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Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature

RATIONALE: PNETs (primitive neuroectodermal tumors) are a family of highly malignant neoplasms characterized by small round cells of neuroepithelial origin. They usually involve bone and soft tissues, and have a higher incidence in childhood. PATIENT CONCERNS: In this case report, we describe the ob...

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Autores principales: De Nola, Rosalba, Di Naro, Edoardo, Schonauer, Luca Maria, Lucarelli, Giuseppe, Battaglia, Michele, Fiore, Maria Grazia, Mastrolia, Salvatore Andrea, Loverro, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943895/
https://www.ncbi.nlm.nih.gov/pubmed/29480840
http://dx.doi.org/10.1097/MD.0000000000009505
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author De Nola, Rosalba
Di Naro, Edoardo
Schonauer, Luca Maria
Lucarelli, Giuseppe
Battaglia, Michele
Fiore, Maria Grazia
Mastrolia, Salvatore Andrea
Loverro, Giuseppe
author_facet De Nola, Rosalba
Di Naro, Edoardo
Schonauer, Luca Maria
Lucarelli, Giuseppe
Battaglia, Michele
Fiore, Maria Grazia
Mastrolia, Salvatore Andrea
Loverro, Giuseppe
author_sort De Nola, Rosalba
collection PubMed
description RATIONALE: PNETs (primitive neuroectodermal tumors) are a family of highly malignant neoplasms characterized by small round cells of neuroepithelial origin. They usually involve bone and soft tissues, and have a higher incidence in childhood. PATIENT CONCERNS: In this case report, we describe the obstetric and oncological outcome of a huge mass diagnosed as a leiomyoma in a 39-year-old pregnant woman who complained of low back pain, dysuria, and urinary frequency at 22 weeks of gestation. DIAGNOSES: During the 25th week of pregnancy, the patient was referred to our hospital at night with severe anemia and suspected hemoperitoneum. She underwent an emergency caesarean section, delivering a female fetus weighing 400 g, with an Apgar score of 7 at 1 minute and 9 at 5 minutes. INTERVENTION: During surgery, we found a huge uterine sarcoma-like metastatic tumor, invading the pelvic peritoneum and parametria bilaterally; the adnexae seemed disease-free. We performed a type B radical hysterectomy, bilateral salpingo-oophorectomy, pelvic peritonectomy, omentectomy, appendectomy, and excision of a bulky lymph node. Seven days after delivery, staging computed tomography (CT) scan demonstrated a large lombo-aortic lymph node compressing the left renal vein and we completed debulking with a second surgery, including diaphragmatic peritonectomy and excision of a huge lymph node by lombo-aortic lymphadenectomy, requiring partial reconstruction of an infiltrated renal vein. OUTCOME: Ten days after the second surgery, echo-color Doppler showed a regular microcirculation in the left kidney. The patient was discharged after 10 days, and the baby after 1 month, both in good health. Histological examination revealed a uterine body cPNET (central primitive neuroectodermal tumor) orienting the clinical management toward chemotherapy with cisplatin and etoposide. LESSONS: PNETs are aggressive neoplasms, usually diagnosed at an advanced stage. Due to their low incidence, universally accepted guidelines are still unavailable. Radical surgery leaving no macroscopic residual disease is mandatory in advanced stages. A good fertility-sparing procedure can be performed only in young women at early stages of disease, when the wish for childbearing is not yet fulfilled.
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spelling pubmed-59438952018-05-15 Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature De Nola, Rosalba Di Naro, Edoardo Schonauer, Luca Maria Lucarelli, Giuseppe Battaglia, Michele Fiore, Maria Grazia Mastrolia, Salvatore Andrea Loverro, Giuseppe Medicine (Baltimore) Research Article RATIONALE: PNETs (primitive neuroectodermal tumors) are a family of highly malignant neoplasms characterized by small round cells of neuroepithelial origin. They usually involve bone and soft tissues, and have a higher incidence in childhood. PATIENT CONCERNS: In this case report, we describe the obstetric and oncological outcome of a huge mass diagnosed as a leiomyoma in a 39-year-old pregnant woman who complained of low back pain, dysuria, and urinary frequency at 22 weeks of gestation. DIAGNOSES: During the 25th week of pregnancy, the patient was referred to our hospital at night with severe anemia and suspected hemoperitoneum. She underwent an emergency caesarean section, delivering a female fetus weighing 400 g, with an Apgar score of 7 at 1 minute and 9 at 5 minutes. INTERVENTION: During surgery, we found a huge uterine sarcoma-like metastatic tumor, invading the pelvic peritoneum and parametria bilaterally; the adnexae seemed disease-free. We performed a type B radical hysterectomy, bilateral salpingo-oophorectomy, pelvic peritonectomy, omentectomy, appendectomy, and excision of a bulky lymph node. Seven days after delivery, staging computed tomography (CT) scan demonstrated a large lombo-aortic lymph node compressing the left renal vein and we completed debulking with a second surgery, including diaphragmatic peritonectomy and excision of a huge lymph node by lombo-aortic lymphadenectomy, requiring partial reconstruction of an infiltrated renal vein. OUTCOME: Ten days after the second surgery, echo-color Doppler showed a regular microcirculation in the left kidney. The patient was discharged after 10 days, and the baby after 1 month, both in good health. Histological examination revealed a uterine body cPNET (central primitive neuroectodermal tumor) orienting the clinical management toward chemotherapy with cisplatin and etoposide. LESSONS: PNETs are aggressive neoplasms, usually diagnosed at an advanced stage. Due to their low incidence, universally accepted guidelines are still unavailable. Radical surgery leaving no macroscopic residual disease is mandatory in advanced stages. A good fertility-sparing procedure can be performed only in young women at early stages of disease, when the wish for childbearing is not yet fulfilled. Wolters Kluwer Health 2018-01-12 /pmc/articles/PMC5943895/ /pubmed/29480840 http://dx.doi.org/10.1097/MD.0000000000009505 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle Research Article
De Nola, Rosalba
Di Naro, Edoardo
Schonauer, Luca Maria
Lucarelli, Giuseppe
Battaglia, Michele
Fiore, Maria Grazia
Mastrolia, Salvatore Andrea
Loverro, Giuseppe
Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title_full Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title_fullStr Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title_full_unstemmed Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title_short Clinical management of a unique case of PNET of the uterus during pregnancy, and review of the literature
title_sort clinical management of a unique case of pnet of the uterus during pregnancy, and review of the literature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943895/
https://www.ncbi.nlm.nih.gov/pubmed/29480840
http://dx.doi.org/10.1097/MD.0000000000009505
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