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1.
Philippine Journal of Obstetrics and Gynecology ; : 214-219, 2023.
Article in English | WPRIM | ID: wpr-998033

ABSTRACT

@#Placental site trophoblastic tumor (PSTT) with uterine arteriovenous malformation (AVM) is a rare and potentially catastrophic occurrence. A high index of suspicion and immunohistochemistry secured the diagnosis. The use of appropriate imaging modalities led to the identification of the extent of the disease. Sequential planned management from neoadjuvant intensive chemotherapy, bilateral uterine artery embolization, and laparotomy, and coordinated among different medical disciplines resulted to a successful definitive treatment. Due to its relatively chemoresistant nature, hysterectomy is the mainstay of treatment. Adjuvant platinum-based intensive chemotherapy has been shown to improve overall survival in patients with metastatic disease and those with poor prognostic factors. This case of PSTT with a typical clinical profile was noteworthy due to the development of a significant AVM, a rare complication of PSTT. This case report included a review of treatment experiences as well as peculiarities that set PSTT apart from the more common gestational trophoblastic diseases.


Subject(s)
Gestational Trophoblastic Disease , Trophoblastic Tumor, Placental Site
2.
Ginecol. obstet. Méx ; 91(8): 631-636, ene. 2023. graf
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1520952

ABSTRACT

Resumen ANTECEDENTES: Las malformaciones arteriovenosas uterinas constituyen una causa infrecuente de hemorragia puerperal, en la bibliografía solo se encontraron 150 casos. Su conocimiento es importante porque son potencialmente mortales y porque se ha registrado un aumento en los últimos años. Suelen estar relacionadas con intervenciones en el útero: legrados, cesáreas o miomectomías o asociadas con neoplasias (enfermedad trofoblástica gestacional o adenocarcinoma endometrial), aunque otras son congénitas. CASO CLÍNICO: Paciente de 32 años, con una conización cervical y ablación de un mioma uterino mediante radiofrecuencia como únicos antecedentes de interés. A los 15 días posteriores a un parto eutócico, que fue el primero en su historial, tuvo un episodio de abundante metrorragia. En el puerperio inmediato tuvo una hemorragia abundante que requirió la transfusión de dos concentrados de hematíes. En la ecografía transvaginal el útero se observó de 22 x 44 mm, que podría corresponder a un cotiledón retenido. Ante la persistencia del sangrado se colocó un taponamiento intracavitario con una sonda de Foley con lo que se consiguió el cese del sangrado. Luego de descartar la embolización de las arterias uterinas debido al gran tamaño de la malformación arteriovenosa, se procedió a la histerectomía total simple por vía laparotómica. CONCLUSIÓN: Las malformaciones arteriovenosas uterinas, aunque son una causa infrecuente de hemorragia puerperal, deben ser sospechadas en virtud de ser potencialmente mortales.


Abstract BACKGROUND: Uterine arteriovenous malformations are a rare cause of puerperal hemorrhage, with only 150 cases reported in the literature. Their knowledge is important because they are life-threatening and because there has been an increase in recent years. They are usually related to interventions in the uterus: curettage, caesarean section or myomectomy or associated with neoplasms (gestational trophoblastic disease or endometrial adenocarcinoma), although others are congenital. CLINICAL CASE: A 32-year-old patient with a cervical conization and ablation of a uterine myoma by radiofrequency as the only history of interest. Fifteen days after a euthecological delivery, which was the first in her history, she had an episode of abundant metrorrhagia. In the immediate postpartum period, she had a heavy hemorrhage that required the transfusion of two red blood cell concentrates. Transvaginal ultrasound showed a uterus measuring 22 x 44 mm, which could correspond to a retained cotyledon. In view of the persistent bleeding, intracavitary tamponade was placed with a Foley catheter, which led to cessation of bleeding. After ruling out embolization of the uterine arteries due to the large size of the arteriovenous malformation, a simple total hysterectomy by laparotomy was performed. CONCLUSION: Uterine arteriovenous malformations, although an infrequent cause of puerperal hemorrhage, should be suspected because they are potentially fatal.

