S. Lastoria et al., IN-VIVO DETECTION OF MALIGNANT THYMIC MASSES BY INDIUM-111-DTPA-D-PHE(1)-OCTREOTIDE SCINTIGRAPHY, The Journal of nuclear medicine, 39(4), 1998, pp. 634-639
Many tumors with neuroendocrine characteristics express high amounts o
f somatostatin receptors that enable in vivo imaging with [(111) In-DT
PA-D-Phe(1)]-octreotide. In this study, we have analyzed the feasibili
ty in detecting and characterizing thymic masses by somatostatin recep
tor scintigraphy (SRS), Methods: Eighteen patients (13 women, 5 men, a
ges 18-78 yr; mean +/- s.d. = 42.1 +/- 17.6 yr) were enrolled in this
study, Eleven patients were studied during diagnosis and seven during
routine follow-up, In seven patients, myasthenia gravis was the presen
ting symptom. SRS was performed within 4 wk after CT and/or MRI, Plana
r and tomographic images were acquired within 24 hr after the injectio
n of approximately 111 MBq of [(111) In-DTPA-D-Phe(1)]-octreotide. The
scintigraphic results were categorized according to the histologic fi
ndings, Results: Histology diagnosed 10 mixed epithelial/lymphoid thym
omas (8 with prevalent epithelial component), 2 thymic carcinomas, 1 t
hymic carcinoid, 1 lymphangioma and 4 thymic hyperplasias. Two thymoma
were Stage I, 3 were Stage II, 2 were Stage III and 5 were Stage IV,
as was the thymic carcinoid. Indium-111-DTPA-D-Phe(1)-octreotide conce
ntrated in primary and/or metastatic sites of thymic tumors, thereby e
nabling successful external gamma imaging of sites greater than 1.5 cm
in size, Tumor-to-lung (T/L) ratios were as high as 7.6-fold (range 1
.7-7.6). Untreated thymomas showed higher T/L (4.34 +/- 1.57) than tre
ated ones (2.68 +/- 1.18). No uptake was detectable in the four patien
ts with benign thymic hyperplasia and the patient with the lymphangiom
a. Conclusion: Indium-111-DTPA-D-Phe(1)-octreotide is avidly concentra
ted within thymic tumors, but it is not concentrated by thymic hyperpl
asia, which allows differential diagnosis. Thus, in patients with myas
thenia gravis, SRS may have a role in characterizing thymic masses, th
ereby overcoming the limits of cross-sectional imaging modalities.