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pseudo meig syndrome

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https://www.readbyqxmd.com/read/27895818/case-of-pseudo-meigs-syndrome-caused-by-gastric-cancer-related-metastatic-ovarian-tumor-with-prolonged-survival
#1
Masaru Okamoto, Kazunori Maeda, Atsushi Yanagitani, Kiwamu Tanaka
A 48-year-old woman presented with bilateral enlarged ovaries, ascites, bilateral pleural effusion, and advanced gastric cancer. Pleural fluid cytology did not reveal malignant cells. Oophorectomy, performed as a palliative procedure, was followed by rapid resolution of the pleural effusion and ascites. The patient was diagnosed with pseudo-Meigs' syndrome, and underwent chemotherapy followed by partial gastrectomy. At the last follow-up, 84 mo following oophorectomy, she was alive, and free of disease recurrence, despite not receiving any further treatment...
November 15, 2016: World Journal of Gastrointestinal Oncology
https://www.readbyqxmd.com/read/27842595/long-term-survival-in-pseudo-meigs-syndrome-caused-by-ovarian-metastases-from-colon-cancer
#2
Yosuke Tajima, Hitoshi Kameyama, Saki Yamada, Ryoma Yagi, Masato Nakano, Masayuki Nagahashi, Yoshifumi Shimada, Jun Sakata, Takashi Kobayashi, Hajime Umezu, Toshifumi Wakai
BACKGROUND: Meigs' syndrome is defined as the co-existence of benign ovarian fibroma or fibroma-like tumor, ascites, and pleural effusion. In contrast, pseudo-Meigs' syndrome is defined as the co-existence of other ovarian or pelvic tumors, ascites, and pleural effusion. In Meigs' and pseudo-Meigs' syndromes, ascites and pleural effusion resolve promptly after the complete resection of the ovarian or pelvic tumor(s). Secondary ovarian tumors from colorectal gastrointestinal metastases rarely cause pseudo-Meigs' syndrome; only 11 cases of pseudo-Meigs' syndrome secondary to colorectal cancers have been reported in the literature...
November 14, 2016: World Journal of Surgical Oncology
https://www.readbyqxmd.com/read/27734419/pseudo-meigs-syndrome-due-to-ovarian-metastases-from-colon-cancer-a-case-report-and-review-of-the-literature
#3
Atsushi Yamamoto, Yoshiaki Miyasaka, Kazushige Furuya, Hideki Watanabe, Masahiro Maruyama, Haruka Nakada, Atsushi Takano, Masao Hada, Hiroshi Nakagomi, Masao Omata, Toshio Oyama
We herein experienced a case with pseudo-Meigs' syndrome that developed both synchronous and metachronous metastases to the ovary from ascending colon cancer. A 57-year-old female visited a hospital for a 2-month history of abdominal distension and voiding difficulty. Massive pleural effusion on the right side and a small amount of left-sided pleural effusion were detected on CT. She underwent emergent laparotomy due to the severe symptom of abdominal distention. The tumor originated from the left ovary, and left-sided oophorectomy was performed...
December 2016: Surgical Case Reports
https://www.readbyqxmd.com/read/27366341/systemic-lupus-erythematosus-presenting-with-massive-ascites-a-case-of-pseudo-pseudo-meigs-syndrome
#4
S McVorran, J Song, V Pochineni, A Abrudescu-Opran
The case presented is consistent with the phenomenon known as Pseudo-Pseudo Meigs Syndrome (PPMS). In it, we describe a young woman with newly diagnosed Systemic Lupus Erythematosus presenting with ascites, pleural effusions, and an elevated CA-125 level. Although rare, and of uncertain etiology, PPMS is becoming increasingly recognized in the literature. It should be considered as a differential diagnosis in such patients, along with the search for malignancy.