3.
Clinical Medicine of China ; (12): 83-87, 2022.
Article in Chinese | WPRIM | ID: wpr-932149

ABSTRACT

Objective:To analyze the clinical characteristics, diagnosis and treatment of acquired uterine arteriovenous malformation (UAVM).Methods:The clinical data of 16 patients with diagnosis of UAVM from January 2014 to March 2021 in Beijing Friendship Hospital, Capital Medical University were enrolled in this retrospective study. The general data of patients were observed and analyzed: age, pregnancy and childbirth, etc. Auxiliary examinations: human chorionic gonadotropin (hCG), B-ultrasound, CT angiography (CTA), magnetic resonance (MRI), digital subtraction angiography (DSA), lesion diameter, resistance index (RI), peak systolic velocity (PSV), treatment and postoperative pathology.Result:Among the 16 patients, hCG was negative in 10 cases and positive in 6 cases. The first abnormal bleeding time was (43.4±36.4) days and (16.0±9.0) days, respectively. The rehospitalization time was (63.3±54.4) days and (48.3±54.0) days. Six patients with massive bleeding were HCG negative. Ultrasound in 16 cases showed mixed echo light mass with rich blood flow in the uterine cavity, and magnetic resonance examination in 14 cases also showed abnormal signals in the uterine cavity or uterine wall. Mass staining was seen in 6 cases by DSA, vein development in advance, contrast medium overflow was seen in 2 cases, and the conclusion of CTA was consistent with DSA in 5 cases. Uterine artery embolization was performed in 5 cases, including 2 cases of massive bleeding, emergency bilateral uterine artery embolization and 3 cases of preventive embolization. Hysteroscopy was performed in 4 cases after embolization, and balloon compression was performed in 1 case because there was no obvious tissue in the uterine cavity. Hysteroscopy were performed in 10 cases without UAE. Mifepristone combined with misoprostol was used in 1 case. Among the 15 patients treated by surgery, 14 cases showed degenerative trophoblasts or villi. During the follow-up, one patient after uterine artery embolization complained of decreased menstruation, and ultrasound considered the possibility of intrauterine adhesion.Conclusion:After termination of pregnancy, imaging examination should be strengthened to guard against the occurrence of UAVM. Once diagnosed, medical intervention should be started as soon as possible to reduce bleeding. There is no standardized treatment for UAVM related to pregnancy. Comprehensive consideration should be given to the clinical manifestations, bleeding situation, lesion location and fertility requirements of the patients.

4.
Philippine Journal of Obstetrics and Gynecology ; : 33-38, 2020.
Article in English | WPRIM | ID: wpr-876630

ABSTRACT

@#Arteriovenous malformations (AVM) are vascular disorders with a mixture of arterial, venous and small capillary-like channels with fistulous connections. Uterine arteriovenous malformations are rare cause of abnormal uterine bleeding with only a few reported cases. They may arise from pregnancy, miscarriage, previous cesarean section or other uterine surgery and gestational trophoblastic disease. Diagnosis can be made through angiography or doppler ultrasonography. Traditionally, uterine AVMs are treated with hysterectomy but with the advances in technology, minimally invasive conservative approaches such as radiologic arterial embolization or laparoscopic uterine artery ligation have become available. We present a case of a 29-year-old, G2P1 (1011) who had a three- month history of heavy, intermittent vaginal bleeding from uterine arteriovenous malformation after a miscarriage. Laparoscopic bilateral uterine artery occlusion, offered a minimally invasive treatment with high symptomatic effectiveness.


Subject(s)
Uterine Artery , Arteriovenous Malformations , Uterine Diseases , Ligation , Uterine Hemorrhage
5.
Ginecol. obstet. Méx ; 85(7): 466-471, mar. 2017. graf
Article in Spanish | LILACS | ID: biblio-953731

ABSTRACT

Resumen ANTECEDENTES: las malformaciones arteriovenosas uterinas constituyen un conjunto de alteraciones de la vascularización endometrial y miometrial que se caracterizan por la formación de comunicaciones heterogéneas y aberrantes entre los territorios arteriales y venosos que tienen como consecuencia cuadros de sangrado genital abundante e inestabilidad hemodinámica. CASO CLÍNICO: paciente que luego de un legrado uterino hemostásico resultó con una fístula arteriovenosa uterina que se trató mediante embolización selectiva de la arteria uterina izquierda; quedó embarazada después de tres meses del procedimiento, no tuvo alteraciones y la evolución perinatal fue satisfactoria. CONCLUSIÓN: el diagnóstico de las malformaciones arteriovenosas es eminentemente clínico, aunque la confirmación depende de las pruebas de imagen. La ecografía con estudio Doppler y la angiografía son las técnicas de elección para el diagnóstico de las lesiones y la planificación del tratamiento a seguir, decisión que dependerá de los deseos reproductivos de la paciente. En la actualidad, el tratamiento de elección para las pacientes que desean embarazarse es la embolización endovascular selectiva, guiada radiológicamente. Los anticonceptivos orales, las técnicas histeroscópicas de resección o la histerectomía son otras opciones terapéuticas que pueden valorarse, en función de los parámetros indicados.


