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Paraurachal paraganglioma
INTRODUCTION: Paragangliomas (PGLs) are frequently reported around the abdominal aorta; however, are extremely rare near the urachus. CASE PRESENTATION: A 78‐year‐old woman was referred to the urology department of our hospital for further examination and treatment of a 1.2‐cm tumor in the lower abd...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436662/ https://www.ncbi.nlm.nih.gov/pubmed/36090947 http://dx.doi.org/10.1002/iju5.12488 |
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author | Tsuruta, Masafumi Goto, Takayuki Kono, Jin Kita, Yuki Masui, Kimihiko Sano, Takeshi Fujimoto, Masakazu Sawada, Atsuro Akamatsu, Shusuke Kobayashi, Takashi |
author_facet | Tsuruta, Masafumi Goto, Takayuki Kono, Jin Kita, Yuki Masui, Kimihiko Sano, Takeshi Fujimoto, Masakazu Sawada, Atsuro Akamatsu, Shusuke Kobayashi, Takashi |
author_sort | Tsuruta, Masafumi |
collection | PubMed |
description | INTRODUCTION: Paragangliomas (PGLs) are frequently reported around the abdominal aorta; however, are extremely rare near the urachus. CASE PRESENTATION: A 78‐year‐old woman was referred to the urology department of our hospital for further examination and treatment of a 1.2‐cm tumor in the lower abdominal wall, a tumor excision was then performed. On immunohistochemical staining, the tumor and supporting cells were positive for chromogranin A and the S 100 protein, respectively, and were diagnosed as PGL. The PGL was thought to be derived from chromaffin cells that migrated to the wall of the urachus during embryonic life and remained even after the wall regressed. CONCLUSION: We report a case of PGL near the urachus that can be explained by the distribution of the sympathetic network around the midline of the lower abdominal wall during embryonic development. Therefore, PGL should be considered in the differential diagnosis of periurachal tumors. |
format | Online Article Text |
id | pubmed-9436662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94366622022-09-09 Paraurachal paraganglioma Tsuruta, Masafumi Goto, Takayuki Kono, Jin Kita, Yuki Masui, Kimihiko Sano, Takeshi Fujimoto, Masakazu Sawada, Atsuro Akamatsu, Shusuke Kobayashi, Takashi IJU Case Rep Case Reports INTRODUCTION: Paragangliomas (PGLs) are frequently reported around the abdominal aorta; however, are extremely rare near the urachus. CASE PRESENTATION: A 78‐year‐old woman was referred to the urology department of our hospital for further examination and treatment of a 1.2‐cm tumor in the lower abdominal wall, a tumor excision was then performed. On immunohistochemical staining, the tumor and supporting cells were positive for chromogranin A and the S 100 protein, respectively, and were diagnosed as PGL. The PGL was thought to be derived from chromaffin cells that migrated to the wall of the urachus during embryonic life and remained even after the wall regressed. CONCLUSION: We report a case of PGL near the urachus that can be explained by the distribution of the sympathetic network around the midline of the lower abdominal wall during embryonic development. Therefore, PGL should be considered in the differential diagnosis of periurachal tumors. John Wiley and Sons Inc. 2022-05-31 /pmc/articles/PMC9436662/ /pubmed/36090947 http://dx.doi.org/10.1002/iju5.12488 Text en © 2022 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Tsuruta, Masafumi Goto, Takayuki Kono, Jin Kita, Yuki Masui, Kimihiko Sano, Takeshi Fujimoto, Masakazu Sawada, Atsuro Akamatsu, Shusuke Kobayashi, Takashi Paraurachal paraganglioma |
title | Paraurachal paraganglioma |
title_full | Paraurachal paraganglioma |
title_fullStr | Paraurachal paraganglioma |
title_full_unstemmed | Paraurachal paraganglioma |
title_short | Paraurachal paraganglioma |
title_sort | paraurachal paraganglioma |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436662/ https://www.ncbi.nlm.nih.gov/pubmed/36090947 http://dx.doi.org/10.1002/iju5.12488 |
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