A case of paratesticular rhabdomyosarcoma in an 18-year-old male is reported. The patient was admitted for swelling of the right scrotum and right inguinal pain. Malignant tumor of the right testis was suspected and a high inguinal orchiectomy was performed. The pathological diagnosis was paratesticular rhabdomyosarcoma. Following retroperitoneal lymph node extirpation, chemotherapy, so-called CYVADIC therapy, consisting of cyclophosphamide, vincristine, adriamycin and dacarbazine was employed in 3 regions. The patient is in good health without recurrence 16 months after the surgery.

Download full-text PDF

Source

Publication Analysis

Top Keywords

case paratesticular
8
paratesticular rhabdomyosarcoma
8
paratesticular rhabdomyosarcoma]
4
rhabdomyosarcoma] case
4
rhabdomyosarcoma 18-year-old
4
18-year-old male
4
male reported
4
reported patient
4
patient admitted
4
admitted swelling
4

Similar Publications

A CASE REPORT OF DISCONTINUED SPLENOGONADAL FUSION MASQUERADED AS PARATESTICULAR TUMOR.

Georgian Med News

November 2024

Department of Surgery, College of Medicine, Qassim University, Buraydah, Saudi Arabia.

Splenogonadal fusion is a rare congenital anomaly characterized by an unusual linkage between ectopic splenic tissue and the gonad, with a higher prevalence observed in the males. While the majority of the splenogonadal fusion cases are associated with cryptorchidism, the patients may have other congenital malformations such as inguinal hernias. Despite being benign and having a rare occurrence, the preoperative diagnosis of splenogonadal fusion is a challenging one.

View Article and Find Full Text PDF

In this case study, we describe a 46-year-old male presenting with a palpable, gradually enlarging scrotal mass persisting over three to four years, ultimately diagnosed as paratesticular leiomyoma, who underwent enucleation of the tumor with no signs of recurrence, two years after surgery. This report underscores the significance of accurate diagnosis to avoid unnecessary treatment. We also emphasize the sequential events and findings, supported by relevant literature review, that contributed to establishing the correct diagnosis and guiding appropriate treatment decisions.

View Article and Find Full Text PDF

Paratesticular adenomatoid tumors are benign and rare neoplasms, and the management of these lesions is challenging as many cases end up in the operation room due to the lack of specific clinical and radiological features to differentiate them from malignant lesions. We report a case of adenomatoid tumor of the tunica albuginea in a 48-year-old male along with a review of the literature for similar cases in the last 10 years.

View Article and Find Full Text PDF
Article Synopsis
  • Paratesticular inflammatory pseudotumor is a rare condition that can look like cancer, making it hard to diagnose and treat.
  • A 52-year-old man experienced pain in his left testicle, followed by back pain and leg stiffness, leading to a surgery called left radical orchiectomy.
  • The biopsy after surgery confirmed the diagnosis, highlighting the importance of histopathological analysis and timely surgical treatment for these benign tumors.
View Article and Find Full Text PDF
Article Synopsis
  • * A young man was found to have a right scrotal mass initially thought to be a solitary fibrous tumor but was later identified as a benign fibrous pseudotumor after thorough examination.
  • * This case underscores the need for detailed diagnostic methods, like advanced imaging and intraoperative evaluations, to prevent unnecessary surgeries and ensure correct treatment of these benign conditions.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!