Abstract BACKGROUND: uterine arteriovenous malformations constitute a group endometrial and myometrial vascularization disorders characterized by the formation of heterogeneous and aberrant communications between the arterial and venous territories, producing abundant genital bleeding pictures as well as hemodynamic instability. CLINICAL CASE: a patient who underwent a hemostatic uterine D&C developed a uterine arteriovenous fistula that was treated through selective embolization of the left uterine artery; she became pregnant after three months of the procedure, she presented a normal pregnancy with satisfactory perinatal outcomes. CONCLUSION: the diagnosis of arteriovenous malformations is mainly clinical, although confirmation depends on imaging tests. A Doppler ultrasound and angiography are the preferred techniques to diagnose lesions and to plan subsequent treatment, a decision that will depend on the patient's reproductive wishes. Currently, the choice treatment for patients who want to become pregnant is a radiologically guided selective endovascular embolization. Oral contraceptives, resection hysteroscopy techniques or hysterectomy are other therapeutic options that may be considered based on the parameters indicated.

6.
Rev. Nac. (Itauguá) ; 8(2): 81-93, dic 2016.
Article in Spanish | LILACS, BDNPAR | ID: biblio-884762

ABSTRACT

RESUMEN La malformación arteriovenosa uterina (MAVU) es una causa poco frecuente de sangrado uterino, dado que en la mayoría de casos cursa de forma asintomática. Las MAVU son dilataciones varicosas arteriovenosas intramiometriales sin afectación capilar. Plantean un reto diagnóstico y terapéutico en el esfuerzo de la preservación de la fertilidad, constituyéndose la embolización como su principal tratamiento. En la actualidad, el estándar de oro para el diagnóstico de esta patología es la angiografía. Sin embargo, las modalidades menos invasivas como la ecografía Doppler color se utilizan cada vez más para el diagnóstico. Se presenta el caso de una mujer de 20 años de edad, con antecedente de embarazo molar y sangrado menstrual excesivo debido a MAVU.


ABSTRACT Uterine arteriovenous malformation (AVMV) is a rare cause of uterine bleeding, since most cases are asymptomatic. The MAVU are intramyometrial arteriovenous variceal dilatations without capillary involvement. They propouse a diagnostic and therapeutic challenge in the effort for preservation of fertility, constituting the embolization its main treatment. At present, the gold standard for the diagnosis of this pathology is angiography. However, less invasive modalities such as color Doppler ultrasound are increasingly used for diagnosis. We present the case of a 20-year-old woman with a history of molar pregnancy and excessive menstrual bleeding due to MAVU.


Subject(s)
Humans , Female , Adult , Young Adult , Arteriovenous Malformations/therapy , Arteriovenous Malformations/diagnostic imaging , Uterine Artery Embolization , Uterine Artery/abnormalities , Angiography , Magnetic Resonance Spectroscopy , Ultrasonography, Doppler, Color , Uterine Artery/diagnostic imaging
7.
Philippine Journal of Obstetrics and Gynecology ; : 29-33, 2016.
Article in English | WPRIM | ID: wpr-632843

ABSTRACT

Arteriovenous Malformations are vascular disorders where there is an abnormal communication between an artery and vein. It can occur anywhere in the body not even sparing the uterus. Uterine Arteriovenous Malformations (AV Malformation) is a rare occurrence with less than 100 cases reported in literature. It can cause significant bleeding leading to anemia and even hypovolemic shock. It may be acquired from previous uterine manipulation such as dilatation and curettage and previous uterine surgeries. Diagnosis is made by angiography or doppler ultrasonography. Definitive treatment is hysterectomy however a less invasive, fertility preserving are uterine vascular occlusion techniques, of which the treatment of choice is Uterine Artery Embolization (UAE). We present our experience with 24 year-old G2P2 (1101) with scarred uterus suffering from recurrent profuse vaginal bleeding suspected to have uterine arteriovenous malformation. Laparoscopic bilateral uterine artery ligation, an alternative, more economical, relatively safe and available treatment option was given to the patient. 


Subject(s)
Humans , Female , Adult , Uterine Artery Embolization , Arteries , Veins , Patients , Curettage , Dilatation , Diagnosis , Angiography , Ultrasonography, Doppler , Hysterectomy
8.
Obstetrics & Gynecology Science ; : 419-423, 2014.
Article in English | WPRIM | ID: wpr-110043

ABSTRACT

Uterine arteriovenous malformation (AVM) is a rare entity in gynecology with fewer than 100 cases reported in the literature. Due to abnormal connection between arteries and veins without an intervening capillary system, recurrent and profuse vaginal bleeding is the most common symptom which can be potentially life-threatening. Uterine AVM can be either congenital or acquired. Acquired AVM is reported as a consequence of previous uterine trauma such as curettage procedures, caesarean section or pelvic surgery. It is also associated with infection, retained product of conception, gestational trophoblastic disease, malignancy and exposure to diethlystilboestrol. We herein report a case of acquired uterine AVM located on the right lateral wall after intrauterine instrumentation for laparoscopic left salpingectomy due to left tubal pregnancy. The patient was successfully treated with embolization.


