The Role of Fine Needle Aspiration of Liver and Spleen in the Staging of Low-Grade Canine Cutaneous Mast Cell Tumor.
FNA
dog
liver
mast cell tumor
spleen
Journal
Veterinary sciences
ISSN: 2306-7381
Titre abrégé: Vet Sci
Pays: Switzerland
ID NLM: 101680127
Informations de publication
Date de publication:
01 Sep 2022
01 Sep 2022
Historique:
received:
18
07
2022
revised:
09
08
2022
accepted:
30
08
2022
entrez:
22
9
2022
pubmed:
23
9
2022
medline:
23
9
2022
Statut:
epublish
Résumé
Clinical staging is a fundamental step in the clinical assessment of canine cutaneous mast cell tumor (cMCT), and it is recommended to evaluate the tumor draining lymph node (eTDLN), perform diagnostic imaging, and fine needle aspiration (FNA) of the spleen and liver to determine the presence of metastatic disease, thereby refining the prognosis. The aim of this retrospective study was to evaluate the prevalence of splenic and hepatic involvement in newly diagnosed canine low-grade cMCT (Patnaik grade I-II, Kiupel low-grade). Medical records of dogs that underwent a clinical staging work-up and surgical excision for a low-grade cMCT between December 2019 and December 2021 were reviewed at five veterinary centers. Only dogs with a histological diagnosis of low-grade cMCT, FNA or histology of the eTDLN, FNA of the spleen and liver, and one year of follow up were included. One hundred and thirty-six dogs met the inclusion criteria. Only 1 out of 136 dogs (0.7%) had the presence of visceral metastases at diagnosis, suggesting that the prevalence of visceral metastases in low-grade cMCT is extremely low. The results of this study are consistent with previous literature and suggest that after a diagnosis of low-grade cMCT, cytology of visceral organs may not represent an essential step in the clinical staging work-up.
Identifiants
pubmed: 36136689
pii: vetsci9090473
doi: 10.3390/vetsci9090473
pmc: PMC9506313
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
J Am Anim Hosp Assoc. 2014 Mar-Apr;50(2):89-95
pubmed: 24446400
Vet Comp Oncol. 2009 Jun;7(2):130-8
pubmed: 19453367
Vet Comp Oncol. 2018 Mar;16(1):28-36
pubmed: 28233400
Vet Comp Oncol. 2018 Dec;16(4):505-510
pubmed: 29893066
Vet J. 2016 Sep;215:43-54
pubmed: 27372911
J Small Anim Pract. 2022 Sep;63(9):661-669
pubmed: 35733233
Front Vet Sci. 2021 Dec 10;8:755258
pubmed: 34957277
J Comp Pathol. 2014 Nov;151(4):329-38
pubmed: 25172053
Vet Pathol. 2011 Jan;48(1):147-55
pubmed: 21062911
Vet Comp Oncol. 2014 Dec;12(4):287-98
pubmed: 23240829
Animals (Basel). 2021 Aug 11;11(8):
pubmed: 34438830
J Am Vet Med Assoc. 2015 Apr 1;246(7):765-9
pubmed: 25794126
Vet Comp Oncol. 2020 Sep;18(3):409-415
pubmed: 31930651
Vet Comp Oncol. 2020 Jun;18(2):239-246
pubmed: 31509648
Vet Pathol. 1984 Sep;21(5):469-74
pubmed: 6435301
Vet Radiol Ultrasound. 2011 Sep-Oct;52(5):548-54
pubmed: 21689203
Vet Comp Oncol. 2014 Mar;12(1):58-66
pubmed: 22577893
Vet Comp Oncol. 2018 Dec;16(4):580-589
pubmed: 30047226
Vet Rec. 2004 Jun 12;154(24):743-6
pubmed: 15224593
J Am Vet Med Assoc. 2001 May 1;218(9):1424-8
pubmed: 11345304
Br Vet J. 1986 Jan-Feb;142(1):1-19
pubmed: 3947927
J Vet Intern Med. 2008 Jul-Aug;22(4):1001-7
pubmed: 18564225
J Vet Intern Med. 2009 Sep-Oct;23(5):1051-7
pubmed: 19656285
Vet Comp Oncol. 2012 Sep;10(3):e1-e29
pubmed: 22882486
Vet Radiol Ultrasound. 2004 Jan-Feb;45(1):51-7
pubmed: 15005361
Vet Comp Oncol. 2021 Sep;19(3):451-462
pubmed: 32840038
Vet Surg. 2021 Jan;50(1):133-141
pubmed: 33169849
Vet Comp Oncol. 2014 Sep;12(3):215-26
pubmed: 22958227
J Am Anim Hosp Assoc. 2011 May-Jun;47(3):210-6
pubmed: 21498594
Vet Clin North Am Small Anim Pract. 2003 May;33(3):473-89, v
pubmed: 12852232
Vet Radiol Ultrasound. 2019 May;60(3):306-315
pubmed: 30786323
Vet Comp Oncol. 2020 Sep;18(3):389-401
pubmed: 31863546
Vet Comp Oncol. 2017 Dec;15(4):1206-1217
pubmed: 27523399
J Am Anim Hosp Assoc. 2011 Jan-Feb;47(1):37-44
pubmed: 21164163