- Login
- Register
- Home/Current Issue
- About the journal
- Editorial board
- Online submission
- Instructions for authors
- Subscriptions
- Foundation Acta Endocrinologica
- Archive
- Contact
Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
Acta Endocrinologica(Bucharest) is live in PubMed Central
Journal Impact Factor - click here.
This Article
Services
Google Scholar
PubMed
Acta Endocrinologica (Buc)
Badan MI, Piciu D
Immunohistochemical Markers and SPECT/CT Somatostatin-Receptor (99MTCTEKTROTYD) Uptake in Well and Moderately Differentiated Neuroendocrine Tumors
Acta Endo (Buc) 2022, 18 (4): 523-530doi: 10.4183/aeb.2022.523
Context. Diagnosis of primary NETs
(neuroendocrine tumors) is challenging and often late due to
tumor heterogeneity, and a wide variety of general symptoms.
Low grade NETs are often indolent and have a good prognosis,
especially in the early stages. Even so, some tumors are
diagnosed using SPECT/CT either in the metastatic stage or
directly as a metastasis with an unknown primary tumor.
Objective. This study aims to characterize well
and moderately differentiated NETs, using Tektrotyd
SPECT/CT imaging as well as from the viewpoint of NET
immunohistochemical biomarker expression.
Design. Patients diagnosed with low grade
neuroendocrine tumors (carcinoids) investigated over a
period of 2 years, using SPECT/CT with 99mTc-EDDA/
HYNIC-Tyr3-Octreotide (Tektrotyd) and confirmed through
at least two immunohistochemical neuroendocrine markers
were evaluated.
Subjects and Methods. Twenty-seven cases with
neuroendocrine tumors were analyzed. Four patients met
the inclusion criteria. Staining intensity was scored using
a weak, moderate, or strong scoring system. CD56 was
quantified using criteria derived from Her2 cell membrane
staining evaluations.
Results. Patients included in the study had two well
differentiated (G1) NETs and two moderately differentiated
(G2) NETs. SPECT/CT with Tektrotyd showed variable
intensity ranging from discreet to strong. All tumors
expressed chromogranin A with at least moderate intensity,
weak to moderate intensity for synaptophysin and variable
CD56 intensity.
Conclusions. Chromogranin A and synaptophysin
staining patterns may aid in primary tumor identification.
CD56 stain intensity showed an inverse correlation with
Tektrotyd uptake in carcinoids. Additional studies merit
further investigation for use in clinical settings.
Keywords: neuroendocrine tumors, Tektrotyd, SPECT/CT, carcinoid, immunohistochemistry.
Correspondence: Marius-Ioan Badan MD, “Iuliu Ha?ieganu” University of Medicine and Pharmacy, Doctoral School, 8 Victor Babe?, Cluj-Napoca, 400347, Romania, E-mail: badan_marius@yahoo.com