Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature

The adrenal gland is a common metastatic site of squamous cell carcinoma (SCC), however primary adrenal SCC has not been reported in literature. In this case report, we presented the first case of primary adrenal SCC. A 53-year-old man presented with chronic right flank pain. Abdominopelvic computed...

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Main Author: Mehdi Kardoust Parizi
Format: Article
Language:English
Published: Karolinum Press 2019-01-01
Series:Prague Medical Report
Subjects:
Online Access:https://pmr.lf1.cuni.cz/120/1/0024/
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spelling doaj-4fda1236d99245d58c0244abe3f096b22020-11-25T03:34:47ZengKarolinum PressPrague Medical Report1214-69942336-29362019-01-011201242910.14712/23362936.2019.8Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of LiteratureMehdi Kardoust Parizi0Department of Urology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, IranThe adrenal gland is a common metastatic site of squamous cell carcinoma (SCC), however primary adrenal SCC has not been reported in literature. In this case report, we presented the first case of primary adrenal SCC. A 53-year-old man presented with chronic right flank pain. Abdominopelvic computed tomography (CT) confirmed left kidney agenesis and a soft tissue density mass measuring about 40×30 mm in the right adrenal gland. Adrenal functional assessment including metanephrine, normetanephrine and vanillyl mandelic acid were normal. The patient underwent surgical resection of right adrenal mass. Pathology report revealed adrenal SCC. Immunohistochemistry evaluation demonstrated positive staining for P63, CK, CD10, CK7, chromogranin, neuron specific enolase, and negative staining for alpha-inhibin, neurofilament, CK20, and tyrosine hydroxylase that were compatible with SCC. All other assessments to find primary site of SCC including upper and lower gastro-intestinal endoscopy, chest CT scan, positron emission tomography scan, and bronchoscopy demonstrated normal findings. To our knowledge, this is the first case of primary adrenal SCC without any evidence of metastatic nature of such adrenal involvement by SCC.https://pmr.lf1.cuni.cz/120/1/0024/Squamous cell carcinomaAdrenalMalignancyAdrenalectomy
collection DOAJ
language English
format Article
sources DOAJ
author Mehdi Kardoust Parizi
spellingShingle Mehdi Kardoust Parizi
Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
Prague Medical Report
Squamous cell carcinoma
Adrenal
Malignancy
Adrenalectomy
author_facet Mehdi Kardoust Parizi
author_sort Mehdi Kardoust Parizi
title Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
title_short Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
title_full Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
title_fullStr Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
title_full_unstemmed Primary Adrenal Squamous Cell Carcinoma in a Single Kidney Patient: Case Report and Review of Literature
title_sort primary adrenal squamous cell carcinoma in a single kidney patient: case report and review of literature
publisher Karolinum Press
series Prague Medical Report
issn 1214-6994
2336-2936
publishDate 2019-01-01
description The adrenal gland is a common metastatic site of squamous cell carcinoma (SCC), however primary adrenal SCC has not been reported in literature. In this case report, we presented the first case of primary adrenal SCC. A 53-year-old man presented with chronic right flank pain. Abdominopelvic computed tomography (CT) confirmed left kidney agenesis and a soft tissue density mass measuring about 40×30 mm in the right adrenal gland. Adrenal functional assessment including metanephrine, normetanephrine and vanillyl mandelic acid were normal. The patient underwent surgical resection of right adrenal mass. Pathology report revealed adrenal SCC. Immunohistochemistry evaluation demonstrated positive staining for P63, CK, CD10, CK7, chromogranin, neuron specific enolase, and negative staining for alpha-inhibin, neurofilament, CK20, and tyrosine hydroxylase that were compatible with SCC. All other assessments to find primary site of SCC including upper and lower gastro-intestinal endoscopy, chest CT scan, positron emission tomography scan, and bronchoscopy demonstrated normal findings. To our knowledge, this is the first case of primary adrenal SCC without any evidence of metastatic nature of such adrenal involvement by SCC.
topic Squamous cell carcinoma
Adrenal
Malignancy
Adrenalectomy
url https://pmr.lf1.cuni.cz/120/1/0024/
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