Solitary fibrous tumors（SFT）is rare Mesenchymal tissue tumor，originally identified and usually found in the pleura，but the incidence of SFT in the spermatic cord is particularly rare.This article reported a case of a 37-year-old patient who was admitted for a right inguinal mass over the past 2 years. Preoperative MR examination showed a right spermatic cord-derived mass. Under spinal anesthesia，excision of the right spermatic cord mass was performed. Postoperative pathological diagnosis was spermatic cord solitary fibrous tumor. Twelve months of follow-up revealed no metastasis and recurrence on imaging examination. Solitary fibrous tumors of the spermatic cord are rare and require a combination of pathological examination and immunohistochemistry to confirm the diagnosis. Once the diagnosis is confirmed，tumor resection should be performed as soon as possible，and benign lesions are also at risk of recurrence，and long-term follow-up is required after surgery.

This article reports a case of a 55-year-old patient who was admitted to the hospital due to an 8-year history of a right epididymal mass and intermittent right scrotal heaviness for 1 month. Preoperative ultrasound examination revealed a right epididymal cyst and right testicular hydrocele. Under general anesthesia, a right epididymal mass resection and right testicular tunica vaginalis inversion procedure were performed. Postoperative pathological diagnosis was epididymal papillary cystadenoma. The patient has been followed up for 1 year with no recurrence and malignancy. Epididymal papillary cystadenoma, a rare benign tumor, lacks specific clinical and imaging features, often leading to misdiagnosis as seminal vesicle cysts or malignant tumors. If associated with von Hippel-Lindau syndrome, bilateral occurrence should be considered to prevent missed diagnosis and treatment delay.

This article reports a case of a 55-year-old patient who was admitted to the hospital due to an 8-year history of a right epididymal mass and intermittent right scrotal heaviness for 1 month. Preoperative ultrasound examination revealed a right epididymal cyst and right testicular hydrocele. Under general anesthesia, a right epididymal mass resection and right testicular tunica vaginalis inversion procedure were performed. Postoperative pathological diagnosis was epididymal papillary cystadenoma. The patient has been followed up for 1 year with no recurrence and malignancy. Epididymal papillary cystadenoma, a rare benign tumor, lacks specific clinical and imaging features, often leading to misdiagnosis as seminal vesicle cysts or malignant tumors. If associated with von Hippel-Lindau syndrome, bilateral occurrence should be considered to prevent missed diagnosis and treatment delay.

Solitary fibrous tumors（SFT）is rare Mesenchymal tissue tumor，originally identified and usually found in the pleura，but the incidence of SFT in the spermatic cord is particularly rare.This article reported a case of a 37-year-old patient who was admitted for a right inguinal mass over the past 2 years. Preoperative MR examination showed a right spermatic cord-derived mass. Under spinal anesthesia，excision of the right spermatic cord mass was performed. Postoperative pathological diagnosis was spermatic cord solitary fibrous tumor. Twelve months of follow-up revealed no metastasis and recurrence on imaging examination. Solitary fibrous tumors of the spermatic cord are rare and require a combination of pathological examination and immunohistochemistry to confirm the diagnosis. Once the diagnosis is confirmed，tumor resection should be performed as soon as possible，and benign lesions are also at risk of recurrence，and long-term follow-up is required after surgery.