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Journal articles on the topic 'Mucinous cystadenoma'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Jacob, Sheba S. K., Ashok Parameswaran, Rajan Santosham, and Rajiv Santosham. "Mucinous cystadenoma of the Thymus presenting as a mediastinal mass in a child." IP Journal of Diagnostic Pathology and Oncology 7, no. 1 (2022): 67–69. http://dx.doi.org/10.18231/j.jdpo.2022.015.

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This is the first case report of a mucinous cystadenoma of the thymus. So this case is reported for awareness that mucinous cystadenomas can occur in the mediastinum with a review of literature and the need for complete surgical excision. A twelve year old girl with a cystic mediastinal mass, presented with dry cough for three weeks. The mass was completely excised as it was huge and causing pressure symptoms. On light microscopy, there was thymic tissue with a mucinous cystadenoma. This is the first report of a mucinous cystadenoma in the thymus. Mucinous cystadenomas can grow into large size

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2

Özcan, Aykut. "Ovarian mucinous cystadenoma recurred 2 years after laparoscopic surgery: A Case Report." Aegean Journal of Obstetrics and Gynecology 4, no. 3 (2023): 65–67. http://dx.doi.org/10.46328/aejog.v4i3.132.

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Objective: Recurrence of ovarian mucinous cystadenomas is very rare. This report describes a case of ovarian mucous cystadenoma in a women that recurred 2 years after surgery. Case presentation: A 22-year-old patient, with a sizable ovarian tumor underwent laparoscopic-assisted cystectomy. On histopathology, the tumor was diagnosed to be an ovarian mucinous cystadenoma. The mucinous cystadenoma recurred 2 years after surgery and subsequently laparoscopic right adnexectomy was performed. Discussion: It has been reported that intraoperative cyst rupture and cystectomy instead of adne

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3

Biswas, Swapan Kumar, Muhammad Mofazzal Hossain, and Arjun Deb. "Mucinous Cystadenoma Arising From Renal Pelvis." Faridpur Medical College Journal 14, no. 2 (2020): 104–6. http://dx.doi.org/10.3329/fmcj.v14i2.48189.

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Primary mucinous cystic tumors occurring in the renal pelvis or the entire pelvicaliceal system are uncommon. Most are mucinous cystadenoma and less frequently mucinous cystadenocarcinomas. In fact, the publications on these neoplasms are limited to a few cases. Because mucinous cystadenomas of kidney are exceedingly rare, little is known about their natural history, pathogenesis and clinicopathologic features. Herein, we describe a case of mucinous cystadenoma arising from the renal pelvis, which resembled hydronephrosis. The patient presented with a history of intermittent dull pain on the l

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4

Ataikiru, Usiwoma Okeroghene, Emil Radu Iacob, Călin Marius Popoiu, Rodica Heredea, Corina Stănciulescu, and Eugen Sorin Boia. "REPETITIVE OVARIAN TORSION AS WARNING SIGN OF SEROUS AND MUCINOUS CYSTADENOMA IN CHILDREN - REPORT OF TWO CASES." Jurnalul Pediatrului XXIII, no. 91-92 (2020): 35–38. http://dx.doi.org/10.37224/jp.2020.9192.06.

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Cystadenomas are surface epithelial-stromal tumors. Although they are the most common type of ovarian tumor, seen mostly from late adolescent age, yet, they remain difficult to accurately diagnose clinically due to their diverse presentations similar to other diseases like functional cyst and appendicitis. We report the cases of two pediatric patients. The first one aged seventeen years and six months old with serous cystadenoma and the second patient aged seventeen years and three months old with mucinous cystadenoma, presenting with abdominal pain in the level of the right iliac fossa and ab

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5

Gupta, Jagdish, Anju Bishnoi, Pallavi Chauhan, and Neeraj Verma. "Diagnostic Odyssey: Unveiling a Giant-infected Mucinous Cystadenoma of the Liver." Haryana Journal of Surgery 1, no. 1 (2025): 20–23. https://doi.org/10.4103/hjs.hjs_6_25.

