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Case Report
26 (
2
); 107-108
doi:
10.4103/0972-3919.90265

A rare case of mature teratoma. Has FDG PET/CT a role to play?

Department of Nuclear Medicine, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh, India
Department of Radiology, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh, India
Department of Surgical Oncology, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh, India
Department of Pathology, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh, India
Department of Medical Oncology, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh, India

Address for correspondence: Dr. Tushar Mohapatra, 2nd floor, B Block, Yashoda Hospital, Somajiguda, Hyderabad, Andhra Pradesh-500 082, India. E-mail: drtushar04@yahoo.co.in

Licence

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Disclaimer:
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Authors describe a very rare case of mature teratoma with malignant transformation, preoperatively suggested by FDG PET/CT study. So the role of CT component in elucidating three embryonal components and hypermetabolism evident on PET part suggesting possible malignant transformation makes PET/CT a valuable modality in evaluation of these rare tumors

Keywords

Computed tomography
FDG PET/CT
teratoma

INTRODUCTION

Mature cystic teratomas account for 10-20% of all ovarian neoplasms and peak incidence in most series is age 20-40 years.[1] They are the most common ovarian germ cell tumor and also the most common ovarian neoplasm in patients younger than 20 years. In approximately 0.2-2% of cases, it may undergo malignant transformation, the majority of which are squamous cell carcinomas.[2] Mature cystic teratomas of the ovary are often discovered as incidental findings and malignancy is often discovered intraoperatively due to presence of nodal disease or on histopathology, after which a proper staging is usually necessary. There is also risk of future recurrence due to intraoperative spillage if malignancy is not known prior to surgery.[3] So a FDG PET/CT study has a role in diagnosis, predicting malignant transformation and preoperative staging. One of important differential diagnosis is intense tracer activity in the well differentiated neuronal component which is highly metabolically active similar to normal brain parenchyma.[4]

CASE REPORT AND IMAGE DESCRIPTION

A 60 year lady presented with abdominal mass underwent PET/CT study as part of the presurgical evaluation. CT scan shows a large abdominal mass arising from the left adnexa, with areas of focal soft tissue densities in the peripheral sheath of a mixed fluid/fat attenuation [Figure 1]. FDG metabolism appears significantly high in the solid components with a SUVmax of 35.18 [Figure 2]. Gross specimen shows embryonal components including hair [Figure 3]. H and E stained section high power (40×) - sheets of polygonal cells with marked neclear pleomorphism, hyperchromasia and abundant eosinophilic cytoplasm. Individual cell keratinization is evident [Figure 4].

A 60 year lady presented with abdominal mass underwent PET/CT study as part of the presurgical evaluation. CT scan shows a large abdominal mass arising from the left adnexa, with areas of focal soft tissue densities in the peripheral sheath of a mixed fluid/fat attenuation
Figure 1 A 60 year lady presented with abdominal mass underwent PET/CT study as part of the presurgical evaluation. CT scan shows a large abdominal mass arising from the left adnexa, with areas of focal soft tissue densities in the peripheral sheath of a mixed fluid/fat attenuation
FDG metabolism appears significantly high in the solid components with a SUVmax of 35.18
Figure 2 FDG metabolism appears significantly high in the solid components with a SUVmax of 35.18
Gross specimen shows embryonal components including hair
Figure 3 Gross specimen shows embryonal components including hair
H and E stained section high power (40×) - sheets of polygonal cells with marked neclear pleomorphism, hyperchromasia and abundant eosinophilic cytoplasm. Individual cell keratinization is evident
Figure 4 H and E stained section high power (40×) - sheets of polygonal cells with marked neclear pleomorphism, hyperchromasia and abundant eosinophilic cytoplasm. Individual cell keratinization is evident

Source of Support: Nil.

Conflict of Interest: None declared.

REFERENCES

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