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Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology

Incisional endometriosis (IE) is a rare entity reported in 0.03–1.08% of women following obstetric or gynecologic surgeries. Most cases reported in literature have appeared after cesarean sections and were often clinically mistaken for hernia, abscess, suture granuloma or lipoma. We hereby report a...

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Detalles Bibliográficos
Autores principales: Veda, P, Srinivasaiah, M
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040086/
https://www.ncbi.nlm.nih.gov/pubmed/21346911
http://dx.doi.org/10.4103/0974-2727.72216
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author Veda, P
Srinivasaiah, M
author_facet Veda, P
Srinivasaiah, M
author_sort Veda, P
collection PubMed
description Incisional endometriosis (IE) is a rare entity reported in 0.03–1.08% of women following obstetric or gynecologic surgeries. Most cases reported in literature have appeared after cesarean sections and were often clinically mistaken for hernia, abscess, suture granuloma or lipoma. We hereby report a case of IE following a second trimester hysterotomy, which was diagnosed by fine needle aspiration cytology (FNAC). Our patient was 26 years old, presenting with a mass over anterior abdominal wall, associated with incapacitating pain during each menstrual cycle. FNAC showed epithelial cells, stromal cells and hemosiderin laden macrophages. Based on the typical history, clinical and cytological features, the diagnosis of IE was established. Wide surgical excision was done and the resulting rectus sheath defect was repaired. Patient was followed for 6 months during which time she was symptom free. This article also reviews the spectrum of cytological features and the rare possibility of malignant transformation that can occur in IE.
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spelling pubmed-30400862011-02-23 Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology Veda, P Srinivasaiah, M J Lab Physicians Case Report Incisional endometriosis (IE) is a rare entity reported in 0.03–1.08% of women following obstetric or gynecologic surgeries. Most cases reported in literature have appeared after cesarean sections and were often clinically mistaken for hernia, abscess, suture granuloma or lipoma. We hereby report a case of IE following a second trimester hysterotomy, which was diagnosed by fine needle aspiration cytology (FNAC). Our patient was 26 years old, presenting with a mass over anterior abdominal wall, associated with incapacitating pain during each menstrual cycle. FNAC showed epithelial cells, stromal cells and hemosiderin laden macrophages. Based on the typical history, clinical and cytological features, the diagnosis of IE was established. Wide surgical excision was done and the resulting rectus sheath defect was repaired. Patient was followed for 6 months during which time she was symptom free. This article also reviews the spectrum of cytological features and the rare possibility of malignant transformation that can occur in IE. Medknow Publications 2010 /pmc/articles/PMC3040086/ /pubmed/21346911 http://dx.doi.org/10.4103/0974-2727.72216 Text en © Journal of Laboratory Physicians http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Veda, P
Srinivasaiah, M
Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title_full Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title_fullStr Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title_full_unstemmed Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title_short Incisional Endometriosis: Diagnosed by Fine Needle Aspiration Cytology
title_sort incisional endometriosis: diagnosed by fine needle aspiration cytology
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040086/
https://www.ncbi.nlm.nih.gov/pubmed/21346911
http://dx.doi.org/10.4103/0974-2727.72216
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