a case report of bilateral adrenal sarcomatoid carcinoma

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ID: 250873
2016
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Abstract
Adrenocortical carcinoma (ACC) is a rare and aggressive malignancy. Sarcomatoid adrenal carcinoma is even more aggressive type of ACC. Bilateral malignant adrenal tumors are extremely rare except for those that represent metastasis from an extra-adrenal organ. Here we report a 53-year-old woman who presented with abdominal pain and weight loss. Abdominal computed tomography revealed bilateral adrenal masses and a mass in her liver. Surgical specimens showed pleomorphic tumor cells with epithelial and spindle cell morphology and immunohistochemical staining was compatible with sarcomatoid carcinoma. Sarcomatoid adrenal carcinoma should be kept in mind during the management of bilateral adrenal masses.
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iyidir2016casea Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Ozlem Turhan Iyidir;Ethem Turgay Cerit;Çiğdem Özkan;Eroğlu Altınova;Ali Rıza Çimen;Sinan Sözen;Mustafa Kerem;Müjde Aktürk;Leyla Memiş;Baloş Törüner;Nuri Çakır;Metin Arslan
Journal Polymers
Year 2016
DOI
10.1155/2016/3768258
URL
http://dx.doi.org/10.1155/2016/3768258
Keywords
surgery

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