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1.
Rev. bras. ginecol. obstet ; 41(2): 124-128, Feb. 2019. graf
Article in English | LILACS | ID: biblio-1003532

ABSTRACT

Abstract Müllerian adenosarcoma is a very rare gynecological disease, comprising 5% of uterine sarcomas. Extragenital localizations are even rarer.We report a very interesting case of a 27-year-old woman complaining of pelvic pain, with a subsequent diagnosis of extragenital Müllerian adenosarcoma. This is the first case reported in the literature with a complete and wide imaging description. Even if rare, Müllerian adenosarcoma should be hypothesized in case of young female patients presenting with suspicious pelvic mass.


Resumo O adenosarcoma Mülleriano é uma doença ginecológica muito rara, compreendendo 5% dos sarcomas uterinos. Localizações extragenitais são ainda mais raras. Relatamos um caso muito interessante de uma mulher de 27 anos queixando-se de dor pélvica com diagnóstico subsequente de adenosarcoma Mülleriano extragenital. Este é o primeiro caso relatado na literatura com uma descrição completa e ampla de imagem. Mesmo que raro, o adenosarcoma Mülleriano deve ser hipotetizado no caso de pacientes jovens do sexo feminino com massa pélvica suspeita.


Subject(s)
Humans , Female , Adult , Pelvic Neoplasms/diagnostic imaging , Adenosarcoma/diagnostic imaging , Ascites/diagnostic imaging , Uterine Neoplasms/diagnostic imaging , Tomography, X-Ray Computed , Ultrasonography , Pelvic Pain/etiology , Pelvic Pain/diagnostic imaging , Diagnosis, Differential , Multimodal Imaging
2.
Rev. cuba. obstet. ginecol ; 44(2): 1-7, abr.-jun. 2018.
Article in Spanish | LILACS, CUMED | ID: biblio-1003944

ABSTRACT

Los sarcomas de útero son un grupo diverso de tumores que constituyen 1 por ciento de las neoplasias del aparato genital femenino. La incidencia mundial es de 0,5 a 3,3 casos por cada 100,000 mujeres por año. Se presenta un caso poco frecuente con diagnóstico de leiomiosarcoma uterino de alto grado y se hace una revisión de la literatura sobre este tema(AU)


Uterine sarcomas are a diverse group of tumors that make up 1 percent of the neoplasms of the female genital tract. The worldwide incidence is from 0.5 to 3.3 cases per 100,000 women per year. A rare case with a diagnosis of high-grade uterine leiomyosarcoma is presented and a review of the literature on this subject is made(AU)


Subject(s)
Humans , Female , Middle Aged , Uterine Neoplasms/complications , Leiomyosarcoma/complications , Sarcoma/diagnosis
3.
Femina ; 45(1): 56-62, mar. 2017. ilus, tab
Article in Portuguese | LILACS | ID: biblio-1050705

ABSTRACT

O Food and Drug Administration (FDA) fez um alerta de segurança em relação ao risco potencial de disseminação de neoplasias malignas pelo uso do morcelador elétrico durante procedimentos minimamente invasivos. Esse artigo visa avaliar as evidências científicas sobre morcelamento uterino em relação ao risco de disseminação de câncer, sendo abordados a incidência de sarcoma uterino entre as mulheres previamente diagnosticadas com doença uterina benigna aparente, a possibilidade de avaliação pré-operatória desse risco, o posicionamento das principais sociedades médicas em relação à utilização do morcelador elétrico e as repercussões na prática clínica após as recomendações do FDA.(AU)


The US Food and Drug Administration (FDA) released a safety communication advising the potential risk of inadvertent spread of cancer cellsafter the use of electrical morcellator in minimally invasive procedures. This article aims to evaluate the scientific evidence regarding the risk of spread of cancer after uterine morcellation, the incidence of uterine sarcoma among women diagnosed with benign uterine disease, the possibility of preoperative assessment of this risk, the main medical societies positions statements regarding theuse of electric morcellation and the FDA recommendation`s impact on clinical practice. A review of the literature and a research of the main medical societies positions statements regarding the use of electric morcellation in minimally invasive surgeries were done.(AU)


Subject(s)
Humans , Female , Sarcoma/surgery , Uterine Cervical Neoplasms/complications , Morcellation/adverse effects , Morcellation/instrumentation , Leiomyoma/surgery , United States Food and Drug Administration , Risk
4.
Int. j. morphol ; 29(4): 1126-1129, dic. 2011. ilus
Article in Spanish | LILACS | ID: lil-626976

ABSTRACT

Los sarcomas uterinos son relativamente raros. El tipo histológico más frecuente es el leiomiosarcoma, seguido por el sarcoma del estroma endometrial. Los rabdomiosarcomas (RMS) son neoplasias malignas con diferenciación muscular esquelética. El rabdomiosarcoma embrionario (RMSE) tipo botrioide es el sarcoma más común de la infancia; con escasos reportes en adultos, afectando la región de cabeza y cuello, tracto genitourinario y extremidades más frecuentemente. En el tracto genitourinario, la vagina es la localización mas frecuente, comprometiendo en raras ocasiones el cuello o fondo uterino. Se presentan las características clínicas y morfológicas de un caso de RMSE uterino tipo botrioide diagnosticado en una paciente de 58 años en la Unidad de Anatomía Patológica del Hospital Hernán Henríquez Aravena de Temuco.


Uterine sarcomas are relatively rare. The most common histological type is leiomyosarcoma, followed by endometrial stromal sarcoma. The rhabdomyosarcoma (RMS) are malignant neoplasms with skeletal muscle differentiation. Embryonal rhabdomyosarcoma (RMSE) type botryoides is the most common in childhood, with few reports in adults, affecting the head and neck region, genitourinary tract and extremities more frequently. In the genitourinary tract, the vagina is the most common location, rarely involving cervix and fundus uterine. Clinical and morphological characteristics are presented of a case of uterine RMSE diagnosed in a 58 year-old woman in the Pathology Unit of the Hernán Henríquez Aravena Hospital in Temuco.


Subject(s)
Humans , Female , Middle Aged , Uterine Neoplasms/pathology , Rhabdomyosarcoma, Embryonal/pathology , Immunohistochemistry , Uterine Neoplasms/diagnosis , Rhabdomyosarcoma, Embryonal/diagnosis
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