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Abstract Hepatic mucinous cystadenomas are rare cystic tumors that account for <5% of all liver cysts. These neoplasms can arise within the hepatic parenchyma or, less commonly, in the extrahepatic bile ducts. They are seen exclusively in females. They are usually symptomatic but occasionally may be detected incidentally. They may present with features of compression of adjacent organs or as dull aching pain. No cases have been reported of hepatic mucinous cystadenoma filled with purulent material. We present the rare case of a giant-infected mucinous cystadenoma of the liver in a young fem

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6

Alasio, Teresa M., James Borin, Kevia Taylor, Natan Bar-Chama, and Pamela D. Unger. "Intratesticular Mucinous Cystadenoma: Immunohistochemical Comparison With Ovarian and Colonic Tissue." Archives of Pathology & Laboratory Medicine 129, no. 3 (2005): 399–402. http://dx.doi.org/10.5858/2005-129-399-imcicw.

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Abstract We report a case of a primary intratesticular mucinous cystadenoma in an asymptomatic 39-year-old man. The mass was found incidentally during a consultation for infertility. Pathologic examination of the orchiectomy specimen revealed a unilocular cyst lined with bland mucinous epithelium and mucinous extravasation, consistent with a diagnosis of mucinous cystadenoma. Foci of bone were also found in association with extensive chronic inflammation. Immunohistochemical stains performed showed immunoreactivity for cytokeratin 7, and nonreactivity for cytokeratin 20, CA125, chromogranin, a

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7

Ye, Feng, Yanli Li, Ying Hu, Caiyun Zhou, Yuting Hu, and Huaizeng Chen. "Stage-Specific Embryonic Antigen 4 Expression in Epithelial Ovarian Carcinoma." International Journal of Gynecologic Cancer 20, no. 6 (2010): 958–64. http://dx.doi.org/10.1111/igc.0b013e3181e6fee1.

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Introduction:Stage-specific embryonic antigen 4 (SSEA-4) is a widely used marker to monitor the differentiation of pluripotent embryonic stem cells. Little is known about the expression pattern of SSEA-4 in solid tumors up to now.Methods:In this study, we investigated the expression of SSEA-4 in 479 cases of various degrees of ovarian epithelial lesions by immunohistochemistry, consisting of 45 normal ovarian epithelia, 110 benign serous ovarian cystadenomas, 68 borderline serous ovarian cystadenomas, 104 invasive serous ovarian carcinomas, 64 benign serous mucinous cystadenomas, 48 borderline

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8

Olimov, B. P., N. S. Balabin, J. V. Kuleznova, et al. "Mucinous Cystadenoma of the Cystic Duct." Journal of oncology: diagnostic radiology and radiotherapy 6, no. 3 (2023): 64–71. http://dx.doi.org/10.37174/2587-7593-2023-6-3-64-71.

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A rare clinical observation of a cystic formation of the biliary system — mucinous cystadenoma of the cystic duct is presented. This type of tumors is benign, but in 20 % of cases their malignancy is described. They are often detected incidentally during routine examination and require surgical treatment, regardless of clinical manifestations. Difficulties in differential diagnosis led to unreasonably long follow-up, ending with malignancy of cystadenomas, which reduces the possibility of radical surgical treatment. Therefore, timely detection and differentiation of biliary mucinous cystadenom

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9

Wilson, Mitchell P., Prayash Katlariwala, June Hwang, and Gavin Low. "Radiographic Features of a Benign Mixed Brenner Tumor and Mucinous Cystadenoma: A Rarely Identified Ovarian Neoplasm on Imaging." Journal of Clinical Imaging Science 10 (April 27, 2020): 22. http://dx.doi.org/10.25259/jcis_1_2020.

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Imaging features of benign mixed Brenner tumor and mucinous cystadenomas are rarely reported. This report aims to describe the case of a benign mixed Brenner tumor and mucinous cystadenoma with a dominant Brenner tumor component and to review the typical imaging features of this ovarian neoplasm.

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10

H., Tamour, Ait Belaid W., Ahbala T., Rabbani K., and Louzi A. "HYDATIC CYST OF THE LIVER OR HEPATIC MUCINOUS CYSTADENOMA." International Journal of Advanced Research 9, no. 11 (2021): 35–39. http://dx.doi.org/10.21474/ijar01/13709.

