Clinics and Practice (Mar 2014)

Primary adrenal sarcomatoid carcinoma

  • Aftab S. Shaikh,
  • Girish D. Bakhshi,
  • Arshad S. Khan,
  • Nilofar M. Jamadar,
  • Aravind Kotresh Nirmala,
  • Arif Ahmed Raza

DOI
https://doi.org/10.4081/cp.2014.604
Journal volume & issue
Vol. 4, no. 1

Abstract

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Adrenal sarcomatoid carcinomas are extremely rare tumors presenting with extensive locoregional spread at the time of diagnosis. Patients succumb to metastases within a couple of months. As a result, very few cases are reported in the literature until now. We present a case of a 62-year old female with non-functional sarcomatoid carcinoma of the right adrenal gland. There was no radiological evidence of locoregional metastases. Patient underwent right adrenalectomy. Follow up after 3 months showed para-aortic lymphadenopathy and similar left adrenal mass on computed tomography. Patient refused further treatment and succumbed to the disease. A brief case report with review of literature is presented.

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