scholarly journals Malignant Pelvic Neoplasm

2020 ◽  
Author(s):  
Keyword(s):  
Pelvic Neoplasm

scholarly journals A case of a rare pelvic neoplasm - unusually large angiofibromas

2021 ◽  
Vol 12 (1) ◽  
pp. 95-98
Author(s):  
I. D. Pokladov ◽  
O. N. Chernova ◽  
A. V. Vazhenin ◽  
R. E. Shtentsel
Keyword(s):  
Differential Diagnosis ◽  
Malignant Tumors ◽  
Great Similarity ◽  
Pelvic Tumors ◽  
Average Size ◽  
The Right ◽  
Pelvic Neoplasm

Pelvic tumors are quite common. Of these, angiofibromas are very rare. It is causes difficulties in differential diagnosis. But getting the right diagnosis is important, given the great similarity with other, often malignant tumors. According to the literature, the average size of angiofibromas does not exceed 12 cm. We present the case of a patient with an unusually large angiofibroma.

A rare pelvic neoplasm is discovered during a routine evaluation

2011 ◽  
Vol 24 (1) ◽  
pp. E7-E9
Author(s):  
Lisa Vieira ◽  
Kevin Cunningham ◽  
Melanie Kim
Keyword(s):  
Pelvic Neoplasm

Internal hemipelvectomy with reconstruction for primary pelvic neoplasm: a systematic review

2014 ◽  
Vol 85 (7-8) ◽  
pp. 553-560 ◽  
Author(s):  
Qing Dong Shao ◽  
Xu Yan ◽  
Jiu Yi Sun ◽  
Tian Ming Xu
Keyword(s):  
Systematic Review ◽  
Internal Hemipelvectomy ◽  
Pelvic Neoplasm

Multifocal polypoid endometriosis in a young woman simulating vaginal and pelvic neoplasm

2010 ◽  
Vol 63 (5) ◽  
pp. 452-454 ◽  
Author(s):  
Seema Kaushal ◽  
Vatsla Dadhwal ◽  
Sandeep R Mathur ◽  
Ruma Ray ◽  
Prashant Durgapal ◽  
...  
Keyword(s):  
Young Women ◽  
Vaginal Bleeding ◽  
Oestrogen Receptor ◽  
Clinical Presentation ◽  
History Of ◽  
Pouch Of Douglas ◽  
Age Range ◽  
Pelvic Neoplasm ◽  
Unopposed Oestrogen ◽  
Polypoid Endometriosis

A 27-year-old nulliparous woman presented with large finger-like projections protruding from her vagina. Intraoperatively there were deposits in the pouch of Douglas. Clinical presentation and history of vaginal bleeding suggested malignancy. Histopathology of both the vaginal and pouch of Douglas masses showed endometrial glands and stroma. There was no architectural complexity or cytological atypia of glands or stroma. Immunohistochemistry for oestrogen receptor, progesterone receptor and CD10 was positive. Based on morphological and immunohistochemical findings, multifocal polypoid endometriosis was diagnosed; this is a recently described entity having a clinical presentation and age range completely different from conventional or non-polypoid endometriosis. Although an association between tamoxifen use, unopposed oestrogen therapy and polypoid endometriosis has been suggested, the patient had no history of tamoxifen or oestrogen intake. Polypoid endometriosis should be part of the differential diagnosis in young women presenting with vaginal growth.

Acute appendicitis mimicking pelvic neoplasm

Urology ◽  
1988 ◽  
Vol 32 (2) ◽  
pp. 124-125
Author(s):  
J.R. Kuntze ◽  
E.C. Park ◽  
B.E. Hardy ◽  
M.H. Herman
Keyword(s):  
Acute Appendicitis ◽  
Pelvic Neoplasm

Nonresectable recurrent pelvic neoplasm

1980 ◽  
Vol 9 (2) ◽  
pp. 177-181 ◽  
Author(s):  
Ted Haas ◽  
Herbert J. Buchsbaum ◽  
Samuel Lifshitz
Keyword(s):  
Pelvic Neoplasm

Giant Pelvic Solitary Fibrous Tumor Obstructing Intestinal and Urinary Tract: A Case Report and Literature Review

2007 ◽  
Vol 73 (5) ◽  
pp. 478-480 ◽  
Author(s):  
Bing Yi ◽  
Chandra Bewtra ◽  
K. Yussef ◽  
Edibaldo Silva
Keyword(s):  
Solitary Fibrous Tumor ◽  
Large Bowel Obstruction ◽  
Complete Resection ◽  
Solitary Fibrous Tumors ◽  
Long Term Follow Up ◽  
High Grade Sarcoma ◽  
Fibrous Tumor ◽  
Pelvic Neoplasm

We are reporting a giant pelvic neoplasm, a rare solitary fibrous tumor that presented with a large bowel obstruction and bilateral ureteral obstruction because of its size and location. Preoperative diagnosis required complex pathological studies to exclude a high-grade sarcoma suspected clinically. Complete resection was required for resolution of obstructive symptoms. Prognosis for solitary fibrous tumors is usually good after complete resection. Recurrence and metastasis may be related to rare aggressive histological features, including nuclear atypia, hypercellularity, greater than four mitoses/10 high power fields, and necrosis. Because histology is not always a reliable predictor of prognosis, careful long-term follow-up is necessary for this tumor. Solitary fibrous tumors (SFTs) are rare spindle cell neoplasms most likely arising from mesenchymal cells. SFTs were originally described in the pleura, the most common site for this tumor; however, extrathoracic SFTs are seemingly diagnosed with increased frequency. We report a case of a giant pelvic SFT that required complicated clinical management.

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