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Mucinous cystadenomas of the liver are rare cystic neoplasms, often mistaken for simple cysts or hydatid cysts of the liver. They are generally benign tumors, often discovered incidentally on imaging or during independent surgeries. Despite their tendency to grow slowly, mucinous cystadenomas of the liver can reach symptomatic dimensions. And given their potential for malignant transformation into mucinous cystadenocarcinomas, a misdiagnosis can have serious secondary consequences. We report the case of a 55-year-old woman with chronic right hypochondrium pain in whom a mucinous cystadenoma of

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11

De Lima Jr, Mario Maciel, Mario Maciel De Lima, and Fabiana Granja. "Primary testicular mucinous cystadenoma: Case report and literature review." Canadian Urological Association Journal 9, no. 11-12 (2015): 814. http://dx.doi.org/10.5489/cuaj.3218.

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Testicular mucinous cystadenomas are rare in urological practice, and their histogenesis, course and management are debated. We report a primary testicular mucinous cystadenoma in a 54-year old male who presented with left testicular swelling and pain. He denied having a history of cryptorchidism, testicular trauma, infections, urinary complaints, or febrile illnesses. He did not have diabetes, but was on treatment for hypertension. The patient underwent a left inguinal radical orchiectomy, and histological examination of the resected tumour confirmed a primary testicular mucinous cystadenoma.

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12

Butt, Umber Irshad, Gulfishan Zameer, Aatiqa Rana, and Sameer Anjum. "Mucinous Cystadenoma of Parotid Gland: A Rare Entity." BioMedica 39, no. 2 (2023): 50–53. http://dx.doi.org/10.24911/biomedica/5-1025.

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<p>Cystadenoma is a benign salivary gland tumor that develops very infrequently. The commonest site for their occurrence is minor salivary glands, where these present as cystic growths with papillary projections. Cystadenomas are often interpreted as mucous retention cysts. Therefore, histopathological confirmation is essential for further treatment and follow-up of the patients, even after the surgery, to keep a check on the recurrence and, in the long run, the exclusion of the possibility of malignant transformation. We report a case of mucinous cystadenoma of the salivary gland occurr

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13

Kulkarni, Jayshree, Manasvi Milind Kulkarni, Shankar Burute, and Rajkumar Salunke. "Massive ovarian mucinous cystadenoma with torsion: A surgical wonder." Indian Journal of Obstetrics and Gynecology Research 11, no. 1 (2024): 124–27. http://dx.doi.org/10.18231/j.ijogr.2024.025.

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Mucinous cystadenomas are some of the commonly encountered ovarian tumors, having huge size which causes pain, pressure, distension, genito urinary symptoms etc. Eventually, these tumors are prone to life threatening complications, like hemorrhage or torsion. These cases may remain asymptomatic for a long period of time. For further diagnosis of symptomatic patients clinical examinations and radiological investigations can be used and help the surgeon in deciding management. We hereby report a case involving a very large mucinous cystadenoma, measuring 25 × 24 centimeter with torsion. The data

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14

Chen, Gau-Yang, and Guan-Chin Tseng. "Mucinous Cystadenoma." New England Journal of Medicine 345, no. 14 (2001): 1041. http://dx.doi.org/10.1056/nejmicm960402.

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15

Schell, Andrew J., Curtis J. Nickel, and Phillip A. Isotalo. "Complex mucinous cystadenoma of undetermined malignant potential of the urachus." Canadian Urological Association Journal 3, no. 4 (2013): 39. http://dx.doi.org/10.5489/cuaj.1139.

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Urachal mucinous neoplasms are rare and include both villousadenomas and invasive adenocarcinomas. These mucinous tumoursshould be completely excised as they can demonstrate aggressiveclinical behaviour, including the development of pseudomyxomaperitonei. We describe a 70-year-old woman who presented witha lower abdominal mass and received a diagnosis of a rare, complexurachal mucinous cystadenoma of undetermined malignant potential.This tumour demonstrated extensive mucin extravasation intoperivesical soft tissue, but was not associated with pseudomyxomaperitonei or any malignancy. Rarely des

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16

S., Shreevidya Bhat Y., Neha Tabassum, Mehvish Anjum, and Nivedita D. "A rare case of mucinous cystedenoma in adoloscence." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 13, no. 9 (2024): 2555–57. http://dx.doi.org/10.18203/2320-1770.ijrcog20242523.

