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Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma

A 43-year-old perimenopausal lady presented with bleeding per vagina and lower abdominal pain. On evaluation, she had cervical polyp, which expelled spontaneously during the per speculum examination. Histopathology revealed malignant mixed Mullerian tumor. Extended hysterectomy with salphingo oophor...

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Autores principales: Prasad, Kishan H L, Makannavar, J H, Shetty, Jayaprakash, Vinutha, Patil, Channappa, Permi, Harish S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118060/
https://www.ncbi.nlm.nih.gov/pubmed/21701666
http://dx.doi.org/10.4103/0974-2727.78569
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author Prasad, Kishan H L
Makannavar, J H
Shetty, Jayaprakash
Vinutha,
Patil, Channappa
Permi, Harish S
author_facet Prasad, Kishan H L
Makannavar, J H
Shetty, Jayaprakash
Vinutha,
Patil, Channappa
Permi, Harish S
author_sort Prasad, Kishan H L
collection PubMed
description A 43-year-old perimenopausal lady presented with bleeding per vagina and lower abdominal pain. On evaluation, she had cervical polyp, which expelled spontaneously during the per speculum examination. Histopathology revealed malignant mixed Mullerian tumor. Extended hysterectomy with salphingo oophorectomy was carried out, which showed bilateral fallopian tube carcinoma and leiomyoma uterus. The patient was treated with carboplatin regime and found to be disease-free for 1 year. This case presented because of a rare combination of the lesions.
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spelling pubmed-31180602011-06-23 Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma Prasad, Kishan H L Makannavar, J H Shetty, Jayaprakash Vinutha, Patil, Channappa Permi, Harish S J Lab Physicians Case Report A 43-year-old perimenopausal lady presented with bleeding per vagina and lower abdominal pain. On evaluation, she had cervical polyp, which expelled spontaneously during the per speculum examination. Histopathology revealed malignant mixed Mullerian tumor. Extended hysterectomy with salphingo oophorectomy was carried out, which showed bilateral fallopian tube carcinoma and leiomyoma uterus. The patient was treated with carboplatin regime and found to be disease-free for 1 year. This case presented because of a rare combination of the lesions. Medknow Publications 2011 /pmc/articles/PMC3118060/ /pubmed/21701666 http://dx.doi.org/10.4103/0974-2727.78569 Text en Copyright: © Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Prasad, Kishan H L
Makannavar, J H
Shetty, Jayaprakash
Vinutha,
Patil, Channappa
Permi, Harish S
Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title_full Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title_fullStr Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title_full_unstemmed Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title_short Uncommon manifestations of Endocervical Malignant Mixed Mullerian Tumor with Incidental Bilateral Fallopian Tube Carcinoma
title_sort uncommon manifestations of endocervical malignant mixed mullerian tumor with incidental bilateral fallopian tube carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118060/
https://www.ncbi.nlm.nih.gov/pubmed/21701666
http://dx.doi.org/10.4103/0974-2727.78569
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