Teratoma involving adrenal gland – A case report and review of literature

Author:

Ban Amit1,Satapara Jay1,Rathod Ketan1,Bahri Nandini1

Affiliation:

1. Department of Radiodiagnosis, Shri M.P. Shah Government Medical College and Shri Gurugobind Singh Government Hospital, P.N. Marg, Jamnagar, Gujarat, India

Abstract

AbstractTeratomas are germ cell tumors which are mainly gonadal in origin. Other common extra-gonadal sites are mediastinal, sacro-coccygeal and pineal regions. Adrenal teratomas are extremely rare and primary adrenal teratomas are even rarer. We reported a case of primary adrenal teratoma in a 60-year-old male. We reviewed literature from 2000 to till date, and found 29 adult cases and 6 paediatric cases of adrenal teratoma. Usually, they are asymptomatic and identified as an incidental finding. Imaging modality such as USG, CT and MRI are useful in diagnosis. Though these tumors are mostly benign, malignant transformation may occur. Treatment includes surgical removal.

Publisher

Georg Thieme Verlag KG

Subject

Radiology Nuclear Medicine and imaging

Reference38 articles.

1. Non-functioning adrenal masses: Incidental discovery on computed tomography;H S Glazer;Am J Roentgenol,1982

2. Primary adrenal teratoma: A case series and review of the literature;L Zhou;Mol Clin Oncol,2018

3. Primary adrenal teratoma: An unusual tumor-Challenges in diagnosis and surgical management;P Ramakant;J Postgrad Med,2018

4. Malignant transformation of a mature teratoma of the adrenal gland: A rare case report and literature review;M Niu;Medicine (Baltimore),2017

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