نتایج جستجو برای: spermatic quality

تعداد نتایج: 754543  

Mohsen Houjjati,

SUMMARY Occurance of Malignant Fihrous Histiocytoma (MFH) of the spermatic cord as a primary source is so rare that since I 967 Just 12 of such cases have heen reported (4,8, 10). MFH is one of the pleomorphic soft tissue Malignant tumors which has been studied for first time by Ozzello and Co workers on 1963. The Tumor ong1nates from primary Mesenchymal cells which have both histocytic & fi...

2014
Gautier Müllhaupt Livio Mordasini Tobias Gramann Vera Ertel Hans-Peter Schmid Dominik Abt

We report on a 44-year-old man who underwent microsurgical inguinal repair for symptomatic varicocele. As an incidental finding during surgery, a yellowish tumor (9 × 5 × 4 mm) was found in the spermatic cord. Histologic examination revealed ectopic adrenocortical tissue. Ectopic adrenocortical tissue in the spermatic cord is known to appear in children and adolescents but is extremely rare in ...

2013
Yu Mi Seo Na-Hye Myung Jeong Hee Hong

The fate of testicular salvage in spermatic cord torsion depends on the duration of ischemia and the degree of torsion. Even though spermatic cord torsion (SCT) can occur at any age, it is rarely reported in older patients. If the physician does not pay close attention to this unusual situation, the lack of suspicion for SCT may result in a missed or delayed diagnosis. We report a very uncommon...

2011
M. S. Papageorgiou G. Dadakas K. Donev

Liposarcomas are malignant tumors derived embryologically from mesodermal tissues. An unusual site of presentation is the spermatic cord, presenting as an inguinal or scrotal mass. We report a rare case of a liposarcoma of the spermatic cord, mimicking a testicular tumor. The patient was operated, and an orchidectomy, including the tumor, was performed. To our knowledge, there are about 185 sim...

2008
Alin Chirindel Felipe Martinez Joseph A. Gagliardi Milton F. Armm

We present the case of a 47-year-old man with testicular tuberculosis without epididymal involvement that simulated neoplasm on sonography. The patient also had evidence of contralateral spermatic cord involvement. The diagnosis was made following transinguinal intrascrotal exploration and excisional biopsy of the left spermatic cord mass and right transinguinal radical orchiectomy. Histopathol...

Journal: :Hinyokika kiyo. Acta urologica Japonica 2007
Ryuichi Taue Hirofumi Izaki Ryouichi Nakanishi Kunihisa Yamaguchi Hiroyoshi Nakatzuji Tomoteru Kishimoto Natsuo Oka Tomoharu Hukumori Masayuki Takahashi Masa-aAki Nishitani Hiro-omi Kanayama

A 56-year-old man was diagnosed with a right testicular tumor. Orchiectomy with high ligation of the spermatic cord was performed. Histological examination revealed leiomyosarcoma of the spermatic cord. Distant metastases were not found. The patient was treated with adjuvant radiation therapy to control the disease, since a high incidence of local recurrence has been reported. The patient had n...

Journal: :The Journal of urology 1971
N S Datta S M Singh B C Bapna

Liposarcoma of the spermatic cord is rare. We report 6 cases with followup ranging from 3 months to 23 years from presentation. Initially 4 liposarcomas were well differentiated and 2 had poorly differentiated components. All 6 patients underwent radical orchiectomy and 3 required additional surgical procedures. Although most liposarcomas of the spermatic cord are of low grade and stage, the pr...

Journal: :Canadian Urological Association journal = Journal de l'Association des urologues du Canada 2007
Pankaj Dangle Doddametikurke R Basavaraj Selina Bhattarai Alan B Paul Chandra Shekhar Biyani

A 51-year-old man presented with a 2-year history of painless lump in the left hemiscrotum. Scrotal examination demonstrated a 3-cm, firm-to-hard mass attached to the left spermatic cord. Scrotal ultrasound scan revealed a heterogeneous mass separate from the left testis and epididymis. An orchidectomy was recommended to the patient; however, he declined surgery and underwent excision biopsy of...

2013
Srinivasa Rao Sirasanagandla Satheesha B. Nayak Raghu Jetti Kumar M. R. Bhat

Duplication of vas deferens is a rare congenital anomaly. All previously reported cases of this rare anomaly were identified during procedures such as orchiepexy, inguinal hernia repair, vasectomy, varicocoelectomy, and radical prostatectomy. Here, we report a case of unilateral duplicated vas deferens noted in an adult cadaver during regular dissection for medical students. The right spermatic...

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