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Mucinous cystadenomas are one of the rarely found benign ovarian neoplasms seen in adolescents. They are commonly known for their massive size causing compressive effects ranging from pressure, pain, bloating, and urinary symptoms. As time passes by, these adnexal masses can lead to severe and fatal complications, such as ovarian torsion or haemorrhage. Accidental findings of these tumours are common as many of these patients are usually asymptomatic. Pelvic examinations and imaging studies can be used to further diagnose symptomatic patients and aid physicians in developing an appropriate cou

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17

Wirtzfeld, Debrah A., Lorne M. Price, Maire A. Duggan, Shaun AC Medlicott, and Francis R. Sutherland. "Mucinous Cystadenoma of the Appendix in a Patient with Systemic Lupus Erthematosus." Canadian Journal of Gastroenterology 12, no. 8 (1998): 573–76. http://dx.doi.org/10.1155/1998/317346.

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A 38-year-old female with systemic lupus erythematosus presented with abdominal pain, diarrhea and iron-deficient anemia. Computed tomogram showed a 2x4 cm inhomogeneous lesion of the right adnexa. An unusual mass was identified extending from the appendiceal orifice at colonoscopy, and an 8 cm tubular appendix, apparently prolapsed into the cecum, was identified at celiotomy. An appendectomy with cecectomy was performed. On cut section, mucin was extruded from the lumen of the appendix. A mucinous neoplasm of the appendix with mucinous dissection to the serosal surface was reported at the tim

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18

Subramony, Charu, Saied Habibpour, and Luis A. Hashimoto. "Retroperitoneal Mucinous Cystadenoma." Archives of Pathology & Laboratory Medicine 125, no. 5 (2001): 691–94. http://dx.doi.org/10.5858/2001-125-0691-rmc.

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Abstract Primary retroperitoneal mucinous cystadenoma is an uncommon tumor found exclusively in women. Herein, we describe a patient who had resection of a large retroperitoneal cystic mass. Histologic, immunohistochemical, and electron microscopic examination of the lining epithelial cells showed features of mesothelial cells in addition to ovarian mucinous cystadenoma. These findings suggest that these tumors arise from inclusions of mesothelial cells and subsequent mucinous metaplasia of the lining cells to form a cystadenoma. Estrogen receptors may be implicated in tumor promotion, explain

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19

Agrawal, Sujan N., Manisha Goyal, and Sanjay Prasad. "Mucinous cystadenoma of both ovaries and appendix: a case report." International Surgery Journal 11, no. 4 (2024): 681–84. http://dx.doi.org/10.18203/2349-2902.isj20240765.

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Epithelial neoplasm of ovaries is common and almost 40% of them are benign. Cystadenoma of ovary is the commonest epithelial neoplasm. They can be serous or mucinous. They arise from the surface epithelium of ovary, some of them may have germ cell origin. They are multilocular. 80% of ovarian mucinous cyst are benign cystadenoma. They are unilateral in 95% of cases. In this case presentation, it was bilateral and appendix was also showing mucinous cystic degeneration. The mucinous cystadenoma of the appendix is the most common mucinous cyst of the appendix, but the definite diagnosis is made a

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20

Honnef, Ingo, Michael Moschopulos, and Thomas Roeren. "Appendiceal Mucinous Cystadenoma." RadioGraphics 28, no. 5 (2008): 1524–27. http://dx.doi.org/10.1148/rg.285075160.

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21

Kehagias, Dimitris T., Eleni E. Karvounis, Alexis Fotopoulos, and Athanassios D. Gouliamos. "Retroperitoneal mucinous cystadenoma." European Journal of Obstetrics & Gynecology and Reproductive Biology 82, no. 2 (1999): 213–15. http://dx.doi.org/10.1016/s0301-2115(98)00254-1.

