusive in 1/9 UGCNBs. The remaining UGCNB contained no mass related tissue and was, therefore, excluded. Histological parameters (i.e., cell organisation, tumour capsular and vascular invasion) were not concordant between 6/8 included UGCNBs and their respective EB. Immunolabelling for thyroglobulin and calcitonin was concordant between all eight included UGCNBs and their respective EB. The remaining evaluated immunohistochemical markers (i.e., cyclooxygenase-2 [COX-2], P-glycoprotein and vascular endothelial growth factor [VEGF]) were concordant between the included UGCNBs and the EBs in 6/8 dogs. To conclude, UGCNBs can be safely obtained in suspected cTCs and enable a reliable diagnosis of the thyroid origin, thyroid cell origin and potential therapeutic markers such as COX-2, P-glycoprotein and VEGF. Subsequently, UGCNB enables clinicians to establish an individually tailored treatment plan in dogs with unresectable TC.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/37017123/