Meigs’ syndrome
Authors:
L. Kristková; M. Zvaríková; O. Bílek; D. Dufek; A. Poprach; M. Holánek
Authors place of work:
Klinika komplexní onkologické péče LF MU a MOÚ Brno
Published in the journal:
Klin Onkol 2022; 35(3): 232-234
Category:
Case Report
doi:
https://doi.org/10.48095/ccko2022232
Summary
Background: Meigs’ syndrome is defined by the presence of a benign ovarian tumor, ascites, and pleural effusion (predominantly on the right side). A characteristic sign of Meigs’ syndrome is the complete disappearance of exudate after surgical resection of the ovarian tumor. Case report: We present a case report of a 58-year-old patient admitted for an advanced ovarian tumor with pleural effusion, ascites, and tumor marker elevation typical for ovarian cancer. Cytological examination of ascites and pleural effusion was repeatedly negative for malignancy. Histopathological examination of the biopsied tissue was concluded as low-grade mesenchymal neoplasia. The second opinion of histopathological examination was concluded as low grade fibroblastic pelvic tumor without the possibility of exact specification. Diagnoses of desmoid fibromatosis and low-grade fibromyxiod sarcoma (less likely) were considered. Surgical resection was indicated, and a large tumor with numerous adhesions to the uterus, bladder, and thin loops with a noticeably thickened peritoneum were perioperatively described. Histologically, left ovarian fibroma with productive peritonitis and sanguine-induced ascites was diagnosed. Due to the clinical findings and the result of the histopathological examination, the case was classified as Meigs’ syndrome. Two months after the surgery, the ascites and pleural effusion disappeared, and the tumor marker levels normalized. Conclusion: The present case report documents that it is always necessary to consider diseases other than those most likely at the outset, as the treatment algorithm and prognosis of these rare diseases may differ significantly.
Keywords:
ovarian neoplasms – Ascites – Pleural effusion – Meigs’ syndrome
Zdroje
1. Meigs JV. Fibroma of the ovary with ascites and hydrothorax – Meigs’ syndrome. Am J Obstet Gynecol 1954; 67 (5): 962–987. doi: 10.1016/0002-9378 (54) 90258-6.
2. Okuda K, Noguchi S, Narumoto O et al. A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion. BMC Pulm Med 2016; 16 (1): 71. doi: 10.1186/s12890-016-0241-1.
3. Yamamoto A, Miyasaka Y, Furuya K et al. Pseudo-Meigs’ syndrome due to ovarian metastases from colon cancer: a case report and review of the literature. Surg Case Rep 2016; 2 (1): 112. doi: 10.1186/s40792-016-0209-7.
4. Ali Y, Parakeh AM, Rao RK et al. Meig’s syndrome: a triad of pleural effusion, abdominal ascites, and benign ovarian fibroma. J Int Transl Med 3 (1): 44–46. doi: 10.11910/2227-6394.2015.03.01.09.
5. Yazdani S, Alijanpoor A, Sharbatdaran M et al. Meigs’ syndrome with elevated serum CA125 in a case of ovarian fibroma/thecoma. Casp J Intern Med 2014; 5 (1): 43–45.
6. Jones OW, Surwit EA. Meigs syndrome and elevated CA 125. Obstet Gynecol 1989; 73 (3 Pt 2): 520–521.
7. Lin JY, Angel C, Sickel JZ. Meigs syndrome with elevated serum CA 125. Obstet Gynecol 1992; 80 (3 Pt 2): 563–566.
8. Krenke R, Maskey-Warzechowska M, Korczynski P et al. Pleural effusion in Meigs’ syndrome – transudate or exudate? Medicine (Baltimore) 2015; 94 (49): e2114. doi: 10.1097/MD.0000000000002114.
9. Lacson A, Alrabeeah A, Gillis D et al. Secondary massive ovarian edema with Meig’s syndrom. Am J Clin Pathol 1989; 91 (5): 597–603. doi: 10.1093/ajcp/91.5.597.
10. Samanth KK, Black WC. Benign ovarian stromal tumors associated with free peritoneal fluid. Am J Obstet Gynecol 1970; 107 (4): 538–545. doi: 10.1016/s0002-9378 (16) 33939-4.
11. Dunn JS, Anderson CD, Method MW et al. Hydropic degenerating leiomyoma presenting as pseudo-Meigs syndrome with elevated CA 125. Obstet Gynecol 1998; 92 (4 Pt 2): 648–649. doi: 10.1016/s0029-7844 (98) 00 130-6.
12. Dalvi SR, Yildirim R, Santoriello D et al. Pseudo-pseudo Meigs’ syndrome in a patient with systemic lupus erythematosus. Lupus 2012; 21 (13): 1463–1466. doi: 10.1177/0961203312461291.
13. Lee SY, Lee SW, Chung WT. Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs’ syndrome in lupus patients: two cases reports and a literature review. Clin Rheumatol 2013; 32 (12): 1823–1826. doi: 10.1007/s10067-013-2362-8.
14. Lanitis S, Sivakumar S, Behranwala K et al. A case of Meigs syndrome mimicking metastatic breast carcinoma. World J Surg Oncol 2009; 7 (1): 10. doi: 10.1186/1477-7819-7-10.
15. Aoshima M, Tanaka H, Takahashi M et al. Meigs’ syndrome due to Brenner tumor mimicking lupus peritonitis in a patient with systemic lupus erythematosus. Am J Gastroenterol 1995; 90 (4): 657–658.
16. Carson SA, Mazur MT. Atypical endometrioid cystadenofibroma with Meigs’ syndrome: ultrastructure and S-phase fraction. Cancer 1982; 49 (3): 472–479. doi: 10.1002/1097-0142 (19820201) 49: 3<472:: aid-cncr2820490314>3.0.co; 2-l.
Štítky
Paediatric clinical oncology Surgery Clinical oncologyČlánok vyšiel v časopise
Clinical Oncology
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