2016: Case Reports in Rheumatology
https://www.readbyqxmd.com/read/27182170/pseudo-meigs-syndrome-secondary-to-metachronous-ovarian-metastases-from-transverse-colon-cancer
#5
Kennoki Kyo, Atsushi Maema, Motoaki Shirakawa, Toshio Nakamura, Kenji Koda, Hidetaro Yokoyama
Pseudo-Meigs' syndrome associated with colorectal cancer is extremely rare. We report here a case of pseudo-Meigs' syndrome secondary to metachronous ovarian metastases from colon cancer. A 65-year-old female with a history of surgery for transverse colon cancer and peritoneal dissemination suffered from metachronous ovarian metastases during treatment with systemic chemotherapy. At first, neither ascites nor pleural effusion was observed, but she later complained of progressive abdominal distention and dyspnea caused by rapidly increasing ascites and pleural effusion and rapidly enlarging ovarian metastases...
May 14, 2016: World Journal of Gastroenterology: WJG
https://www.readbyqxmd.com/read/26721055/metastatic-radioiodine-avid-struma-ovarii-associated-with-pseudo-meigs-syndrome
#6
Saima Riaz, Humayun Bashir, Aamna Hassan, Aamir Ali Syed, Mudassar Hussain, Saba Imtiaz
We report a case of 21 years old lady who presented with ascites, left adnexal mass and elevated CA-125. With suspicion of ovarian malignancy, she underwent left salpingo-oophorectomy with omental biopsy. Histopathology revealed: 'follicular variant of papillary thyroid carcinoma arising in struma ovarii' with metastatic papillary thyroid carcinoma in omental and peritoneal nodules. Patient underwent total thyroidectomy followed by radioactive iodine therapy for metastatic omental and peritoneal disease. Post-therapy whole body scan, revealed extensive I-131 avid disease metastatic disease involving the chest, abdomen, pelvis and the musculoskeletal system...
July 2015: Journal of Ayub Medical College, Abbottabad: JAMC
https://www.readbyqxmd.com/read/26656338/pleural-effusion-in-meigs-syndrome-transudate-or-exudate-systematic-review-of-the-literature
#7
REVIEW
Rafal Krenke, Marta Maskey-Warzechowska, Piotr Korczynski, Monika Zielinska-Krawczyk, Joanna Klimiuk, Ryszarda Chazan, Richard W Light
Although Meigs' syndrome is regarded as a well-defined entity, contradictory data on pleural fluid characteristics have been presented, with some papers classifying it as a transudate, whereas others stating that it is an exudate.The aims of the study were: (1) to evaluate pleural fluid characteristics in patients with Meigs' syndrome and (2) to analyze the prevalence of transudative and exudative pleural effusion in relation to the applied definition of the syndrome.We performed a search through medical databases (MEDLINE, EMBASE, SCOPUS, and GOOGLE SCHOLAR) to identify papers on Meigs' syndrome published between 1940 and 2013...
December 2015: Medicine (Baltimore)
https://www.readbyqxmd.com/read/26489588/-a-case-of-pseudo-meigs-syndrome-associated-with-metachronous-ovarian-metastasis-from-ascending-colon-cancer
#8
Takafumi Yachi, Shinsuke Nishikawa, Tomohisa Tokura, Masahiro Iwama, Takanobu Akaishi, Minoru Umehara, Yutaka Umehara, Akihiko Murata, Kenichi Takahashi, Takayuki Morita
We experienced a case of pseudo-Meigs syndrome associated with metachronous metastasis to the ovary from ascending colon cancer. A 65-year-old woman underwent curative surgery for ascending colon cancer at another hospital. A follow-up CT carried out 3 months after the surgery revealed a right ovarian tumor and a large amount of ascites. The patient was diagnosed with ovarian metastasis from ascending colon cancer with carcinomatous peritonitis. Palliative care was recommended, and she presented at our department for a second opinion...
