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Incisional carcinoma of Mullerian Origin: A case report and review of literature

Primary incisional carcinoma (PIC) is a rare, delayed complication of surgery, usually attributed to the malignant transformation of endometriosis. We report a case of incisional carcinoma with nodal metastases in a 55-year-old woman, 18 years after cesarean section. She underwent extirpative surger...

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Autores principales: Bedell, Sabrina, Chang, Zenas, Burt, Cassaundra, Khalifa, Mahmoud A., Argenta, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262414/
https://www.ncbi.nlm.nih.gov/pubmed/32490125
http://dx.doi.org/10.1016/j.gore.2020.100588
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author Bedell, Sabrina
Chang, Zenas
Burt, Cassaundra
Khalifa, Mahmoud A.
Argenta, Peter A.
author_facet Bedell, Sabrina
Chang, Zenas
Burt, Cassaundra
Khalifa, Mahmoud A.
Argenta, Peter A.
author_sort Bedell, Sabrina
collection PubMed
description Primary incisional carcinoma (PIC) is a rare, delayed complication of surgery, usually attributed to the malignant transformation of endometriosis. We report a case of incisional carcinoma with nodal metastases in a 55-year-old woman, 18 years after cesarean section. She underwent extirpative surgery, including hysterectomy and bilateral salpingo-oophorectomy, without intraperitoneal disease identifed. Adjuvant treatment included sandwiched platinum-based chemotherapy (carboplatin and paclitaxel) and radiation. She remains disease-free 8 months after completing therapy. We identified 46 additional reported cases. Of these, >90% had undergone an “endometrium-exposing” surgery, most commonly cesarean section; while no cases followed adnexal-only surgery. The median time between antecedent surgery and presentation was 18 years. At presentation, tumors were often large (median 8 cm), and symptomatic with pain (63%) and/or mass (26%). Serum CA125 levels were commonly, albeit slightly, elevated (median 57U/ml (IQR 22–96, Range 6–1690)). Lymph node metastases were common (35%), with most following a vulvar-type spread pattern (inguinal first). Most patients (63%) were treated with chemotherapy +/− radiation. Approximately 50% of patients recurred promptly (median < 6 months), but long-term survival was reported following combined chemotherapy/radiation. Lymph node metastases portended a shorter disease-free interval, with 73% of cases recurring (median 5 months) despite chemotherapy-based treatment. These data suggest that some incisional carcinomas may result from displacement of healthy endometrium followed by delayed malignant transformation. Chemotherapy-only and radiation-only treatments are attended by modest prognosis. Taken together, these data suggest there is both need and potential avenues for improved prevention, detection, and treatment of this condition.
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spelling pubmed-72624142020-06-01 Incisional carcinoma of Mullerian Origin: A case report and review of literature Bedell, Sabrina Chang, Zenas Burt, Cassaundra Khalifa, Mahmoud A. Argenta, Peter A. Gynecol Oncol Rep Case Report Primary incisional carcinoma (PIC) is a rare, delayed complication of surgery, usually attributed to the malignant transformation of endometriosis. We report a case of incisional carcinoma with nodal metastases in a 55-year-old woman, 18 years after cesarean section. She underwent extirpative surgery, including hysterectomy and bilateral salpingo-oophorectomy, without intraperitoneal disease identifed. Adjuvant treatment included sandwiched platinum-based chemotherapy (carboplatin and paclitaxel) and radiation. She remains disease-free 8 months after completing therapy. We identified 46 additional reported cases. Of these, >90% had undergone an “endometrium-exposing” surgery, most commonly cesarean section; while no cases followed adnexal-only surgery. The median time between antecedent surgery and presentation was 18 years. At presentation, tumors were often large (median 8 cm), and symptomatic with pain (63%) and/or mass (26%). Serum CA125 levels were commonly, albeit slightly, elevated (median 57U/ml (IQR 22–96, Range 6–1690)). Lymph node metastases were common (35%), with most following a vulvar-type spread pattern (inguinal first). Most patients (63%) were treated with chemotherapy +/− radiation. Approximately 50% of patients recurred promptly (median < 6 months), but long-term survival was reported following combined chemotherapy/radiation. Lymph node metastases portended a shorter disease-free interval, with 73% of cases recurring (median 5 months) despite chemotherapy-based treatment. These data suggest that some incisional carcinomas may result from displacement of healthy endometrium followed by delayed malignant transformation. Chemotherapy-only and radiation-only treatments are attended by modest prognosis. Taken together, these data suggest there is both need and potential avenues for improved prevention, detection, and treatment of this condition. Elsevier 2020-05-22 /pmc/articles/PMC7262414/ /pubmed/32490125 http://dx.doi.org/10.1016/j.gore.2020.100588 Text en © 2020 Published by Elsevier Inc. 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 Case Report
Bedell, Sabrina
Chang, Zenas
Burt, Cassaundra
Khalifa, Mahmoud A.
Argenta, Peter A.
Incisional carcinoma of Mullerian Origin: A case report and review of literature
title Incisional carcinoma of Mullerian Origin: A case report and review of literature
title_full Incisional carcinoma of Mullerian Origin: A case report and review of literature
title_fullStr Incisional carcinoma of Mullerian Origin: A case report and review of literature
title_full_unstemmed Incisional carcinoma of Mullerian Origin: A case report and review of literature
title_short Incisional carcinoma of Mullerian Origin: A case report and review of literature
title_sort incisional carcinoma of mullerian origin: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262414/
https://www.ncbi.nlm.nih.gov/pubmed/32490125
http://dx.doi.org/10.1016/j.gore.2020.100588
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