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Abdominal wall endometriosis (AWE): Two case reports and literature review

INTRODUCTION AND IMPORTANCE: Endometriosis is one of the most frequent gynecologic disorders, clinically confirmed or suspected in one of nine women by the age of 44 years. Its location of occurrence can be classified into intra and extra pelvic. Abdominal wall endometriosis (AWE) is one of its rare...

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Autores principales: Christina, Natalia Maria, Candrawinata, Valeska Siulinda, Lie, Hendry, Godam, Kezia Imanuella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384551/
https://www.ncbi.nlm.nih.gov/pubmed/37459697
http://dx.doi.org/10.1016/j.ijscr.2023.108495
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author Christina, Natalia Maria
Candrawinata, Valeska Siulinda
Lie, Hendry
Godam, Kezia Imanuella
author_facet Christina, Natalia Maria
Candrawinata, Valeska Siulinda
Lie, Hendry
Godam, Kezia Imanuella
author_sort Christina, Natalia Maria
collection PubMed
description INTRODUCTION AND IMPORTANCE: Endometriosis is one of the most frequent gynecologic disorders, clinically confirmed or suspected in one of nine women by the age of 44 years. Its location of occurrence can be classified into intra and extra pelvic. Abdominal wall endometriosis (AWE) is one of its rare location, with frequency of 0.04 to 5.5 %. Furthermore there are only a few cases of AWE in Indonesia that have been reported. CASE PRESENTATION: Here we present two Indonesian patients at a General Hospital in Tangerang, Indonesia. The first patient, 26 years old, complained of an umbilical mass 2 years after caesarean section. The second patient, 36 years old, complained of an umbilical mass since 8 months, with no history of prior surgery. Both patients had pre-operative ultrasonography (US) and underwent wide local excision. Histopathology examination with presence of endometrial glandular components and endometrial-like stroma confirmed the diagnosis of AWE. CLINICAL DISCUSSION: AWE is defined as any endometrial tissue found superficial to the peritoneum, locating most commonly at umbilical, inguinal area, and anterior abdominal wall. Pre-operative diagnostic tools include abdominal ultrasonography (US) or abdominopelvic computed tomography (CT) scan. Since treatment with medications is usually not effective, surgical treatment is recommended, along with confirmation by histopathological examination. CONCLUSION: Diagnosis of AWE should be suspected in all women with symptoms of an abdominal mass and cyclic pain, especially if the patient had history of surgery at the abdominal region. AWE is quite rare, but its symptoms can affect quality of life. Hence, a multi-disciplinary approach is necessary, with the strongly recommended treatment of wide local excision to prevent recurrence and malignant transformation.
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spelling pubmed-103845512023-07-30 Abdominal wall endometriosis (AWE): Two case reports and literature review Christina, Natalia Maria Candrawinata, Valeska Siulinda Lie, Hendry Godam, Kezia Imanuella Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Endometriosis is one of the most frequent gynecologic disorders, clinically confirmed or suspected in one of nine women by the age of 44 years. Its location of occurrence can be classified into intra and extra pelvic. Abdominal wall endometriosis (AWE) is one of its rare location, with frequency of 0.04 to 5.5 %. Furthermore there are only a few cases of AWE in Indonesia that have been reported. CASE PRESENTATION: Here we present two Indonesian patients at a General Hospital in Tangerang, Indonesia. The first patient, 26 years old, complained of an umbilical mass 2 years after caesarean section. The second patient, 36 years old, complained of an umbilical mass since 8 months, with no history of prior surgery. Both patients had pre-operative ultrasonography (US) and underwent wide local excision. Histopathology examination with presence of endometrial glandular components and endometrial-like stroma confirmed the diagnosis of AWE. CLINICAL DISCUSSION: AWE is defined as any endometrial tissue found superficial to the peritoneum, locating most commonly at umbilical, inguinal area, and anterior abdominal wall. Pre-operative diagnostic tools include abdominal ultrasonography (US) or abdominopelvic computed tomography (CT) scan. Since treatment with medications is usually not effective, surgical treatment is recommended, along with confirmation by histopathological examination. CONCLUSION: Diagnosis of AWE should be suspected in all women with symptoms of an abdominal mass and cyclic pain, especially if the patient had history of surgery at the abdominal region. AWE is quite rare, but its symptoms can affect quality of life. Hence, a multi-disciplinary approach is necessary, with the strongly recommended treatment of wide local excision to prevent recurrence and malignant transformation. Elsevier 2023-07-14 /pmc/articles/PMC10384551/ /pubmed/37459697 http://dx.doi.org/10.1016/j.ijscr.2023.108495 Text en © 2023 The Authors. Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Christina, Natalia Maria
Candrawinata, Valeska Siulinda
Lie, Hendry
Godam, Kezia Imanuella
Abdominal wall endometriosis (AWE): Two case reports and literature review
title Abdominal wall endometriosis (AWE): Two case reports and literature review
title_full Abdominal wall endometriosis (AWE): Two case reports and literature review
title_fullStr Abdominal wall endometriosis (AWE): Two case reports and literature review
title_full_unstemmed Abdominal wall endometriosis (AWE): Two case reports and literature review
title_short Abdominal wall endometriosis (AWE): Two case reports and literature review
title_sort abdominal wall endometriosis (awe): two case reports and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384551/
https://www.ncbi.nlm.nih.gov/pubmed/37459697
http://dx.doi.org/10.1016/j.ijscr.2023.108495
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