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22

Sheen-Chen, Shyr-Ming, and Hock-Liew Eng. "Retroperitoneal Mucinous Cystadenoma." Digestive Diseases and Sciences 51, no. 4 (2006): 752–53. http://dx.doi.org/10.1007/s10620-006-3202-3.

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23

Pennell, Timothy C., and John P. Gusdon. "Retroperitoneal mucinous cystadenoma." American Journal of Obstetrics and Gynecology 160, no. 5 (1989): 1229–31. http://dx.doi.org/10.1016/0002-9378(89)90201-9.

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24

Arribas, Dolores, Alfonso Cay, Alberto Latorre, Elena C�rdoba, Fernando Mart�nez, and Javier Lagos. "Retroperitoneal mucinous cystadenoma." Archives of Gynecology and Obstetrics 270, no. 4 (2003): 292–93. http://dx.doi.org/10.1007/s00404-003-0515-8.

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25

Rouchaud, A., L. Glas, M. Gayet, and M. F. Bellin. "Appendiceal mucinous cystadenoma." Diagnostic and Interventional Imaging 95, no. 1 (2014): 113–16. http://dx.doi.org/10.1016/j.diii.2013.07.015.

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26

Uschuplich, Vedran, John R. Hilsenbeck, and Claude R. Velasco. "Paratesticular Mucinous Cystadenoma Arising From an Oviduct-Like Müllerian Remnant: A Case Report and Review of the Literature." Archives of Pathology & Laboratory Medicine 130, no. 11 (2006): 1715–17. http://dx.doi.org/10.5858/2006-130-1715-pmcafa.

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Abstract A mucinous cystadenoma of the paratestis arising from an unequivocal oviduct-like structure in an 18-year-old man is reported. Mucinous cystadenomas of the testis and paratestis are extremely rare benign tumors of controversial origin. The diagnosis may be challenging and is of clinical importance because these lesions may mimic a teratoma, and teratomas in postpubertal males carry a malignant potential regardless of the degree of maturation. A few case reports and reviews of testicular and paratesticular mucinous neoplasms resembling ovarian tumors have suggested the possibility of a

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27

Park, Guppeum, Soe Lwin Aye, Sobirjon Mamarajabov, and Hwunjae Lee. "A case study of pancreatic cystadenomas in an old woman." Journal of Medical Imaging 7, no. 1 (2024): 29–34. https://doi.org/10.31916/sjmi2024-01-05.

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Serous cystadenoma of the pancreas is a rare, benign neoplasm that is often discovered incidentally during imaging studies for unrelated health concerns. These tumors are typically asymptomatic and characterized by multiple small cysts filled with clear serous fluid. Despite their benign nature, accurate diagnosis is crucial to distinguish them from other pancreatic cystic lesions, particularly those with malignant potential, such as mucinous cystadenomas, pseudocysts, and intraductal papillary mucinous neoplasms (IPMN). This report presents a case of a 67- year-old female who was referred for

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Nuțu, Vlad, Eugen Târcoveanu, Ana-Maria Axentioi, et al. "Tumors in a pandemic era: giant ovarian mucinous cystadenomas." Jurnalul de Chirurgie 18, no. 2 (2022): 148–56. http://dx.doi.org/10.7438/jsurg.2022.02.06.

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Tumors in the pandemic era: giant ovarian mucinous cystadenoma. Mucinous cystadenoma is a benign tumor of the ovary originating from the surface epithelium of the ovary, characterized by mucin production. They represent 10-15% of ovarian tumors. The borderline variety represents 10% of mucinous cystadenomas. They can reach very large sizes. We present the case of a patient, aged 65, hospitalized at the end of pandemics with a giant abdominal cystic tumor (diameter 40 cm) with compression disorders. He had a subtotal hysterectomy for uterine fibroids at the age of 25. Laboratory tests are withi

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De Vis, Maarten, Stefanie Brock, Stefan Cosyns, and Brigitte Velkeniers. "A rare cause of postmenopausal hyperandrogenism." BMJ Case Reports 14, no. 1 (2021): e237505. http://dx.doi.org/10.1136/bcr-2020-237505.