Subject(s)
Female , Humans , Pregnancy , Arteries , Arteriovenous Malformations , Capillaries , Cesarean Section , Curettage , Fertilization , Gestational Trophoblastic Disease , Gynecology , Laparoscopy , Pregnancy, Tubal , Salpingectomy , Uterine Hemorrhage , Veins
9.
Yonsei Medical Journal ; : 367-373, 2014.
Article in English | WPRIM | ID: wpr-19553

ABSTRACT

PURPOSE: To evaluate the technical feasibility and clinical outcome of bilateral uterine artery embolization (UAE) as a first-line therapeutic option for bleeding uterine arteriovenous malformation (AVM). MATERIALS AND METHODS: Between 2002 and 2012, 19 patients were diagnosed with acquired uterine AVM clinically and through imaging studies. The clinical characteristics, angiographic features, technical success rate of embolization, procedure-related complications, imaging, and clinical follow-up data were assessed. Clinical success was defined as immediate symptomatic resolution with disappearance of vascular abnormality on subsequent imaging studies. RESULTS: A total of 20 bilateral UAE, with or without embolization of extra-uterine feeders, were performed as the first-line treatment. Technical and clinical success rate was 90.0% (18/20) and 89.5% (17/19), respectively. Embolization was incomplete in two patients who had residual extra-uterine fine feeders to the AVM or a procedure-related complication (ruptured uterine artery); the former showed slow regression of the vascular malformation during the observation period, while the latter underwent a successful second bilateral UAE. Immediate clinical success was achieved in the remaining 17 patients after a single session and no recurrence of bleeding was found. Recovery to normal menstrual cycle was seen in all 17 patients with clinical success within one or two months, two of whom subsequently had uneventful intrauterine pregnancies carried to term. CONCLUSION: Bilateral UAE is a safe and effective first-line therapeutic option for the management of bleeding uterine AVMs. However, incomplete embolization due to unembolizable feeders or difficult access into the uterine artery may lead to suboptimal treatment.


Subject(s)
Female , Humans , Pregnancy , Arteriovenous Malformations , Follow-Up Studies , Hemorrhage , Menstrual Cycle , Methods , Recurrence , Uterine Artery Embolization , Uterine Artery , Vascular Malformations
10.
Article in Spanish | LILACS-Express | LILACS, LIPECS | ID: biblio-1522504

ABSTRACT

Se comunica el caso de una paciente que cursó con hemorragia uterina anormal debida a malformación arteriovenosa uterina adquirida, relacionada con un aborto y curetaje en los meses anteriores. El diagnóstico se realizó mediante ecografía Doppler y Doppler con reconstrucción 3D. Posteriormente fue manejada de manera expectante y con anticonceptivos, resolviéndose el sangrado.


The case of a patient with abnormal uterine bleeding due to acquired uterine arteriovenous malformation related to dilatation and curettage for abortion in previous months is reported. Diagnosis was done by ultrasound Doppler and Doppler 3D reconstruction. Expectant treatment and contraceptives solved the problem.

11.
Journal of the Korean Neurological Association ; : 37-41, 2012.
Article in Korean | WPRIM | ID: wpr-211785

ABSTRACT

Piriformis syndrome is a rare entrapment neuropathy in which the sciatic nerve is compromised by the piriformis muscle or other local structures. We report a case of sciatic and gluteal nerve lesions with infarction of the piriformis muscle following internal iliac artery embolization of the bilateral uterine vascular malformation. The surgical intervention revealed anatomical variation of the right sciatic nerve. To our knowledge, this is the first case of piriformis syndrome following endovascular treatment of uterine vascular malformation in Korea.


Subject(s)
Arteriovenous Malformations , Iliac Artery , Infarction , Korea , Muscles , Nerve Compression Syndromes , Piriformis Muscle Syndrome , Sciatic Nerve , Vascular Malformations
12.
Korean Journal of Obstetrics and Gynecology ; : 2039-2043, 1998.
Article in Korean | WPRIM | ID: wpr-206099

ABSTRACT

Uterine arteriovenous malformation is a rare gynecologic condition, which is sometimes accompanied torrential vaginal bleeding and it can be aggravated with diagnostic dilatation and curettage. For proper management of vaginal bleeding, accurate diagnosis should be achieved before the intervention. In the past, the diagnosis was made retrospectively after hysterectomy, however recently it may be made by noninvasive method such as Doppler ultrasonogram before management. We have experienced 3 cases of uterine arteriovenous malformation, of which 2 cases were diagnosed with Doppler ultrasonogram.


Subject(s)
Female , Arteriovenous Malformations , Diagnosis , Dilatation and Curettage , Hysterectomy , Retrospective Studies , Ultrasonography , Uterine Hemorrhage
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