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1.
Taiwan J Obstet Gynecol ; 60(6): 1116-1120, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34794749

ABSTRACT

OBJECTIVE: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare. CASE REPORT: A 56-year-old perimenopausal woman presented with abdominal distention and abnormal vaginal spotting. Ultrasound and abdominal computed tomography showed a complex cystic mass in the left ovary accompanied with bilateral pleural effusion and ascites. The patient underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, left pelvic lymph node dissection, omentectomy and appendectomy. Final histopathological diagnosis was adult-type GCT. The patient had postoperative hormone and anti-angiogenesis agent therapy with free of disease. CONCLUSION: Ovarian cystic complex mass accompanied with ascites and pleural effusion often results from malignant ovarian tumors or benign ovarian fibroma. Based on the aforementioned report, the rare types of ovarian tumors, such as adult-type granulosa cell tumor of the ovary should be taken into consideration.


Subject(s)
Ascites/diagnosis , Granulosa Cell Tumor/complications , Meigs Syndrome/pathology , Ovary/pathology , Antineoplastic Agents, Hormonal/therapeutic use , Ascites/surgery , Bevacizumab/therapeutic use , Cytoreduction Surgical Procedures , Female , Gonadotropin-Releasing Hormone/agonists , Goserelin/therapeutic use , Granulosa Cell Tumor/therapy , Humans , Laparotomy , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Middle Aged , Ovarian Neoplasms/complications , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/therapy , Pleural Effusion/etiology , Salpingo-oophorectomy , Treatment Outcome
2.
Transplant Proc ; 52(8): 2527-2529, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32276839

ABSTRACT

Ascites is the excessive accumulation of fluid in the peritoneal cavity and predominantly caused by liver cirrhosis, cancers, or heart failure. In this study, a 31-year-old woman with chronic renal failure of unknown etiology treated with hemodialysis and peritoneal dialysis was often hospitalized because of ascites, which appeared 4 years after the second kidney transplantation. The patient was regularly (every 2-3 weeks) treated with paracentesis. Peritoneal fluid tested negative for bacterial (including atypical) and fungal infections and tuberculosis. Doppler ultrasound and liver FibroScan did not show any irregularities. Computed tomography (CT) revealed an enlarged left ovary. A high level of CA 125 was found. The second diagnostic laparoscopy revealed no changes in the ovaries, and there were no tumor cells. Diagnostics were extended, but no deviations were revealed. Suspecting drug etiology, mycophenolic acid was discontinued, bringing no improvement. Diagnostic tests caused suspicion of Meigs' syndrome; therefore, oophorectomy of left ovary was conducted, revealing numerous small cysts filled with serous fluid, without tumor cells in the ovary or peritoneal fluid. Despite the procedure performed, ascites was recurrent. Five month later, ascites spontaneously stopped growing. Paracentesis to decompress ascites was no longer required. There were 9 paracenteses performed from oophorectomy (the latest on May 23, 2019). The need for repetitive paracentesis, significantly reducing the patient's quality of life, required diagnosis for casuistic diseases. The described case is atypical because of the confusing etiology of ascites and its spontaneous cessation. Despite numerous examinations and recession of ascites, the cause of the problem is not entirely clear.


Subject(s)
Ascites/etiology , Kidney Failure, Chronic/complications , Kidney Transplantation/adverse effects , Meigs Syndrome/etiology , Postoperative Complications/etiology , Adult , Ascites/therapy , Female , Humans , Kidney Failure, Chronic/therapy , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Paracentesis , Postoperative Complications/therapy , Quality of Life , Renal Dialysis , Tomography, X-Ray Computed , Ultrasonography
3.
World J Surg Oncol ; 7: 10, 2009 Jan 22.
Article in English | MEDLINE | ID: mdl-19161612

