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bladder/сарком

Веза се чува у привремену меморију
Страна 1 од 468 резултати

Bladder conservation for muscle-invasive bladder cancer.

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In the UK alone, approximately 10,000 patients are diagnosed with bladder cancer each year. Of these, muscle-invasive bladder cancer stage T2 or T3 accounts for 10-15%, with the remainder being non-muscle-invasive tumors, dealt with by local intravesical treatment. This group of patients are often

Leiomyosarcoma in urinary bladder after cyclophosphamide therapy for retinoblastoma and review of bladder sarcomas.

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We report an unusual case of a leiomyosarcoma of the urinary bladder after chemotherapy for retinoblastoma and the results of a review of the published reports of bladder sarcomas. A 22-year-old man presented with hematuria and was found to have a mass in his urinary bladder on computed tomography.

Immunoblastic sarcoma of the bladder.

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We describe the first case of immunoblastic sarcoma of the bladder. Urologists should be aware of this entity arising in organs that are prone to chronic antigenic stimulation. Treatment consists of radiotherapy for localized lesions and combination chemotherapy for more advanced disease.

An isolated bladder endometriosis misdiagnosed as a bladder tumor.

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Urinary bladder endometriosis as a part of deep infiltrating pelvic endometriosis is well known, but isolated bladder involvement is very rare. A 36-year-old woman, who had two cesarean sections, was complaining of dysuria, frequency and burning micturition. MRI showed a tissular mass probably

[Uncommon bladder tumours].

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Bladder tumours are frequent with around 10,000 new cases each year in France. Less than 500 of these cases are not transitional cell carcinoma, the most frequent pathological aspect. The identification of these pathological patterns requires an initial biopsy through transurethral resection.

Bladder management in children with genitourinary sarcoma.

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Between 1977 and 1991, 14 patients were treated for genitourinary sarcoma (mean age, 7.4 years). The primary site was bladder in six patients, prostate in five, and vagina in three. Histological study showed embryonal rhabdomyosarcoma in 12 and leiomyosarcoma in 2 children. Initial therapy included

[Treatment of five cases of bladder sarcoma].

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Five cases of bladder sarcoma were treated at our Department between January, 1972 and December, 1981. These cases accounted for only 1.5% of the bladder tumors (335 cases) diagnosed during the same period. The patients ranged from 11 months to 67 years old. There were 2 males and 3 females.

Sarcoma of the urinary bladder and prostate in children.

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The survival rate has been improved for rhabdomyosarcoma of all sites in children by combining surgery, radiation and chemotherapy. However, very few children are alive today who have had sarcoma of the prostate. The prognosis appears to be better for sarcoma of the bladder than for sarcoma of the

Management of adult sarcomas of the bladder and prostate.

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Historically, survival of patients with adult pelvic sarcoma of the bladder and prostate has been poor. Between November 1974 and November 1984 we treated 11 patients with leiomyosarcoma: 7 with primary bladder and 4 with prostate tumors. Patients with nonbulky disease underwent surgical resection

Review on gall bladder myeloid sarcoma: a great masquerader

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Pain in abdomen has wide differentials and narrowing down the clinical possibilities depends on type of pain, location, characterization which is usually assisted by imaging studies. Cholecystitis and cholelithiasis are amongst the common causes of acute abdomen. This study reviews the literature

Granulocytic sarcoma of the urinary bladder in a pediatric patient.

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Granulocytic sarcoma (GS) is a rare tumor consisting of immature cells of granulocytic lineage. It is also called chloroma, referring to the green color of the tumor caused by high levels of myeloperoxidase in the cells. GS is often associated with acute myeloblastic leukemia. We report the case of

Angiosarcoma of the bladder: a review.

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OBJECTIVE To present a new case of angiosarcoma of the bladder, review 9 other previously reported cases, and discuss the unique features of our case with regard to presentation, treatment, and clinical course of patients with this exceedingly rare tumor. The utility of multimodality therapy is

Recent advances in pediatric bladder malignancies.

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Urothelial pediatric neoplasms are relatively rare. Papillary urothelial neoplasms of low malignant potential (PUNLMPs) and rhabdomyosarcoma (RMS) are the most common bladder malignancies in the pediatric population. Clinical presentation encompasses macroscopic hematuria or lower urinary tract

Malignant mesodermal (mesenchymal) tumors of bladder.

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Malignant mesodermal tumors originating in the bladder are rare. Only a few cases could be found in large series of autopsies or in gathered series of primary retroperitoneal space tumors. Sarcomas originating in the bladder wall grow rapidly and usually infiltrate into neighboring tissues. Two cass

Myxoid malignant fibrous histiocytoma of the bladder.

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Although the most common soft tissue sarcoma of adulthood, malignant fibrous histiocytoma (MFH) is an extremely rare tumor of the urinary bladder. Only three well-documented cases have been reported in the world literature. The patient presented in this report represents the first case of the myxoid
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