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We present an unusual case of mucinous cystadenoma presenting with severe virilisation in a postmenopausal woman. A 71-year-old woman was referred to our outpatient endocrinology clinic because of rapidly progressive androgenic alopecia, clitoromegaly and male pattern pubic hair growth for 1 year. Her medical history was unremarkable. The serum testosterone level was 3.35 µg/L (normal range, <0.4 µg/L), and the dehydroepiandrosterone sulfate level was 267 µg/L (normal range, 100–800 µg/L). MRI of the abdomen revealed a 4×4 cm cystic ovarian mass. A bilateral salpingo-oophorectomy was perfor

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30

Annal, Anjana, Zareena A. Khalid, and Swati Francis. "The treatment approach of a 12 kg giant ovarian mucinous cystadenoma in a 13-year-old: a case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 10, no. 2 (2021): 758. http://dx.doi.org/10.18203/2320-1770.ijrcog20210072.

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Epithelial ovarian tumours are rare in the adolescent age group, accounting for less than 15% of overall ovarian malignancy. Of this, one-fourth of them are mucinous in nature. Mucinous cystadenomas, being precursors of borderline and invasive ovarian tumours, can reach to size as large as 15-30 cm in diameter without having malignant potential. Also, intraoperative management of such large abdominal mass can be challenging. We present a case of a giant unilateral 12 kg mucinous cystadenoma in a 13-year-old young girl, that grew over a period of 1 year. She underwent left salpingo-oophorectomy

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Anuradha, Ananthaneni, Undavalli Suresh Babu, Penumala Vignatha, and Bagalad S. Bhavana. "Papillary mucous cystadenoma of parotid gland." International Journal of Scientific Reports 3, no. 12 (2017): 322. http://dx.doi.org/10.18203/issn.2454-2156.intjscirep20175387.

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<p>Cystadenomas are rare benign salivary gland tumours characterised by prominent epithelium-lined papillary projections into the cystic spaces. Cystadenoma accounts for 2% of all salivary gland tumors, occurring most commonly in major salivary glands. Histopathologically there are two variants, papillary and mucinous variant. However very few cases are being reported in literature. We report a case of papillary cystadenoma occuring in parotid gland in a 28 year old male patient. Clinically, it presents as a soft, fluctuant, sessile and non-tender swelling measuring about 4×3.5 cm in dia

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Bajaj, Anubha. "The Muculent Bleb-Mucinous Cystic Neoplasm-Hepatobiliary Region." Cell & Cellular Life Sciences Journal 9, no. 1 (2024): 1–3. http://dx.doi.org/10.23880/cclsj-16000201.

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Mucinous cystic neoplasm configures as a cystic neoplasm incriminating the hepatic parenchyma. Tumour is constituted of multi-locular or cystic cavity layered with mucinous or biliary type epithelium encompassed within an ovarian type stroma. The cystic lesion appears non communicative with adjoining bile ducts. Additionally designated as hepatobiliary cystadenoma, biliary cystadenoma or cystadenoma with mesenchymal stroma, neoplasms associated with invasive carcinoma component may be denominated as hepatobiliary cystadenocarcinoma.

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Rabie, Mohammad Ezzedien, Mubarak Al Shraim, Mohammad Saad Al Skaini, et al. "Mucus Containing Cystic Lesions “Mucocele” of the Appendix: The Unresolved Issues." International Journal of Surgical Oncology 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/139461.

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Background. Mucocele of the appendix is a rare condition, the pathological classification and management strategy of which have not been standardized yet.Aim. To report on our management of appendiceal mucocele, highlighting the pitfalls and possible means for avoiding them.Materials and Methods. Our registries were reviewed to retrieve cases of appendiceal mucocele, encountered in the period from July 2008 to May 2013.Results. We had 9 cases, three males and sex females, with a median age of 62 years. Abdominal ultrasound (US) and computerized axial tomography scan (CT) suspected the diagnosi

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Gupta, Jagdish, and Archit Gupta. "Ruptured primary mucinous cystadenoma of spleen leading to mucinous ascites." BMJ Case Reports 12, no. 11 (2019): e231212. http://dx.doi.org/10.1136/bcr-2019-231212.