ABSTRACT

BACKGROUND: Adnexal masses are not uncommon in patients with breast cancer. Breast cancer and ovarian malignancies are known to be associated. In patients with breast cancer and co-existing pleural effusions, ascites and adnexal masses, the probability of disseminated disease is high. Nevertheless, benign ovarian masses can mimic this clinical picture when they are associated with Meigs' syndrome making the work-up and management of these patients challenging. To our knowledge, there are no similar reports in the literature and therefore we present this case to highlight this entity. CASE PRESENTATION: A 56-year old woman presented with a 4 cm, grade 2, invasive ductal carcinoma of her left breast. Pre-treatment staging investigations showed a 13.5 cm mass in her left ovary, a small amount of ascites and a large right pleural effusion. Serum tumour markers showed a raised CA125 supporting the malignant nature of the ovarian mass. The cytology from the pleural effusion was indeterminate but thoracoscopic biopsy failed to show malignancy. The patient was strongly against mastectomy and she was commenced on neo-adjuvant Letrozole 2.5 mg daily with a view to perform breast conserving surgery. After a good response to the hormone manipulation, the patient had breast conserving surgery, axillary sampling and laparoscopic excision of the ovarian mass which was eventually found to be a benign ovarian fibroma. CONCLUSION: Despite the high probability of disseminated malignancy when an ovarian mass associated with ascites if found in a patient with a breast cancer and pleural effusion, clinicians should be aware about rare benign syndromes, like Meigs', which may mimic a similar picture and mislead the diagnosis and management plan.


Subject(s)
Breast Neoplasms/diagnosis , Carcinoma, Ductal, Breast/diagnosis , Fibroma/diagnosis , Meigs Syndrome/diagnosis , Ovarian Neoplasms/diagnosis , Antineoplastic Agents/therapeutic use , Breast Neoplasms/blood , CA-125 Antigen/blood , Carcinoma, Ductal, Breast/blood , Diagnosis, Differential , Female , Fibroma/drug therapy , Gynecologic Surgical Procedures , Humans , Letrozole , Mastectomy , Meigs Syndrome/blood , Meigs Syndrome/therapy , Middle Aged , Nitriles/therapeutic use , Ovarian Neoplasms/drug therapy , Pleural Effusion/diagnosis , Pleural Effusion/drug therapy , Triazoles/therapeutic use
4.
Kurume Med J ; 56(3-4): 85-7, 2009.
Article in English | MEDLINE | ID: mdl-20505286

ABSTRACT

A 61-year-old otherwise healthy woman presented with gradually worsening exertional dyspnea. Routine examinations revealed bilateral pleural effusion with no other notable cardiopulmonary diseases. Systemic examinations showed ascites and a pelvic tumor, which turned out to be right ovarian endometrioid adenocarcinoma. Surgical removal and chemotherapy against the ovarian cancer resulted in disappearance of the ascites and pleural effusion, establishing a diagnosis of pseudo-Meigs'syndrome. It is common for reported cases of pseudo-Meigs' syndrome to initially present with dyspnea, therefore it is important to consider this disorder when attempting a differential diagnosis in female patients presenting with dyspnea without other noticeable conditions.


Subject(s)
Dyspnea/etiology , Meigs Syndrome/complications , CA-125 Antigen/blood , Female , Humans , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Membrane Proteins/blood , Middle Aged
5.
Gastroenterol Clin Biol ; 32(3): 261-4, 2008 Mar.
Article in French | MEDLINE | ID: mdl-18353585

ABSTRACT

Ascites and/or pleural effusion with ovarian metastases in colorectal cancer are usually related to peritoneal carcinomatosis. Pseudo-Meigs syndrome is a characterized by non-malignant ascites and/or pleural effusion caused by pelvic tumors other than solid benign ovarian tumors. We treated two patients who developed this syndrome in a context of colorectal cancer. After ovarian metastasis resection, ascites and pleural diffusion disappeared. In the presence of acellular ascites with ovarian metastases from colorectal cancer, diagnosis of pseudo-Meigs syndrome may allow surgical treatment with curative intent.


