scholarly journals A Rare Case of Adenomatoid Tumor of the Adrenal Gland

2013 ◽  
Vol 74 (11) ◽  
pp. 3201-3205
Author(s):  
Masahiro SHIBATA ◽  
Yatsuka HIBI ◽  
Kimio OGAWA ◽  
Yoshimi SHIMIZU ◽  
Chikara KAGAWA ◽  
...  
Keyword(s):  
Adrenal Gland ◽  
Rare Case ◽  
Adenomatoid Tumor

scholarly journals Adenomatoid tumor of adrenal gland: A rare case report

2013 ◽  
Vol 56 (3) ◽  
pp. 319 ◽  
Author(s):  
Sheng Zhang ◽  
SanYan Li ◽  
Xingfu Wang
Keyword(s):  
Case Report ◽  
Adrenal Gland ◽  
Rare Case ◽  
Adenomatoid Tumor ◽  
Rare Case Report

18F-FDG PET/CT of a Rare Case of an Adenomatoid Tumor of the Adrenal Gland

2020 ◽  
Vol 45 (7) ◽  
pp. e331-e333
Author(s):  
Matthieu Dietz ◽  
Sophie Neyrand ◽  
Anthony Dhomps ◽  
Myriam Decaussin-Petrucci ◽  
Jeremie Tordo
Keyword(s):  
Adrenal Gland ◽  
Fdg Pet ◽  
Rare Case ◽  
Adenomatoid Tumor ◽  
Pet Ct ◽  
18F Fdg ◽  
Fdg Pet Ct

Cystic lymphangioma-like adenomatoid tumor of the adrenal gland: report a rare case from Lao PDR

Pathology ◽  
2014 ◽  
Vol 46 ◽  
pp. S72
Author(s):  
Thitsamay Luangxay ◽  
Bounleuang Kousonh ◽  
Phetsamone Arounlangsy ◽  
Phaengvilay Xaysomphet ◽  
Prawat Nitiyanant ◽  
...  
Keyword(s):  
Adrenal Gland ◽  
Rare Case ◽  
Lao Pdr ◽  
Cystic Lymphangioma ◽  
Adenomatoid Tumor

scholarly journals Isolated hydatid cyst of adrenal gland with hypertension mimicking Conn's syndrome: a very rare case

2016 ◽  
pp. 3071-3073 ◽  
Author(s):  
Tarun Chaudhary ◽  
Shikhar Agrawal ◽  
Manoj Biswas ◽  
Rajeev Sarpal ◽  
Nadia Shirazi
Keyword(s):  
Adrenal Gland ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Conn’S Syndrome

scholarly journals A Case Report of Adenomatoid Tumor of the Adrenal Gland Mimicking an Adrenal Metastasis from Sigmoid Colon Cancer

2010 ◽  
Vol 43 (4) ◽  
pp. 472-478
Author(s):  
Akio Shiomi ◽  
Yusuke Kinugasa ◽  
Syuji Saito ◽  
Yousuke Hashimoto ◽  
Hiroyuki Tomioka ◽  
...  
Keyword(s):  
Colon Cancer ◽  
Case Report ◽  
Adrenal Gland ◽  
Sigmoid Colon ◽  
Adrenal Metastasis ◽  
Sigmoid Colon Cancer ◽  
Adenomatoid Tumor

Composite Adenomatoid Tumor and Myelolipoma of Adrenal Gland: Report of 2 Cases

2008 ◽  
Vol 132 (2) ◽  
pp. 265-267
Author(s):  
Elizabeth R. Timonera ◽  
Maria Emilia Paiva ◽  
Jose Manuel Lopes ◽  
Catarina Eloy ◽  
Theodore van der Kwast ◽  
...  
Keyword(s):  
Adrenal Gland ◽  
Incidental Findings ◽  
Adrenal Glands ◽  
Adenomatoid Tumor

Abstract Adenomatoid tumor and myelolipoma are benign, hormonally inactive tumors that are often incidental findings in the adrenal glands. Myelolipoma is more common than adenomatoid tumor in this location but both are rare, and as yet, the pathogenesis of both remains unclear. We report 2 cases of composite adenomatoid tumor and myelolipoma, incidentally found in the adrenal gland on investigation for other diseases. To our knowledge, composite adenomatoid tumor and myelolipoma of adrenal gland has not been previously reported.

scholarly journals Sarcomatoid carcinoma of adrenal gland: a rare case report

2019 ◽  
Vol 10 (1) ◽  
pp. 73-75
Author(s):  
Israt Rezwana ◽  
Sourav Sarkar ◽  
Rushda Sharmin Binte Rouf ◽  
Sultana Marufa Shefin ◽  
SM Ashrafuzzaman
Keyword(s):  
Adrenal Gland ◽  
Rare Case ◽  
Adrenal Glands ◽  
Malignant Tumors ◽  
Sarcomatoid Carcinoma ◽  
Endocrine Dysfunction ◽  
Diagnostic Challenge ◽  
Atypical Symptoms ◽  
Rare Case Report ◽  
New Onset

Adrenal sarcomatoid carcinoma (ASC) are very rare and aggressive malignant tumors of adrenal glands containing both epithelial (carcinomatous) and mesenchymal (sarcomatous) components. ASC presents a diagnostic challenge due to its atypical symptoms and histological patterns which influence treatment.At the time of diagnosis, a large percentage of patients are already at the metastatic stage and succumb within a few months. Here, we report a case of functional sarcomatoid carcinoma in right adrenal gland in a 37-year-old female, who presented with new onset hypertension. The patient underwent right sided adrenalectomy and she was alive at the time of writing the current report.To the best of our knowledge, ASC reported in literature to date showed only few patient presented with endocrine hypersecretion and only one patient presented with both hypertension and endocrine dysfunction. So, our case is the rarest among the rare. Birdem Med J 2020; 10(1): 73-75

Cystic Lymphangioma-like Adenomatoid Tumor of the Adrenal Gland: Case Presentation and Review of the Literature

2009 ◽  
Vol 16 (6) ◽  
pp. 424-432 ◽  
Author(s):  
Michele Bisceglia ◽  
Illuminato Carosi ◽  
Alfredo Scillitani ◽  
Gianandrea Pasquinelli
Keyword(s):  
Adrenal Gland ◽  
Cystic Lymphangioma ◽  
Adenomatoid Tumor ◽  
Review Of The Literature ◽  
Case Presentation

scholarly journals Adenomatoid tumor of the adrenal gland mimicking an echinococcus cyst of the liver – A case report

2008 ◽  
Vol 6 (6) ◽  
pp. 485-487 ◽  
Author(s):  
Martin Hoffmann ◽  
Süleyman Yedibela ◽  
Arno Dimmler ◽  
Werner Hohenberger ◽  
Thomas Meyer
Keyword(s):  
Case Report ◽  
Adrenal Gland ◽  
Adenomatoid Tumor ◽  
Echinococcus Cyst
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