J Korean Soc Radiol.  2017 Sep;77(3):187-191. 10.3348/jksr.2017.77.3.187.

Primary Presacral Neuroendocrine Tumor: A Case Report and Review of MRI Findings

Affiliations
  • 1Department of Radiology, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea. leenk77@hanmail.net
  • 2Department of Pathology, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea.
  • 3Department of Obstetrics and Gynecology, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea.

Abstract

Primary presacral neuroendocrine tumor (NET) is extremely rare. Furthermore, its preoperative diagnosis is very difficult, and its imaging characteristics are not well described. We report the case of a 70-year-old female with presacral NET, and describe its imaging features on diffusion-weighted magnetic resonance imaging.


MeSH Terms

Aged
Diagnosis
Diffusion Magnetic Resonance Imaging
Female
Humans
Magnetic Resonance Imaging*
Neuroendocrine Tumors*
Sacrum

Figure

  • Fig. 1 A 70-year-old woman presented with primary presacral neuroendocrine tumor. A. Contrast-enhanced CT reveals an 8 cm-sized presacral mass (arrow) which abutted the sacrum without bony erosion or destruction. The mass is well-defined, solid with heterogeneous enhancement and it shows internal cystic degeneration and calcification. B. Sagittal T2-weighted image (left) shows a presacral mass with pressure erosion and bone marrow change (arrow) in the sacrum. The mass shows heterogeneous intermediate signal intensity on T2-weighted image (left), hypointensity on T1-weighted image (middle), and avid enhancement on contrast-enhanced T1-weighted image (right). Focal hyperintense foci (arrowheads) within the mass are noted on T1- and T2-weighted images. C. The tumor exhibits hyperintensity on diffusion-weighted image (left) at a b value of 1000 s/mm2 with a low apparent diffusion coefficient (ADC) value (mean, 0.632 × 10−3 mm2/sec) on the ADC map (right). D. Photomicrograph of the tumor cells (left, hematoxylin and eosin stain, × 200) shows an infiltrative border in the background of fibrotic stroma. Tumor shows monomorphic, plasmacytoid neuroendocrine cells, with insular, solid and trabecular growth patterns. Immunohistochemical examinations show approximately 15% increase in the Ki-67 labeling index (middle, × 400) and positivity for synaptophysin (right, × 200). E. Positron emission tomography-CT shows multiple pulmonary nodules, which are suspicious for metastasis.


Reference

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