Subject(s)
Adenocarcinoma/pathology , Adenocarcinoma/secondary , Colorectal Neoplasms/pathology , Meigs Syndrome/therapy , Ovarian Neoplasms/secondary , Adenocarcinoma/therapy , Adult , Chemotherapy, Adjuvant , Female , Humans , Meigs Syndrome/diagnosis , Ovarian Neoplasms/therapy , Ovariectomy
6.
Bratisl Lek Listy ; 108(3): 158-60, 2007.
Article in English | MEDLINE | ID: mdl-17682545

ABSTRACT

The triad of ascites, hydrothorax in association with a benign ovarian tumor is defined as Meig's syndrome. It is a rare clinical entity. A case of a 62 year-old woman whith dyspnoe, abdominal discomfort and ascites is presented. Clinical and ultrasonographic findings revealed extended palpable pelvic mass originating from the ovaries and ascites as well as hydrothorax of the left lung by chest radiography. The treatment method was surgical intervention. Cytomorphologic studies were positive for malignacy and adenocarcinoma cells were confirmed. The pathogenesis of the pleural and ascites fluids and the importance of CA-125 are discussed (Fig. 2, Ref. 21).


Subject(s)
Meigs Syndrome/diagnosis , Adenocarcinoma/complications , Adenocarcinoma/diagnosis , Adenocarcinoma/secondary , Adenocarcinoma/surgery , Female , Humans , Meigs Syndrome/therapy , Middle Aged , Ovarian Neoplasms/complications , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/pathology , Ovarian Neoplasms/surgery
7.
Gynecol Oncol ; 105(3): 796-800, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17433421

ABSTRACT

OBJECTIVES: To report various descriptions of the combination of a benign genital tumour with pleural and/or abdominal effusion throughout the years and to determine the paternity of this syndrome, commonly known as Meigs' syndrome. METHODS: A systematic review of the literature from 1728 to 2004. RESULTS: Before 1880, publications were rare and limited to clinical and anatomical descriptions drawing no conclusions between the cause and effect of this condition and even less about its management. Demons described the syndrome between 1887 and 1902. He was the first to specify that removal of the tumour (benign ovarian cyst, solid ovarian tumour, fibroma of the broad ligament) was essential for the patient to be cured of the effusions and that it was wrong to postpone surgery. In 1937, Meigs arrived at the same findings concerning ovarian fibromas and granulosa cell tumours, hence the name of Demons-Meigs which was given to this syndrome with the agreement of Meigs. Current literature reports on pseudosyndromes of Demons-Meigs including genital malignancies with negative cytology. These entities should not be called Demons or Meigs pseudosyndromes. Inversely, all benign tumours of the genital tract should be included in Demons syndrome, even if Demons did not actually encounter any during his years of practice, but it was in the spirit of his observations. CONCLUSION: Demons' syndrome includes all benign genital tumours, the Demons-Meigs eponym is reserved for the description of ovarian fibromas and granulosa cell tumours, and the Demons' pseudosyndrome includes all other entities.


Subject(s)
Meigs Syndrome/history , England , Female , France , History, 18th Century , History, 19th Century , History, 20th Century , Humans , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Middle Aged
8.
Breast Cancer ; 13(4): 344-8, 2006.
Article in English | MEDLINE | ID: mdl-17146160

ABSTRACT

We report a rare case of pseudo-Meigs' syndrome due to metastasis of breast cancer to both ovaries. A 34-year-old woman with exertional dyspnea was admitted to our hospital. Before entry the patient had undergone radical mastectomy for left breast cancer in June 1998. Resection and reconstruction of the chest wall for recurrence of the breast cancer had been performed in April 2001. Right pleural effusion was found on admission to our hospital in October 2002. Continuous thoracic drainage obtained 500-2000 ml of fluid per day. Cytologic results were both normal and benign, and cultures for bacteria and acid-fast bacilli were negative. During treatment of the pleural effusion, which proved to be cryptogenic and intractable, a huge pelvic tumor was found. The primary site was unknown. Surgery was performed in November 2002, and tumors were removed from both ovaries. The right pleural effusion vanished after surgery. Pseudo-Meigs' syndrome with metastasis of breast cancer to both ovaries was diagnosed. The patient died of cachexia related to the carcinoma in January 2005.


