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Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report

Splenic metastasis is generally not a common clinical event. However, metastasis to the spleen from adrenal pheochromocytoma is extremely rare and has not been reported in literature. This report presents a case of a 58 year-old male patient who developed spleen-only metastases in July 2007. The pat...

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Autor principal: Duan, Xiao-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719189/
https://www.ncbi.nlm.nih.gov/pubmed/23882428
http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.009
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author Duan, Xiao-Feng
author_facet Duan, Xiao-Feng
author_sort Duan, Xiao-Feng
collection PubMed
description Splenic metastasis is generally not a common clinical event. However, metastasis to the spleen from adrenal pheochromocytoma is extremely rare and has not been reported in literature. This report presents a case of a 58 year-old male patient who developed spleen-only metastases in July 2007. The patient had a previous history of left epinephroectomy for adrenal pheochromocytoma in January 2003. Abdominal computed tomography demonstrated multiple enhancing lesions suggestive of metastases; thus splenectomy was performed. Pathological examinations confirmed the diagnosis of splenic metastases from pheochromocytoma. The patient was alive without recurrence 48 months after splenectomy. This study is the first report on splenic metastasis from previous adrenal pheochromocytoma, and long-term survival was achieved by splenectomy. A history of malignancy indicates a high index of suspicion for splenic metastasis, and long-term survival can be achieved by splenectomy for spleen-only metastasis.
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spelling pubmed-37191892013-07-23 Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report Duan, Xiao-Feng Cancer Biol Med Case Report Splenic metastasis is generally not a common clinical event. However, metastasis to the spleen from adrenal pheochromocytoma is extremely rare and has not been reported in literature. This report presents a case of a 58 year-old male patient who developed spleen-only metastases in July 2007. The patient had a previous history of left epinephroectomy for adrenal pheochromocytoma in January 2003. Abdominal computed tomography demonstrated multiple enhancing lesions suggestive of metastases; thus splenectomy was performed. Pathological examinations confirmed the diagnosis of splenic metastases from pheochromocytoma. The patient was alive without recurrence 48 months after splenectomy. This study is the first report on splenic metastasis from previous adrenal pheochromocytoma, and long-term survival was achieved by splenectomy. A history of malignancy indicates a high index of suspicion for splenic metastasis, and long-term survival can be achieved by splenectomy for spleen-only metastasis. Chinese Anti-Cancer Association 2013-06 /pmc/articles/PMC3719189/ /pubmed/23882428 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.009 Text en 2013 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Duan, Xiao-Feng
Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title_full Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title_fullStr Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title_full_unstemmed Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title_short Splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
title_sort splenectomy for splenic metastases from malignant adrenal pheochromocytoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719189/
https://www.ncbi.nlm.nih.gov/pubmed/23882428
http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.009
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