Absence of hepatic activity in lymphoscintigraphy performed with Tc-99m-Nanoscan.


Journal

Nuclear medicine communications
ISSN: 1473-5628
Titre abrégé: Nucl Med Commun
Pays: England
ID NLM: 8201017

Informations de publication

Date de publication:
Jun 2020
Historique:
pubmed: 14 4 2020
medline: 10 2 2021
entrez: 14 4 2020
Statut: ppublish

Résumé

For assessment of lower extremity swelling using lymphoscintigraphy, several nuclear medicine departments in the UK have recently switched from Tc-Nanocoll to Tc-Nanoscan. The aim of the study was to compare quantitative and semiquantitative features of lymphoscintigraphy between these two tracers. Twenty patients received Tc-Nanocoll and 20 received Tc-Nanoscan either side of the switch-over in our department. Tracers were compared with respect to visualisation of the liver, para-aortic lymph nodes and urine (all graded by consensus from 0 to 3; invisible-to-very prominent); and with respect to ilio-inguinal nodal quantification and ratio of liver-to-summed bilateral ilio-inguinal nodal activity at 120 min postinjection (L/N120). Scans were deemed abnormal when there was lymph diversion through skin or deep system, no activity in ilio-inguinal nodes at 60 min or negligible ilio-inguinal activity (<5%, left plus right) at 120 min. Liver was visualised in 18/20 Tc-Nanocoll but only 3/20 Tc-Nanoscan scans. Moreover, para-aortic activity was less prominent after Tc-Nanoscan. Urinary activity was more prominent after Tc-Nanocoll. There were 9/20 patients with stomach activity after Tc-Nanocoll compared with 1/20 after Tc-Nanoscan. Urinary and stomach activities correlated. There was an elevated L/N120, and therefore a suspicion of peripheral lympho-venous communication, in the single Tc-Nanoscan patient who displayed prominent hepatic activity. Hepatic activity is the result of accumulation of colloidal degradation products generated in lymph nodes, rather than intact colloid. Tc-Nanoscan gives less hepatic activity than Tc-Nanocoll because it is more resistant to intranodal degradation. Peripheral lymphovenous communication remains a possible alternative route for activity to reach the liver.

Identifiants

pubmed: 32282635
doi: 10.1097/MNM.0000000000001181
pii: 00006231-202006000-00003
doi:

Substances chimiques

Technetium Tc 99m Aggregated Albumin 0
technetium Tc 99m nanocolloid 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

505-509

Références

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Peters AM, Fowler JC, Britton TB, Solanki CK, Ballinger JR, Ravichandran D, et al. Functional variation in lymph node arrangements within the axilla. Lymphat Res Biol. 2009; 7:139–144
Stamp GF, Peters AM. Peripheral lymphovenous communication in lymphoedema. Nucl Med Commun. 2012; 33:701–707
Soares MM, Keramida G, Glass DM, Mortimer PS, Peters AM. Lymph proteins may access peripheral blood without entering thoracic duct in patients with lymphatic dysfunction. J Vasc Surg Venous Lymphat Disord. 2016; 4:215–220
Keramida G, Winterman N, Wroe E, Aplin M, Peters AM. Importance of accurate ilio-inguinal quantification in lower extremity lymphoscintigraphy. Nucl Med Commun. 2017; 38:209–214
Altman DG. Practical Statistics for Medical Research. 1991, London: Chapman and Hall
Mikata A, Niki R. Permeability of postcapillary venules of the lymph node. An electron microscopic study. Exp Mol Pathol. 1971; 14:289–305
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Chisholm PM, Danpure HJ, Healey G, Osman S. Cell damage resulting from the labeling of rat lymphocytes and hela S3 cells with in-111 oxine. J Nucl Med. 1979; 20:1308–1311
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Auteurs

Adeel Syed (A)

Department of Nuclear Medicine, King's College Hospital.

Danielle Levart (D)

Department of Nuclear Medicine, King's College Hospital.

Manuela Vadrucci (M)

Department of Nuclear Medicine, King's College Hospital.

Victoria Gibson (V)

Department of Nuclear Medicine, Guy's and St Thomas' Hospitals Foundation Trusts, London, UK.

A Michael Peters (AM)

Department of Nuclear Medicine, King's College Hospital.

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