Subject(s)
Breast Neoplasms/pathology , Carcinoma, Ductal, Breast/pathology , Meigs Syndrome/etiology , Ovarian Neoplasms/secondary , Adult , Breast Neoplasms/surgery , Carcinoma, Ductal, Breast/surgery , Dyspnea/etiology , Fatal Outcome , Female , Humans , Mastectomy , Meigs Syndrome/therapy , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/surgery
9.
Int J Gynecol Cancer ; 16 Suppl 1: 315-8, 2006.
Article in English | MEDLINE | ID: mdl-16515612

ABSTRACT

Meigs' syndrome is the association of ovarian fibroma, pleural effusion, and ascites. Meigs' syndrome with marked elevation of CA125 is an unusual clinical condition reported in 27 cases in the literature. The patient was a 46-year-old woman with right pleural effusion, ascites, ovarian tumor, and CA125 level of 1808 U/mL. Tomography revealed ascites and bilobate pelvic tumor of approximately 25 cm. The diagnosis of advanced epithelial ovarian cancer was considered, and the patient was treated with chemotherapy. Three chemotherapy schemes were applied due to the total lack of response in tumor volume; however, CA125 decreased to 90 U/mL. Thus, surgery was performed with resection of 25 cm of the left ovarian tumor, with intact capsule and without implants; the result of histopathologic analysis was fibroma. Postoperative CA125 was 11 U/mL. Patients with elevated CA125 and ascites cytology positive for malignancy must be cautiously treated due to the possibility of false positives, even if the probability is low. Therefore, minimally invasive surgery for biopsy collection must be considered. Although the association between ovarian tumor, pleural effusion, ascites, and marked elevation of CA125 is highly indicative of epithelial ovarian cancer, Meigs' syndrome must be considered in the differential diagnosis.


Subject(s)
Adenocarcinoma/therapy , Antineoplastic Agents/administration & dosage , Meigs Syndrome/therapy , Adenocarcinoma/blood , CA-125 Antigen/blood , Carboplatin/administration & dosage , Deoxycytidine/administration & dosage , Deoxycytidine/analogs & derivatives , Female , Gynecologic Surgical Procedures , Humans , Meigs Syndrome/blood , Middle Aged , Paclitaxel/administration & dosage , Vinblastine/administration & dosage , Vinblastine/analogs & derivatives , Vinorelbine , Gemcitabine
11.
Contracept Fertil Sex ; 27(1): 47-50, 1999 Jan.
Article in French | MEDLINE | ID: mdl-10071447

ABSTRACT

Regarding a original observation of the Deimons-Meigs syndrome, the authors have derived, from a review of the literature, the main clinicals and etiopathogenics characteristics, and tried to discuss the terms and conditions of a therapeutic treatment appropriate to such a situation.


Subject(s)
CA-125 Antigen/analysis , Meigs Syndrome/diagnosis , Aged , Female , Humans , Meigs Syndrome/surgery , Meigs Syndrome/therapy , Treatment Outcome
12.
Rev Pneumol Clin ; 55(5): 280-2, 1999 Oct.
Article in French | MEDLINE | ID: mdl-10637894

ABSTRACT

Two main benign diseases of the ovary which can simulate advanced stage cancer of the ovary are described. The first is Meigs' syndrome, a triad of benign ovarian tumor, usually an ovarian fibroma, ascitis, and pleural effusion with complete disappearance of serous exsudative effusions with surgical resection of the ovarian tumor. The second is ovarian hyperstimulation syndrome following ovulation induction with exogenous gonotropins for the treatment of infertility. This syndrome associates significant ovarian enlargement, hyperestrogenism and latent or clinically patent serous exsudative effusions; it usually resolves with suggestive measures and rest.


