Results 11 to 20 of about 24,009 (201)

A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature [PDF]

open access: yesCase Reports in Medicine, 2011
Primary renal mucinous cystadenocarcinoma is a very rare lesion of kidney which originates from the metaplasia of the renal pelvic uroepithelium. Only one case with primary mucinous cystadenocarcinoma has been reported in the English literature.
Abdulkadir Tepeler   +6 more
doaj   +3 more sources

Recurrent Pneumonia Due to an Appendiceal Mucinous Cystadenocarcinoma: A Rare Presentation of a Rare Malignancy

open access: yesClinical Medicine Insights: Oncology, 2009
Mucinous cystadenocarcinoma of the appendix is a rare malignancy. This is a report of a 74-year-old man who presented with recurrent pneumonia which turned out to be a postobstructive pneumonia complicating a large mucinous cystadenocarcinoma of the ...
Karin G. Gerritsen   +6 more
doaj   +4 more sources

Mucinous cystadenocarcinoma of renal pelvis presenting as pyonephrosis

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2014
Mucinous cystadenocarcinoma of renal pelvis is a rare epithelial tumor with poor prognosis. It is postulated to arise from metaplastic glandular mucosa in response to chronic irritation, and comprises less than 0.3% of total renal pelvic tumors.
Rashmi D Patel   +2 more
doaj   +2 more sources

MUCINOUS CYSTADENOCARCINOMA

open access: yesGomal Journal of Medical Sciences, 2018
A 55 years old lady presented to Gynecology outpatient of MMM Teaching Hospital, D.I.Khan in January 2018 with history of abdominal mass. Her abdominal hysterectomy was done one year back. On examination a huge cystic mass reaching up to the xiphisternum
Sadia Anwar, Nasim Saba
doaj   +2 more sources

Primary pulmonary mucinous cystadenocarcinoma presenting as a complex bronchocele: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2009
Introduction Primary pulmonary mucinous cystadenocarcinoma is a rare variety of lung cancer. It is characterized pathologically by copious mucin production predominantly in the extracellular space. This tumour has a remarkably favorable prognosis.
Raza Syed Arsalan   +4 more
doaj   +2 more sources

Primary retroperitoneal mucinous cystadenocarcinoma in a male patient

open access: yesIndian Journal of Pathology and Microbiology, 2016
Primary retroperitoneal mucinous neoplasms are extremely rare tumors. Less than sixty cases have been reported in international literature until date, with striking female predominance.
Anuj Khurana   +2 more
doaj   +2 more sources

Ovarian Mucinous Cystadenocarcinoma with Virilization

open access: yesGynecologic Oncology, 2002
Background. Ovarian neoplasms, other than sex cord–stromal tumors, are rare causes of hyperandrogenism. Only two cases of primary mucinous carcinomas associated with virilization have been reported. Case.
Nezhat, Farr   +3 more
core   +3 more sources

A rare pleural mucinous cystadenocarcinoma mimicking loculated empyema initially: A case report

open access: yesIndian Journal of Radiology and Imaging, 2013
We report a case of pleural mucinous cystadenocarcinoma which was mistaken to be a loculated empyema on chest CT. To the best of our knowledge, this entity has never been previously reported in literature.
Sung Min Moon   +3 more
doaj   +2 more sources

Mucinous cystadenocarcinoma of breast in a 69-year-old woman with positive hormone receptors, the first case reported

open access: yesCaspian Journal of Internal Medicine, 2021
Background: Mucinous cystadenocarcinoma is a relatively uncommon histological subtype of breast cancer that is a cystic form of papillary mucinous carcinoma.  It is regularly negative for estrogen and progesterone receptors and it is most often diagnosed
Ghodsieh Kamrani   +5 more
doaj   +1 more source

Primary Pulmonary Mucinous Cystadenocarcinoma: A Case Report [PDF]

open access: yesCase Reports in Medicine, 2011
Primary pulmonary mucinous cystadenocarcinoma (PMCAC) is an extremely rare cystic neoplasm. A case of a 56-year-old male with a cystic lesion of the right lower lobe is described.
Andreas Efstathiou   +6 more
doaj   +2 more sources

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