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Mucinous cystadenoma are rare benign mucin-producing tumours. Primary mucinous neoplasms most commonly involve ovary, pancreas or appendix. They may rupture to produce mucous ascites/pseudomyxoma peritonei. We are describing a 51-year-old man who presented to us with symptomatic gallstone disease but during preoperative ultrasound was found to have cystic lesions in spleen with free fluid in the abdomen. Splenectomy and drainage of mucin were done. Histopathology was done and a final diagnosis of primary mucinous cystadenoma of spleen with mucinous ascites was made.

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Mishina, Ana, Ludmila Velenciuc, Eugenia Crivceanscaia, and V. Petrovici. "GIANT OVARIAN MUCINOUS CYSTADENOMA." Arta Medica 86, no. 1 (2023): 67–71. https://doi.org/10.5281/zenodo.7830984.

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<strong>Objectives. </strong>Mucinous ovarian tumors are a variant of epithelial neoplasms and constitute from 10% to 15% of the structure of primary ovarian neoplasms. <strong>Case presentation. </strong>Giant mucinous ovarian tumors are a rather rare phenomenon and are presented in the specialized literature as sporadic observations. Given the rarity of giant mucinous ovarian tumors, we present our own clinical observation. Patient C., 24 years old, was hospitalized for surgical treatment with detected giant volume formation for 5 months. It causes pain in the lower abdomen, the increase in

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Mishra, Pragnya P., Anuradha Calicut Kini Rao, Madan K, and Siddhartha Biswas. "A rare collision tumor of ovary – Mucinous cystadenoma with adult granulosa cell tumor." Indian Journal of Pathology and Oncology 9, no. 1 (2022): 68–70. http://dx.doi.org/10.18231/j.ijpo.2022.014.

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Though collision tumors have been reported earlier like serous cystadenoma and mature cystic teratoma, combination of mucinous cystadenoma and adult granulosa cell tumor is rarely reported in the literature. Collision tumors lack the histological cellular intermingling which is seen in composite tumors. Both involve two morphologically and immunohistochemically distinct neoplasms coexisting within a single organ. Mucinous cystadenoma is a benign cystic surface epithelial tumor of ovary. Granulosa cell tumor(GCT) is a low grade malignancy arising from sex cord stromal cells of ovary and need a

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37

Wang, Diping, and Norbert Sule. "Mucinous Cystadenoma of the Urachus and Review of Current Classification of Urachal Mucinous Cystic Neoplasms." Archives of Pathology & Laboratory Medicine 143, no. 2 (2018): 258–63. http://dx.doi.org/10.5858/arpa.2017-0319-rs.

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Urachal neoplasms are uncommon and represent a minor portion of bladder tumors. According to the recently updated World Health Organization classification (2016), these tumors are classified as adenomas, adenocarcinomas, nonglandular neoplasms, and mixed carcinomas. The mucinous cystic neoplasms represent a small percentage of urachal tumors with morphologic spectrum ranging from benign mucinous cystadenoma to borderline mucinous cystic tumor of low malignant potential and to malignant mucinous cystadenocarcinoma. Benign urachal mucinous cystic adenomas are exceedingly rare, and only a few cas

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Mosimann, F., C. Ribaux, and P. Schnyder. "Cystic Neoplasms of the Exocrine Pancreas." HPB Surgery 2, no. 3 (1990): 165–75. http://dx.doi.org/10.1155/1990/24762.

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Cystic neoplasms of the pancreas are rare and their diagnosis and treatment can be difficult. This report details 7 patients who had histologically proven serous cystadenoma4, mucinous cystadenoma2 and cystadeno carcinoma1. Computed tomography and sonography allowed excellent preoperative assessment but to attempt a distinction between the histological variants may be hazardous. Two tumours were only autopsy findings and 5 patients underwent laparotomy. It is confirmed that potentially malignant mucinous cystadenomas and cytadenocarcinomas should be resected whenever possible; serous cystadeno

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Bhatia, P. K., Kirti Savyasacchi Goyal, Himanshu Tanwar, and Prakash Biswas. "Primary retroperitoneum mucinous cystadenoma." International Surgery Journal 7, no. 2 (2020): 554. http://dx.doi.org/10.18203/2349-2902.isj20200318.

