Translate this page into:
99m-Technetium-Labeled Red Blood Cells' Single-Photon Emission Computed Tomography/Computed Tomography in Situs Ambiguous with Polysplenia
Address for correspondence: Dr. Selin Kesim, Department of Nuclear Medicine, Marmara University Istanbul Pendik Training and Research Hospital, Muhsin Yazıcıoğlu Street, TR-34899, Üstkaynarca, Pendik, Istanbul, Turkey. E-mail: selinkesim@yandex.com
-
Received: ,
Accepted: ,
This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
This article was originally published by Wolters Kluwer - Medknow and was migrated to Scientific Scholar after the change of Publisher.
Abstract
Situs ambiguous or heterotaxy syndrome is defined as the abnormal arrangement of organs and vessels within the body. Herein, we present an 8-year-old girl with growing right-sided suprarenal masses mimicking adrenal tumors. Technetium-99-m-radiolabeled red blood cells' planar images were inconclusive for the diagnosis of splenic tissue in the right side. Single-photon emission computed tomography/computed tomography imaging clearly identified right-sided functioning spleens and confirmed the diagnosis of situs ambiguous with polysplenia.
Keywords
Heterotaxy syndrome
polysplenia
selective spleen scintigraphy
single-photon emission computed tomography/computed tomography
situs ambiguous
technetium-99m-labeled red blood cells
The term “situs” means “position, site, and location.”[1] Situs solitus is the normal positioning of organs and vessels within the body. Situs inversus represents anatomic arrangement that is the mirror image of situs solitus. The condition which is called situs ambiguous or heterotaxy syndrome is less common, and it refers to visceral malposition and dismorphism. The two main subgroups of situs ambiguous are situs ambiguous with polysplenia and situs ambiguous with asplenia.[123] Although the cases are classified into two main groups, it should be remembered that this anomaly has no pathognomonic feature and a single description is not possible.[45] Multiple spleens of variable size and number, bilateral bilobar lungs, centrally located liver, and dextrocardia are the most common anomalies; also, the stomach may be right sided in up to 75% of children with polysplenia that are typically in the same side with stomach along the greater curvature as in our case.[26] [Figure 1] A segmental or individualized approach has been recommended with the use of specific anatomic labels for describing patients with heterotaxy syndrome to achieve the best clinical management knowing the clinical risks caused by malposition.[1] SSS is useful in characterizing an incidentally detected mass as functional splenic tissue.[789] It should be kept in mind that right-sided spleen tissue can mimic adrenal tumors and is more likely to be misdiagnosed as an adrenal tumor because of its growing in time, especially in children.[10] Although there are some studies in the literature using Tc-99m sulfur colloid in pediatric patients, damaged red blood cell (dRBC) scintigraphy is less commonly used in children because of its technical difficulties and special radiopharmaceutical preparation. However, dRBC has advantages over sulfur colloid in differential diagnosis due to its high specificity to splenic tissue.[911] Single-photon emission computed tomography/computed tomography gives valuable information if there are multiple or small lesions, where planar spleen scan images are inconclusive, especially in the presence of overlapping activity [Figure 2].


Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References
- Situs revisited: Imaging of the heterotaxy syndrome. Radiographics. 1999;19:837-52.
- [Google Scholar]
- Abdominal manifestations of situs anomalies in adults. Radiographics. 2002;22:1439-56.
- [Google Scholar]
- Extended hemi-hepatectomy with portal vein reconstruction in a patient with situs ambiguous. Case Rep Gastroenterol. 2008;2:76-82.
- [Google Scholar]
- Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer. Medicine (Baltimore). 2017;96:e8599.
- [Google Scholar]
- Two apparent suprarenal masses. Two cases in children: Heterotaxy syndrome with spleen lying in suprarenal space and gastric duplication cyst lying in suprarenal space. Pediatr Radiol. 2000;30:400-3.
- [Google Scholar]
- Procedure guideline for hepatic and splenic imaging. Society of nuclear medicine. J Nucl Med. 1998;39:1114-6.
- [Google Scholar]
- Right-sided spleen with partial situs inversus of the abdominal viscera: Visualization of the spleen by dynamic and static 99mTc-sulfur colloid imaging and 51Cr-labeled red blood cell sequestration imaging. Clin Nucl Med. 1979;4:425-6.
- [Google Scholar]
- Technetium-99m-sulfur colloid SPECT imaging in infants with suspected heterotaxy syndrome. J Nucl Med. 1995;36:1368-71.
- [Google Scholar]
- An unusual right-sided suprarenal accessory spleen misdiagnosed as an atypical pheochromocytoma. Urology. 2017;110:e1-e2.
- [Google Scholar]
