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Mucinous Cystadenocarcinoma of the Breast: The Challenge of Diagnosing a Rare Entity

open access: yesRare Tumors, 2017
Mucinous cystadenocarcinoma is an extremely rare variant of primary breast tumor which is histologically similar to mucinous cystadenocarcinoma of the ovary and pancreas. Herein we report a case of a 63 years old woman diagnosed with diverse histological
Nektarios Koufopoulos
exaly   +5 more sources

Primary retroperitoneal mucinous cystadenocarcinoma with transition from the mesothelium [PDF]

open access: yesIJU Case Reports, 2020
Introduction Mucinous cystic neoplasms are uncommon among the tumors that develop in the retroperitoneum. We report a case of primary retroperitoneal mucinous cystadenocarcinoma with pathological considerations.
Naohiro Fujimoto, Ikko Tomisaki
exaly   +3 more sources

Primary mucinous cystadenocarcinoma of the spleen: a case report and literature review [PDF]

open access: yesFrontiers in Medicine
BackgroundTumors of the spleen are uncommon, and most represent metastases from primary organs. Primary mucinous cystadenocarcinoma of the spleen is an extremely rare tumor.
Bo Zhou, Canyang Zhan, Sheng Yan
doaj   +2 more sources

Mucinous cystadenocarcinoma of the breast: a new entity with broad differentials—a case report [PDF]

open access: yesJournal of the Egyptian National Cancer Institute, 2022
Background Mucinous cystadenocarcinoma is a rare and recently described primary breast cancer with strikingly similar histomorphology to ovarian, pancreatic, and gastrointestinal counterparts.
Kanwalpreet Kaur   +3 more
doaj   +2 more sources

Mucinous cystadenocarcinoma of the ovary in a 14-year-old girl: a case report and literature review [PDF]

open access: yesBMC Women's Health, 2023
Background Ovarian epithelial tumors are common in adults, and their peak incidence of onset is over 40 years of age. In children, most ovarian tumors are germ cell-derived, whereas epithelial tumors are rare and mostly benign.
Qiong Li   +4 more
doaj   +2 more sources

Giant ovarian mucinous cystadenocarcinoma: A case report [PDF]

open access: yesClinical Case Reports, 2022
Giant ovarian tumors are rare in the present day due to the early diagnosis and treatment. However, owing to the large size, it can often compress the inferior vena cava and sudden decompression of it during the removal can lead to hemodynamic ...
Bibek Man Shrestha   +9 more
doaj   +2 more sources

Mature cystic teratoma with co-existent mucinous cystadenocarcinoma: describing a diagnostic challenge—a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Mature cystic teratoma co-existing with a mucinous cystadenocarcinoma is a rare tumor that few cases have been reported until now. In these cases, either a benign teratoma is malignantly transformed into adenocarcinoma or a collision tumor is ...
Mahboobeh Chahkandi   +4 more
doaj   +2 more sources

Case report: Short-course hypofractionated radiation therapy combined with immune checkpoint inhibitors for the treatment of advanced ovarian mucinous cystadenocarcinoma [PDF]

open access: yesFrontiers in Oncology
BackgroundOvarian mucinous cystadenocarcinoma is a rare subtype of ovarian epithelial carcinoma that is resistant to platinum-based chemotherapy and has a poor prognosis, and there is no standard treatment plan for patients for whom multiline treatment ...
Xinan Wan   +4 more
doaj   +2 more sources

Ovarian mucinous cystadenocarcinoma in an 11-year-old girl

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Epithelial ovarian tumors are extremely rare in the pediatric age group. Mucinous cystadenocarcinoma in children, a rare form of epithelial tumor, is a malignant cystic ovarian neoplasm.
Reham S. Alsereihi   +2 more
doaj   +1 more source

Mucinous carcinoma of the breast: distinctive histopathologic and genetic characteristics [PDF]

open access: yesKosin Medical Journal, 2022
Mucinous carcinoma is a rare histologic type of breast cancer that, when classified with favorable histology, can be treated with different therapeutic options.
Minjung Jung
doaj   +1 more source

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