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Primary retroperitoneal mucinous cystadenomas (PRMCs) are observed more frequently in women with no specific symptoms. A 35 Years old female patient presented with Intermittent abdominal pain in her left flank associated with fullness in abdomen. CECT confirmed a well-defined smoothly marginated homogenous non-enhancing unilocular cystic lesion in retroperitoneum in left lumbar region, separated from the pancreas, left kidney and ovary. On Laprotomy, the retroperitoneal tumor was completely removed, without spillage of its contents.

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Lee, Seok Youn, and Weon Cheol Han. "Primary Retroperitoneal Mucinous Cystadenoma." Annals of Coloproctology 32, no. 1 (2016): 33. http://dx.doi.org/10.3393/ac.2016.32.1.33.

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Lai, Eric C. H., K. M. Chung, and W. Y. Lau. "Primary retroperitoneal mucinous cystadenoma." ANZ Journal of Surgery 76, no. 6 (2006): 537. http://dx.doi.org/10.1111/j.1445-2197.2006.03768.x.

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Matsuo, Toshihiro, Norman Yusuke Kimura, Shinzo Takamori, and Kazuo Shirouzu. "Recurrent pulmonary mucinous cystadenoma." European Journal of Cardio-Thoracic Surgery 28, no. 1 (2005): 176–77. http://dx.doi.org/10.1016/j.ejcts.2005.04.006.

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Zevallos Quiroz, Julio César, Francisco Javier Toran Monserrat, Fernando Jesús de Santiago Urquijo, Enrique Pedro Cormenzana Lizarribar, and José María Arrinda Yeregui. "Primary Retroperitoneal Mucinous Cystadenoma." Cirugía Española (English Edition) 94, no. 6 (2016): 365–66. http://dx.doi.org/10.1016/j.cireng.2016.06.001.

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Díaz de Liaño, A., E. Olivera, C. Artieda, C. Yárnoz, and H. Ortiz. "Intrahepatic mucinous biliary cystadenoma." Clinical and Translational Oncology 9, no. 10 (2007): 678–80. http://dx.doi.org/10.1007/s12094-007-0122-4.

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Gupta, Sanjay, Rajeev Sharma, Ashok K. Attri, and Ravinder Kaur. "Mucinous cystadenoma of appendix." Indian Journal of Surgery 70, no. 5 (2008): 254–55. http://dx.doi.org/10.1007/s12262-008-0074-0.

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Wu, Jingjun, Ailian Liu, Anliang Chen, and Pengxin Zhang. "Urachal borderline mucinous cystadenoma." Medicine 96, no. 47 (2017): e8740. http://dx.doi.org/10.1097/md.0000000000008740.

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Nardi, Walter Sebastián, Pablo Dezanzo, and Sergio Damián Quildrian. "Primary retroperitoneal mucinous cystadenoma." International Journal of Surgery Case Reports 39 (2017): 218–20. http://dx.doi.org/10.1016/j.ijscr.2017.08.029.

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Rifki Jai, S., R. Bouffetal, F. Chehab, D. Khaiz, and A. Bouzidi. "Primary retroperitoneal mucinous cystadenoma." Archives of Gynecology and Obstetrics 280, no. 3 (2009): 479–83. http://dx.doi.org/10.1007/s00404-008-0925-8.

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Grover, Dr A. S., Dr Abhitesh Singh, Dr Guramritpal Singh, and Dr Sumeet Mahajan. "Appendiceal Mucinous Cystadenoma – An Incidental Finding." Scholars Journal of Medical Case Reports 4, no. 7 (2016): 534–36. http://dx.doi.org/10.21276/sjmcr.2016.4.7.23.

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Gaffoor, Nidha, Archana Shetty, Aparna Muralidhar, and N. Nagendra Prasad. "Mesenteric mucinous cystadenoma: a diagnostic conundrum." New Indian Journal of OBGYN 9, no. 2 (2023): 394–97. http://dx.doi.org/10.21276/obgyn.2023.9.2.40.

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