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Usefulness of combined imaging with 68Ga-DOTATOC PET/CT and spleen scintigraphy in differentiating a neuroendocrine tumour of the pancreatic tail from splenic lesions in a patient with posttraumatic splenosis
Utilidad de la imagen combinada de PET/TC con 68Ga-DOTATOC y gammagrafía de bazo para la diferenciación entre tumor neuroendocrino de la cola del páncreas y lesiones esplénicas en un paciente con esplenosis post-traumática
Johanna Maffey-Steffan, Christian Uprimny
Corresponding author
, Roy Moncayo, Alexander Stephan Kroiss, Irene Johanna Virgolini
Department of Nuclear Medicine, Medical University Innsbruck, Austria
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We report on a patient diagnosed with renal cell carcinoma who revealed several lesions in the abdomen on staging CT consistent with splenosis after splenectomy&#46; In addition an unclear lesion in the pancreatic tail was found&#44; a distinction between a neuroendocrine tumour and an intrapancreatic splenosis foci was not possible with CT&#46; <span class="elsevierStyleSup">68</span>Ga-DOTATOC PET&#47;CT could not yield a differentiation&#44; showing high tracer accumulation in the pancreatic lesion as well as in the areas of splenosis&#46; However&#44; spleen scintigraphy did not demonstrate an increased tracer uptake in the pancreatic lesion ruling out spleen tissue and rendering the diagnosis of a neuroendocrine tumour very likely&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 52 year-old patient was referred to our clinic for evaluation of a previously diagnosed lesion in the left kidney&#44; highly suspicious for renal cell carcinoma on contrast enhanced CT &#40;ceCT&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a> blue arrow&#41;&#44; subsequently resected and histologically confirmed as light cell carcinoma&#46; Multiple lesions with contrast enhancement in the abdomen and in the pelvis were found on staging CT &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a> green arrows&#41;&#46; As the patient underwent splenectomy due to traumatic rupture of the spleen several years before&#44; these lesions were interpreted as splenosis&#44; a condition occurring in up to 66&#37; of patients after splenectomy because of trauma&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">1</span></a> In addition&#44; CT revealed a lesion in the pancreatic tail with a diameter of 19<span class="elsevierStyleHsp" style=""></span>mm&#44; showing similar characteristics as splenic tissue &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a> red arrow&#41;&#46; However&#44; a clear differentiation of another splenic foci and a malignant tumour was not possible&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">As CT could not rule out a neuroendocrine tumour and Chromogranin A was slightly elevated &#40;110&#46;9<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;l&#41; a <span class="elsevierStyleSup">68</span>Ga-DOTATOC PET&#47;CT scan with low-dose CT was performed after the resection of the renal tumour&#44; histologically classified as a clear cell carcinoma&#44; grade II&#44; pT1pN0&#46; Somatostatin receptor imaging with the PET tracer <span class="elsevierStyleSup">68</span>Ga-DOTATOC has been proven to constitute a very sensitive method in the diagnosis of well differentiated neuroendocrine tumours showing higher sensitivity than conventional somatostatin receptor scintigraphy in this indication&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">2</span></a> In our patient the pancreatic lesion revealed a markedly increased tracer accumulation on <span class="elsevierStyleSup">68</span>Ga-DOTATOC-PET&#47;CT with a maximum standardised uptake value &#40;SUV<span class="elsevierStyleInf">max</span>&#41; of 28&#46;9&#46; However&#44; the areas of splenosis also showed a similar tracer uptake with an almost identical SUV<span class="elsevierStyleInf">max</span> of 33&#46;9&#44; measured in the largest lesion in the paragastral region&#46; A final diagnosis was not possible due to the physiologically increased expression of somatostatin receptors in the red pulpa of splenic tissue as can be visualised by somatostatin receptor scintigraphy&#44; sometimes mimicking neuroendocrine tumour lesions &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">As a further diagnostic step a <span class="elsevierStyleSup">99m</span>Tc heat-denatured red blood cell SPECT&#47;CT scan was conducted&#46; This method has been proven to establish a very specific exam in the detection of splenosis and accessory spleen<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">3</span></a> and seems to be very helpful in distinguishing pancreatic neuroendocrine tumours from intrapancreatic accessory spleen tissue&#46; MIP image of the patient showed multiple lesions with high tracer uptake in the abdomen &#40;green arrows&#41; corresponding to the known lesions diagnosed as splenosis on diagnostic CT&#46; In contrast the lesion in the pancreatic tail did not demonstrate an increased tracer accumulation &#40;red arrow pointing at the site of the lesion on low-dose CT&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; This finding with markedly elevated somatostatin receptor expression on <span class="elsevierStyleSup">68</span>Ga-DOTATOC PET&#47;CT and negative result on spleen scintigraphy is not compatible with a splenic lesion and consistent with a well differentiated neuroendocrine tumour&#46; Unfortunately no histologic confirmation was available as the patient did not consent to perform a biopsy&#46; However&#44; on a follow-up CT-scan performed 22 months after the base-line the pancreatic lesion increased in size from 16 to 21<span class="elsevierStyleHsp" style=""></span>mm&#44; rendering the diagnosis of a slowly growing malignant tumour very likely&#44; as it is the case in well differentiated neuroendocroine tumours&#46; This case highlights the complementary information obtained from spleen scintigraphy and <span class="elsevierStyleSup">68</span>Ga-DOTATOC PET&#47;CT&#46; Both modalities should be applied in the diagnostic work-up of patients with splenosis and accessory spleens in whom neuroendocrine tumours are suspected prior to biopsy and&#47;or operation&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflict of interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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