Sertoli Cell Tumor
Sertoli Cell Tumor is a rare type of sex cord-stromal tumor that originates from the Sertoli cells in the testes, which are crucial for sperm development. While typically benign, understanding this condition is vital for timely diagnosis and effective management.

Key Takeaways
- Sertoli Cell Tumor is a rare testicular tumor originating from Sertoli cells, usually benign.
- Symptoms can include a palpable testicular mass and, rarely, hormonal effects like feminization.
- Diagnosis involves physical examination, imaging studies, and definitive biopsy.
- The primary treatment for Sertoli Cell Tumor is surgical removal of the affected testicle.
- Prognosis is generally excellent, especially for benign tumors.
What is Sertoli Cell Tumor?
A Sertoli Cell Tumor is an uncommon neoplasm derived from the Sertoli cells, which are supportive cells found in the seminiferous tubules of the testes. These tumors are part of a broader category known as sex cord-stromal tumors. They are significantly rarer than germ cell tumors, accounting for less than 1% of all testicular tumors. While most Sertoli Cell Tumors are benign, a small percentage can exhibit malignant characteristics, necessitating careful evaluation and follow-up. They can occur at any age, from infancy to adulthood, though they are more frequently observed in young to middle-aged adults. The exact cause of these tumors is often unknown, but some cases have been linked to genetic syndromes or conditions like Peutz-Jeghers syndrome.
Recognizing Sertoli Cell Tumor: Symptoms and Diagnosis
Recognizing Sertoli cell tumor symptoms often begins with the detection of a testicular mass. This mass is typically painless and may be discovered during a self-examination or a routine physical exam. In some cases, the tumor may produce hormones, particularly estrogen, which can lead to specific symptoms. For instance, in males, increased estrogen levels might cause feminizing effects such as gynecomastia (breast enlargement) or decreased libido. In prepubertal boys, hormonal activity could lead to precocious puberty. However, many individuals remain asymptomatic until the tumor grows large enough to be palpable.
The process of Sertoli cell tumor diagnosis typically involves several steps. Initial evaluation includes a thorough physical examination to assess the testicular mass. Imaging studies are crucial, with ultrasound being the primary tool to characterize the mass, determine its size, and differentiate it from other testicular conditions. Further imaging like CT scans or MRI may be used to check for potential spread if malignancy is suspected, though this is rare. Blood tests to measure hormone levels (e.g., estrogen, testosterone) can provide supportive evidence, especially if feminizing symptoms are present. However, a definitive diagnosis requires a biopsy, usually performed during surgical exploration, where tissue is examined by a pathologist to confirm the presence of Sertoli cells and assess for any malignant features.
- Common Symptoms:
- Painless testicular mass or swelling
- Testicular discomfort or heaviness (less common)
- Hormonal Symptoms (less common):
- Gynecomastia (breast enlargement)
- Decreased libido or erectile dysfunction
- Precocious puberty in children
Treatment Options for Sertoli Cell Tumor
The primary Sertoli cell tumor treatment is surgical removal of the affected testicle, a procedure known as radical inguinal orchiectomy. This approach is standard due to the potential for malignancy and the difficulty in definitively ruling out cancer without pathological examination of the entire tumor. For most benign tumors, surgery is curative, and no further treatment is typically required. The decision for additional treatment depends heavily on the pathological findings, including tumor size, presence of necrosis, and mitotic activity, which indicate the tumor’s aggressiveness.
In the rare instances where a Sertoli Cell Tumor is found to be malignant and has spread beyond the testicle, additional therapies such as chemotherapy or radiation therapy may be considered. However, the effectiveness of these treatments for malignant Sertoli Cell Tumors is less well-established compared to other types of testicular cancers, and treatment plans are highly individualized. Regular follow-up with imaging and tumor markers is essential after treatment to monitor for recurrence, particularly for tumors with atypical features or those deemed malignant. The prognosis for individuals with Sertoli Cell Tumor is generally excellent, especially for the vast majority of cases that are benign and confined to the testicle.