October 2015: Gan to Kagaku Ryoho. Cancer & Chemotherapy
https://www.readbyqxmd.com/read/26466694/pseudo-meigs-syndrome-caused-by-a-krukenberg-tumour-of-gastric-cancer
#9
Takahiro Horimatsu, Shin'ichi Miyamoto, Yoko Mashimo, Hiroshi Okabe, Yoshiki Mikami, Tsutomu Chiba, Manabu Muto
A 50-year-old woman who presented with a one-month history of abdominal fullness and dyspnoea was admitted to our hospital. Esophagogastroduodenoscopy showed the scirrhous-type gastric cancer on the greater curvature of the gastric body. Computed tomography revealed bilateral large ovarian tumours with massive right pleural effusion and ascites. A repeated cytological examination of pleural effusion and ascites revealed no malignant cells. The definitive diagnosis of pseudo-Meigs' syndrome was made by confirming the fact that pleural effusion and ascites disappeared after bilateral oophorectomy...
2015: Internal Medicine
https://www.readbyqxmd.com/read/26377236/a-case-of-mixed-connective-tissue-disease-with-pseudo-pseudo-meigs-syndrome-ppms-like-features
#10
C K Cheah, S Ramanujam, N Mohd Noor, C Gandhi, Beryl A D Souza, S C Gun
Pseudo-pseudo Meigs' syndrome (PPMS) has been reported to be a rare presentation of patients with systemic lupus erythematosus (SLE). However, such a presentation is not common in other forms of connective tissue disease. We presented a case of gross ascites, pleural effusion, and marked elevation of CA-125 level (PPMS-like features) that led to a diagnosis of MCTD. The patient responded to systemic steroid therapy.
February 2016: Lupus
https://www.readbyqxmd.com/read/26334600/pseudo-meig-s-syndrome-in-a-woman-on-ulipristal-acetate
#11
Barry Sanders
No abstract text is available yet for this article.
June 2015: Journal of Obstetrics and Gynaecology Canada: JOGC, Journal D'obstétrique et Gynécologie du Canada: JOGC
https://www.readbyqxmd.com/read/26148741/serous-cystadenoma-and-fibrothecoma-a-rare-combination-in-collision-tumor-of-ovary-with-pseudo-meigs-syndrome
#12
Shirish S Chandanwale, Sukanya S Pal, Harsh B Kumar, Amit B Sammi
No abstract text is available yet for this article.
March 2015: Journal of Pathology and Translational Medicine
https://www.readbyqxmd.com/read/26137781/-benign-ovarian-pathology-findings-in-pre-operative-and-intra-operative-signs-suggestive-of-malignancy-case-series
#13
Hristamian Armand, Veselka Hristamian
Case 1--22 year old patient with dense permagnum adult teratoma, ascites, ipsilateral hydro-ureter and hydro-nephrosis, elevated C -125 level a pseudo- military peritoneal spread. Case 2--19 -year old patient with endometrial kystoma, originating at the uterine fundus with with elevated C-125 levels. Case 3--22 year old patient with monstrous tecoma permagnum, ascites and concomitant pleural effusions as in Meigs syndrome. Case 4--66 year old patient, multiparous with granular cell tumor, recurrent uterine bleeds and endometrial poliposis, with ambiguous C-125 level and congenital uterus bicornis bicolis anomaly...
2015: Akusherstvo i Ginekologii︠a︡
https://www.readbyqxmd.com/read/25891047/cellular-leiomyoma-with-necrosis-and-mucinous-degeneration-presenting-as-pseudo-meigs-syndrome-with-elevated-ca125
#14
Ruiying Dong, Chengjuan Jin, Qing Zhang, Xingsheng Yang, Beihua Kong
Pseudo-Meigs' syndrome is a syndrome rarely caused by leiomyomas. Elevated CA125 usually suggests malignancy of the ovary. No reported case of pseudo-Meigs' syndrome presenting with necrosis and mucinous degeneration of uterine cellular leiomyomas (CLs) and an elevated CA125 level was found upon a PubMed search. A 37-year-old woman presenting with massive ascites, bilateral pleural effusions and a pelvic mass measuring 20 x 18 x 10 cm is described. The pre-operative serum CA125 was 920.4 U/ml. After total abdominal hysterectomy and partial omentumectomy, the final pathologic diagnosis was CL with focal hemorrhage, necrosis and mucinous degeneration...
