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A rare case of spontaneous rupture of epithelioid angiomyolipoma

A male patient, 40 years of age, arrived at our Institute with diffuse abdominal tenderness, right flank pain, hematuria and early stage of hemorrhagic shock with anemia and initial hypotension. The immediate clinical history revealed no significant previous trauma, only subsequently was reported in...

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Autores principales: Benincasa, Alfonso, Pinto, Angelo, Lamberti, Francesco, Fristachi, Raffaele, Della Pepa, Chiara, Benincasa, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024590/
https://www.ncbi.nlm.nih.gov/pubmed/33850730
http://dx.doi.org/10.1016/j.eucr.2021.101645
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author Benincasa, Alfonso
Pinto, Angelo
Lamberti, Francesco
Fristachi, Raffaele
Della Pepa, Chiara
Benincasa, Giuseppe
author_facet Benincasa, Alfonso
Pinto, Angelo
Lamberti, Francesco
Fristachi, Raffaele
Della Pepa, Chiara
Benincasa, Giuseppe
author_sort Benincasa, Alfonso
collection PubMed
description A male patient, 40 years of age, arrived at our Institute with diffuse abdominal tenderness, right flank pain, hematuria and early stage of hemorrhagic shock with anemia and initial hypotension. The immediate clinical history revealed no significant previous trauma, only subsequently was reported inconstant pain in the right flank for 4–5 days with pallor and asthenia, signs and symptoms that the patient had not investigated. Abdominal CT scan with angiographic evaluation was performed showing right kidney mass and perirenal fluid collection by blood component. Immediate nephrectomy was performed and histopathological and further immunohistochemical study, revealed the epithelioid variant of angiomyolipoma.
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spelling pubmed-80245902021-04-12 A rare case of spontaneous rupture of epithelioid angiomyolipoma Benincasa, Alfonso Pinto, Angelo Lamberti, Francesco Fristachi, Raffaele Della Pepa, Chiara Benincasa, Giuseppe Urol Case Rep Oncology A male patient, 40 years of age, arrived at our Institute with diffuse abdominal tenderness, right flank pain, hematuria and early stage of hemorrhagic shock with anemia and initial hypotension. The immediate clinical history revealed no significant previous trauma, only subsequently was reported inconstant pain in the right flank for 4–5 days with pallor and asthenia, signs and symptoms that the patient had not investigated. Abdominal CT scan with angiographic evaluation was performed showing right kidney mass and perirenal fluid collection by blood component. Immediate nephrectomy was performed and histopathological and further immunohistochemical study, revealed the epithelioid variant of angiomyolipoma. Elsevier 2021-03-19 /pmc/articles/PMC8024590/ /pubmed/33850730 http://dx.doi.org/10.1016/j.eucr.2021.101645 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Benincasa, Alfonso
Pinto, Angelo
Lamberti, Francesco
Fristachi, Raffaele
Della Pepa, Chiara
Benincasa, Giuseppe
A rare case of spontaneous rupture of epithelioid angiomyolipoma
title A rare case of spontaneous rupture of epithelioid angiomyolipoma
title_full A rare case of spontaneous rupture of epithelioid angiomyolipoma
title_fullStr A rare case of spontaneous rupture of epithelioid angiomyolipoma
title_full_unstemmed A rare case of spontaneous rupture of epithelioid angiomyolipoma
title_short A rare case of spontaneous rupture of epithelioid angiomyolipoma
title_sort rare case of spontaneous rupture of epithelioid angiomyolipoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024590/
https://www.ncbi.nlm.nih.gov/pubmed/33850730
http://dx.doi.org/10.1016/j.eucr.2021.101645
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