Subject(s)
Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Ovarian Hyperstimulation Syndrome/diagnosis , Ovarian Hyperstimulation Syndrome/therapy , Female , Humans , Meigs Syndrome/etiology , Ovarian Hyperstimulation Syndrome/classification , Ovarian Hyperstimulation Syndrome/etiology , Risk Factors , Severity of Illness Index
14.
Ginecol. obstet. Méx ; 62(8): 217-21, ago. 1994. tab, ilus
Article in Spanish | LILACS | ID: lil-198922

ABSTRACT

Se describe el caso de una paciente con síndrome de Meigs atendida en el Instituto Nacional de Perinatología (SSa), con la triada clásica de derrame pleural, ascitis y tumor benigno del ovario (fibroma). Se resolvió con manejo quirúrgico de salpingooforectomía, actualmente la paciente está curada. Se hace mención a la etiopatogenia del hidrotórax y el líquido libre en cavidad abdominal, que hasta la fecha no es clara


Subject(s)
Humans , Female , Adult , Meigs Syndrome/therapy
15.
Minerva Ginecol ; 45(5): 263-6, 1993 May.
Article in Italian | MEDLINE | ID: mdl-8351065

ABSTRACT

The co-existence of pelvic tumor, hydrothorax and ascites has been known since the last century. The features of this disease were described by Meigs and Cass in 1937; in the same year Roads named it Meigs syndrome. According to the original description this syndrome only included, as pelvic involvement, an ovarian neoplasm; at present it is accepted that hydrothorax and the ascites can also be associated with a uterine tumor, like a fibroma. The existence of either an ovarian or a uterine neoplasm distinguishes the typical Meigs syndrome from a pseudo-Meigs syndrome. The most likely pathogenesis of Meigs syndrome ascribes the formation of the peritoneal and pleural effusion to the filtration of interstitial fluid in the peritoneum through the tumor capsule, and the diffusion to the pleural space, generally at the right side, through the diaphragm lymphatic vessels and the foramen of Bochdalek. Dockerty reported that at least 40% of ovarian tumors had a diameter of more than 6 cm when associated with hydrothorax and ascites. The entity of pleural and peritoneal effusion can be moderate or massive. The effusions generally derive from a transudative process, but they can occasionally contain blood cells. The connection between the pelvic tumor and the effusion is demonstrated by the regression of the latter when the neoplasm is excised. When the pelvic tumor has an ovarian location it derives from the connective tissue of the hilus, it appears during fertile age and has a slow growth, the clinical signs becoming evident in elder age.


Subject(s)
Hydrothorax/etiology , Meigs Syndrome/complications , Ovarian Neoplasms/complications , Aged , Ascites/etiology , Ascites/radiotherapy , Drainage , Female , Humans , Hydrothorax/diagnosis , Hydrothorax/therapy , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/radiotherapy , Tetracycline/therapeutic use , Tomography, X-Ray Computed
16.
Zhonghua Yi Xue Za Zhi (Taipei) ; 44(5): 322-4, 1989 Nov.
Article in English | MEDLINE | ID: mdl-2634472

ABSTRACT

Bilateral ovarian fibromas combined with as and hydrothorax is a rare disorder. A case of bilateral ovarian fibromas combined with ascites and hyrothorax is presented. The ascites and hydrothorax disappeared spontaneously after removal of the ovarian tumors.


Subject(s)
Meigs Syndrome/pathology , Aged , Aged, 80 and over , Female , Humans , Meigs Syndrome/diagnosis , Meigs Syndrome/therapy
17.
Poumon Coeur ; 37(4): 265-7, 1981.
Article in French | MEDLINE | ID: mdl-7312757

ABSTRACT

Thoracoscopy, a diagnostic method of high precision, may be considered to be a lifesaving gesture in certain dramatic situations. It offers the possibility of a precise diagnosis and effective therapeutic measures, which may be performed endoscopically. Such dramatic situations are represented above all by haemopneumothorax, high tension spontaneous pneumothorax and fulminating pleural effusions, as in Meigs syndrome. Pathology involved may range from traumatic, degenerative or inflammatory conditions to tumours of pathognomic malformations. A number of clinical cases spectacular by virtue of their clinical features, endoscopic diagnosis and successful treatment in dramatic circumstances, are presented.


Subject(s)
Hemopneumothorax/diagnosis , Meigs Syndrome/diagnosis , Thoracoscopy , Adult , Emergencies , Female , Hemopneumothorax/therapy , Humans , Male , Meigs Syndrome/therapy , Middle Aged
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