June 2015: Oncology Reports
https://www.readbyqxmd.com/read/25789033/coexistence-of-benign-struma-ovarii-pseudo-meigs-syndrome-and-elevated-serum-ca-125-case-report-and-review-of-the-literature
#15
Chengjuan Jin, Ruiying Dong, Hualei Bu, Mingyuan Yuan, Youzhong Zhang, Beihua Kong
Struma ovarii is an uncommon ovarian teratoma comprised predominantly of mature thyroid tissue. The combination of pseudo-Meigs' syndrome, and elevation of CA 125 to the struma ovarii is a rare condition that can mimic ovarian malignancy. We reported a case of benign struma ovarii, presenting with the clinical features of advanced ovarian carcinoma: complex pelvic mass, gross ascites, bilateral pleural effusion and markedly elevated serum CA 125 levels. The patient underwent total abdominal hysterectomy and bilateral salpingo-oophorectomy...
April 2015: Oncology Letters
https://www.readbyqxmd.com/read/25396010/-pseudo-meigs-syndrome-report-of-a-case
#16
Benjelloun Hanane, Morad Sanaa, Zaghba Nahid, Bakhatar Abdelaziz, Yassine Najiba, Bahlaoui Abdelkrim
No abstract text is available yet for this article.
2014: Pan African Medical Journal
https://www.readbyqxmd.com/read/25056475/concentrated-ascites-re-infusion-therapy-for-pseudo-meigs-syndrome-complicated-by-massive-ascites-in-large-pedunculated-uterine-leiomyoma
#17
Yukie Yonehara, Shintaro Yanazume, Masaki Kamio, Shinichi Togami, Takashi Tasaki, Tsutomu Douchi
Pseudo-Meigs' syndrome accompanied by massive ascites in uterine leiomyoma is rare. We encountered a rare case of a 37-year-old, nulliparous woman with a lower abdominal tumor and severe abdominal distention due to massive ascites. Serum cancer antigen 125 and vascular endothelial growth factor levels were elevated to 1007.9 U/mL and 103 pg/mL, respectively. She was tentatively diagnosed with ovarian cancer. Emergency concentrated ascites re-infusion therapy was performed to improve dyspnea, abdominal pain, and her preoperative respiratory condition...
July 2014: Journal of Obstetrics and Gynaecology Research
https://www.readbyqxmd.com/read/24612300/pseudo-meigs-syndrome-associated-with-hydropic-degenerating-uterine-leiomyoma-a-case-report
#18
Tomoko Oguma, Noriyuki Yamasaki, Kentaro Nakanishi, Dan Kinoshita, Tamae Mitsuhashi, Shoko Nakagawa
Pseudo-Meigs' syndrome secondary to uterine leiomyoma is a rare entity. A 50-year-old Japanese woman presented with a 3-month history of shortness of breath. Chest X-ray and magnetic resonance imaging revealed massive right pleural effusion, ascites and a large subserosal uterine myoma. She underwent a total abdominal hysterectomy with bilateral salpingo-oophorectomy. The pathology was consistent with a benign leiomyoma. The ascites and pleural effusion rapidly disappeared postoperatively. The serum interleukin-6 level was 3...
April 2014: Journal of Obstetrics and Gynaecology Research
https://www.readbyqxmd.com/read/24359073/pseudo-meigs-syndrome-secondary-to-endodermal-sinus-tumour
#19
T Song, M K Kim, M-L Kim, B S Yoon, S J Seong, J-Y Kim
No abstract text is available yet for this article.
January 2014: Journal of Obstetrics and Gynaecology: the Journal of the Institute of Obstetrics and Gynaecology
https://www.readbyqxmd.com/read/24359072/massive-ascites-caused-by-a-large-pedunculated-subserosal-uterine-leiomyoma-that-has-feeding-arteries-from-peripheral-tissues-and-exhibits-elevated-ca125-a-case-report-of-atypical-pseudo-meigs-syndrome
#20
H-K Yip, L-W Huang, Y-H Lin, J-L Hwang
No abstract text is available yet for this article.
January 2014: Journal of Obstetrics and Gynaecology: the Journal of the Institute of Obstetrics and Gynaecology
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